Dr Derek Morris

BSc, Ph.D

Contact Details

Senior Lecturer
Biochemistry
Room 106
Arts/Science Building
South Campus
E: DEREK.MORRIS@nuigalway.ie
 
researcher
 

Biography

Dr Derek Morris is a geneticist and his area of expertise is the identification of risk genes for psychiatric disorders. He graduated with a B.Sc. in Biotechnology from the National University of Ireland (NUI), Galway in 1998. In 2001, he completed his PhD in molecular genetics at Cardiff University. He subsequently joined the Neuropsychiatric Genetics Research Group in Trinity College Dublin (TCD) as a research fellow, was awarded a Health Research Board Postdoctoral Career Development Research Fellowship in 2003 and was appointed Lecturer in Molecular Psychiatry in 2006. Using Science Foundation Ireland funding, he set up TrinSeq, the first next-generation sequencing lab in Ireland in 2008. In 2013, Dr Morris moved to NUI Galway where he is Lecturer in Biomedical Science and a PI in the Neuroimaging and Cognitive Genomics (NICOG) Centre. His group has built on the genome-wide association studies (GWAS) by taking new risk genes forward for in-depth phenotypic analysis to understand how they contribute to abnormal brain function and illness. Genetic studies in the areas of epigenetic regulation, cognition, neuroimaging and numerous collaborations have produced a series of senior author manuscripts for Dr Morris in high impact psychiatry journals (e.g. Molecular Psychiatry, Biological Psychiatry) and genetics journals (e.g. American Journal of Human Genetics, Human Molecular Genetics). Dr Morris is involved in international consortia undertaking GWAS that have identified new risk genes for psychosis and related phneotypes. This high-profile work has resulted in multiple publications in Nature, Science and Cell. Involvement in these consortia has helped him establish a world-wide network of collaborators. In total, Dr Morris has 221 peer-reviewed publications (29 as first or senior author) that have generated 39,227 citations (29,255 since 2015) and his h index is 76 (Google Scholar 2020). Dr Morris is a former President of the Irish Society of Human Genetics (2014-16). He was awarded the NUIG President’s Award for Research Excellence in 2017 and was ranked in the top 1% of Highly Cited Researchers for 2018 (Clarivate Analytics).





Peer Reviewed Journals

  Year Publication
(2020) 'Childhood Trauma, Brain Structure and Emotion Recognition in Patients with Schizophrenia and Healthy Participants'
Rokita KI;Holleran L;Dauvermann MR;Mothersill D;Holland J;Costello L;Kane R;McKernan D;Morris DW;Kelly JP;Corvin A;Hallahan B;McDonald C;Donohoe G; (2020) 'Childhood Trauma, Brain Structure and Emotion Recognition in Patients with Schizophrenia and Healthy Participants'. Social Cognitive And Affective Neuroscience, [DOI] [Details]
(2020) 'The genetic architecture of the human cerebral cortex'
Grasby KL;Jahanshad N;Painter JN;Colodro-Conde L;Bralten J;Hibar DP;Lind PA;Pizzagalli F;Ching CRK;McMahon MAB;Shatokhina N;Zsembik LCP;Thomopoulos SI;Zhu AH;Strike LT;Agartz I;Alhusaini S;Almeida MAA;Alnæs D;Amlien IK;Andersson M;Ard T;Armstrong NJ;Ashley-Koch A;Atkins JR;Bernard M;Brouwer RM;Buimer EEL;Bülow R;Bürger C;Cannon DM;Chakravarty M;Chen Q;Cheung JW;Couvy-Duchesne B;Dale AM;Dalvie S;de Araujo TK;de Zubicaray GI;de Zwarte SMC;den Braber A;Doan NT;Dohm K;Ehrlich S;Engelbrecht HR;Erk S;Fan CC;Fedko IO;Foley SF;Ford JM;Fukunaga M;Garrett ME;Ge T;Giddaluru S;Goldman AL;Green MJ;Groenewold NA;Grotegerd D;Gurholt TP;Gutman BA;Hansell NK;Harris MA;Harrison MB;Haswell CC;Hauser M;Herms S;Heslenfeld DJ;Ho NF;Hoehn D;Hoffmann P;Holleran L;Hoogman M;Hottenga JJ;Ikeda M;Janowitz D;Jansen IE;Jia T;Jockwitz C;Kanai R;Karama S;Kasperaviciute D;Kaufmann T;Kelly S;Kikuchi M;Klein M;Knapp M;Knodt AR;Krämer B;Lam M;Lancaster TM;Lee PH;Lett TA;Lewis LB;Lopes-Cendes I;Luciano M;Macciardi F;Marquand AF;Mathias SR;Melzer TR;Milaneschi Y;Mirza-Schreiber N;Moreira JCV;Mühleisen TW;Müller-Myhsok B;Najt P;Nakahara S;Nho K;Olde Loohuis LM;Orfanos DP;Pearson JF;Pitcher TL;Pütz B;Quidé Y;Ragothaman A;Rashid FM;Reay WR;Redlich R;Reinbold CS;Repple J;Richard G;Riedel BC;Risacher SL;Rocha CS;Mota NR;Salminen L;Saremi A;Saykin AJ;Schlag F;Schmaal L;Schofield PR;Secolin R;Shapland CY;Shen L;Shin J;Shumskaya E;Sønderby IE;Sprooten E;Tansey KE;Teumer A;Thalamuthu A;Tordesillas-Gutiérrez D;Turner JA;Uhlmann A;Vallerga CL;van der Meer D;van Donkelaar MMJ;van Eijk L;van Erp TGM;van Haren NEM;van Rooij D;van Tol MJ;Veldink JH;Verhoef E;Walton E;Wang M;Wang Y;Wardlaw JM;Wen W;Westlye LT;Whelan CD;Witt SH;Wittfeld K;Wolf C;Wolfers T;Wu JQ;Yasuda CL;Zaremba D;Zhang Z;Zwiers MP;Artiges E;Assareh AA;Ayesa-Arriola R;Belger A;Brandt CL;Brown GG;Cichon S;Curran JE;Davies GE;Degenhardt F;Dennis MF;Dietsche B;Djurovic S;Doherty CP;Espiritu R;Garijo D;Gil Y;Gowland PA;Green RC;Häusler AN;Heindel W;Ho BC;Hoffmann WU;Holsboer F;Homuth G;Hosten N;Jack CR;Jang M;Jansen A;Kimbrel NA;Kolskår K;Koops S;Krug A;Lim KO;Luykx JJ;Mathalon DH;Mather KA;Mattay VS;Matthews S;Mayoral Van Son J;McEwen SC;Melle I;Morris DW;Mueller BA;Nauck M;Nordvik JE;Nöthen MM;O'Leary DS;Opel N;Martinot MP;Pike GB;Preda A;Quinlan EB;Rasser PE;Ratnakar V;Reppermund S;Steen VM;Tooney PA;Torres FR;Veltman DJ;Voyvodic JT;Whelan R;White T;Yamamori H;Adams HHH;Bis JC;Debette S;Decarli C;Fornage M;Gudnason V;Hofer E;Ikram MA;Launer L;Longstreth WT;Lopez OL;Mazoyer B;Mosley TH;Roshchupkin GV;Satizabal CL;Schmidt R;Seshadri S;Yang Q; ; ; ; ; ; ;Alvim MKM;Ames D;Anderson TJ;Andreassen OA;Arias-Vasquez A;Bastin ME;Baune BT;Beckham JC;Blangero J;Boomsma DI;Brodaty H;Brunner HG;Buckner RL;Buitelaar JK;Bustillo JR;Cahn W;Cairns MJ;Calhoun V;Carr VJ;Caseras X;Caspers S;Cavalleri GL;Cendes F;Corvin A;Crespo-Facorro B;Dalrymple-Alford JC;Dannlowski U;de Geus EJC;Deary IJ;Delanty N;Depondt C;Desrivières S;Donohoe G;Espeseth T;Fernández G;Fisher SE;Flor H;Forstner AJ;Francks C;Franke B;Glahn DC;Gollub RL;Grabe HJ;Gruber O;Håberg AK;Hariri AR;Hartman CA;Hashimoto R;Heinz A;Henskens FA;Hillegers MHJ;Hoekstra PJ;Holmes AJ;Hong LE;Hopkins WD;Hulshoff Pol HE;Jernigan TL;Jönsson EG;Kahn RS;Kennedy MA;Kircher TTJ;Kochunov P;Kwok JBJ;Le Hellard S;Loughland CM;Martin NG;Martinot JL;McDonald C;McMahon KL;Meyer-Lindenberg A;Michie PT;Morey RA;Mowry B;Nyberg L;Oosterlaan J;Ophoff RA;Pantelis C;Paus T;Pausova Z;Penninx BWJH;Polderman TJC;Po (2020) 'The genetic architecture of the human cerebral cortex'. Science, 367 (6484) [DOI] [Details]
(2020) 'Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults'
Hofer E;Roshchupkin GV;Adams HHH;Knol MJ;Lin H;Li S;Zare H;Ahmad S;Armstrong NJ;Satizabal CL;Bernard M;Bis JC;Gillespie NA;Luciano M;Mishra A;Scholz M;Teumer A;Xia R;Jian X;Mosley TH;Saba Y;Pirpamer L;Seiler S;Becker JT;Carmichael O;Rotter JI;Psaty BM;Lopez OL;Amin N;van der Lee SJ;Yang Q;Himali JJ;Maillard P;Beiser AS;DeCarli C;Karama S;Lewis L;Harris M;Bastin ME;Deary IJ;Veronica Witte A;Beyer F;Loeffler M;Mather KA;Schofield PR;Thalamuthu A;Kwok JB;Wright MJ;Ames D;Trollor J;Jiang J;Brodaty H;Wen W;Vernooij MW;Hofman A;Uitterlinden AG;Niessen WJ;Wittfeld K;Bülow R;Völker U;Pausova Z;Bruce Pike G;Maingault S;Crivello F;Tzourio C;Amouyel P;Mazoyer B;Neale MC;Franz CE;Lyons MJ;Panizzon MS;Andreassen OA;Dale AM;Logue M;Grasby KL;Jahanshad N;Painter JN;Colodro-Conde L;Bralten J;Hibar DP;Lind PA;Pizzagalli F;Stein JL;Thompson PM;Medland SE; ;Sachdev PS;Kremen WS;Wardlaw JM;Villringer A;van Duijn CM;Grabe HJ;Longstreth WT;Fornage M;Paus T;Debette S;Arfan Ikram M;Schmidt H;Schmidt R;Seshadri S; (2020) 'Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults'. Nature Communications, 11 (1) [DOI] [Details]
(2020) 'Genes influenced by MEF2C contribute to neurodevelopmental disease via gene expression changes that affect multiple types of cortical excitatory neurons'
Cosgrove D;Whitton L;Fahey L;Broin PÓ;Donohoe G;Morris DW; (2020) 'Genes influenced by MEF2C contribute to neurodevelopmental disease via gene expression changes that affect multiple types of cortical excitatory neurons'. Human Molecular Genetics, [DOI] [ARAN Link] [Details]
(2017) 'Genetic correlation between amyotrophic lateral sclerosis and schizophrenia'
McLaughlin, RL;Schijven, D;van Rheenen, W;van Eijk, KR;O'Brien, M;Kahn, RS;Ophoff, RA;Goris, A;Bradley, DG;Al-Chalabi, A;van den Berg, LH;Luykx, JJ;Hardiman, O;Veldink, JH (2017) 'Genetic correlation between amyotrophic lateral sclerosis and schizophrenia'. Nature Communications, 8 [DOI] [Details]
(2017) 'Novel genetic loci associated with hippocampal volume'
Hibar, DP;Adams, HHH;Jahanshad, N;Chauhan, G;Stein, JL;Hofer, E;Renteria, ME;Bis, JC;Arias-Vasquez, A;Ikram, MK;Desrivieres, S;Vernooij, MW;Abramovic, L;Alhusaini, S;Amin, N;Andersson, M;Arfanakis, K;Aribisala, BS;Armstrong, NJ;Athanasiu, L;Axelsson, T;Beecham, AH;Beiser, A;Bernard, M;Blanton, SH;Bohlken, MM;Boks, MP;Bralten, J;Brickman, AM;Carmichael, O;Chakravarty, MM;Chen, Q;Ching, CRK;Chouraki, V;Cuellar-Partida, G;Crivello, F;Den Braber, A;Doan, NT;Ehrlich, S;Giddaluru, S;Goldman, AL;Gottesman, RF;Grimm, O;Griswold, ME;Guadalupe, T;Gutman, BA;Hass, J;Haukvik, UK;Hoehn, D;Holmes, AJ;Hoogman, M;Janowitz, D;Jia, T;Jorgensen, KN;Karbalai, N;Kasperaviciute, D;Kim, S;Klein, M;Kraemer, B;Lee, PH;Liewald, DCM;Lopez, LM;Luciano, M;Macare, C;Marquand, AF;Matarin, M;Mather, KA;Mattheisen, M;McKay, DR;Milaneschi, Y;Maniega, SM;Nho, K;Nugent, AC;Nyquist, P;Loohuis, LMO;Oosterlaan, J;Papmeyer, M;Pirpamer, L;Putz, B;Ramasamy, A;Richards, JS;Risacher, SL;Roiz-Santianez, R;Rommelse, N;Ropele, S;Rose, EJ;Royle, NA;Rundek, T;Samann, PG;Saremi, A;Satizabal, CL;Schmaal, L;Schork, AJ;Shen, L;Shin, J;Shumskaya, E;Smith, AV;Sprooten, E;Strike, LT;Teumer, A;Tordesillas-Gutierrez, D;Toro, R;Trabzuni, D;Trompet, S;Vaidya, D;Van der Grond, J;Van der Lee, SJ;Van der Meer, D;Van Donkelaar, MMJ;Van Eijk, KR;Van Erp, TGM;Van Rooij, D;Walton, E;Westlye, LT;Whelan, CD;Windham, BG;Winkler, AM;Wittfeld, K;Woldehawariat, G;Wolf, C;Wolfers, T;Yanek, LR;Yang, JY;Zijdenbos, A;Zwiers, MP;Agartz, I;Almasy, L;Ames, D;Amouyel, P;Andreassen, OA;Arepalli, S;Assareh, AA;Barral, S;Bastin, ME;Becker, DM;Becker, JT;Bennett, DA;Blangero, J;van Bokhoven, H;Boomsma, DI;Brodaty, H;Brouwer, RM;Brunner, HG;Buckner, RL;Buitelaar, JK;Bulayeva, KB;Cahn, W;Calhoun, VD;Cannon, DM;Cavalleri, GL;Cheng, CY;Cichon, S;Cookson, MR;Corvin, A;Crespo-Facorro, B;Curran, JE;Czisch, M;Dale, AM;Davies, GE;De Craen, AJM;De Geus, EJC;De Jager, PL;De Zubicaray, GI;Deary, IJ;Debette, S;DeCarli, C;Delanty, N;Depondt, C;DeStefano, A;Dillman, A;Djurovic, S;Donohoe, G;Drevets, WC;Duggirala, R;Dyer, TD;Enzinger, C;Erk, S;Espeseth, T;Fedko, IO;Fernandez, G;Ferrucci, L;Fisher, SE;Fleischman, DA;Ford, I;Fornage, M;Foroud, TM;Fox, PT;Francks, C;Fukunaga, M;Gibbs, JR;Glahn, DC;Gollub, RL;Goring, HHH;Green, RC;Gruber, O;Gudnason, V;Guelfi, S;Haberg, AK;Hansell, NK;Hardy, J;Hartman, CA;Hashimoto, R;Hegenscheid, K;Heinz, A;Le Hellard, S;Hernandez, DG;Heslenfeld, DJ;Ho, BC;Hoekstra, PJ;Hoffmann, W;Hofman, A;Holsboer, F;Homuth, G;Hosten, N;Hottenga, JJ;Huentelman, M;Pol, HEH;Ikeda, M;Jack, CR;Jenkinson, M;Johnson, R;Jonsson, EG;Jukema, JW;Kahn, RS;Kanai, R;Kloszewska, I;Knopman, DS;Kochunov, P;Kwok, JB;Lawrie, SM;Lemaitre, H;Liu, XM;Longo, DL;Lopez, OL;Lovestone, S;Martinez, O;Martinot, JL;Mattay, VS;McDonald, C;McIntosh, AM;McMahon, FJ;McMahon, KL;Mecocci, P;Melle, I;Meyer-Lindenberg, A;Mohnke, S;Montgomery, GW;Morris, DW;Mosley, TH;Muhleisen, TW;Muller-Myhsok, B;Nalls, MA;Nauck, M;Nichols, TE;Niessen, WJ;Nothen, MM;Nyberg, L;Ohi, K;Olvera, RL;Ophoff, RA;Pandolfo, M;Paus, T;Pausova, Z;Penninx, BWJH;Pike, GB;Potkin, SG;Psaty, BM;Reppermund, S;Rietschel, M;Roffman, JL;Romanczuk-Seiferth, N;Rotter, JI;Ryten, M;Sacco, RL;Sachdev, PS;Saykin, AJ;Schmidt, R;Schmidt, H;Schofield, PR;Sigursson, S;Simmons, A;Singleton, A;Sisodiya, SM;Smith, C;Smoller, JW;Soininen, H;Steen, VM;Stott, DJ;Sussmann, JE;Thalamuthu, A;Toga, AW;Traynor, BJ;Troncoso, J;Tsolaki, M;Tzourio, C;Uitterlinden, AG;Hernandez, MCV;Van der Brug, M;van der Lugt, A;van der Wee, NJA;Van Haren, NEM;van't Ent, D;Van Tol, MJ;Vardarajan, BN;Vellas, B;Veltman, DJ;Volzke, H;Walter, H;Wardlaw, JM;Wassink, TH;Weale, ME;Weinberger, DR;Weiner, MW;Wen, W;Westman, E;White, T;Wong, TY;Wright, CB;Zielke, RH;Zonderman, AB;Martin, NG;Van Duijn, CM;Wright, MJ;Longstreth, WT;Schumann, G;Grabe, HJ;Franke, B;Launer, LJ;Medland, SE;Seshadri, S;Thompson, PM;Ikram, MA (2017) 'Novel genetic loci associated with hippocampal volume'. Nature Communications, 8 [DOI] [Details]
(2017) 'Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study'
Hawi, Z;Cummins, TDR;Tong, J;Arcos-Burgos, M;Zhao, Q;Matthews, N;Newman, DP;Johnson, B;Vance, A;Heussler, HS;Levy, F;Easteal, S;Wray, NR;Kenny, E;Morris, D;Kent, L;Gill, M;Bellgrove, MA (2017) 'Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study'. Molecular Psychiatry, 22 :580-584 [DOI] [Details]
(2017) 'GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium'
Trampush, JW;Yang, MLZ;Yu, J;Knowles, E;Davies, G;Liewald, DC;Starr, JM;Djurovic, S;Melle, I;Sundet, K;Christoforou, A;Reinvang, I;DeRosse, P;Lundervold, AJ;Steen, VM;Espeseth, T;Raikkonen, K;Widen, E;Palotie, A;Eriksson, JG;Giegling, I;Konte, B;Roussos, P;Giakoumaki, S;Burdick, KE;Payton, A;Ollier, W;Horan, M;Chiba-Falek, O;Attix, DK;Need, AC;Cirulli, ET;Voineskos, AN;Stefanis, NC;Avramopoulos, D;Hatzimanolis, A;Arking, DE;Smyrnis, N;Bilder, RM;Freimer, NA;Cannon, TD;London, E;Poldrack, RA;Sabb, FW;Congdon, E;Conley, ED;Scult, MA;Dickinson, D;Straub, RE;Donohoe, G;Morris, D;Corvin, A;Gill, M;Hariri, AR;Weinberger, DR;Pendleton, N;Bitsios, P;Rujescu, D;Lahti, J;Le Hellard, S;Keller, MC;Andreassen, OA;Deary, IJ;Glahn, DC;Malhotra, AK;Lencz, T (2017) 'GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium'. Molecular Psychiatry, 22 :336-345 [DOI] [Details]
(2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'
Cosgrove, D;Harold, D;Mothersill, O;Anney, R;Hill, MJ;Bray, NJ;Blokland, G;Petryshen, T;Richards, A;Mantripragada, K;Owen, M;O'Donovan, MC;Gill, M;Corvin, A;Morris, DW;Donohoe, G (2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'. Translational Psychiatry, 7 [DOI] [Details]
(2016) 'Schizophrenia risk from complex variation of complement component 4'
Sekar, A;Bialas, AR;de Rivera, H;Davis, A;Hammond, TR;Kamitaki, N;Tooley, K;Presumey, J;Baum, M;Van Doren, V;Genovese, G;Rose, SA;Handsaker, RE;Daly, MJ;Carroll, MC;Stevens, B;McCarroll, SA (2016) 'Schizophrenia risk from complex variation of complement component 4'. Nature, 530 [DOI] [Details]
(2016) 'Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept'
Franke, B;Stein, JL;Ripke, S;Anttila, V;Hibar, DP;van Hulzen, KJE;Arias-Vasquez, A;Smoller, JW;Nichols, TE;Neale, MC;McIntosh, AM;Lee, P;McMahon, FJ;Meyer-Lindenberg, A;Mattheisen, M;Andreassen, OA;Gruber, O;Sachdev, PS;Roiz-Santianez, R;Saykin, AJ;Ehrlich, S;Mather, KA;Turner, JA;Wright, MJ;O'Donovan, MC;Thompson, PM;Neale, BM;Medland, SE;Sullivan, PF (2016) 'Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept'. Nature Neuroscience, 19 [DOI] [Details]
(2016) 'Single-Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression'
Tozzi, L;Carballedo, A;Wetterling, F;McCarthy, H;O'Keane, V;Gill, M;Morris, D;Fahey, C;Meaney, J;Frodl, T (2016) 'Single-Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression'. Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology, 41 :487-497 [DOI] [Details]
(2016) 'No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study'
Johnson, EC;Bjelland, DW;Howrigan, DP;Abdellaoui, A;Breen, G;Borglum, A;Cichon, S;Degenhardt, F;Forstner, AJ;Frank, J;Genovese, G;Heilmann-Heimbach, S;Herms, S;Hoffman, P;Maier, W;Mattheisen, M;Morris, D;Mowry, B;Mueller-Mhysok, B;Neale, B;Nenadic, I;Noethen, MM;O'Dushlaine, C;Rietschel, M;Ruderfer, DM;Rujescu, D;Schulze, TG;Simonson, MA;Stahl, E;Strohmaier, J;Witt, SH;Sullivan, PF;Keller, MC (2016) 'No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study'. Plos Genetics, 12 [DOI] [Details]
(2015) 'Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment'
Trampush, JW;Lencz, T;Knowles, E;Davies, G;Guha, S;Pe'er, I;Liewald, DC;Starr, JM;Djurovic, S;Melle, I;Sundet, K;Christoforou, A;Reinvang, I;Mukherjee, S;DeRosse, P;Lundervold, A;Steen, VM;John, M;Espeseth, T;Raikkonen, K;Widen, E;Palotie, A;Eriksson, JG;Giegling, I;Konte, B;Ikeda, M;Roussos, P;Giakoumaki, S;Burdick, KE;Payton, A;Ollier, W;Horan, M;Scult, M;Dickinson, D;Straub, RE;Donohoe, G;Morris, D;Corvin, A;Gill, M;Hariri, A;Weinberger, DR;Pendleton, N;Iwata, N;Darvasi, A;Bitsios, P;Rujescu, D;Lahti, J;Le Hellard, S;Keller, MC;Andreassen, OA;Deary, IJ;Glahn, DC;Malhotra, AK (2015) 'Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, 168 :363-373 [DOI] [Details]
(2015) 'Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder'
Maier, R;Moser, G;Chen, GB;Ripke, S;Coryell, W;Potash, JB;Scheftner, WA;Shi, JX;Weissman, MM;Hultman, CM;Landen, M;Levinson, DF;Kendler, KS;Smoller, JW;Wray, NR;Lee, SH (2015) 'Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder'. American Journal Of Human Genetics, 96 :283-294 [DOI] [Details]
(2015) 'LD Score regression distinguishes confounding from polygenicity in genome-wide association studies'
Bulik-Sullivan, BK;Loh, PR;Finucane, HK;Ripke, S;Yang, J;Patterson, N;Daly, MJ;Price, AL;Neale, BM (2015) 'LD Score regression distinguishes confounding from polygenicity in genome-wide association studies'. Nature Genetics, 47 [DOI] [Details]
(2015) 'Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis'
Loh, PR;Bhatia, G;Gusev, A;Finucane, HK;Bulik-Sullivan, BK;Pollack, SJ;de Candia, TR;Lee, SH;Wray, NR;Kendler, KS;O'Donovan, MC;Neale, BM;Patterson, N;Price, AL (2015) 'Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis'. Nature Genetics, 47 [DOI] [Details]
(2015) 'Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways'
O'Dushlaine, C;Rossin, L;Lee, PH;Duncan, L;Parikshak, NN;Newhouse, S;Ripke, S;Neale, BM;Purcell, SM;Posthuma, D;Nurnberger, JI;Lee, SH;Faraone, SV;Perlis, RH;Mowry, BJ;Thapar, A;Goddard, ME;Witte, JS;Absher, D;Agartz, I;Akil, H;Amin, F;Andreassen, OA;Anjorin, A;Anney, R;Anttila, V;Arking, DE;Asherson, P;Azevedo, MH;Backlund, L;Badner, JA;Bailey, AJ;Banaschewski, T;Barchas, JD;Barnes, MR;Barrett, TB;Bass, N;Battaglia, A;Bauer, M;Bayes, M;Bellivier, F;Bergen, SE;Berrettini, W;Betancur, C;Bettecken, T;Biederman, J;Binder, EB;Black, DW;Blackwood, DHR;Bloss, CS;Boehnke, M;Boomsma, DI;Breuer, R;Bruggeman, R;Cormican, P;Buccola, NG;Buitelaar, JK;Bunney, WE;Buxbaum, JD;Byerley, WF;Byrne, EM;Caesar, S;Cahn, W;Cantor, RM;Casas, M;Chakravarti, A;Chambert, K;Choudhury, K;Cichon, S;Mattheisen, M;Cloninger, CR;Collier, DA;Cook, EH;Coon, H;Cormand, B;Corvin, A;Coryell, WH;Craig, DW;Craig, IW;Crosbie, J;Cuccaro, ML;Curtis, D;Czamara, D;Datta, S;Dawson, G;Day, R;De Geus, EJ;Degenhardt, F;Djurovic, S;Donohoe, GJ;Doyle, AE;Duan, J;Dudbridge, F;Duketis, E;Ebstein, RP;Edenberg, HJ;Elia, J;Ennis, S;Etain, B;Fanous, A;Farmer, AE;Ferrier, IN;Flicldnger, M;Fombonne, E;Foroud, T;Frank, J;Franke, B;Fraser, C;Freedman, R;Freimer, NB;Freitag, CM;Friedl, M;Frisen, L;Gailagher, L;Gejman, PV;Georgieva, L;Gershon, ES;Giegling, I;Gill, M;Gordon, SD;Gordon-Smith, K;Green, EK;Greenwood, TA;Grice, DE;Gross, M;Grozeva, D;Guan, W;Gurling, H;De Haan, L;Haines, JL;Hakonarson, H;Hallmayer, J;Hamilton, SP;Hamshere, ML;Hansen, TF;Hartmann, AM;Hautzinger, M;Heath, AC;Henders, AK;Herms, S;Hickie, IB;Hipolito, M;Hoefels, S;Holsboer, F;Hoogendijk, WJ;Hottenga, JJ;Hultman, CM;Hus, V;Ingason, A;Ising, M;Jamain, S;Jones, EG;Jones, I;Jones, L;Tzeng, JY;Kahler, AK;Kahn, RS;Kandaswamy, R;Keller, MC;Kennedy, JL;Kenny, E;Kent, L;Kim, YJ;Kirov, GK;Klauck, SM;Klei, L;Knowles, JA;Kohli, MA;Koller, DL;Konte, B;Korszun, A;Krabbendam, L;Krasucki, R;Kuntsi, J;Kwan, P;Landen, M;Langstrom, N;Lathrop, M;Lawrence, J;Lawson, WB;Leboyer, M;Ledbetter, DH;Lencz, T;Lesch, KP;Levinson, DF;Lewis, CM;Li, J;Lichtenstein, P;Lieberman, JA;Lin, DY;Linszen, DH;Liu, CY;Lohoff, FW;Loo, SK;Lord, C;Lowe, JK;Lucae, S;MacIntyre, DJ;Madden, PAF;Maestrini, E;Magnusson, PKE;Mahon, PB;Maier, W;Malhotra, AK;Mane, SM;Martin, CL;Martin, NG;Matthews, K;Mattingsdal, M;McCarroll, SA;McGhee, KA;McGough, JJ;McGrath, PJ;McGuffin, P;McInnis, MG;McIntosh, A;McKinney, R;McLean, AW;McMahon, FJ;McMahon, WM;McQuillin, A;Medeiros, H;Medland, SE;Meier, S;Melle, I;Meng, F;Meyer, J;Middeldorp, CM;Middleton, L;Milanova, V;Miranda, A;Monaco, AP;Montgomery, GW;Moran, JL;Moreno-De-Luca, D;Morken, G;Morris, DW;Morrow, EM;Moskvina, V;Muglia, P;Muhleisen, TW;Muir, WJ;Muller-Myhsok, B;Murtha, M;Myers, RM;Myin-Germeys, I;Neale, MC;Nelson, SF;Nievergelt, CM;Nikolov, I;Nimgaonkar, V;Nolen, WA;Nothen, MM;Nwulia, EA;Nyholt, DR;Oades, RD;Olincy, A;Oliveira, G;Olsen, L;Ophoff, RA;Osby, U;Owen, MJ;Palotie, A;Parr, JR;Paterson, AD;Pato, CN;Pato, MT;Penninx, BW;Pergadia, ML;Pericak-Vance, MA;Pickard, BS;Pimm, J;Piven, J;Potash, JB;Poustka, F;Propping, P;Puri, V;Quested, DJ;Quinn, EM;Ramos-Quiroga, JA;Rasmussen, HB;Raychaudhuri, S;Rehnstrom, K;Reif, A;Ribases, M;Rice, JP;Rietschel, M;Roeder, K;Roeyers, H;Rothenberger, A;Rouleau, G;Ruderfer, D;Rujescu, D;Sanders, AR;Sanders, SJ;Santangelo, SL;Sergeant, JA;Schachar, R;Schalling, M;Schatzberg, AF;Scheftner, WA;Schellenberg, GD;Scherer, SW;Schork, NJ;Schulze, TG;Schumacher, J;Schwarz, M;Scolnick, E;Scott, LJ;Shi, JX;Shilling, PD;Shyn, SI;Silverman, JM;Slager, SL;Smalley, SL;Smit, JH;Smith, EN;Sonuga-Barke, EJS;Cair, DS;State, M;Steffens, M;Steinhausen, HC;Strauss, JS;Strohmaier, J;Stroup, TS;Sutdiffe, JS;Szatmari, P;Szelinger, S;Thirumalai, S;Thompson, RC;Todorov, AA;Tozzi, F;Treutlein, J;Uhr, M;Van den Oord, EJCG;Van Grootheest, G;Van Os, J;Vicente, AM;Vieland, VJ;Vincent, JB;Visscher, PM;Walsh, CA;Wassink, TH;Watson, SJ;Weissman, MM;Werge, T;Wienker, TF;Wijsman, EM;Willemsen, G;Williams, N;Willsey, AJ;Wi (2015) 'Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways'. Nature Neuroscience, 18 :199-209 [DOI] [Details]
(2015) 'Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores'
Vilhjalmsson, BJ;Yang, J;Finucane, HK;Gusev, A;Lindstrom, S;Ripke, S;Genovese, G;Loh, PR;Bhatia, G;Do, R;Hayeck, T;Won, HH;Kathiresan, S;Pato, M;Pato, C;Tamimi, R;Stahl, E;Zaitlen, N;Pasaniuc, B;Belbin, G;Kenny, EE;Schierup, MH;De Jager, P;Patsopouos, NA;Mc Carroll, S;Daly, M;Purce, S;Chasman, D;Neale, B;Goddard, M;Visscher, PM;Kraft, P;Patterson, N;Price, AL (2015) 'Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores'. American Journal Of Human Genetics, 97 :576-592 [DOI] [Details]
(2014) 'Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population'
Douglas, AP;Vance, DR;Kenny, EM;Morris, DW;Maxwell, AP;McKnight, AJ (2014) 'Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population'. Scientific Reports, 4 [DOI] [Details]
(2014) 'Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases'
Gusev, A;Lee, SH;Trynka, G;Finucane, H;Vilhjalmsson, BJ;Xu, H;Zang, CZ;Ripke, S;Bulik-Sullivan, B;Stahl, E;Kahler, AK;Hultman, CM;Purcell, SM;McCarroll, SA;Daly, M;Pasaniuc, B;Sullivan, PF;Neale, BM;Wray, NR;Raychaudhuri, S;Price, AL (2014) 'Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases'. American Journal Of Human Genetics, 95 :535-552 [DOI] [Details]
(2012) 'Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia'
Strange, A;Riley, BP;Spencer, CCA;Morris, DW;Pirinen, M;O'Dushlaine, CT;Su, Z;Maher, BS;Freeman, C;Cormican, P;Bellenguez, C;Kenny, EM;Band, G;Wormley, B;Donohoe, G;Dilthey, A;Moutsianas, L;Quinn, E;Edkins, S;Judge, R;Coleman, K;Hunt, S;Tropea, D;Roche, S;Cummings, L;Kelleher, E;McKeon, P;Dinan, T;McDonald, C;Murphy, KC;O'Callaghan, E;O'Neill, FA;Waddington, JL;Walsh, D;Giannoulatou, E;Langford, C;Deloukas, P;Gray, E;Dronov, S;Potter, S;Pearson, R;Vukcevic, D;Tashakkori-Ghanbaria, A;Blackwell, JM;Bramon, E;Brown, MA;Casas, JP;Duncanson, A;Jankowski, J;Markus, HS;Mathew, CG;Palmer, CNA;Plomin, R;Rautanen, A;Sawcer, SJ;Trembath, RC;Viswanathan, AC;Wood, NW;Stone, J;Scolnick, E;Purcell, S;Sklar, P;Ripke, S;Walters, J;Owen, MJ;O'Donovan, MC;Peltonen, L;McVean, G;Kendler, KS;Gill, M;Donnelly, P;Corvin, A (2012) 'Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia'. Biological Psychiatry, 72 :620-628 [DOI] [Details]
(2014) 'Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)'
Lencz, T;Knowles, E;Davies, G;Guha, S;Liewald, DC;Starr, JM;Djurovic, S;Melle, I;Sundet, K;Christoforou, A;Reinvang, I;Mukherjee, S;DeRosse, P;Lundervold, A;Steen, VM;John, M;Espeseth, T;Raikkonen, K;Widen, E;Palotie, A;Eriksson, JG;Giegling, I;Konte, B;Ikeda, M;Roussos, P;Giakoumaki, S;Burdick, KE;Payton, A;Ollier, W;Horan, M;Donohoe, G;Morris, D;Corvin, A;Gill, M;Pendleton, N;Iwata, N;Darvasi, A;Bitsios, P;Rujescu, D;Lahti, J;Hellard, SL;Keller, MC;Andreassen, OA;Deary, IJ;Glahn, DC;Malhotra, AK (2014) 'Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)'. Molecular Psychiatry, 19 :168-174 [DOI] [Details]
(2014) 'Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients'
Mothersill O, Morris DW, Kelly S, Rose EJ, Bokde A, Reilly R, Gill M, Corvin AP, Donohoe G. (2014) 'Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients'. Schizophrenia Research, [Details]
(2014) 'Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants'
Kelly S, Morris DW, Mothersill O, Rose EJ, Fahey C, O'Brien C, O'Hanlon E, Gill M, Corvin AP, Donohoe G. (2014) 'Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants'. Neuroscience Letters, [Details]
(2014) 'Effects of MIR137 on fronto-amygdala functional connectivity'
Mothersill O, Morris DW, Kelly S, Rose EJ, Fahey C, O'Brien C, Lyne R, Reilly R, Gill M, Corvin AP, Donohoe G. (2014) 'Effects of MIR137 on fronto-amygdala functional connectivity'. Neuroimage, [Details]
(2015) 'Mutational analysis of the insulin-like growth factor 1 receptor tyrosine kinase domain in non-small cell lung cancer patients'
Gately, K,Forde, L,Gray, S,Morris, D,Corvin, A,Tewari, P,O'Byrne, K (2015) 'Mutational analysis of the insulin-like growth factor 1 receptor tyrosine kinase domain in non-small cell lung cancer patients'. Molecular And Clinical Oncology, 3 :1073-1079 [DOI] [Details]
(2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'
Cosgrove D, Mothersill O, Kendall K, Konte B, Harold D, Giegling I, Hartmann A, Richards A, Mantripragada K; Wellcome Trust Case Control Consortium, Owen MJ, O'Donovan MC, Gill M, Rujescu D, Walters J, Corvin A, Morris DW, Donohoe G. (2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'. Neuropsychopharmacology, [Details]
(2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'
Mothersill, O;Tangney, N;Morris, DW;McCarthy, H;Frodl, T;Gill, M;Corvin, A;Donohoe, G (2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'. Schizophrenia Research, 184 :52-58 [DOI] [Details]
(2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'
Cosgrove, D,Mothersill, O,Kendall, K,Konte, B,Harold, D,Giegling, I,Hartmann, A,Richards, A,Mantripragada, K,Owen, MJ,O'Donovan, MC,Gill, M,Rujescu, D,Walters, J,Corvin, A,Morris, DW,Donohoe, G,Wellcome Trust Case Control Consor (2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'. Neuropsychopharmacology, 42 :2612-2622 [DOI] [Details]
(2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'
Cosgrove, D,Harold, D,Mothersill, O,Anney, R,Hill, MJ,Bray, NJ,Blokland, G,Petryshen, T,Richards, A,Mantripragada, K,Owen, M,O'Donovan, MC,Gill, M,Corvin, A,Morris, DW,Donohoe, G,Wellcome Trust Case Control (2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'. Translational Psychiatry, 7 [DOI] [Details]
(2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'
Mothersill O, Tangney N, Morris DW, McCarthy H, Frodl T, Gill M, Corvin A, Donohoe G. (2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'. Schizophrenia Research, [Details]
(2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'
Cosgrove, D;Mothersill, O;Kendall, K;Konte, B;Harold, D;Giegling, I;Hartmann, A;Richards, A;Mantripragada, K;Owen, MJ;O'Donovan, MC;Gill, M;Rujescu, D;Walters, J;Corvin, A;Morris, DW;Donohoe, G (2017) 'Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory'. Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology, 42 :2612-2622 [DOI] [Details]
(2017) 'Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets'
Lam, M,Trampush, JW,Yu, J,Knowles, E,Davies, G,Liewald, DC,Starr, JM,Djurovic, S,Melle, I,Sundet, K,Christoforou, A,Reinvang, I,DeRosse, P,Lundervold, AJ,Steen, VM,Espeseth, T,Raikkonen, K,Widen, E,Palotie, A,Eriksson, JG,Giegling, I,Konte, B,Roussos, P,Giakoumaki, S,Burdick, KE,Payton, A,Ollier, W,Chiba-Falek, O,Attix, DK,Need, AC,Cirulli, ET,Voineskos, AN,Stefanis, NC,Avramopoulos, D,Hatzimanolis, A,Arking, DE,Smyrnis, N,Bilder, RM,Freimer, NA,Cannon, TD,London, E,Poldrack, RA,Sabb, FW,Congdon, E,Conley, ED,Scult, MA,Dickinson, D,Straub, RE,Donohoe, G,Morris, D,Corvin, A,Gill, M,Hariri, AR,Weinberger, DR,Pendleton, N,Bitsios, P,Rujescu, D,Lahti, J,Le Hellard, S,Keller, MC,Andreassen, OA,Deary, IJ,Glahn, DC,Malhotra, AK,Lencz, T (2017) 'Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets'. Cell Reports, 21 :2597-2613 [DOI] [Details]
(2017) 'GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium'
Trampush, JW,Yang, MLZ,Yu, J,Knowles, E,Davies, G,Liewald, DC,Starr, JM,Djurovic, S,Melle, I,Sundet, K,Christoforou, A,Reinvang, I,DeRosse, P,Lundervold, AJ,Steen, VM,Espeseth, T,Raikkonen, K,Widen, E,Palotie, A,Eriksson, JG,Giegling, I,Konte, B,Roussos, P,Giakoumaki, S,Burdick, KE,Payton, A,Ollier, W,Horan, M,Chiba-Falek, O,Attix, DK,Need, AC,Cirulli, ET,Voineskos, AN,Stefanis, NC,Avramopoulos, D,Hatzimanolis, A,Arking, DE,Smyrnis, N,Bilder, RM,Freimer, NA,Cannon, TD,London, E,Poldrack, RA,Sabb, FW,Congdon, E,Conley, ED,Scult, MA,Dickinson, D,Straub, RE,Donohoe, G,Morris, D,Corvin, A,Gill, M,Hariri, AR,Weinberger, DR,Pendleton, N,Bitsios, P,Rujescu, D,Lahti, J,Le Hellard, S,Keller, MC,Andreassen, OA,Deary, IJ,Glahn, DC,Malhotra, AK,Lencz, T (2017) 'GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium'. Molecular Psychiatry, 22 :336-345 [DOI] [Details]
(2017) 'Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study'
Hawi, Z,Cummins, TDR,Tong, J,Arcos-Burgos, M,Zhao, Q,Matthews, N,Newman, DP,Johnson, B,Vance, A,Heussler, HS,Levy, F,Easteal, S,Wray, NR,Kenny, E,Morris, D,Kent, L,Gill, M,Bellgrove, MA (2017) 'Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study'. Molecular Psychiatry, 22 :580-584 [DOI] [Details]
(2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'
McCarthy-Jones, S;Smailes, D;Corvin, A;Gill, M;Morris, DW;Dinan, TG;Murphy, KC;O'Neill, FA;Waddington, JL;Donohoe, G;Dudley, R (2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'. Psychiatry Research, 252 :154-160 [DOI] [Details]
(2017) 'Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects'
Marshall, CR;Marshall, CR;Howrigan, DP;Merico, D;Thiruvahindrapuram, B;Wu, WT;Greer, DS;Antaki, D;Shetty, A;Holmans, PA;Pinto, D;Gujral, M;Brandler, WM;Malhotra, D;Wang, ZZ;Fajarado, KVF;Maile, MS;Ripke, S;Agartz, I;Albus, M;Alexander, M;Amin, F;Atkins, J;Bacanu, SA;Belliveau, RA;Bergen, SE;Ertalan, M;Bevilacqua, E;Bigdeli, TB;Black, DW;Bruggeman, R;Buccola, NG;Buckner, RL;Bulik-Sullivan, B;Byerley, W;Cahn, W;Cai, GQ;Cairns, MJ;Campion, D;Cantor, RM;Carr, VJ;Carrera, N;Catts, SV;Chambert, KD;Cheng, W;Cloninger, CR;Cohen, D;Cormican, P;Craddock, N;Crespo-Facorro, B;Crowley, JJ;Curtis, D;Davidson, M;Davis, KL;Degenhardt, F;Del Favero, J;DeLisi, LE;Dikeos, D;Dinan, T;Djurovic, S;Donohoe, G;Drapeau, E;Duan, J;Dudbridge, F;Eichhammer, P;Eriksson, J;Escott-Price, V;Essioux, L;Fanous, AH;Farh, KH;Farrell, MS;Frank, J;Franke, L;Freedman, R;Freimer, NB;Friedman, JI;Forstner, AJ;Fromer, M;Genovese, G;Georgieva, L;Gershon, ES;Giegling, I;Giusti-Rodriguez, P;Godard, S;Goldstein, JI;Gratten, J;de Haan, L;Hamshere, ML;Hansen, M;Hansen, T;Haroutunian, V;Hartmann, AM;Henskens, FA;Herms, S;Hirschhorn, JN;Hoffinann, P;Hofman, A;Huang, H;Ikeda, M;Joa, I;Kahler, AK;Kahn, RS;Kalaydjieva, L;Karjalainen, J;Kavanagh, D;Keller, MC;Kelly, BJ;Kennedy, JL;Kim, Y;Knowles, JA;Konte, B;Laurent, C;Lee, P;Lee, SH;Legge, SE;Lerer, B;Levy, DL;Liang, KY;Lieberman, J;Lonnqvist, J;Loughland, CM;Magnusson, PKE;Maher, BS;Maier, W;Mallet, J;Mattheisen, M;Mattingsdal, M;McCarley, RW;McDonald, C;McIntosh, AM;Meier, S;Meijer, CJ;Melle, I;Mesholam-Gately, RI;Metspalu, A;Michie, PT;Milani, L;Milanova, V;Mokrab, Y;Morris, DW;Muller-Myhsok, B;Murphy, KC;Murray, RM;Myin-Germeys, I;Nenadic, I;Nertney, DA;Nestadt, G;Nicodemus, KK;Nisenbaum, L;Nordin, A;O'Callaghan, E;O'Dushlaine, C;Oh, SY;Olincy, A;Olsen, L;O'Neill, FA;Van Os, J;Pantelis, C;Papadimitriou, GN;Parkhomenko, E;Pato, MT;Paunio, T;Perkins, DO;Pers, TH;Pietilainen, O;Pimm, J;Pocklington, AJ;Powell, J;Price, A;Pulver, AE;Purcell, SM;Quested, D;Rasmussen, HB;Reichenberg, A;Reimers, MA;Richards, AL;Roffman, JL;Roussos, P;Ruderfer, DM;Salomaa, V;Sanders, AR;Savitz, A;Schall, U;Schulze, TG;Schwab, SG;Scolnick, EM;Scott, RJ;Seidman, LJ;Shi, JX;Silverman, JM;Smoller, JW;Soderman, E;Spencer, CCA;Stahl, EA;Strengman, E;Strohmaier, J;Stroup, TS;Suvisaari, J;Svrakic, DM;Szatkiewicz, JP;Thirumalai, S;Tooney, PA;Veijola, J;Visscher, PM;Waddington, J;Walsh, D;Webb, BT;Weiser, M;Wildenauer, DB;Williams, NM;Williams, S;Witt, SH;Wolen, AR;Wormley, BK;Wray, NR;Wu, JQ;Zai, CC;Adolfsson, R;Andreassen, OA;Blackwood, DHR;Bramon, E;Buxbaum, JD;Cichon, S;Collier, DA;Corvin, A;Daly, MJ;Darvasi, A;Domenici, E;Esko, T;Gejman, PV;Gill, M;Gurling, H;Hultman, CM;Iwata, N;Jablensky, AV;Jonsson, EG;Kendler, KS;Kirov, G;Knight, J;Levinson, DF;Li, QQS;McCarroll, SA;McQuillin, A;Moran, JL;Mowry, BJ;Nothen, MM;Ophoff, RA;Owen, MJ;Palotie, A;Pato, CN;Petryshen, TL;Posthuma, D;Rietschel, M;Riley, BP;Rujescu, D;Sklar, P;St Clair, D;Walters, JTR;Werge, T;Siillivan, PF;O'Donovan, MC;Scherer, SW;Neale, BM;Sebat, J (2017) 'Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects'. Nature Genetics, 49 :27-35 [DOI] [Details]
(2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'
Mothersill, O,Tangney, N,Morris, DW,McCarthy, H,Frodl, T,Gill, M,Corvin, A,Donohoe, G (2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'. Schizophrenia Research, 184 :52-58 [DOI] [Details]
(2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'
Cosgrove D, Harold D, Mothersill O, Anney R, Hill MJ, Bray NJ, Blokland G, Petryshen T; Wellcome Trust Case Control Consortium, Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, Morris DW, Donohoe G. (2017) 'MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls'. Translational Psychiatry, [Details]
(2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'
McCarthy-Jones, S,Smailes, D,Corvin, A,Gill, M,Morris, DW,Dinan, TG,Murphy, KC,O'Neill, FA,Waddington, JL,Donohoe, G,Dudley, R,Australian Schizophrenia Res Bank (2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'. Psychiatry Research, 252 :154-160 [DOI] [Details]
(2018) 'The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project'
Blokland, GAM;del Re, EC;Mesholam-Gately, RI;Jovicich, J;Trampush, J;Keshavan, MS;DeLisi, LE;Walters, JTR;Turner, JA;Malhotra, AK;Lencz, T;Shenton, ME;Voineskos, AN;Rujescu, D;Giegling, I;Kahnv, RS;Roffman, JL;Holt, DJ;Ehrlich, S;Kikinis, Z;Dazzan, P;Murray, RM;Di Forti, M;Lee, J;Sim, K;Lam, M;Wolthusen, RPF;de Zwarte, SMC;Walton, E;Cosgrove, D;Kelly, S;Maleki, N;Osiecki, L;Picchioni, MM;Bramon, E;Russo, M;David, AS;Mondelli, V;Reinders, AATS;Falcone, MA;Hartmann, AM;Konte, B;Morris, DW;Gill, M;Corvin, AP;Cahn, W;Ho, NF;Liu, JJ;Keefe, RSE;Gollub, RL;Manoach, DS;Calhoun, VD;Schulz, SC;Sponheim, SR;Goff, DC;Buka, SL;Cherkerzian, S;Thermenos, HW;Kubicki, M;Nestor, PG;Dickie, EW;Vassos, E;Ciufolini, S;Marques, TR;Crossley, NA;Purcell, SM;Smoller, JW;van Haren, NEM;Toulopoulou, T;Donohoe, G;Goldstein, JM;Seidman, LJ;McCarley, RW;Petryshen, TL (2018) 'The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project'. Schizophrenia Research, 195 :306-317 [DOI] [Details]
(2018) 'Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment'
Whitton, L;Apostolova, G;Rieder, D;Dechant, G;Rea, S;Donohoe, G;Morris, DW (2018) 'Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment'. Plos Genetics, 14 [DOI] [Details]
(2018) 'The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project'
Blokland, GAM,del Re, EC,Mesholam-Gately, RI,Jovicich, J,Trampush, J,Keshavan, MS,DeLisi, LE,Walters, JTR,Turner, JA,Malhotra, AK,Lencz, T,Shenton, ME,Voineskos, AN,Rujescu, D,Giegling, I,Kahnv, RS,Roffman, JL,Holt, DJ,Ehrlich, S,Kikinis, Z,Dazzan, P,Murray, RM,Di Forti, M,Lee, J,Sim, K,Lam, M,Wolthusen, RPF,de Zwarte, SMC,Walton, E,Cosgrove, D,Kelly, S,Maleki, N,Osiecki, L,Picchioni, MM,Bramon, E,Russo, M,David, AS,Mondelli, V,Reinders, AATS,Falcone, MA,Hartmann, AM,Konte, B,Morris, DW,Gill, M,Corvin, AP,Cahn, W,Ho, NF,Liu, JJ,Keefe, RSE,Gollub, RL,Manoach, DS,Calhoun, VD,Schulz, SC,Sponheim, SR,Goff, DC,Buka, SL,Cherkerzian, S,Thermenos, HW,Kubicki, M,Nestor, PG,Dickie, EW,Vassos, E,Ciufolini, S,Marques, TR,Crossley, NA,Purcell, SM,Smoller, JW,van Haren, NEM,Toulopoulou, T,Donohoe, G,Go (2018) 'The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project'. Schizophrenia Research, 195 :306-317 [DOI] [Details]
(2018) 'Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes'
Ruderfer, DM;Ripke, S;McQuillin, A;Boocock, J;Stahl, EA;Pavlides, JMW;Mullins, N;Charney, AW;Ori, APS;Loohuis, LMO;Domenici, E;Di Florio, A;Papiol, S;Kalman, JL;Trubetskoy, V;Adolfsson, R;Agartz, I;Agerbo, E;Akil, H;Albani, D;Albus, M;Alda, M;Alexander, M;Alliey-Rodriguez, N;Als, TD;Amin, F;Anjorin, A;Arranz, MJ;Awasthi, S;Bacanu, SA;Badner, JA;Baekvad-Hansen, M;Bakker, S;Band, G;Barchas, JD;Barroso, I;Bass, N;Bauer, M;Baune, BT;Begemann, M;Bellenguez, C;Belliveau, RA;Bellivier, F;Bender, S;Bene, J;Bergen, SE;Berrettini, WH;Bevilacqua, E;Biernacka, JM;Bigdeli, TB;Black, DW;Blackburn, H;Blackwell, JM;Blackwood, DHR;Pedersen, CB;Boehnke, M;Boks, M;Borglum, AD;Bramon, E;Breen, G;Brown, MA;Bruggeman, R;Buccola, NG;Buckner, RL;Budde, M;Bulik-Sullivan, B;Bumpstead, SJ;Bunney, W;Burmeister, M;Buxbaum, JD;Bybjerg-Grauholm, J;Byerley, W;Cahn, W;Cai, GQ;Cairns, MJ;Campion, D;Cantor, RM;Carr, VJ;Carrera, N;Casas, JP;Casas, M;Catts, SV;Cervantes, P;Chambert, KD;Chan, RCK;Chen, EYH;Chen, RYL;Cheng, W;Cheung, EFC;Chong, SA;Clarke, TK;Cloninger, CR;Cohen, D;Cohen, N;Coleman, JRI;Collier, DA;Cormican, P;Coryell, W;Craddock, N;Craig, DW;Crespo-Facorro, B;Crowley, JJ;Cruceanu, C;Curtis, D;Czerski, PM;Dale, AM;Daly, MJ;Dannlowski, U;Darvasi, A;Davidson, M;Davis, KL;de Leeuw, CA;Degenhardt, F;Del Favero, J;DeLisi, LE;Deloukas, P;Demontis, D;DePaulo, JR;di Forti, M;Dikeos, D;Dinan, T;Djurovic, S;Dobbyn, AL;Donnelly, P;Donohoe, G;Drapeau, E;Dronov, S;Duan, J;Dudbridge, F;Duncanson, A;Edenberg, H;Edkins, S;Ehrenreich, H;Eichhammer, P;Elvsashagen, T;Eriksson, J;Escott-Price, V;Esko, T;Essioux, L;Etain, B;Fan, CC;Farh, KH;Farrell, MS;Flickinger, M;Foroud, TM;Forty, L;Frank, J;Franke, L;Fraser, C;Freedman, R;Freeman, C;Freimer, NB;Friedman, JI;Fromer, M;Frye, MA;Fullerton, JM;Gade, K;Garnham, J;Gaspar, HA;Gejman, PV;Genovese, G;Georgieva, L;Giambartolomei, C;Giannoulatou, E;Giegling, I;Gill, M;Gillman, M;Pedersen, MG;Giusti-Rodriguez, P;Godard, S;Goes, F;Goldstein, JI;Gopal, S;Gordon, SD;Gordon-Smith, K;Gratten, J;Gray, E;Green, EK;Green, MJ;Greenwood, TA;Grigoroiu-Serbanescu, M;Grove, J;Guan, WH;Gurling, H;Parra, JGM;Gwilliam, R;de Haan, L;Hall, J;Hall, MH;Hammer, C;Hammond, N;Hamshere, ML;Hansen, M;Hansen, T;Haroutunian, V;Hartmann, AM;Hauser, J;Hautzinger, M;Heilbronner, U;Hellenthal, G;Henskens, FA;Herms, S;Hipolito, M;Hirschhorn, JN;Hoffmann, P;Hollegaard, MV;Hougaard, DM;Huang, HL;Huckins, L;Hultman, CM;Hunt, SE;Ikeda, M;Iwata, N;Iyegbe, C;Jablensky, AV;Jamain, S;Jankowski, J;Jayakumar, A;Joa, I;Jones, I;Jones, LA;Jonsson, EG;Julia, A;Jureus, A;Kahler, AK;Kahn, RS;Kalaydjieva, L;Kandaswamy, R;Karachanak-Yankova, S;Karjalainen, J;Karlsson, R;Kavanagh, D;Keller, MC;Kelly, BJ;Kelsoe, J;Kennedy, JL;Khrunin, A;Kim, Y;Kirov, G;Kittel-Schneider, S;Klovins, J;Knight, J;Knott, SV;Knowles, JA;Kogevinas, M;Konte, B;Kravariti, E;Kucinskas, V;Kucinskiene, ZA;Kupka, R;Kuzelova-Ptackova, H;Landen, M;Langford, C;Laurent, C;Lawrence, J;Lawrie, S;Lawson, WB;Leber, M;Leboyer, M;Lee, PH;Keong, JLC;Legge, SE;Lencz, T;Lerer, B;Levinson, DF;Levy, SE;Lewis, CM;Li, JZ;Li, MX;Li, QQS;Li, T;Liang, KY;Liddle, J;Lieberman, J;Limborska, S;Lin, K;Linszen, DH;Lissowska, J;Liu, CY;Liu, JY;Lonnqvist, J;Loughland, CM;Lubinski, J;Lucae, S;Macek, M;MacIntyre, DJ;Magnusson, PKE;Maher, BS;Mahon, PB;Maier, W;Malhotra, AK;Mallet, J;Malt, UF;Markus, HS;Marsal, S;Martin, NG;Mata, I;Mathew, CG;Mattheisen, M;Mattingsdal, M;Mayoral, F;McCann, OT;McCarley, RW;McCarroll, SA;McCarthy, MI;McDonald, C;McElroy, SL;McGuffin, P;McInnis, MG;McIntosh, AM;Mckay, JD;McMahon, FJ;Medeiros, H;Medland, SE;Meier, S;Meijer, CJ;Melegh, B;Melle, I;Meng, F;Mesholam-Gately, RI;Metspalu, A;Michie, PT;Milani, L;Milanova, V;Mitch-Ell, PB;Mokrab, Y;Montgomery, GW;Moran, JL;Morken, G;Morris, DW;Mors, O;Mortensen, PB;Mowry, BJ;Muhleisen, TW;Muller-Myhsok, B;Murphy, KC;Murray, RM;Myers, RM;Myin-Germeys, I;Neale, BM;Nelis, M;Nenadic, I;Nertney, DA;Nestadt, G;Nicodemus, KK;Nievergelt, CM;Nikitina-Zake, L;Nimgaonkar, V;Nis (2018) 'Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes'. Cell, 173 [DOI] [Details]
(2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'
Cosgrove, D,Mothersill, DO,Whitton, L,Harold, D,Kelly, S,Holleran, L,Holland, J,Anney, R,Richards, A,Mantripragada, K,Owen, M,O'Donovan, MC,Gill, M,Corvin, A,Morris, DW,Donohoe, G,Wellcome Trust Case Control (2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'. American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 177 :369-376 [DOI] [Details]
(2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'
Cosgrove D, Mothersill DO, Whitton L, Harold D, Kelly S, Holleran L, Holland J, Anney R; Wellcome Trust Case Control Consortium, Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, Morris DW, Donohoe G (2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'. American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, [Details]
(2018) 'Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment'
Whitton, L,Apostolova, G,Rieder, D,Dechant, G,Rea, S,Donohoe, G,Morris, DW (2018) 'Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment'. Plos Genetics, 14 [DOI] [Details]
(2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'
Cosgrove, D;Mothersill, DO;Whitton, L;Harold, D;Kelly, S;Holleran, L;Holland, J;Anney, R;Richards, A;Mantripragada, K;Owen, M;O'Donovan, MC;Gill, M;Corvin, A;Morris, DW;Donohoe, G (2018) 'Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, 177 :369-376 [DOI] [Details]
(2018) 'Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation'
Donohoe, G,Holland, J,Mothersill, D,McCarthy-Jones, S,Cosgrove, D,Harold, D,Richards, A,Mantripragada, K,Owen, MJ,O'Donovan, MC,Gill, M,Corvin, A,Morris, DW,WTCCC2 (2018) 'Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation'. Psychological Medicine, 48 :1608-1615 [DOI] [Details]
(2018) 'Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function'
Davies, G;Lam, M;Harris, SE;Trampush, JW;Luciano, M;Hill, WD;Hagenaars, SP;Ritchie, SJ;Marioni, RE;Fawns-Ritchie, C;Liewald, DCM;Okely, JA;Ahola-Olli, AV;Barnes, CLK;Bertram, L;Bis, JC;Burdick, KE;Christoforou, A;DeRosse, P;Djurovic, S;Espeseth, T;Giakoumaki, S;Giddaluru, S;Gustavson, DE;Hayward, C;Hofer, E;Ikram, MA;Karlsson, R;Knowles, E;Lahti, J;Leber, M;Li, S;Mather, KA;Melle, I;Morris, D;Oldmeadow, C;Palviainen, T;Payton, A;Pazoki, R;Petrovic, K;Reynolds, CA;Sargurupremraj, M;Scholz, M;Smith, JA;Smith, AV;Terzikhan, N;Thalamuthu, A;Trompet, S;Lee, SJD;Ware, EB;Windham, BG;Wright, MJ;Yang, J;Yu, J;Ames, D;Amin, N;Amouyel, P;Andreassen, OA;Armstrong, NJ;Assareh, AA;Attia, JR;Attix, D;Avramopoulos, D;Bennett, DA;Boehmer, AC;Boyle, PA;Brodaty, H;Campbell, H;Cannon, TD;Cirulli, ET;Congdon, E;Conley, ED;Corley, J;Cox, SR;Dale, AM;Dehghan, A;Dick, D;Dickinson, D;Eriksson, JG;Evangelou, E;Faul, JD;Ford, I;Freimer, NA;Gao, H;Giegling, I;Gillespie, NA;Gordon, SD;Gottesman, RF;Griswold, ME;Gudnason, V;Harris, TB;Hartmann, AM;Hatzimanolis, A;Heiss, G;Holliday, EG;Joshi, PK;Kahonen, M;Kardia, SLR;Karlsson, I;Kleineidam, L;Knopman, DS;Kochan, NA;Konte, B;Kwok, JB;Hellard, S;Lee, T;Lehtimaki, T;Li, SC;Liu, T;Koini, M;London, E;LongstrethJr, WT;Lopez, OL;Loukola, A;Luck, T;Lundervold, AJ;Lundquist, A;Lyytikainen, LP;Martin, NG;Montgomery, GW;Murray, AD;Need, AC;Noordam, R;Nyberg, L;Ollier, W;Papenberg, G;Pattie, A;Polasek, O;Poldrack, RA;Psaty, BM;Reppermund, S;Riedel-Heller, SG;Rose, RJ;Rotter, JI;Roussos, P;Rovio, SP;Saba, Y;Sabb, FW;Sachdev, PS;Satizabal, CL;Schmid, M;Scott, RJ;Scult, MA;Simino, J;Slagboom, PE;Smyrnis, N;Soumare, A;Stefanis, NC;Stott, DJ;Straub, RE;Sundet, K;Taylor, AM;Taylor, KD;Tzoulaki, I;Tzourio, C;Uitterlinden, A;Vitart, V;Voineskos, AN;Kaprio, J;Wagner, M;Wagner, H;Weinhold, L;Wen, KH;Widen, E;Yang, Q;Zhao, W;Adams, HHH;Arking, DE;Bilder, RM;Bitsios, P;Boerwinkle, E;Chiba-Falek, O;Corvin, A;Jager, PL;Debette, S;Donohoe, G;Elliott, P;Fitzpatrick, AL;Gill, M;Glahn, DC;Hagg, S;Hansell, NK;Hariri, AR;Ikram, MK;Jukema, JW;Vuoksimaa, E;Keller, MC;Kremen, WS;Launer, L;Lindenberger, U;Palotie, A;Pedersen, NL;Pendleton, N;Porteous, DJ;Raikkonen, K;Raitakari, OT;Ramirez, A;Reinvang, I;Rudan, I;Rujescu, D;Schmidt, R;Schmidt, H;Schofield, PW;Schofield, PR;Starr, JM;Steen, VM;Trollor, JN;Turner, ST;Duijn, CM;Villringer, A;Weinberger, DR;Weir, DR;Wilson, JF;Malhotra, A;McIntosh, AM;Gale, CR;Seshadri, S;MosleyJr, TH;Bressler, J;Lencz, T;Deary, IJ (2018) 'Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function'. Nature Communications, 9 [DOI] [Details]
(2018) 'Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium'
van Erp, TGM;Walton, E;Hibar, DP;Schmaal, L;Jiang, WH;Glahn, DC;Pearlson, GD;Yao, NL;Fukunaga, M;Hashimoto, R;Okada, N;Yamamori, H;Bustillo, JR;Clark, VP;Agartz, I;Mueller, BA;Cahn, W;de Zwarte, SMC;Pol, HEH;Kahn, RS;Ophoff, RA;van Haren, NEM;Andreassen, OA;Dale, AM;Doan, NT;Gurholt, TP;Hartberg, CB;Haukvik, UK;Jorgensen, KN;Lagerberg, TV;Melle, I;Westlye, LT;Gruber, O;Kraemer, B;Richter, A;Zilles, D;Calhoun, VD;Crespo-Facorro, B;Roiz-Santianez, R;Tordesillas-Gutierrez, D;Loughland, C;Carr, VJ;Catts, S;Cropley, VL;Fullerton, JM;Green, MJ;Henskens, FA;Jablensky, A;Lenroot, RK;Mowry, BJ;Michie, PT;Pantelis, C;Quide, Y;Schall, U;Scott, RJ;Cairns, MJ;Seal, M;Tooney, PA;Rasser, PE;Cooper, G;Weickert, CS;Weickert, TW;Morris, DW;Hong, E;Kochunov, P;Beard, LM;Gur, RE;Gur, RC;Satterthwaite, TD;Wolf, DH;Belger, A;Brown, GG;Ford, JM;Macciardi, F;Mathalon, DH;O'Leary, DS;Potkin, SG;Preda, A;Voyvodic, J;Lim, KO;McEwen, S;Yang, FD;Tan, YL;Tan, SP;Wang, ZR;Fan, FM;Chen, JX;Xiang, H;Tang, SY;Guo, H;Wan, P;Wei, D;Bockholt, HJ;Ehrlich, S;Wolthusen, RPF;King, MD;Shoemaker, JM;Sponheim, SR;De Haan, L;Koenders, L;Machielsen, MW;van Amelsvoort, T;Veltman, DJ;Assogna, F;Banaj, N;de Rossi, P;Iorio, M;Piras, F;Spalletta, G;McKenna, PJ;Pomarol-Clotet, E;Salvador, R;Corvin, A;Donohoe, G;Kelly, S;Whelan, CD;Dickie, EW;Rotenberg, D;Voineskos, AN;Ciufolini, S;Radua, J;Dazzan, P;Murray, R;Marques, TR;Simmons, A;Borgwardt, S;Egloff, L;Harrisberger, F;Riecher-Rossler, A;Smieskova, R;Alpert, KI;Wang, L;Jonsson, EG;Koops, S;Sommer, IEC;Bertolino, A;Bonvino, A;Di Giorgio, A;Neilson, E;Mayer, AR;Stephen, JM;Kwon, JS;Yun, JY;Cannon, DM;McDonald, C;Lebedeva, I;Tomyshev, AS;Akhadov, T;Kaleda, V;Fatouros-Bergman, H;Flyckt, L;Busatto, GF;Rosa, PGP;Serpa, MH;Zanetti, MV;Hoschl, C;Skoch, A;Spaniel, F;Tomecek, D;Hagenaars, SP;McIntosh, AM;Whalley, HC;Lawrie, SM;Knochel, C;Oertel-Knochel, V;Stablein, M;Howells, FM;Stein, DJ;Temmingh, HS;Uhlmann, A;Lopez-Jaramillo, C;Dima, D;McMahon, A;Faskowitz, JI;Gutman, BA;Jahanshad, N;Thompson, PM;Turner, JA (2018) 'Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium'. Biological Psychiatry, 84 :644-654 [DOI] [Details]
(2018) 'GWAS and eQTL analysis identifies a SNP associated with both residual feed intake and GFRA2 expression in beef cattle'
Higgins, MG,Fitzsimons, C,McClure, MC,McKenna, C,Conroy, S,Kenny, DA,McGee, M,Waters, SM,Morris, DW (2018) 'GWAS and eQTL analysis identifies a SNP associated with both residual feed intake and GFRA2 expression in beef cattle'. Scientific Reports, 8 [DOI] [Details]
(2018) 'Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation'
Donohoe G, Holland J, Mothersill D, McCarthy-Jones S, Cosgrove D, Harold D, Richards A, Mantripragada K, Owen MJ, O'Donovan MC; WTCCC2, Gill M, Corvin A, Morris DW. (2018) 'Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation'. Psychological Medicine, [ARAN Link] [Details]
(2018) 'Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis'
Rees E, Carrera N, Morgan J, Hambridge K, Escott-Price V, Pocklington A, Richards A, Partinas A, GROUP Investigators, McDonald C, Donohoe G, Morris D, Kenny E, Kelleher E, Gill M, Corvin A, Kirov G, Walters J, Holmans P, Owen M, O'Donovan M. (2018) 'Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis'. Biological Psychiatry, [DOI] [Details]
(2018) 'DNA methylation differences at the glucocorticoid receptor gene in depression are related to functional alterations in hypothalamic-pituitary-adrenal axis activity and to early life emotional abuse'
Farrell, C,Doolin, K,O'Leary, N,Jairaj, C,Roddy, D,Tozzi, L,Morris, D,Harkin, A,Frodl, T,Nemoda, Z,Szyf, M,Booij, L,O'Keane, V (2018) 'DNA methylation differences at the glucocorticoid receptor gene in depression are related to functional alterations in hypothalamic-pituitary-adrenal axis activity and to early life emotional abuse'. Psychiatry Research, 265 :341-348 [DOI] [Details]
(2019) 'Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis'
Rees, E;Carrera, N;Morgan, J;Hambridge, K;Escott-Price, V;Pocklington, AJ;Richards, AL;Pardinas, AF;McDonald, C;Donohoe, G;Morris, DW;Kenny, E;Kelleher, E;Gill, M;Corvin, A;Kirov, G;Walters, JTR;Holmans, P;Owen, MJ;O'Donovan, MC;Alizadeh, BZ;van Amelsvoort, T;Bartels-Velthuis, AA;van Beveren, NJ;Bruggeman, R;Cahn, W;de Haan, L;Delespaul, P;Meijer, CJ;Myin-Germeys, I;Kahn, RS;Schirmbeck, F;Simons, CJP;van Haren, NE;van Os, J;van Winkel, R;Luykx, JJ (2019) 'Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis'. Biological Psychiatry, 85 :554-562 [DOI] [Details]
(2019) 'A COGNITIVE AND MOLECULAR ANALYSIS OF SDCCAG8, A SCHIZOPHRENIA RISK GENE THAT FUNCTIONS IN THE CENTROSOME'
Flynn, M,Whitton, L,Corvin, A,Harold, D,Gill, M,Donohoe, G,Morrison, C,Morris, D (2019) 'A COGNITIVE AND MOLECULAR ANALYSIS OF SDCCAG8, A SCHIZOPHRENIA RISK GENE THAT FUNCTIONS IN THE CENTROSOME'. European Neuropsychopharmacology, 29 :876-877 [DOI] [Details]
(2019) 'The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia'
Richards AL;Pardiñas AF;Frizzati A;Tansey KE;Lynham AJ;Holmans P;Legge SE;Savage JE;Agartz I;Andreassen OA;Blokland GAM;Corvin A;Cosgrove D;Degenhardt F;Djurovic S;Espeseth T;Ferraro L;Gayer-Anderson C;Giegling I;van Haren NE;Hartmann AM;Hubert JJ;Jönsson EG;Konte B;Lennertz L;Olde Loohuis LM;Melle I;Morgan C;Morris DW;Murray RM;Nyman H;Ophoff RA; ;van Os J; ; ;Petryshen TL;Quattrone D;Rietschel M;Rujescu D;Rutten BPF;Streit F;Strohmaier J;Sullivan PF;Sundet K;Wagner M;Escott-Price V;Owen MJ;Donohoe G;O'Donovan MC;Walters JTR; (2019) 'The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia'. Schizophrenia Bulletin, [DOI] [Details]
(2019) 'Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability'
Cera I, Whitton L, Donohoe G, Morris D, Dechant G, Apostolova G. (2019) 'Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability'. Plos Genetics, 15 (2):1-21 [DOI] [Details]
(2019) 'Beyond C4: Analysis of the complement gene pathway shows enrichment for IQ in patients with psychotic disorders and healthy controls'
Holland, JF,Cosgrove, D,Whitton, L,Harold, D,Corvin, A,Gill, M,Mothersill, DO,Morris, DW,Donohoe, G (2019) 'Beyond C4: Analysis of the complement gene pathway shows enrichment for IQ in patients with psychotic disorders and healthy controls'. Genes Brain And Behavior, [DOI] [Details]
(2019) 'Beyond C4: Analysis of the complement gene pathway shows enrichment for IQ in patients with psychotic disorders and healthy controls'
Holland, JF;Cosgrove, D;Whitton, L;Harold, D;Corvin, A;Gill, M;Mothersill, DO;Morris, DW;Donohoe, G (2019) 'Beyond C4: Analysis of the complement gene pathway shows enrichment for IQ in patients with psychotic disorders and healthy controls'. Genes Brain And Behavior, [DOI] [Details]
(2019) 'The effect of breed and diet type on the global transcriptome of hepatic tissue in beef cattle divergent for feed efficiency'
Higgins, MG;Kenny, DA;Fitzsimons, C;Blackshields, G;Coyle, S;McKenna, C;McGee, M;Morris, DW;Waters, SM (2019) 'The effect of breed and diet type on the global transcriptome of hepatic tissue in beef cattle divergent for feed efficiency'. BMC Genomics, 20 [DOI] [Details]
(2019) 'GENETIC RISK VARIANTS INTERACTING WITH MIR137: EFFECTS ON COGNITION, BRAIN STRUCTURE AND BRAIN FUNCTION IN PATIENTS AND HEALTHY PARTICIPANTS'
Donohoe, G,Cosgrove, D,Motherills, D,Harold, D,Kelly, S,Holleran, L,Holland, J,Anney, R,Richards, A,Owen, M,O'Donovan, M,Gill, M,Corvin, A,Morris, D,Wellcome Trust CCC (2019) 'GENETIC RISK VARIANTS INTERACTING WITH MIR137: EFFECTS ON COGNITION, BRAIN STRUCTURE AND BRAIN FUNCTION IN PATIENTS AND HEALTHY PARTICIPANTS'. European Neuropsychopharmacology, 29 :729-730 [DOI] [Details]
(2019) 'Beyond C4: Analysis Of The Complement Gene Pathway Shows Enrichment For IQ In Patients With Psychotic Disorders And Healthy Controls'
Holland JF;Cosgrove D;Whitton L;Harold D;Corvin A;Gill M;Mothershill D;Morris DW;Donohoe G; (2019) 'Beyond C4: Analysis Of The Complement Gene Pathway Shows Enrichment For IQ In Patients With Psychotic Disorders And Healthy Controls'. Genes Brain And Behavior, [DOI] [Details]
(2019) 'The effect of breed and diet type on the global transcriptome of hepatic tissue in beef cattle divergent for feed efficiency'
Higgins, MG,Kenny, DA,Fitzsimons, C,Blackshields, G,Coyle, S,McKenna, C,McGee, M,Morris, DW,Waters, SM (2019) 'The effect of breed and diet type on the global transcriptome of hepatic tissue in beef cattle divergent for feed efficiency'. BMC Genomics, 20 [DOI] [Details]
(2019) 'THE IMMUNE 8: IMPAIRED COGNITION IN SCHIZOPHRENIA RELATED TO GENETIC, ENVIRONMENTAL, AND IMMUNE INTERACTIONS IN IRISH AND UK COHORTS'
Holland, J,Morris, D,Cosgrove, D,Harold, D,Mothershill, OD,Corvin, A,Donohoe, G (2019) 'THE IMMUNE 8: IMPAIRED COGNITION IN SCHIZOPHRENIA RELATED TO GENETIC, ENVIRONMENTAL, AND IMMUNE INTERACTIONS IN IRISH AND UK COHORTS'. European Neuropsychopharmacology, 29 :879-880 [DOI] [Details]
(2019) 'COMMON AND RARE RISK VARIANTS MAP TO GENES WITH SIMILAR CHARACTERISTICS IN BOTH SCHIZOPHRENIA AND EDUCATIONAL ATTAINMENT'
Whitton, L,Sohedein, MNA,Donohoe, G,Morris, D (2019) 'COMMON AND RARE RISK VARIANTS MAP TO GENES WITH SIMILAR CHARACTERISTICS IN BOTH SCHIZOPHRENIA AND EDUCATIONAL ATTAINMENT'. European Neuropsychopharmacology, 29 :937-938 [DOI] [Details]
(2019) 'Gene expression imputation across multiple brain regions provides insights into schizophrenia risk'
Huckins, LM;Dobbyn, A;Ruderfer, DM;Hoffman, G;Wang, WQ;Pardinas, AF;Rajagopal, VM;Als, TD;Nguyen, HT;Girdhar, K;Boocock, J;Roussos, P;Fromer, M;Kramer, R;Domenici, E;Gamazon, ER;Purcell, S;Demontis, D;Borglum, AD;Walters, JTR;O'Donovan, MC;Sullivan, P;Owen, MJ;Devlin, B;Sieberts, SK;Cox, NJ;Im, HK;Sklar, P;Stahl, EA;Johnson, JS;Shah, HR;Klein, LL;Dang, KK;Logsdon, BA;Mahajan, MC;Mangravite, LM;Toyoshiba, H;Gur, RE;Hahn, CG;Schadt, E;Lewis, DA;Haroutunian, V;Peters, MA;Lipska, BK;Buxbaum, JD;Hirai, K;Perumal, TM;Essioux, L;Rajagopal, VM;Mattheisen, M;Grove, J;Werge, T;Mortensen, PB;Pedersen, CB;Agerbo, E;Pedersen, MG;Mors, O;Nordentoft, M;Hougaard, DM;Bybjerg-Grauholm, J;Baekvad-Hansen, M;Hansen, CS;Ripke, S;Neale, BM;Corvin, A;Farh, KH;Holmans, PA;Lee, P;Bulik-Sullivan, B;Collier, DA;Huang, HL;Pers, TH;Agartz, I;Albus, M;Alexander, M;Amin, F;Bacanu, SA;Begemann, M;Belliveau, RA;Bene, J;Bergen, SE;Bevilacqua, E;Bigdeli, TB;Black, DW;Bruggeman, R;Buccola, NG;Buckner, RL;Byerley, W;Cahn, W;Cai, GQ;Campion, D;Cantor, RM;Carr, VJ;Carrera, N;Catts, SV;Chambert, KD;Chan, RCK;Chen, RYL;Chen, EYH;Cheng, W;Cheung, EFC;Chong, SA;Cloninger, CR;Cohen, D;Cohen, N;Cormican, P;Craddock, N;Crowley, JJ;Curtis, D;Davidson, M;Davis, KL;Degenhardt, F;Del Favero, J;Dikeos, D;Dinan, T;Djurovic, S;Donohoe, G;Drapeau, E;Duan, J;Dudbridge, F;Durmishi, N;Eichhammer, P;Eriksson, J;Escott-Price, V;Essioux, L;Fanous, AH;Farrell, MS;Frank, J;Franke, L;Freedman, R;Freimer, NB;Friedl, M;Friedman, JI;Fromer, M;Genovese, G;Georgieva, L;Giegling, I;Giusti-Rodriguez, P;Godard, S;Goldstein, JI;Golimbet, V;Gopal, S;Gratten, J;de Haan, L;Hammer, C;Hamshere, ML;Hansen, M;Hansen, T;Haroutunian, V;Hartmann, AM;Henskens, FA;Herms, S;Hirschhorn, JN;Hoffmann, P;Hofman, A;Hollegaard, MV;Ikeda, M;Joa, I;Julia, A;Kahn, RS;Kalaydjieva, L;Karachanak-Yankova, S;Karjalainen, J;Kavanagh, D;Keller, MC;Kennedy, JL;Khrunin, A;Kim, Y;Klovins, J;Knowles, JA;Konte, B;Kucinskas, V;Kucinskiene, ZA;Kuzelova-Ptackova, H;Kahler, AK;Laurent, C;Keong, JLC;Lee, SH;Legge, SE;Lerer, B;Li, MX;Li, T;Liang, KY;Lieberman, J;Limborska, S;Loughland, CM;Lubinski, J;Lonnqvist, J;Macek, M;Magnusson, PKE;Maher, BS;Maier, W;Mallet, J;Marsal, S;Mattingsdal, M;McCarley, RW;McDonald, C;McIntosh, AM;Meier, S;Meijer, CJ;Melegh, B;Melle, I;Mesholam-Gately, RI;Metspalu, A;Michie, PT;Milani, L;Milanova, V;Mokrab, Y;Morris, DW;Mors, O;Murphy, KC;Murray, RM;Myin-Germeys, I;Muller-Myhsok, B;Nelis, M;Nenadic, I;Nertney, DA;Nestadt, G;Nicodemus, KK;Nikitina-Zake, L;Nisenbaum, L;Nordin, A;O'Callaghan, E;O'Dushlaine, C;O'Neill, FA;Oh, SY;Olincy, A;Olsen, L;Van Os, J;Pantelis, C;Papadimitriou, GN;Papiol, S;Parkhomenko, E;Pato, MT;Paunio, T;Pejovic-Milovancevic, M;Perkins, DO;Pietilainen, O;Pimm, J;Pocklington, AJ;Powell, J;Price, A;Pulver, AE;Purcell, SM;Quested, D;Rasmussen, HB;Reichenberg, A;Reimers, MA;Richards, AL;Roffman, JL;Ruderfer, DM;Salomaa, V;Sanders, AR;Schall, U;Schubert, CR;Schulze, TG;Schwab, SG;Scolnick, EM;Scott, RJ;Seidman, LJ;Shi, JX;Sigurdsson, E;Silagadze, T;Silverman, JM;Sim, K;Slominsky, P;Smoller, JW;So, HC;Spencer, CCA;Stefansson, H;Steinberg, S;Stogmann, E;Straub, RE;Strengman, E;Strohmaier, J;Stroup, TS;Subramaniam, M;Suvisaari, J;Svrakic, DM;Szatkiewicz, JP;Soderman, E;Thirumalai, S;Toncheva, D;Tosato, S;Veijola, J;Waddington, J;Walsh, D;Wang, D;Wang, Q;Webb, BT;Weiser, M;Wildenauer, DB;Williams, NM;Williams, S;Witt, SH;Wolen, AR;Wong, EHM;Wormley, BK;Xi, HS;Zai, CC;Zheng, XB;Zimprich, F;Wray, NR;Stefansson, K;Visscher, PM;Adolfsson, R;Andreassen, OA;Blackwood, DHR;Bramon, E;Buxbaum, JD;Borglum, AD;Cichon, S;Darvasi, A;Domenici, E;Ehrenreich, H;Esko, T;Gejman, PV;Gill, M;Gurling, H;Hultman, CM;Iwata, N;Jablensky, AV;Jonsson, EG;Kendler, KS;Kirov, G;Knight, J;Lencz, T;Levinson, DF;Li, QQS;Liu, JJ;Malhotra, AK;McCarroll, SA;McQuillin, A;Moran, JL;Mortensen, PB;Mowry, BJ;Nothen, MM;Ophoff, RA;Owen, MJ;Palotie, A;Pato, CN;Petryshen, TL;Posthuma, D;Rietschel, M;Riley, BP;Rujescu, D;Sham, PC;St Clair (2019) 'Gene expression imputation across multiple brain regions provides insights into schizophrenia risk'. Nature Genetics, 51 [DOI] [Details]
(2019) 'Population-based identity-by descent mapping combined with exome sequencing to detect rare risk variants for Schizophrenia'
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, WaltersJ; Wellcome Trust Case Control Consortium2; Schiophrena Working Group of the Psychiatric Genomics Consortium, Donohoe G, Gill M, Corvin A, Morris DW. (2019) 'Population-based identity-by descent mapping combined with exome sequencing to detect rare risk variants for Schizophrenia'. Am J Med, 180 (3):223-231 [DOI] [Details]
(2019) 'Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways'
Lam M;Hill WD;Trampush JW;Yu J;Knowles E;Davies G;Stahl E;Huckins L;Liewald DC;Djurovic S;Melle I;Sundet K;Christoforou A;Reinvang I;DeRosse P;Lundervold AJ;Steen VM;Espeseth T;Räikkönen K;Widen E;Palotie A;Eriksson JG;Giegling I;Konte B;Hartmann AM;Roussos P;Giakoumaki S;Burdick KE;Payton A;Ollier W;Chiba-Falek O;Attix DK;Need AC;Cirulli ET;Voineskos AN;Stefanis NC;Avramopoulos D;Hatzimanolis A;Arking DE;Smyrnis N;Bilder RM;Freimer NA;Cannon TD;London E;Poldrack RA;Sabb FW;Congdon E;Conley ED;Scult MA;Dickinson D;Straub RE;Donohoe G;Morris D;Corvin A;Gill M;Hariri AR;Weinberger DR;Pendleton N;Bitsios P;Rujescu D;Lahti J;Le Hellard S;Keller MC;Andreassen OA;Deary IJ;Glahn DC;Malhotra AK;Lencz T; (2019) 'Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways'. American Journal Of Human Genetics, 105 (2) [DOI] [Details]
(2019) 'Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia'
Harold, D;Connolly, S;Riley, BP;Kendler, KS;McCarthy, SE;McCombie, WR;Richards, A;Owen, MJ;O'Donovan, MC;Walters, J;Donnelly, P;Bates, L;Barroso, I;Blackwell, JM;Bramon, E;Brown, MA;Casas, JP;Corvin, A;Deloukas, P;Duncanson, A;Jankowski, J;Markus, HS;Mathew, CG;Palmer, CNA;Plomin, R;Rautanen, A;Sawcer, SJ;Trembath, RC;Viswanathan, AC;Wood, NW;Spencer, CCA;Band, G;Bellenguez, C;Freeman, C;Hellenthal, G;Giannoulatou, E;Hopkins, L;Pirinen, M;Pearson, R;Strange, A;Su, Z;Vukcevic, D;Langford, C;Hunt, SE;Edkins, S;Gwilliam, R;Blackburn, H;Bumpstead, SJ;Dronov, S;Gillman, M;Gray, E;Hammond, N;Jayakumar, A;McCann, OT;Liddle, J;Potter, SC;Ravindrarajah, R;Ricketts, M;Waller, M;Weston, P;Widaa, S;Whittaker, P;Ripke, S;Neale, BM;Corvin, A;Walters, JTR;Farh, KH;Holmans, PA;Lee, P;Bulik-Sullivan, B;Collier, DA;Huang, H;Pers, TH;Agartz, I;Agerbo, E;Albus, M;Alexander, ML;Amin, F;Bacanu, SA;Begemann, M;Belliveau, RA;Bene, J;Bergen, SE;Bevilacqua, E;Bigdeli, TB;Black, DW;Bruggeman, R;Buccola, NG;Buckner, RL;Byerley, W;Cahn, W;Cai, GQ;Campion, D;Cantor, RM;Carr, VJ;Carrera, N;Catts, SV;Chambert, KD;Chan, RCK;Chan, RYL;Chen, EYH;Cheng, W;Cheung, EFC;Chong, SA;Cloninger, CR;Cohen, D;Cohen, N;Cormican, P;Craddock, N;Crowley, JJ;Curtis, D;Davidson, M;Davis, KL;Degenhardt, F;Del Favero, J;Demontis, D;Dikeos, D;Dinan, T;Djurovic, S;Donohoe, G;Drapeau, E;Duan, J;Dudbridge, F;Durmishi, N;Eichhammer, P;Eriksson, J;Escott-Price, V;Essioux, L;Fanous, AH;Farrell, MS;Frank, J;Franke, L;Freedman, R;Freimer, NB;Friedl, M;Friedman, JI;Fromer, M;Genovese, G;Georgieva, L;Giegling, I;Giusti-Rodriguez, P;Godard, S;Goldstein, JI;Golimbet, V;Gopal, S;Gratten, J;de Haan, L;Hammer, C;Hamshere, ML;Hansen, M;Hansen, T;Haroutunian, V;Hartmann, AM;Henskens, FA;Herms, S;Hirschhorn, JN;Hoffmann, P;Hofman, A;Hollegaard, MV;Hougaard, DM;Ikeda, M;Joa, I;Julia, A;Kalaydjieva, L;Karachanak-Yankova, S;Karjalainen, J;Kavanagh, D;Keller, MC;Kennedy, JL;Khrunin, A;Kim, Y;Klovins, J;Knowles, JA;Konte, B;Kucinskas, V;Kucinskiene, ZA;Kuzelova-Ptackova, H;Kahler, AK;Laurent, C;Lee, J;Lee, SH;Legge, SE;Lerer, B;Li, MX;Li, T;Liang, KY;Lieberman, J;Limborska, S;Loughland, CM;Lubinski, J;Lonnqvist, J;Macek, M;Magnusson, PKE;Maher, BS;Maier, W;Mallet, J;Marsal, S;Mattheisen, M;Mattingsdal, M;McCarley, RW;McDonald, C;McIntosh, AM;Meier, S;Meijer, CJ;Melegh, B;Melle, I;Mesholam-Gately, RI;Metspalu, A;Michie, PT;Milani, L;Milanova, V;Mokrab, Y;Morris, DW;Mors, O;Murphy, KC;Murray, RM;Myin-Germeys, I;Muller-Myhsok, B;Nelis, M;Nenadic, I;Nertney, DA;Nestadt, G;Nicodemus, KK;Nikitina-Zake, L;Nisenbaum, L;Nordin, A;O'Callaghan, E;O'Dushlaine, C;O'Neill, FA;Oh, SY;Olincy, A;Olsen, L;Van Os, J;Pantelis, C;Papadimitriou, GN;Papiol, S;Parkhomenko, E;Pato, MT;Paunio, T;Pejovic-Milovancevic, M;Perkins, DO;Pietilainen, O;Pimm, J;Pocklington, AJ;Price, A;Pulver, AE;Purcell, SM;Quested, D;Rasmussen, HB;Reichenberg, A;Reimers, MA;Richards, AL;Roffman, JL;Roussos, P;Ruderfer, DM;Salomaa, V;Sanders, AR;Schall, U;Schubert, CR;Schulze, TG;Schwab, SG;Scolnick, EM;Scott, RJ;Seidman, LJ;Shi, JX;Sigurdsson, E;Silagadze, T;Silverman, JM;Sim, K;Slominsky, P;Smoller, JW;So, HC;Spencer, CCA;Stahl, EA;Stefansson, H;Steinberg, S;Stogmann, E;Straub, RE;Strengman, E;Strohmaier, J;Stroup, TS;Subramaniam, M;Suvisaari, J;Svrakic, DM;Szatkiewicz, JP;Soderman, E;Thirumalai, S;Toncheva, D;Tosato, S;Veijola, J;Waddington, J;Walsh, D;Wang, D;Wang, Q;Webb, BT;Weiser, M;Wildenauer, DB;Williams, NM;Williams, S;Witt, SH;Wolen, AR;Wong, EHM;Wormley, BK;Xi, HS;Zai, CC;Zheng, XB;Zimprich, F;Wray, NR;Stefansson, K;Visscher, PM;Adolfsson, R;Andreassen, OA;Blackwood, DHR;Bramon, E;Buxbaum, JD;Borglum, AD;Darvasi, A;Domenici, E;Ehrenreich, H;Esko, T;Gejman, PV;Gill, M;Gurling, H;Hultman, CM;Iwata, N;Jablensky, AV;Jonsson, EG;Kendler, KS;Kirov, G;Knight, J;Lencz, T;Levinson, DF;Li, QQS;Liu, JJ;Malhotra, AK;McCarroll, SA;McQuillin, A;Moran, JL;Mortensen, PB;Mowry, BJ;Owen, MJ;Palotie, A;Pato, CN;Petryshen, TL;Posthuma, D;Riley, BP;Rujescu, D;S (2019) 'Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, 180 :223-231 [DOI] [Details]
(2019) 'Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability'
Cera, I,Whitton, L,Donohoe, G,Morris, DW,Dechant, G,Apostolova, G (2019) 'Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability'. Plos Genetics, 15 [DOI] [Details]
(2020) 'Altered gene regulation as a candidate mechanism by which ciliopathy gene SDCCAG8 contributes to schizophrenia and cognitive function'
Flynn M;Whitton L;Donohoe G;Morrison CG;Morris DW; (2020) 'Altered gene regulation as a candidate mechanism by which ciliopathy gene SDCCAG8 contributes to schizophrenia and cognitive function'. Human Molecular Genetics, 29 (3) [DOI] [Details]
(2020) 'The Relationship Between White Matter Microstructure and General Cognitive Ability in Patients With Schizophrenia and Healthy Participants in the ENIGMA Consortium'
Holleran L;Kelly S;Alloza C;Agartz I;Andreassen OA;Arango C;Banaj N;Calhoun V;Cannon D;Carr V;Corvin A;Glahn DC;Gur R;Hong E;Hoschl C;Howells FM;James A;Janssen J;Kochunov P;Lawrie SM;Liu J;Martinez C;McDonald C;Morris D;Mothersill D;Pantelis C;Piras F;Potkin S;Rasser PE;Roalf D;Rowland L;Satterthwaite T;Schall U;Spalletta G;Spaniel F;Stein DJ;Uhlmann A;Voineskos A;Zalesky A;van Erp TGM;Turner JA;Deary IJ;Thompson PM;Jahanshad N;Donohoe G; (2020) 'The Relationship Between White Matter Microstructure and General Cognitive Ability in Patients With Schizophrenia and Healthy Participants in the ENIGMA Consortium'. American Journal Of Psychiatry, [DOI] [Details]
(2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer'
McVeigh, UM,McVeigh, TP,Curran, C,Miller, N,Morris, DW,Kerin, MJ (2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer'. Irish Journal Of Medical Science, [DOI] [Details]
(2020) 'Cognitive Genomics: Recent Advances and Current Challenges'
Fitzgerald J;Morris DW;Donohoe G; (2020) 'Cognitive Genomics: Recent Advances and Current Challenges'. Current Psychiatry Reports, 22 (1) [DOI] [Details]
(2020) 'Effects of early life adversity on immune function and cognitive performance: results from the ALSPAC cohort'
Holland, JF;Khandaker, GM;Dauvermann, MR;Morris, D;Zammit, S;Donohoe, G (2020) 'Effects of early life adversity on immune function and cognitive performance: results from the ALSPAC cohort'. Social Psychiatry And Psychiatric Epidemiology, [DOI] [Details]
(2020) 'Genes regulated byBCL11Bduring T-cell development are enriched for de novo mutations found in schizophrenia patients'
Fahey, L,Donohoe, G,Broin, PO,Morris, DW (2020) 'Genes regulated byBCL11Bduring T-cell development are enriched for de novo mutations found in schizophrenia patients'. American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, [DOI] [ARAN Link] [Details]
(2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer'
McVeigh, UM;McVeigh, TP;Curran, C;Miller, N;Morris, DW;Kerin, MJ (2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer'. Irish Journal of Medical Science, [DOI] [Details]
(2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer (Feb, 10.1007/s11845-020-02174-x, 2020)'
McVeigh, UM;McVeigh, TP;Curran, C;Miller, N;Morris, DW;Kerin, MJ (2020) 'Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer (Feb, 10.1007/s11845-020-02174-x, 2020)'. Irish Journal of Medical Science, [DOI] [Details]
(2020) 'Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia'
Sønderby IE;Gústafsson Ó;Doan NT;Hibar DP;Martin-Brevet S;Abdellaoui A;Ames D;Amunts K;Andersson M;Armstrong NJ;Bernard M;Blackburn N;Blangero J;Boomsma DI;Bralten J;Brattbak HR;Brodaty H;Brouwer RM;Bülow R;Calhoun V;Caspers S;Cavalleri G;Chen CH;Cichon S;Ciufolini S;Corvin A;Crespo-Facorro B;Curran JE;Dale AM;Dalvie S;Dazzan P;de Geus EJC;de Zubicaray GI;de Zwarte SMC;Delanty N;den Braber A;Desrivières S;Donohoe G;Draganski B;Ehrlich S;Espeseth T;Fisher SE;Franke B;Frouin V;Fukunaga M;Gareau T;Glahn DC;Grabe H;Groenewold NA;Haavik J;Håberg A;Hashimoto R;Hehir-Kwa JY;Heinz A;Hillegers MHJ;Hoffmann P;Holleran L;Hottenga JJ;Hulshoff HE;Ikeda M;Jahanshad N;Jernigan T;Jockwitz C;Johansson S;Jonsdottir GA;Jönsson EG;Kahn R;Kaufmann T;Kelly S;Kikuchi M;Knowles EEM;Kolskår KK;Kwok JB;Hellard SL;Leu C;Liu J;Lundervold AJ;Lundervold A;Martin NG;Mather K;Mathias SR;McCormack M;McMahon KL;McRae A;Milaneschi Y;Moreau C;Morris D;Mothersill D;Mühleisen TW;Murray R;Nordvik JE;Nyberg L;Olde Loohuis LM;Ophoff R;Paus T;Pausova Z;Penninx B;Peralta JM;Pike B;Prieto C;Pudas S;Quinlan E;Quintana DS;Reinbold CS;Marques TR;Reymond A;Richard G;Rodriguez-Herreros B;Roiz-Santiañez R;Rokicki J;Rucker J;Sachdev P;Sanders AM;Sando SB;Schmaal L;Schofield PR;Schork AJ;Schumann G;Shin J;Shumskaya E;Sisodiya S;Steen VM;Stein DJ;Steinberg S;Strike L;Teumer A;Thalamuthu A;Tordesillas-Gutierrez D;Turner J;Ueland T;Uhlmann A;Ulfarsson MO;van 't Ent D;van der Meer D;van Haren NEM;Vaskinn A;Vassos E;Walters GB;Wang Y;Wen W;Whelan CD;Wittfeld K;Wright M;Yamamori H;Zayats T;Agartz I;Westlye LT;Jacquemont S;Djurovic S;Stefánsson H;Stefánsson K;Thompson P;Andreassen OA; ; (2020) 'Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia'. Molecular Psychiatry, 25 (3) [DOI] [Details]
(2020) 'Genes regulated byBCL11Bduring T-cell development are enriched for de novo mutations found in schizophrenia patients'
Fahey, L;Donohoe, G;Broin, PO;Morris, DW (2020) 'Genes regulated byBCL11Bduring T-cell development are enriched for de novo mutations found in schizophrenia patients'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, [DOI] [Details]
(2020) 'Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study'
Foley C;Heron EA;Harold D;Walters J;Owen M;O'Donovan M;Sebat J;Kelleher E;Mooney C;Durand A;Pinto C;Cormican P;Morris D;Donohoe G;Gill M;Gallagher L;Corvin A; (2020) 'Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study'. British Journal Of Psychiatry, [DOI] [Details]
(2020) 'Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults'
Rokita, KI;Dauvermann, MR;Mothersill, D;Holleran, L;Holland, J;Costello, L;Cullen, C;Kane, R;McKernan, D;Morris, DW;Kelly, J;Gill, M;Corvin, A;Hallahan, B;McDonald, C;Donohoe, G (2020) 'Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults'. Journal of clinical psychology, [DOI] [Details]
(2020) 'Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults'
Rokita, KI,Dauvermann, MR,Mothersill, D,Holleran, L,Holland, J,Costello, L,Cullen, C,Kane, R,McKernan, D,Morris, DW,Kelly, J,Gill, M,Corvin, A,Hallahan, B,McDonald, C,Donohoe, G (2020) 'Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults'. Journal of clinical psychology, [DOI] [Details]
(2020) 'Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls'
Holland, JF;Cosgrove, D;Whitton, L;Harold, D;Corvin, A;Gill, M;Mothersill, DO;Morris, DW;Donohoe, G (2020) 'Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, [DOI] [Details]
(2020) 'Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls'
Holland, JF,Cosgrove, D,Whitton, L,Harold, D,Corvin, A,Gill, M,Mothersill, DO,Morris, DW,Donohoe, G (2020) 'Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls'. American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, [DOI] [Details]
(2016) 'Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness'
Bigdeli TB;Ripke S;Bacanu SA;Lee SH;Wray NR;Gejman PV;Rietschel M;Cichon S;St Clair D;Corvin A;Kirov G;McQuillin A;Gurling H;Rujescu D;Andreassen OA;Werge T;Blackwood DH;Pato CN;Pato MT;Malhotra AK;O'Donovan MC;Kendler KS;Fanous AH; Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) 'Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 171B (2):276-289 [Details]
(2016) 'Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex'
Guadalupe T;Mathias SR;vanErp TG;Whelan CD;Zwiers MP;Abe Y;Abramovic L;Agartz I;Andreassen OA;Arias-Vásquez A;Aribisala BS;Armstrong NJ;Arolt V;Artiges E;Ayesa-Arriola R;Baboyan VG;Banaschewski T;Barker G;Bastin ME;Baune BT;Blangero J;Bokde AL;Boedhoe PS;Bose A;Brem S;Brodaty H;Bromberg U;Brooks S;Büchel C;Buitelaar J;Calhoun VD;Cannon DM;Cattrell A;Cheng Y;Conrod PJ;Conzelmann A;Corvin A;Crespo-Facorro B;Crivello F;Dannlowski U;de Zubicaray GI;de Zwarte SM;Deary IJ;Desrivières S;Doan NT;Donohoe G;Dørum ES;Ehrlich S;Espeseth T;Fernández G;Flor H;Fouche JP;Frouin V;Fukunaga M;Gallinat J;Garavan H;Gill M;Suarez AG;Gowland P;Grabe HJ;Grotegerd D;Gruber O;Hagenaars S;Hashimoto R;Hauser TU;Heinz A;Hibar DP;Hoekstra PJ;Hoogman M;Howells FM;Hu H;Hulshoff Pol HE;Huyser C;Ittermann B;Jahanshad N;Jönsson EG;Jurk S;Kahn RS;Kelly S;Kraemer B;Kugel H;Kwon JS;Lemaitre H;Lesch KP;Lochner C;Luciano M;Marquand AF;Martin NG;Martínez-Zalacaín I;Martinot JL;Mataix-Cols D;Mather K;McDonald C;McMahon KL;Medland SE;Menchón JM;Morris DW;Mothersill O;Maniega SM;Mwangi B;Nakamae T;Nakao T;Narayanaswaamy JC;Nees F;Nordvik JE;Onnink AM;Opel N;Ophoff R;Paillère Martinot ML;Papadopoulos Orfanos D;Pauli P;Paus T;Poustka L;Reddy JY;Renteria ME;Roiz-Santiáñez R;Roos A;Royle NA;Sachdev P;Sánchez-Juan P;Schmaal L;Schumann G;Shumskaya E;Smolka MN;Soares JC;Soriano-Mas C;Stein DJ;Strike LT;Toro R;Turner JA;Tzourio-Mazoyer N;Uhlmann A;Hernández MV;van den Heuvel OA;van der Meer D;van Haren NE;Veltman DJ;Venkatasubramanian G;Vetter NC;Vuletic D;Walitza S;Walter H;Walton E;Wang Z;Wardlaw J;Wen W;Westlye LT;Whelan R;Wittfeld K;Wolfers T;Wright MJ;Xu J;Xu X;Yun JY;Zhao J;Franke B;Thompson PM;Glahn DC;Mazoyer B;Fisher SE;Francks C (2016) 'Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex'. Brain Imaging And Behavior, [Details]
(2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'
McCarthy-Jones S;Smailes D;Corvin A;Gill M;Morris DW;Dinan TG;Murphy KC;Anthony O Neill F;Waddington JL;Australian Schizophrenia Research Bank;Donohoe G;Dudley R (2017) 'Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders'. Psychiatry Research, 252 :154-160 [DOI] [Details]
(2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'
Mothersill O;Tangney N;Morris DW;McCarthy H;Frodl T;Gill M;Corvin A;Donohoe G (2017) 'Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia'. Schizophrenia Research, 184 :52-58 [DOI] [Details]
(2015) 'MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia'
Patel VS;Kelly S;Wright C;Gupta CN;Arias-Vasquez A;Perrone-Bizzozero N;Ehrlich S;Wang L;Bustillo JR;Morris D;Corvin A;Cannon DM;McDonald C;Donohoe G;Calhoun VD;Turner JA; (2015) 'MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia'. Neuroscience Letters, 602 :44-49 [DOI] [Details]
(2015) 'New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis'
Lee SH, Byrne EM, Hultman CM, Kähler A, Vinkhuyzen AA, Ripke S, Andreassen OA, Frisell T, Gusev A, Hu X, Karlsson R, Mantzioris VX, McGrath JJ, Mehta D, Stahl EA, Zhao Q, Kendler KS, Sullivan PF, Price AL, O'Donovan M, Okada Y, Mowry BJ, Raychaudhuri S, Wray NR; Schizophrenia Working Group of the Psychiatric Genomics Consortium and Rheumatoid Arthritis Consortium International; Schizophrenia Working Group of the Psychiatric Genomics Consortium authors, Byerley W, Cahn W, Cantor RM, Cichon S, Cormican P, Curtis D, Djurovic S, Escott-Price V, Gejman PV, Georgieva L, Giegling I, Hansen TF, Ingason A, Kim Y, Konte B, Lee PH, McIntosh A, McQuillin A, Morris DW, Nöthen MM, O'Dushlaine C, Olincy A, Olsen L, Pato CN, Pato MT, Pickard BS, Posthuma D, Rasmussen HB, Rietschel M, Rujescu D, Schulze TG, Silverman JM, Thirumalai S, Werge T; Schizophrenia Working Group of the Psychiatric Genomics Consortium collaborators, Agartz I, Amin F, Azevedo MH, Bass N, Black DW, Blackwood DH, Bruggeman R, Buccola NG, Choudhury K, Cloninger RC, Corvin A, Craddock N, Daly MJ, Datta S, Donohoe GJ, Duan J, Dudbridge F, Fanous A, Freedman R, Freimer NB, Friedl M, Gill M, Gurling H, De Haan L, Hamshere ML, Hartmann AM, Holmans PA, Kahn RS, Keller MC, Kenny E, Kirov GK, Krabbendam L, Krasucki R, Lawrence J, Lencz T, Levinson DF, Lieberman JA, Lin DY, Linszen DH, Magnusson PK, Maier W, Malhotra AK, Mattheisen M, Mattingsdal M, McCarroll SA, Medeiros H, Melle I, Milanova V, Myin-Germeys I, Neale BM, Ophoff RA, Owen MJ, Pimm J, Purcell SM, Puri V, Quested DJ, Rossin L, Ruderfer D, Sanders AR, Shi J, Sklar P, St Clair D, Scott Stroup T, Van Os J, Visscher PM, Wiersma D, Zammit S; Rheumatoid Arthritis Consortium International authors, Louis Bridges S Jr, Choi HK, Coenen MJ, de Vries N, Dieud P, Greenberg JD, Huizinga TW, Padyukov L, Siminovitch KA, Tak PP, Worthington J; Rheumatoid Arthritis Consortium International collaborators, De Jager PL, Denny JC, Gregersen PK, Klareskog L, Mariette X, Plenge RM, van Laar M, van Riel P. (2015) 'New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis'. International Journal Of Epidemiology, [Details]
(2015) 'Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis'
Bowes, J,Budu-Aggrey, A,Huffmeier, U,Uebe, S,Steel, K,Hebert, HL,Wallace, C,Massey, J,Bruce, IN,Bluett, J,Feletar, M,Morgan, AW,Marzo-Ortega, H,Donohoe, G,Morris, DW,Helliwell, P,Ryan, AW,Kane, D,Warren, RB,Korendowych, E,Alenius, GM,Giardina, E,Packham, J,McManus, R,FitzGerald, O,McHugh, N,Brown, MA,Ho, P,Behrens, F,Burkhardt, H,Reis, A,Barton, A (2015) 'Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis'. Nature Communications, 6 [DOI] [Details]
(2015) 'Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms'
Baurecht, H,Hotze, M,Brand, S,Buning, C,Cormican, P,Corvin, A,Ellinghaus, D,Ellinghaus, E,Esparza-Gordillo, J,Folster-Holst, R,Franke, A,Gieger, C,Hubner, N,Illig, T,Irvine, AD,Kabesch, M,Lee, YAE,Lieb, W,Marenholz, I,McLean, WHI,Morris, DW,Mrowietz, U,Nair, R,Nothen, MM,Novak, N,O'Regan, GM,Schreiber, S,Smith, C,Strauch, K,Stuart, PE,Trembath, R,Tsoi, LC,Weichenthal, M,Barker, J,Elder, JT,Weidinger, S,Cordell, HJ,Brown, SJ,PAGE Consortium (2015) 'Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms'. American Journal Of Human Genetics, 96 :104-120 [DOI] [Details]
(2015) 'Common genetic variants influence human subcortical brain structures'
Hibar DP;Stein JL;Renteria ME;Arias-Vasquez A;Desrivières S;Jahanshad N;Toro R;Wittfeld K;Abramovic L;Andersson M;Aribisala BS;Armstrong NJ;Bernard M;Bohlken MM;Boks MP;Bralten J;Brown AA;Chakravarty MM;Chen Q;Ching CR;Cuellar-Partida G;den Braber A;Giddaluru S;Goldman AL;Grimm O;Guadalupe T;Hass J;Woldehawariat G;Holmes AJ;Hoogman M;Janowitz D;Jia T;Kim S;Klein M;Kraemer B;Lee PH;Olde Loohuis LM;Luciano M;Macare C;Mather KA;Mattheisen M;Milaneschi Y;Nho K;Papmeyer M;Ramasamy A;Risacher SL;Roiz-Santiañez R;Rose EJ;Salami A;Sämann PG;Schmaal L;Schork AJ;Shin J;Strike LT;Teumer A;van Donkelaar MM;van Eijk KR;Walters RK;Westlye LT;Whelan CD;Winkler AM;Zwiers MP;Alhusaini S;Athanasiu L;Ehrlich S;Hakobjan MM;Hartberg CB;Haukvik UK;Heister AJ;Hoehn D;Kasperaviciute D;Liewald DC;Lopez LM;Makkinje RR;Matarin M;Naber MA;McKay DR;Needham M;Nugent AC;Pütz B;Royle NA;Shen L;Sprooten E;Trabzuni D;van der Marel SS;van Hulzen KJ;Walton E;Wolf C;Almasy L;Ames D;Arepalli S;Assareh AA;Bastin ME;Brodaty H;Bulayeva KB;Carless MA;Cichon S;Corvin A;Curran JE;Czisch M;de Zubicaray GI;Dillman A;Duggirala R;Dyer TD;Erk S;Fedko IO;Ferrucci L;Foroud TM;Fox PT;Fukunaga M;Gibbs JR;Göring HH;Green RC;Guelfi S;Hansell NK;Hartman CA;Hegenscheid K;Heinz A;Hernandez DG;Heslenfeld DJ;Hoekstra PJ;Holsboer F;Homuth G;Hottenga JJ;Ikeda M;Jack CR;Jenkinson M;Johnson R;Kanai R;Keil M;Kent JW;Kochunov P;Kwok JB;Lawrie SM;Liu X;Longo DL;McMahon KL;Meisenzahl E;Melle I;Mohnke S;Montgomery GW;Mostert JC;Mühleisen TW;Nalls MA;Nichols TE;Nilsson LG;Nöthen MM;Ohi K;Olvera RL;Perez-Iglesias R;Pike GB;Potkin SG;Reinvang I;Reppermund S;Rietschel M;Romanczuk-Seiferth N;Rosen GD;Rujescu D;Schnell K;Schofield PR;Smith C;Steen VM;Sussmann JE;Thalamuthu A;Toga AW;Traynor BJ;Troncoso J;Turner JA;Valdés Hernández MC;van 't Ent D;van der Brug M;van der Wee NJ;van Tol MJ;Veltman DJ;Wassink TH;Westman E;Zielke RH;Zonderman AB;Ashbrook DG;Hager R;Lu L;McMahon FJ;Morris DW;Williams RW;Brunner HG;Buckner RL;Buitelaar JK;Cahn W;Calhoun VD;Cavalleri GL;Crespo-Facorro B;Dale AM;Davies GE;Delanty N;Depondt C;Djurovic S;Drevets WC;Espeseth T;Gollub RL;Ho BC;Hoffmann W;Hosten N;Kahn RS;Le Hellard S;Meyer-Lindenberg A;Müller-Myhsok B;Nauck M;Nyberg L;Pandolfo M;Penninx BW;Roffman JL;Sisodiya SM;Smoller JW;van Bokhoven H;van Haren NE;Völzke H;Walter H;Weiner MW;Wen W;White T;Agartz I;Andreassen OA;Blangero J;Boomsma DI;Brouwer RM;Cannon DM;Cookson MR;de Geus EJ;Deary IJ;Donohoe G;Fernández G;Fisher SE;Francks C;Glahn DC;Grabe HJ;Gruber O;Hardy J;Hashimoto R;Hulshoff Pol HE;Jönsson EG;Kloszewska I;Lovestone S;Mattay VS;Mecocci P;McDonald C;McIntosh AM;Ophoff RA;Paus T;Pausova Z;Ryten M;Sachdev PS;Saykin AJ;Simmons A;Singleton A;Soininen H;Wardlaw JM;Weale ME;Weinberger DR;Adams HH;Launer LJ;Seiler S;Schmidt R;Chauhan G;Satizabal CL;Becker JT;Yanek L;van der Lee SJ;Ebling M;Fischl B;Longstreth WT;Greve D;Schmidt H;Nyquist P;Vinke LN;van Duijn CM;Xue L;Mazoyer B;Bis JC;Gudnason V;Seshadri S;Ikram MA; ; ; ; ; ;Martin NG;Wright MJ;Schumann G;Franke B;Thompson PM;Medland SE; (2015) 'Common genetic variants influence human subcortical brain structures'. Nature, 520 (7546):224-229 [DOI] [Details]
(2015) 'BDNF Val66Met polymorphism in patterns of neural activation in individuals with MDD and healthy controls'
Lisiecka, DM,O'Hanlon, E,Fagan, AJ,Carballedo, A,Morris, D,Suckling, J,Frodl, T (2015) 'BDNF Val66Met polymorphism in patterns of neural activation in individuals with MDD and healthy controls'. Journal Of Affective Disorders, 184 :239-244 [DOI] [Details]
(2016) 'Novel genetic loci underlying human intracranial volume identified through genome-wide association'
Adams, HHH;Hibar, DP;Chouraki, V;Stein, JL;Nyquist, PA;Renteria, ME;Trompet, S;Arias-Vasquez, A;Seshadri, S;Desrivieres, S;Beecham, AH;Jahanshad, N;Wittfeld, K;Van der Lee, SJ;Abramovic, L;Alhusaini, S;Amin, N;Andersson, M;Arfanakis, K;Aribisala, BS;Armstrong, NJ;Athanasiu, L;Axelsson, T;Beiser, A;Bernard, M;Bis, JC;Blanken, LME;Blanton, SH;Bohlken, MM;Boks, MP;Bralten, J;Brickman, AM;Carmichael, O;Chakravarty, MM;Chauhan, G;Chen, Q;Ching, CRK;Cuellar-Partida, G;Den Braber, A;Doan, NT;Ehrlich, S;Filippi, I;Ge, T;Giddaluru, S;Goldman, AL;Gottesman, RF;Greven, CU;Grimm, O;Griswold, ME;Guadalupe, T;Hass, J;Haukvik, UK;Hilal, S;Hofer, E;Hoehn, D;Holmes, AJ;Hoogman, M;Janowitz, D;Jia, T;Kasperaviciute, D;Kim, S;Klein, M;Kraemer, B;Lee, PH;Liao, J;Liewald, DCM;Lopez, LM;Luciano, M;Macare, C;Marquand, A;Matarin, M;Mather, KA;Mattheisen, M;Mazoyer, B;Mckay, DR;McWhirter, R;Milaneschi, Y;Mirza-Schreiber, N;Muetzel, RL;Maniega, SM;Nho, K;Nugent, AC;Loohuis, LMO;Oosterlaan, J;Papmeyer, M;Pappa, I;Pirpamer, L;Pudas, S;Puetz, B;Rajan, KB;Ramasamy, A;Richards, JS;Risacher, SL;Roiz-Santianez, R;Rommelse, N;Rose, EJ;Royle, NA;Rundek, T;Samann, PG;Satizabal, CL;Schmaal, L;Schork, AJ;Shen, L;Shin, J;Shumskaya, E;Smith, AV;Sprooten, E;Strike, LT;Teumer, A;Thomson, R;Tordesillas-Gutierrez, D;Toro, R;Trabzuni, D;Vaidya, D;Van der Grond, J;Van der Meer, D;Van Donkelaar, MMJ;Van Eijk, KR;Van Erp, TGM;Van Rooij, D;Walton, E;Westlye, LT;Whelan, CD;Windham, BG;Winkler, AM;Woldehawariat, G;Wolf, C;Wolfers, T;Xu, B;Yanek, LR;Yang, JY;Zijdenbos, A;Zwiers, MP;Agartz, I;Aggarwal, NT;Almasy, L;Ames, D;Amouyel, P;Andreassen, OA;Arepalli, S;Assareh, AA;Barral, S;Bastin, ME;Becker, DM;Becker, JT;Bennett, DA;Blangero, J;van Bokhoven, H;Boomsma, DI;Brodaty, H;Brouwer, RM;Brunner, HG;Buckner, RL;Buitelaar, JK;Bulayeva, KB;Cahn, W;Calhoun, VD;Cannon, DM;Cavalleri, GL;Chen, C;Cheng, CY;Cichon, S;Cookson, MR;Corvin, A;Crespo-Facorro, B;Curran, JE;Czisch, M;Dale, AM;Davies, GE;De Geus, EJC;De Jager, PL;de Zubicaray, GI;Delanty, N;Depondt, C;DeStefano, AL;Dillman, A;Djurovic, S;Donohoe, G;Drevets, WC;Duggirala, R;Dyer, TD;Erk, S;Espeseth, T;Evans, DA;Fedko, I;Fernandez, G;Ferrucci, L;Fisher, SE;Fleischman, DA;Ford, I;Foroud, TM;Fox, PT;Francks, C;Fukunaga, M;Gibbs, JR;Glahn, DC;Gollub, RL;Goring, HHH;Grabe, HJ;Green, RC;Gruber, O;Gudnason, V;Guelfi, S;Hansell, NK;Hardy, J;Hartman, CA;Hashimoto, R;Hegenscheid, K;Heinz, A;Le Hellard, S;Hernandez, DG;Heslenfeld, DJ;Ho, BC;Hoekstra, PJ;Hoffmann, W;Hofman, A;Holsboer, F;Homuth, G;Hosten, N;Hottenga, JJ;Pol, HEH;Ikeda, M;Ikram, MK;Jack, CR;Jenldnson, M;Johnson, R;Jonsson, EG;Jukema, JW;Kahn, RS;Kanai, R;Kloszewska, I;Knopman, DS;Kochunov, P;Kwok, JB;Lawrie, SM;Lemaitre, H;Liu, XM;Longo, DL;Longstreth, WT;Lopez, OL;Lovestone, S;Martinez, O;Martinot, JL;Mattay, VS;McDonald, C;McIntosh, AM;McMahon, KL;McMahon, FJ;Mecocci, P;Melle, I;Meyer-Lindenberg, A;Mohnke, S;Montgomery, GW;Morris, DW;Mosley, TH;Muhleisen, TW;Muller-Myhsok, B;Nalls, MA;Nauck, M;Nichols, TE;Niessen, WJ;Nothen, MM;Nyberg, L;Ohi, K;Olvera, RL;Ophoff, RA;Pandolfo, M;Paus, T;Pausova, Z;Penninx, BWJH;Pike, GB;Potkin, SG;Psaty, BM;Reppermund, S;Rietschel, M;Roffman, JL;Romanczuk-Seiferth, N;Rotter, JI;Ryten, M;Sacco, RL;Sachdev, PS;Saykin, AJ;Schmidt, R;Schofield, PR;Sigurdsson, S;Simmons, A;Singleton, A;Sisodiya, SM;Smith, C;Smoller, JW;Soininen, H;Srikanth, V;Steen, VM;Stott, DJ;Sussmann, JE;Thalamuthu, A;Tiemeier, H;Toga, AW;Traynor, BJ;Troncoso, J;Turner, JA;Tzourio, C;Uitterlinden, AG;Hernandez, MCV;Van der Brug, M;Van der Lugt, A;Van der Wee, NJA;Van Duijn, CM;Van Haren, NEM;Van't Ent, D;Van Tol, MJ;Vardarajan, BN;Veltman, DJ;Vernooij, MW;Volzke, H;Walter, H;Wardlaw, JM;Wassink, TH;Weale, ME;Weinberger, DR;Weiner, MW;Wen, W;Westman, E;White, T;Wong, TY;Wright, CB;Zielke, HR;Zonderman, AB;Deary, IJ;DeCarli, C;Schmidt, H;Martin, NG;De Craen, AJM;Wright, MJ;Launer, LJ;Schumann, G;Fornage, M;Franke, B;Debette, S;Medland, SE;Ikram, MA;Thompson, PM (2016) 'Novel genetic loci underlying human intracranial volume identified through genome-wide association'. Nature Neuroscience, 19 :1569-1582 [DOI] [Details]
(2016) 'Cognitive Analysis of Schizophrenia Risk Genes That Function as Epigenetic Regulators of Gene Expression'
Whitton, L;Cosgrove, D;Clarkson, C;Harold, D;Kendall, K;Richards, A;Mantripragada, K;Owen, MJ;O'Donovan, MC;Walters, J;Hartmann, A;Konte, B;Rujescu, D;Gill, M;Corvin, A;Rea, S;Donohoe, G;Morris, DW (2016) 'Cognitive Analysis of Schizophrenia Risk Genes That Function as Epigenetic Regulators of Gene Expression'. American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics, 171 :1170-1179 [DOI] [ARAN Link] [Details]
(2016) 'Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium'
van Erp TG;Hibar DP;Rasmussen JM;Glahn DC;Pearlson GD;Andreassen OA;Agartz I;Westlye LT;Haukvik UK;Dale AM;Melle I;Hartberg CB;Gruber O;Kraemer B;Zilles D;Donohoe G;Kelly S;McDonald C;Morris DW;Cannon DM;Corvin A;Machielsen MW;Koenders L;de Haan L;Veltman DJ;Satterthwaite TD;Wolf DH;Gur RC;Gur RE;Potkin SG;Mathalon DH;Mueller BA;Preda A;Macciardi F;Ehrlich S;Walton E;Hass J;Calhoun VD;Bockholt HJ;Sponheim SR;Shoemaker JM;van Haren NE;Pol HE;Ophoff RA;Kahn RS;Roiz-Santiañez R;Crespo-Facorro B;Wang L;Alpert KI;Jönsson EG;Dimitrova R;Bois C;Whalley HC;McIntosh AM;Lawrie SM;Hashimoto R;Thompson PM;Turner JA; (2016) 'Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium'. Molecular Psychiatry, 21 (4):547-553 [DOI] [Details]
(2016) 'Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci'
Coleman, C,Quinn, EM,Ryan, AW,Conroy, J,Trimble, V,Mahmud, N,Kennedy, N,Corvin, AP,Morris, DW,Donohoe, G,O'Morain, C,MacMathuna, P,Byrnes, V,Kiat, C,Trynka, G,Wijmenga, C,Kelleher, D,Ennis, S,Anney, RJL,McManus, R (2016) 'Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci'. European Journal Of Human Genetics, 24 :291-297 [DOI] [Details]
(2016) 'Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women'
Mehta D, Tropf FC, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson PK, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, Visscher PM, McGrath JJ, Mills MC, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium, LifeLines Cohort Study, and TwinsUK, Andreassen OA, Bramon E, Bruggeman R, Buxbaum JD, Cairns MJ, Cantor RM, Cloninger CR, Cohen D, Crespo-Facorro B, Darvasi A, DeLisi LE, Dinan T, Djurovic S, Donohoe G, Drapeau E, Escott-Price V, Freimer NB, Georgieva L, de Haan L, Henskens FA, Joa I, Julià A, Khrunin A, Lerer B, Limborska S, Loughland CM, Macek M Jr, Magnusson PK, Marsal S, McCarley RW, McIntosh AM, McQuillin A, Melegh B, Michie PT, Morris DW, Murphy KC, Myin-Germeys I, Olincy A, Van Os J, Pantelis C, Posthuma D, Quested D, Schall U, Scott RJ, Seidman LJ, Toncheva D, Tooney PA, Waddington J, Weinberger DR, Weiser M, Wu JQ. (2016) 'Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women'. Jama Psychiatry, [Details]
(2015) 'DNA methylation of the serotonin transporter gene in peripheral cells and stress-related changes in hippocampal volume: a study in depressed patients and healthy controls'
Booij L, Szyf M, Carballedo A, Frey EM, Morris D, Dymov S, Vaisheva F, Ly V, Fahey C, Meaney J, Gill M, Frodl T (2015) 'DNA methylation of the serotonin transporter gene in peripheral cells and stress-related changes in hippocampal volume: a study in depressed patients and healthy controls'. Plos One, 10 (3) [DOI] [Details]
(2015) 'Translation of 5' leaders is pervasive in genes resistant to eIF2 repression'
Andreev DE, O'Connor PB, Fahey C, Kenny EM, Terenin IM, Dmitriev SE, Cormican P, Morris DW, Shatsky IN, Baranov PV (2015) 'Translation of 5' leaders is pervasive in genes resistant to eIF2 repression'. eLife, 4 [DOI] [Details]
(2015) 'DNA methylation of the serotonin transporter gene (SLC6A4) is associated with brain function involved in processing emotional stimuli'
Frodl T, Szyf M, Carballedo A, Ly V, Dymov S, Vaisheva F, Morris D, Fahey C, Meaney J, Gill M, Booij L (2015) 'DNA methylation of the serotonin transporter gene (SLC6A4) is associated with brain function involved in processing emotional stimuli'. Journal Of Psychiatry & Neuroscience, 40 (2) [Details]
(2014) 'An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis'
Morris, D. W.,Pearson, R. D.,Cormican, P.,Kenny, E. M.,O'Dushlaine, C. T.,Perreault, L. P.,Giannoulatou, E.,Tropea, D.,Maher, B. S.,Wormley, B.,Kelleher, E.,Fahey, C.,Molinos, I.,Bellini, S.,Pirinen, M.,Strange, A.,Freeman, C.,Thiselton, D. L.,Elves, R. L.,Regan, R.,Ennis, S.,Dinan, T. G.,McDonald, C.,Murphy, K. C.,O'Callaghan, E.,Waddington, J. L.,Walsh, D.,O'Donovan, M.,Grozeva, D.,Craddock, N.,Stone, J.,Scolnick, E.,Purcell, S.,Sklar, P.,Coe, B.,Eichler, E. E.,Ophoff, R.,Buizer, J.,Szatkiewicz, J.,Hultman, C.,Sullivan, P.,Gurling, H.,McQuillin, A.,St Clair, D.,Rees, E.,Kirov, G.,Walters, J.,Blackwood, D.,Johnstone, M.,Donohoe, G.,O'Neill, F. A.,Kendler, K. S.,Gill, M.,Riley, B. P.,Spencer, C. C.,Corvin, A. (2014) 'An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis'. Hum Mol Genet, 23 (1212):3316-26 [ARAN Link] [Details]
(2014) 'Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants'
Kelly, S.,Morris, D. W.,Mothersill, O.,Rose, E. J.,Fahey, C.,O'Brien, C.,O'Hanlon, E.,Gill, M.,Corvin, A. P.,Donohoe, G. (2014) 'Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants'. Neurosci Lett, 574 :6-10 [Details]
(2014) 'De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability'
McCarthy, S. E.,Gillis, J.,Kramer, M.,Lihm, J.,Yoon, S.,Berstein, Y.,Mistry, M.,Pavlidis, P.,Solomon, R.,Ghiban, E.,Antoniou, E.,Kelleher, E.,O'Brien, C.,Donohoe, G.,Gill, M.,Morris, D. W.,McCombie, W. R.,Corvin, A. (2014) 'De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability'. Mol Psychiatry, 19 (66):652-8 [Details]
(2014) 'Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene'
Luo, X. J.,Li, M.,Huang, L.,Steinberg, S.,Mattheisen, M.,Liang, G.,Donohoe, G.,Shi, Y.,Chen, C.,Yue, W.,Alkelai, A.,Lerer, B.,Li, Z.,Yi, Q.,Rietschel, M.,Cichon, S.,Collier, D. A.,Tosato, S.,Suvisaari, J.,Rujescu, D.,Golimbet, V.,Silagadze, T.,Durmishi, N.,Milovancevic, M. P.,Stefansson, H.,Schulze, T. G.,Nothen, M. M.,Lyne, R.,Morris, D. W.,Gill, M.,Corvin, A.,Zhang, D.,Dong, Q.,Moyzis, R. K.,Stefansson, K.,Sigurdsson, E.,Hu, F.,Su, B.,Gan, L. (2014) 'Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene'. Mol Psychiatry, 19 (77):774-83 [Details]
(2014) 'The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data'
Thompson, P. M.,Stein, J. L.,Medland, S. E.,Hibar, D. P.,Vasquez, A. A.,Renteria, M. E.,Toro, R.,Jahanshad, N.,Schumann, G.,Franke, B.,Wright, M. J.,Martin, N. G.,Agartz, I.,Alda, M.,Alhusaini, S.,Almasy, L.,Almeida, J.,Alpert, K.,Andreasen, N. C.,Andreassen, O. A.,Apostolova, L. G.,Appel, K.,Armstrong, N. J.,Aribisala, B.,Bastin, M. E.,Bauer, M.,Bearden, C. E.,Bergmann, O.,Binder, E. B.,Blangero, J.,Bockholt, H. J.,Boen, E.,Bois, C.,Boomsma, D. I.,Booth, T.,Bowman, I. J.,Bralten, J.,Brouwer, R. M.,Brunner, H. G.,Brohawn, D. G.,Buckner, R. L.,Buitelaar, J.,Bulayeva, K.,Bustillo, J. R.,Calhoun, V. D.,Cannon, D. M.,Cantor, R. M.,Carless, M. A.,Caseras, X.,Cavalleri, G. L.,Chakravarty, M. M.,Chang, K. D.,Ching, C. R.,Christoforou, A.,Cichon, S.,Clark, V. P.,Conrod, P.,Coppola, G.,Crespo-Facor (2014) 'The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data'. Brain Imaging Behav, 8 (22):153-82 [Details]
(2014) 'Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)'
Lencz, T.,Knowles, E.,Davies, G.,Guha, S.,Liewald, D. C.,Starr, J. M.,Djurovic, S.,Melle, I.,Sundet, K.,Christoforou, A.,Reinvang, I.,Mukherjee, S.,DeRosse, P.,Lundervold, A.,Steen, V. M.,John, M.,Espeseth, T.,Raikkonen, K.,Widen, E.,Palotie, A.,Eriksson, J. G.,Giegling, I.,Konte, B.,Ikeda, M.,Roussos, P.,Giakoumaki, S.,Burdick, K. E.,Payton, A.,Ollier, W.,Horan, M.,Donohoe, G.,Morris, D.,Corvin, A.,Gill, M.,Pendleton, N.,Iwata, N.,Darvasi, A.,Bitsios, P.,Rujescu, D.,Lahti, J.,Hellard, S. L.,Keller, M. C.,Andreassen, O. A.,Deary, I. J.,Glahn, D. C.,Malhotra, A. K. (2014) 'Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)'. Mol Psychiatry, 19 (22):168-74 [Details]
(2014) 'Common variant at 16p11.2 conferring risk of psychosis'
Steinberg, S.,de Jong, S.,Mattheisen, M.,Costas, J.,Demontis, D.,Jamain, S.,Pietilainen, O. P.,Lin, K.,Papiol, S.,Huttenlocher, J.,Sigurdsson, E.,Vassos, E.,Giegling, I.,Breuer, R.,Fraser, G.,Walker, N.,Melle, I.,Djurovic, S.,Agartz, I.,Tuulio-Henriksson, A.,Suvisaari, J.,Lonnqvist, J.,Paunio, T.,Olsen, L.,Hansen, T.,Ingason, A.,Pirinen, M.,Strengman, E.,Hougaard, D. M.,Orntoft, T.,Didriksen, M.,Hollegaard, M. V.,Nordentoft, M.,Abramova, L.,Kaleda, V.,Arrojo, M.,Sanjuan, J.,Arango, C.,Etain, B.,Bellivier, F.,Meary, A.,Schurhoff, F.,Szoke, A.,Ribolsi, M.,Magni, V.,Siracusano, A.,Sperling, S.,Rossner, M.,Christiansen, C.,Kiemeney, L. A.,Franke, B.,van den Berg, L. H.,Veldink, J.,Curran, S.,Bolton, P.,Poot, M.,Staal, W.,Rehnstrom, K.,Kilpinen, H.,Freitag, C. M.,Meyer, J.,Magnusson, P.,Saemund (2014) 'Common variant at 16p11.2 conferring risk of psychosis'. Mol Psychiatry, 19 (11):108-14 [Details]
(2014) 'Evidence that duplications of 22q11.2 protect against schizophrenia'
Rees, E.,Kirov, G.,Sanders, A.,Walters, J. T.,Chambert, K. D.,Shi, J.,Szatkiewicz, J.,O'Dushlaine, C.,Richards, A. L.,Green, E. K.,Jones, I.,Davies, G.,Legge, S. E.,Moran, J. L.,Pato, C.,Pato, M.,Genovese, G.,Levinson, D.,Duan, J.,Moy, W.,Goring, H. H.,Morris, D.,Cormican, P.,Kendler, K. S.,O'Neill, F. A.,Riley, B.,Gill, M.,Corvin, A.,Craddock, N.,Sklar, P.,Hultman, C.,Sullivan, P. F.,Gejman, P. V.,McCarroll, S. A.,O'Donovan, M. C.,Owen, M. J. (2014) 'Evidence that duplications of 22q11.2 protect against schizophrenia'. Mol Psychiatry, 19 (11):37-40 [Details]
(2014) 'Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci'
Andreassen, O. A.,Harbo, H. F.,Wang, Y.,Thompson, W. K.,Schork, A. J.,Mattingsdal, M.,Zuber, V.,Bettella, F.,Ripke, S.,Kelsoe, J. R.,Kendler, K. S.,O'Donovan, M. C.,Sklar, P.,McEvoy, L. K.,Desikan, R. S.,Lie, B. A.,Djurovic, S.,Dale, A. M. (2014) 'Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci'. Mol Psychiatry, [Details]
(2014) 'Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style'
Rose, E. J.,Hargreaves, A.,Morris, D.,Fahey, C.,Tropea, D.,Cummings, E.,Caltagirone, C.,Bossu, P.,Chiapponi, C.,Piras, F.,Spalletta, G.,Gill, M.,Corvin, A.,Donohoe, G. (2014) 'Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style'. Br J Psychiatry, 204 (22):115-21 [Details]
(2014) 'Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways'
Rolfe, R. A.,Nowlan, N. C.,Kenny, E. M.,Cormican, P.,Morris, D. W.,Prendergast, P. J.,Kelly, D.,Murphy, P. (2014) 'Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways'. BMC Genomics, 15 [Details]
(2014) 'The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals'
Rose EJ, Morris DW, Fahey C, Cannon D, McDonald C, Scanlon C, Kelly S, Gill M, Corvin A, Donohoe G (2014) 'The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals'. Journal Of Medical Genetics, 165 (6):467-471 [DOI] [Details]
(2014) 'Genome-wide association studies: findings at the major histocompatibility complex locus in psychosis'
Corvin, A.,Morris, D. W. (2014) 'Genome-wide association studies: findings at the major histocompatibility complex locus in psychosis'. Biol Psychiatry, 75 (44):276-83 [Details]
(2014) 'CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1'
Rees, E.,Walters, J. T.,Chambert, K. D.,O'Dushlaine, C.,Szatkiewicz, J.,Richards, A. L.,Georgieva, L.,Mahoney-Davies, G.,Legge, S. E.,Moran, J. L.,Genovese, G.,Levinson, D.,Morris, D. W.,Cormican, P.,Kendler, K. S.,O'Neill, F. A.,Riley, B.,Gill, M.,Corvin, A.,Sklar, P.,Hultman, C.,Pato, C.,Pato, M.,Sullivan, P. F.,Gejman, P. V.,McCarroll, S. A.,O'Donovan, M. C.,Owen, M. J.,Kirov, G. (2014) 'CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1'. Hum Mol Genet, 23 (66):1669-76 [Details]
(2014) 'Effects of MIR137 on fronto-amygdala functional connectivity'
Mothersill, O.,Morris, D. W.,Kelly, S.,Rose, E. J.,Fahey, C.,O'Brien, C.,Lyne, R.,Reilly, R.,Gill, M.,Corvin, A. P.,Donohoe, G. (2014) 'Effects of MIR137 on fronto-amygdala functional connectivity'. Neuroimage, 90 :189-95 [Details]
(2014) 'Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway'
Nicodemus, K. K.,Hargreaves, A.,Morris, D.,Anney, R.,Gill, M.,Corvin, A.,Donohoe, G. (2014) 'Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway'. JAMA Psychiatry, 71 (77):778-85 [Details]
(2014) 'Effects of ZNF804A on auditory P300 response in schizophrenia'
O'Donoghue, T.,Morris, D. W.,Fahey, C.,Da Costa, A.,Moore, S.,Cummings, E.,Leicht, G.,Karch, S.,Hoerold, D.,Tropea, D.,Foxe, J. J.,Gill, M.,Corvin, A.,Donohoe, G. (2014) 'Effects of ZNF804A on auditory P300 response in schizophrenia'. Transl Psychiatry, 4 [Details]
(2014) 'Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample'
Fahey, C.,Byrne, S.,McLaughlin, R.,Kenna, K.,Shatunov, A.,Donohoe, G.,Gill, M.,Al-Chalabi, A.,Bradley, D. G.,Hardiman, O.,Corvin, A. P.,Morris, D. W. (2014) 'Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample'. Neurobiol Aging, 35 (66) [Details]
(2014) 'Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders'
Kenny, E. M.,Cormican, P.,Furlong, S.,Heron, E.,Kenny, G.,Fahey, C.,Kelleher, E.,Ennis, S.,Tropea, D.,Anney, R.,Corvin, A. P.,Donohoe, G.,Gallagher, L.,Gill, M.,Morris, D. W. (2014) 'Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders'. Mol Psychiatry, 19 (88):872-9 [ARAN Link] [Details]
(2014) 'Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients'
Mothersill, O.,Morris, D. W.,Kelly, S.,Rose, E. J.,Bokde, A.,Reilly, R.,Gill, M.,Corvin, A. P.,Donohoe, G. (2014) 'Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients'. Schizophr Res, 157 (1-31-3):225-30 [Details]
(2014) 'Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility'
Li, M.,Luo, X. J.,Rietschel, M.,Lewis, C. M.,Mattheisen, M.,Muller-Myhsok, B.,Jamain, S.,Leboyer, M.,Landen, M.,Thompson, P. M.,Cichon, S.,Nothen, M. M.,Schulze, T. G.,Sullivan, P. F.,Bergen, S. E.,Donohoe, G.,Morris, D. W.,Hargreaves, A.,Gill, M.,Corvin, A.,Hultman, C.,Toga, A. W.,Shi, L.,Lin, Q.,Shi, H.,Gan, L.,Meyer-Lindenberg, A.,Czamara, D.,Henry, C.,Etain, B.,Bis, J. C.,Ikram, M. A.,Fornage, M.,Debette, S.,Launer, L. J.,Seshadri, S.,Erk, S.,Walter, H.,Heinz, A.,Bellivier, F.,Stein, J. L.,Medland, S. E.,Arias Vasquez, A.,Hibar, D. P.,Franke, B.,Martin, N. G.,Wright, M. J.,Su, B. (2014) 'Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility'. Mol Psychiatry, 19 (44):452-61 [Details]
(2014) 'No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset'
Heron, E. A.,Cormican, P.,Donohoe, G.,O'Neill, F. A.,Kendler, K. S.,Riley, B. P.,Gill, M.,Corvin, A. P.,Morris, D. W. (2014) 'No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset'. Schizophr Res, 154 (1-31-3):79-82 [Details]
(2013) 'Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs'
Lee, S. H., S. Ripke, et al. (2013) 'Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs'. Nature Genetics, 45 (9):984-994 [Details]
(2013) 'Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing'
Kenna, K. P.,McLaughlin, R. L.,Byrne, S.,Elamin, M.,Heverin, M.,Kenny, E. M.,Cormican, P.,Morris, D. W.,Donaghy, C. G.,Bradley, D. G.,Hardiman, O. (2013) 'Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing'. J Med Genet, 50 (1111):776-83 [Details]
(2013) 'The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up'
Walters, J. T.,Rujescu, D.,Franke, B.,Giegling, I.,Vasquez, A. A.,Hargreaves, A.,Russo, G.,Morris, D. W.,Hoogman, M.,Da Costa, A.,Moskvina, V.,Fernandez, G.,Gill, M.,Corvin, A.,O'Donovan, M. C.,Donohoe, G.,Owen, M. J. (2013) 'The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up'. Am J Psychiatry, 170 (88):877-85 [Details]
(2013) 'Schizophrenia genetic variants are not associated with intelligence'
van Scheltinga, A. F.,Bakker, S. C.,van Haren, N. E.,Derks, E. M.,Buizer-Voskamp, J. E.,Cahn, W.,Ripke, S.,Ophoff, R. A.,Kahn, R. S. (2013) 'Schizophrenia genetic variants are not associated with intelligence'. Psychol Med, 43 (1212):2563-70 [Details]
(2013) 'Genetic schizophrenia risk variants jointly modulate total brain and white matter volume'
Terwisscha van Scheltinga, A. F.,Bakker, S. C.,van Haren, N. E.,Derks, E. M.,Buizer-Voskamp, J. E.,Boos, H. B.,Cahn, W.,Hulshoff Pol, H. E.,Ripke, S.,Ophoff, R. A.,Kahn, R. S. (2013) 'Genetic schizophrenia risk variants jointly modulate total brain and white matter volume'. Biol Psychiatry, 73 (66):525-31 [Details]
(2013) 'All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs'
Schork, A. J.,Thompson, W. K.,Pham, P.,Torkamani, A.,Roddey, J. C.,Sullivan, P. F.,Kelsoe, J. R.,O'Donovan, M. C.,Furberg, H.,Schork, N. J.,Andreassen, O. A.,Dale, A. M. (2013) 'All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs'. PLoS Genet, 9 (44) [Details]
(2013) 'Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253'
Rose, E. J.,Morris, D. W.,Hargreaves, A.,Fahey, C.,Greene, C.,Garavan, H.,Gill, M.,Corvin, A.,Donohoe, G. (2013) 'Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253'. Am J Med Genet B Neuropsychiatr Genet, 162B (66):530-7 [Details]
(2013) 'Social dysfunction in schizophrenia: an investigation of the GAF scale's sensitivity to deficits in social cognition'
Robertson, D. A.,Hargreaves, A.,Kelleher, E. B.,Morris, D.,Gill, M.,Corvin, A.,Donohoe, G. (2013) 'Social dysfunction in schizophrenia: an investigation of the GAF scale's sensitivity to deficits in social cognition'. Schizophr Res, 146 (1-31-3):363-5 [Details]
(2013) 'Genome-wide association analysis identifies 13 new risk loci for schizophrenia'
Ripke, S.,O'Dushlaine, C.,Chambert, K.,Moran, J. L.,Kahler, A. K.,Akterin, S.,Bergen, S. E.,Collins, A. L.,Crowley, J. J.,Fromer, M.,Kim, Y.,Lee, S. H.,Magnusson, P. K.,Sanchez, N.,Stahl, E. A.,Williams, S.,Wray, N. R.,Xia, K.,Bettella, F.,Borglum, A. D.,Bulik-Sullivan, B. K.,Cormican, P.,Craddock, N.,de Leeuw, C.,Durmishi, N.,Gill, M.,Golimbet, V.,Hamshere, M. L.,Holmans, P.,Hougaard, D. M.,Kendler, K. S.,Lin, K.,Morris, D. W.,Mors, O.,Mortensen, P. B.,Neale, B. M.,O'Neill, F. A.,Owen, M. J.,Milovancevic, M. P.,Posthuma, D.,Powell, J.,Richards, A. L.,Riley, B. P.,Ruderfer, D.,Rujescu, D.,Sigurdsson, E.,Silagadze, T.,Smit, A. B.,Stefansson, H.,Steinberg, S.,Suvisaari, J.,Tosato, S.,Verhage, M.,Walters, J. T.,Levinson, D. F.,Gejman, P. V.,Laurent, C.,Mowry, B. J.,O'Donovan, M. C.,Pulver, A. (2013) 'Genome-wide association analysis identifies 13 new risk loci for schizophrenia'. Nat Genet, 45 (1010):1150-9 [Details]
(2013) 'Relationship between the COMT-Val158Met and BDNF-Val66Met polymorphisms, childhood trauma and psychotic experiences in an adolescent general population sample'
Ramsay, H.,Kelleher, I.,Flannery, P.,Clarke, M. C.,Lynch, F.,Harley, M.,Connor, D.,Fitzpatrick, C.,Morris, D. W.,Cannon, M. (2013) 'Relationship between the COMT-Val158Met and BDNF-Val66Met polymorphisms, childhood trauma and psychotic experiences in an adolescent general population sample'. PLoS One, 8 (1111) [Details]
(2013) 'Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data'
Quinn, E. M.,Cormican, P.,Kenny, E. M.,Hill, M.,Anney, R.,Gill, M.,Corvin, A. P.,Morris, D. W. (2013) 'Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data'. PLoS One, 8 (33) [Details]
(2013) 'The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis'
Hargreaves, A.,Anney, R.,O'Dushlaine, C.,Nicodemus, K. K.,Gill, M.,Corvin, A.,Morris, D.,Donohoe, G. (2013) 'The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis'. Psychol Med, :1-11 [Details]
(2013) 'Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC'
Hamshere, M. L.,Walters, J. T.,Smith, R.,Richards, A. L.,Green, E.,Grozeva, D.,Jones, I.,Forty, L.,Jones, L.,Gordon-Smith, K.,Riley, B.,O'Neill, F. A.,Kendler, K. S.,Sklar, P.,Purcell, S.,Kranz, J.,Morris, D.,Gill, M.,Holmans, P.,Craddock, N.,Corvin, A.,Owen, M. J.,O'Donovan, M. C. (2013) 'Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC'. Mol Psychiatry, 18 (66):708-12 [Details]
(2013) 'Implication of a rare deletion at distal 16p11.2 in schizophrenia'
Guha, S.,Rees, E.,Darvasi, A.,Ivanov, D.,Ikeda, M.,Bergen, S. E.,Magnusson, P. K.,Cormican, P.,Morris, D.,Gill, M.,Cichon, S.,Rosenfeld, J. A.,Lee, A.,Gregersen, P. K.,Kane, J. M.,Malhotra, A. K.,Rietschel, M.,Nothen, M. M.,Degenhardt, F.,Priebe, L.,Breuer, R.,Strohmaier, J.,Ruderfer, D. M.,Moran, J. L.,Chambert, K. D.,Sanders, A. R.,Shi, J.,Kendler, K.,Riley, B.,O'Neill, T.,Walsh, D.,Malhotra, D.,Corvin, A.,Purcell, S.,Sklar, P.,Iwata, N.,Hultman, C. M.,Sullivan, P. F.,Sebat, J.,McCarthy, S.,Gejman, P. V.,Levinson, D. F.,Owen, M. J.,O'Donovan, M. C.,Lencz, T.,Kirov, G. (2013) 'Implication of a rare deletion at distal 16p11.2 in schizophrenia'. JAMA Psychiatry, 70 (33):253-60 [Details]
(2013) 'Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253'
Donohoe, G.,Walters, J.,Hargreaves, A.,Rose, E. J.,Morris, D. W.,Fahey, C.,Bellini, S.,Cummins, E.,Giegling, I.,Hartmann, A. M.,Moller, H. J.,Muglia, P.,Owen, M. J.,Gill, M.,O'Donovan, M. C.,Tropea, D.,Rujescu, D.,Corvin, A. (2013) 'Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253'. Genes, Brain And Behaviour, 12 (22):203-9 [Details]
(2013) 'Additive genetic variation in schizophrenia risk is shared by populations of African and European descent'
de Candia, T. R.,Lee, S. H.,Yang, J.,Browning, B. L.,Gejman, P. V.,Levinson, D. F.,Mowry, B. J.,Hewitt, J. K.,Goddard, M. E.,O'Donovan, M. C.,Purcell, S. M.,Posthuma, D.,Visscher, P. M.,Wray, N. R.,Keller, M. C. (2013) 'Additive genetic variation in schizophrenia risk is shared by populations of African and European descent'. Am J Hum Genet, 93 (33):463-70 [Details]
(2013) 'Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137'
Cummings, E.,Donohoe, G.,Hargreaves, A.,Moore, S.,Fahey, C.,Dinan, T. G.,McDonald, C.,O'Callaghan, E.,O'Neill, F. A.,Waddington, J. L.,Murphy, K. C.,Morris, D. W.,Gill, M.,Corvin, A. (2013) 'Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137'. Neurosci Lett, 532 :33-8 [Details]
(2013) 'Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume'
Carballedo, A.,Morris, D.,Zill, P.,Fahey, C.,Reinhold, E.,Meisenzahl, E.,Bondy, B.,Gill, M.,Moller, H. J.,Frodl, T. (2013) 'Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume'. Am J Med Genet B Neuropsychiatr Genet, 162B (22):183-90 [Details]
(2013) 'Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors'
Andreassen, O. A.,Djurovic, S.,Thompson, W. K.,Schork, A. J.,Kendler, K. S.,O'Donovan, M. C.,Rujescu, D.,Werge, T.,van de Bunt, M.,Morris, A. P.,McCarthy, M. I.,Roddey, J. C.,McEvoy, L. K.,Desikan, R. S.,Dale, A. M. (2013) 'Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors'. Am J Hum Genet, 92 (22):197-209 [Details]
(2013) 'Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis'
(2013) 'Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis'. Lancet, 381 (98759875):1371-9 [Details]
(2012) 'Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia'
(2012) 'Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia'. Biol Psychiatry, 72 (88):620-8 [Details]
(2012) 'Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms'
Badner, J. A.,Koller, D.,Foroud, T.,Edenberg, H.,Nurnberger, J. I., Jr.,Zandi, P. P.,Willour, V. L.,McMahon, F. J.,Potash, J. B.,Hamshere, M.,Grozeva, D.,Green, E.,Kirov, G.,Jones, I.,Jones, L.,Craddock, N.,Morris, D.,Segurado, R.,Gill, M.,Sadovnick, D.,Remick, R.,Keck, P.,Kelsoe, J.,Ayub, M.,MacLean, A.,Blackwood, D.,Liu, C. Y.,Gershon, E. S.,McMahon, W.,Lyon, G. J.,Robinson, R.,Ross, J.,Byerley, W. (2012) 'Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms'. Mol Psychiatry, 17 (88):818-26 [Details]
(2012) 'Effect of genetic variant in BICC1 on functional and structural brain changes in depression'
Bermingham, R.,Carballedo, A.,Lisiecka, D.,Fagan, A.,Morris, D.,Fahey, C.,Donohoe, G.,Meaney, J.,Gill, M.,Frodl, T. (2012) 'Effect of genetic variant in BICC1 on functional and structural brain changes in depression'. Neuropsychopharmacology, 37 (1313):2855-62 [Details]
(2012) 'Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met-allele of the Val66Met brain-derived neurotrophic factor genotype'
Carballedo, A.,Amico, F.,Ugwu, I.,Fagan, A. J.,Fahey, C.,Morris, D.,Meaney, J. F.,Leemans, A.,Frodl, T. (2012) 'Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met-allele of the Val66Met brain-derived neurotrophic factor genotype'. Am J Med Genet B Neuropsychiatr Genet, 159B (55):537-48 [Details]
(2012) 'Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results'
Collins, A. L.,Kim, Y.,Sklar, P.,O'Donovan, M. C.,Sullivan, P. F. (2012) 'Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results'. Psychol Med, 42 (33):607-16 [Details]
(2012) 'Avian resistance to Campylobacter jejuni colonization is associated with an intestinal immunogene expression signature identified by mRNA sequencing'
Connell, S.,Meade, K. G.,Allan, B.,Lloyd, A. T.,Kenny, E.,Cormican, P.,Morris, D. W.,Bradley, D. G.,O'Farrelly, C. (2012) 'Avian resistance to Campylobacter jejuni colonization is associated with an intestinal immunogene expression signature identified by mRNA sequencing'. PLoS One, 7 (88) [Details]
(2012) 'Insulin-like growth factor 1 (IGF1) and its active peptide (1-3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms'
Corvin, A. P.,Molinos, I.,Little, G.,Donohoe, G.,Gill, M.,Morris, D. W.,Tropea, D. (2012) 'Insulin-like growth factor 1 (IGF1) and its active peptide (1-3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms'. Neurosci Lett, 520 (11):51-6 [Details]
(2012) 'Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia'
Delaney, C.,McGrane, J.,Cummings, E.,Morris, D. W.,Tropea, D.,Gill, M.,Corvin, A.,Donohoe, G. (2012) 'Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia'. Schizophr Res, 140 (1-31-3):232-6 [Details]
(2012) 'Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis'
Derks, E. M.,Vorstman, J. A.,Ripke, S.,Kahn, R. S.,Ophoff, R. A. (2012) 'Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis'. PLoS One, 7 (66) [Details]
(2012) 'Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits'
Donohoe, G.,Duignan, A.,Hargreaves, A.,Morris, D. W.,Rose, E.,Robertson, D.,Cummings, E.,Moore, S.,Gill, M.,Corvin, A. (2012) 'Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits'. Bipolar Disord, 14 (77):743-8 [Details]
(2012) 'Global endometrial transcriptomic profiling: transient immune activation precedes tissue proliferation and repair in healthy beef cows'
Foley, C.,Chapwanya, A.,Creevey, C. J.,Narciandi, F.,Morris, D.,Kenny, E. M.,Cormican, P.,Callanan, J. J.,O'Farrelly, C.,Meade, K. G. (2012) 'Global endometrial transcriptomic profiling: transient immune activation precedes tissue proliferation and repair in healthy beef cows'. BMC Genomics, 13 [Details]
(2012) 'Functional investigation of a schizophrenia GWAS signal at the CDC42 gene'
Gilks, W. P.,Hill, M.,Gill, M.,Donohoe, G.,Corvin, A. P.,Morris, D. W. (2012) 'Functional investigation of a schizophrenia GWAS signal at the CDC42 gene'. World Journal Of Biological Psychiatry, 13 (77):550-4 [Details]
(2012) 'ZNF804A and social cognition in patients with schizophrenia and healthy controls'
Hargreaves, A.,Morris, D. W.,Rose, E.,Fahey, C.,Moore, S.,Cummings, E.,Tropea, D.,Gill, M.,Corvin, A.,Donohoe, G. (2012) 'ZNF804A and social cognition in patients with schizophrenia and healthy controls'. Mol Psychiatry, 17 (22):118-9 [Details]
(2012) 'Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia'
Jablensky, A.,Angelicheva, D.,Donohoe, G. J.,Cruickshank, M.,Azmanov, D. N.,Morris, D. W.,McRae, A.,Weickert, C. S.,Carter, K. W.,Chandler, D.,Alexandrov, B.,Usheva, A.,Morar, B.,Verbrugghe, P. L.,Filipovska, A.,Rackham, O.,Bishop, A. R.,Rasmussen, K. O.,Dragovic, M.,Cooper, M.,Phillips, M.,Badcock, J.,Bramon-Bosch, E.,Almeida, O. P.,Flicker, L.,Gill, M.,Corvin, A.,MacGregor, S.,Kalaydjieva, L. (2012) 'Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia'. Molecular Psychiatry, 17 (1212):1328-39 [Details]
(2012) 'Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia'
Lips, E. S.,Cornelisse, L. N.,Toonen, R. F.,Min, J. L.,Hultman, C. M.,Holmans, P. A.,O'Donovan, M. C.,Purcell, S. M.,Smit, A. B.,Verhage, M.,Sullivan, P. F.,Visscher, P. M.,Posthuma, D. (2012) 'Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia'. Mol Psychiatry, 17 (1010):996-1006 [Details]
(2012) 'Neurotrophic tyrosine kinase polymorphism impacts white matter connections in patients with major depressive disorder'
Murphy, M. L.,Carballedo, A.,Fagan, A. J.,Morris, D.,Fahey, C.,Meaney, J.,Frodl, T. (2012) 'Neurotrophic tyrosine kinase polymorphism impacts white matter connections in patients with major depressive disorder'. Biol Psychiatry, 72 (88):663-70 [Details]
(2012) 'A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception'
O'Donoghue, T.,Morris, D. W.,Fahey, C.,Da Costa, A.,Foxe, J. J.,Hoerold, D.,Tropea, D.,Gill, M.,Corvin, A.,Donohoe, G. (2012) 'A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception'. Hum Brain Mapp, 33 (55):1202-11 [Details]
(2012) 'Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain'
Richards, A. L.,Jones, L.,Moskvina, V.,Kirov, G.,Gejman, P. V.,Levinson, D. F.,Sanders, A. R.,Purcell, S.,Visscher, P. M.,Craddock, N.,Owen, M. J.,Holmans, P.,O'Donovan, M. C. (2012) 'Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain'. Mol Psychiatry, 17 (22):193-201 [Details]
(2012) 'The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals'
Rose, E. J.,Greene, C.,Kelly, S.,Morris, D. W.,Robertson, I. H.,Fahey, C.,Jacobson, S.,O'Doherty, J.,Newell, F. N.,McGrath, J.,Bokde, A.,Garavan, H.,Frodl, T.,Gill, M.,Corvin, A. P.,Donohoe, G. (2012) 'The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals'. Neuroimage, 60 (11):614-22 [Details]
(2012) 'The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function'
Rose, E. J.,Morris, D. W.,Fahey, C.,Robertson, I. H.,Greene, C.,O'Doherty, J.,Newell, F. N.,Garavan, H.,McGrath, J.,Bokde, A.,Tropea, D.,Gill, M.,Corvin, A. P.,Donohoe, G. (2012) 'The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function'. Twin Res Hum Genet, 15 (33):296-303 [Details]
(2012) 'Identification of common variants associated with human hippocampal and intracranial volumes'
Stein, J. L.,Medland, S. E.,Vasquez, A. A.,Hibar, D. P.,Senstad, R. E.,Winkler, A. M.,Toro, R.,Appel, K.,Bartecek, R.,Bergmann, O.,Bernard, M.,Brown, A. A.,Cannon, D. M.,Chakravarty, M. M.,Christoforou, A.,Domin, M.,Grimm, O.,Hollinshead, M.,Holmes, A. J.,Homuth, G.,Hottenga, J. J.,Langan, C.,Lopez, L. M.,Hansell, N. K.,Hwang, K. S.,Kim, S.,Laje, G.,Lee, P. H.,Liu, X.,Loth, E.,Lourdusamy, A.,Mattingsdal, M.,Mohnke, S.,Maniega, S. M.,Nho, K.,Nugent, A. C.,O'Brien, C.,Papmeyer, M.,Putz, B.,Ramasamy, A.,Rasmussen, J.,Rijpkema, M.,Risacher, S. L.,Roddey, J. C.,Rose, E. J.,Ryten, M.,Shen, L.,Sprooten, E.,Strengman, E.,Teumer, A.,Trabzuni, D.,Turner, J.,van Eijk, K.,van Erp, T. G.,van Tol, M. J.,Wittfeld, K.,Wolf, C.,Woudstra, S.,Aleman, A.,Alhusaini, S.,Almasy, L.,Binder, E. B.,Brohawn, D. G.,C (2012) 'Identification of common variants associated with human hippocampal and intracranial volumes'. Nat Genet, 44 (55):552-61 [Details]
(2012) 'A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia'
Jia, P.,Wang, L.,Fanous, A. H.,Chen, X.,Kendler, K. S.,Zhao, Z. (2012) 'A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia'. J Med Genet, 49 (22):96-103 [Details]
(2012) 'Runs of homozygosity implicate autozygosity as a schizophrenia risk factor'
Keller, M. C.,Simonson, M. A.,Ripke, S.,Neale, B. M.,Gejman, P. V.,Howrigan, D. P.,Lee, S. H.,Lencz, T.,Levinson, D. F.,Sullivan, P. F. (2012) 'Runs of homozygosity implicate autozygosity as a schizophrenia risk factor'. PLoS Genet, 8 (44) [Details]
(2012) 'Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs'
Lee, S. H.,DeCandia, T. R.,Ripke, S.,Yang, J.,Sullivan, P. F.,Goddard, M. E.,Keller, M. C.,Visscher, P. M.,Wray, N. R. (2012) 'Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs'. Nat Genet, 44 (33):247-50 [Details]
(2011) 'GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia'
Chen, X.,Lee, G.,Maher, B. S.,Fanous, A. H.,Chen, J.,Zhao, Z.,Guo, A.,van den Oord, E.,Sullivan, P. F.,Shi, J.,Levinson, D. F.,Gejman, P. V.,Sanders, A.,Duan, J.,Owen, M. J.,Craddock, N. J.,O'Donovan, M. C.,Blackman, J.,Lewis, D.,Kirov, G. K.,Qin, W.,Schwab, S.,Wildenauer, D.,Chowdari, K.,Nimgaonkar, V.,Straub, R. E.,Weinberger, D. R.,O'Neill, F. A.,Walsh, D.,Bronstein, M.,Darvasi, A.,Lencz, T.,Malhotra, A. K.,Rujescu, D.,Giegling, I.,Werge, T.,Hansen, T.,Ingason, A.,Noethen, M. M.,Rietschel, M.,Cichon, S.,Djurovic, S.,Andreassen, O. A.,Cantor, R. M.,Ophoff, R.,Corvin, A.,Morris, D. W.,Gill, M.,Pato, C. N.,Pato, M. T.,Macedo, A.,Gurling, H. M.,McQuillin, A.,Pimm, J.,Hultman, C.,Lichtenstein, P.,Sklar, P.,Purcell, S. M.,Scolnick, E.,St Clair, D.,Blackwood, D. H.,Kendler, K. S. (2011) 'GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia'. Molecular Psychiatry, 16 (1111):1117-29 [Details]
(2011) 'Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detection'
Kenny, E. M.,Cormican, P.,Gilks, W. P.,Gates, A. S.,O'Dushlaine, C. T.,Pinto, C.,Corvin, A. P.,Gill, M.,Morris, D. W. (2011) 'Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detection'. Dna Research, 18 (11):31-8 [Details]
(2011) 'Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder'
Williams, H. J.,Norton, N.,Dwyer, S.,Moskvina, V.,Nikolov, I.,Carroll, L.,Georgieva, L.,Williams, N. M.,Morris, D. W.,Quinn, E. M.,Giegling, I.,Ikeda, M.,Wood, J.,Lencz, T.,Hultman, C.,Lichtenstein, P.,Thiselton, D.,Maher, B. S.,Malhotra, A. K.,Riley, B.,Kendler, K. S.,Gill, M.,Sullivan, P.,Sklar, P.,Purcell, S.,Nimgaonkar, V. L.,Kirov, G.,Holmans, P.,Corvin, A.,Rujescu, D.,Craddock, N.,Owen, M. J.,O'Donovan, M. C. (2011) 'Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder'. Molecular Psychiatry, 16 (44):429-41 [Details]
(2011) 'Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia'
Vacic, V.,McCarthy, S.,Malhotra, D.,Murray, F.,Chou, H. H.,Peoples, A.,Makarov, V.,Yoon, S.,Bhandari, A.,Corominas, R.,Iakoucheva, L. M.,Krastoshevsky, O.,Krause, V.,Larach-Walters, V.,Welsh, D. K.,Craig, D.,Kelsoe, J. R.,Gershon, E. S.,Leal, S. M.,Dell Aquila, M.,Morris, D. W.,Gill, M.,Corvin, A.,Insel, P. A.,McClellan, J.,King, M. C.,Karayiorgou, M.,Levy, D. L.,DeLisi, L. E.,Sebat, J. (2011) 'Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia'. Nature, 471 (73397339):499-503 [Details]
(2011) 'Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology'
Runker, A. E.,O'Tuathaigh, C.,Dunleavy, M.,Morris, D. W.,Little, G. E.,Corvin, A. P.,Gill, M.,Henshall, D. C.,Waddington, J. L.,Mitchell, K. J. (2011) 'Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology'. PLoS One, 6 (1111) [Details]
(2011) 'Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility'
O'Dushlaine, C.,Kenny, E.,Heron, E.,Donohoe, G.,Gill, M.,Morris, D.,Corvin, A. (2011) 'Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility'. Molecular Psychiatry, 16 (33):286-92 [Details]
(2011) 'Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation'
Hill, M. J.,Kenny, E.,Roche, S.,Morris, D. W.,Corvin, A.,Hawi, Z.,Gill, M.,Anney, R. J. (2011) 'Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation'. Psychiatric Genetics, 21 (66):281-6 [Details]
(2011) 'Assessment of inactivating stop codon mutations in forty Saccharomyces cerevisiae strains: implications for [PSI] prion- mediated phenotypes'
Fitzpatrick, D. A.,O'Brien, J.,Moran, C.,Hasin, N.,Kenny, E.,Cormican, P.,Gates, A.,Morris, D. W.,Jones, G. W. (2011) 'Assessment of inactivating stop codon mutations in forty Saccharomyces cerevisiae strains: implications for [PSI] prion- mediated phenotypes'. PLoS One, 6 (1212) [Details]
(2011) 'A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809'
Donohoe, G.,Walters, J.,Morris, D. W.,Da Costa, A.,Rose, E.,Hargreaves, A.,Maher, K.,Hayes, E.,Giegling, I.,Hartmann, A. M.,Moller, H. J.,Muglia, P.,Moskvina, V.,Owen, M. J.,O'Donovan, M. C.,Gill, M.,Corvin, A.,Rujescu, D. (2011) 'A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809'. Schizophrenia Research, 125 (2-32-3):304-6 [Details]
(2011) 'ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia'
Donohoe, G.,Rose, E.,Frodl, T.,Morris, D.,Spoletini, I.,Adriano, F.,Bernardini, S.,Caltagirone, C.,Bossu, P.,Gill, M.,Corvin, A. P.,Spalletta, G. (2011) 'ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia'. Neuroimage, 54 (33):2132-7 [Details]
(2011) 'Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder'
Dagdan, E.,Morris, D. W.,Campbell, M.,Hill, M.,Rothermundt, M.,Kastner, F.,Hohoff, C.,von Eiff, C.,Krakowitzky, P.,Gill, M.,McKeon, P.,Roche, S. (2011) 'Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 156B (66):691-9 [Details]
(2011) 'Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia'
Chen, J.,Lee, G.,Fanous, A. H.,Zhao, Z.,Jia, P.,O'Neill, A.,Walsh, D.,Kendler, K. S.,Chen, X. (2011) 'Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia'. Schizophr Res, 131 (1-31-3):43-51 [Details]
(2011) 'First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotype'
Casey, J.,Kawaguchi, R.,Morrissey, M.,Sun, H.,McGettigan, P.,Nielsen, J. E.,Conroy, J.,Regan, R.,Kenny, E.,Cormican, P.,Morris, D. W.,Tormey, P.,Chroinin, M. N.,Kennedy, B. N.,Lynch, S.,Green, A.,Ennis, S. (2011) 'First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotype'. Human Mutation, 32 (1212):1417-26 [Details]
(2011) 'Genetic classification of populations using supervised learning'
Bridges, M.,Heron, E. A.,O'Dushlaine, C.,Segurado, R.,Morris, D.,Corvin, A.,Gill, M.,Pinto, C. (2011) 'Genetic classification of populations using supervised learning'. Plos One, 6 (55) [Details]
(2011) 'Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4'
Psychiatric GWAS Consortium Bipolar Disorder Working Group (2011) 'Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4'. Nature Genetics, 43 (1010):977-83 [Details]
(2011) 'Genome-wide association study identifies five new schizophrenia loci'
(2011) 'Genome-wide association study identifies five new schizophrenia loci'. Nat Genet, 43 (1010):969-76 [Details]
(2010) 'Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia'
Donohoe, G.,Frodl, T.,Morris, D.,Spoletini, I.,Cannon, D. M.,Cherubini, A.,Caltagirone, C.,Bossu, P.,McDonald, C.,Gill, M.,Corvin, A. P.,Spalletta, G. (2010) 'Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia'. Neuropsychopharmacology, 35 (22):368-73 [Details]
(2010) 'Replicated genetic evidence supports a role for HOMER2 in schizophrenia'
Gilks, W. P.,Allott, E. H.,Donohoe, G.,Cummings, E.,Gill, M.,Corvin, A. P.,Morris, D. W. (2010) 'Replicated genetic evidence supports a role for HOMER2 in schizophrenia'. Neuroscience Letters, 468 (33):229-33 [Details]
(2010) 'The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypes'
Donohoe, G.,Morris, D. W.,Corvin, A. (2010) 'The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypes'. Schizophrenia Bulletin, 36 (55):904-9 [Details]
(2010) 'Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression'
Quinn, E. M.,Hill, M.,Anney, R.,Gill, M.,Corvin, A. P.,Morris, D. W. (2010) 'Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression'. Bipolar Disorders, 12 (44):440-5 [Details]
(2010) 'Population structure and genome-wide patterns of variation in Ireland and Britain'
O'Dushlaine, C. T.,Morris, D.,Moskvina, V.,Kirov, G.,Consortium, I. S.,Gill, M.,Corvin, A.,Wilson, J. F.,Cavalleri, G. L. (2010) 'Population structure and genome-wide patterns of variation in Ireland and Britain'. European Journal Of Human Genetics, 18 (1111):1248-54 [Details]
(2010) 'Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha'
Carroll, L. S.,Williams, N. M.,Moskvina, V.,Russell, E.,Norton, N.,Williams, H. J.,Peirce, T.,Georgieva, L.,Dwyer, S.,Grozeva, D.,Greene, E.,Farmer, A.,McGuffin, P.,Morris, D. W.,Corvin, A.,Gill, M.,Rujescu, D.,Sham, P.,Holmans, P.,Jones, I.,Kirov, G.,Craddock, N.,O'Donovan, M. C.,Owen, M. J. (2010) 'Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha'. Molecular Psychiatry, 15 (1111):1101-11 [Details]
(2010) 'BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia'
Spalletta, G.,Morris, D. W.,Angelucci, F.,Rubino, I. A.,Spoletini, I.,Bria, P.,Martinotti, G.,Siracusano, A.,Bonaviri, G.,Bernardini, S.,Caltagirone, C.,Bossu, P.,Donohoe, G.,Gill, M.,Corvin, A. P. (2010) 'BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia'. European Psychiatry, 25 (66):311-3 [Details]
(2010) 'Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia'
Walters, J. T.,Corvin, A.,Owen, M. J.,Williams, H.,Dragovic, M.,Quinn, E. M.,Judge, R.,Smith, D. J.,Norton, N.,Giegling, I.,Hartmann, A. M.,Moller, H. J.,Muglia, P.,Moskvina, V.,Dwyer, S.,O'Donoghue, T.,Morar, B.,Cooper, M.,Chandler, D.,Jablensky, A.,Gill, M.,Kaladjieva, L.,Morris, D. W.,O'Donovan, M. C.,Rujescu, D.,Donohoe, G. (2010) 'Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia'. Archives Of General Psychiatry, 67 (77):692-700 [Details]
(2010) 'Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function'
Raychaudhuri, S.,Korn, J. M.,McCarroll, S. A.,International Schizophrenia Consortium,Altshuler, D.,Sklar, P.,Purcell, S.,Daly, M. J. (2010) 'Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function'. Plos Genetics, 6 (99) [Details]
(2010) 'Clinical symptomatology and the psychosis risk gene ZNF804A'
Cummings, E.,Donohoe, G.,McDonald, C.,Dinan, T. G.,O'Neill, F. A.,O'Callaghan, E.,Waddington, J. L.,Murphy, K. C.,Gill, M.,Morris, D. W.,Corvin, A. (2010) 'Clinical symptomatology and the psychosis risk gene ZNF804A'. Schizophrenia Research, 122 (1-31-3):273-5 [Details]
(2010) 'Genetic Differences between Five European Populations'
Moskvina, V.,Smith, M.,Ivanov, D.,Blackwood, D.,StClair, D.,Hultman, C.,Toncheva, D.,Gill, M.,Corvin, A.,O'Dushlaine, C.,Morris, D. W.,Wray, N. R.,Sullivan, P.,Pato, C.,Pato, M. T.,Sklar, P.,Purcell, S.,Holmans, P.,O'Donovan, M. C.,Owen, M. J.,Kirov, G. (2010) 'Genetic Differences between Five European Populations'. Heredity, 70 (22):141-9 [Details]
(2009) 'Does the ability to sustain attention underlie symptom severity in schizophrenia?'
O'Grada, C.,Barry, S.,McGlade, N.,Behan, C.,Haq, F.,Hayden, J.,O'Donoghue, T.,Peel, R.,Morris, D. W.,O'Callaghan, E.,Gill, M.,Corvin, A. P.,Dinan, T. G.,Donohoe, G. (2009) 'Does the ability to sustain attention underlie symptom severity in schizophrenia?'. Schizophrenia Research, 107 (2-32-3):319-23 [Details]
(2009) 'The SNP ratio test: pathway analysis of genome-wide association datasets'
O'Dushlaine, C.,Kenny, E.,Heron, E. A.,Segurado, R.,Gill, M.,Morris, D. W.,Corvin, A. (2009) 'The SNP ratio test: pathway analysis of genome-wide association datasets'. Bioinformatics, 25 (2020):2762-3 [Details]
(2009) 'Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects'
Donohoe, G.,Walters, J.,Morris, D. W.,Quinn, E. M.,Judge, R.,Norton, N.,Giegling, I.,Hartmann, A. M.,Moller, H. J.,Muglia, P.,Williams, H.,Moskvina, V.,Peel, R.,O'Donoghue, T.,Owen, M. J.,O'Donovan, M. C.,Gill, M.,Rujescu, D.,Corvin, A. (2009) 'Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects'. Archives Of General Psychiatry, 66 (1010):1045-54 [Details]
(2009) 'Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions'
Raychaudhuri, S.,Plenge, R. M.,Rossin, E. J.,Ng, A. C.,International Schizophrenia Consortium,Purcell, S. M.,Sklar, P.,Scolnick, E. M.,Xavier, R. J.,Altshuler, D.,Daly, M. J. (2009) 'Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions'. Plos Genetics, 5 (66) [Details]
(2009) 'Support for the involvement of large copy number variants in the pathogenesis of schizophrenia'
Kirov, G.,Grozeva, D.,Norton, N.,Ivanov, D.,Mantripragada, K. K.,Holmans, P.,International Schizophrenia Consortium,Craddock, N.,Owen, M. J.,O'Donovan, M. C. (2009) 'Support for the involvement of large copy number variants in the pathogenesis of schizophrenia'. Human Molecular Genetics, 18 (88):1497-503 [Details]
(2009) 'Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2'
O'Donovan, M. C.,Norton, N.,Williams, H.,Peirce, T.,Moskvina, V.,Nikolov, I.,Hamshere, M.,Carroll, L.,Georgieva, L.,Dwyer, S.,Holmans, P.,Marchini, J. L.,Spencer, C. C.,Howie, B.,Leung, H. T.,Giegling, I.,Hartmann, A. M.,Moller, H. J.,Morris, D. W.,Shi, Y.,Feng, G.,Hoffmann, P.,Propping, P.,Vasilescu, C.,Maier, W.,Rietschel, M.,Zammit, S.,Schumacher, J.,Quinn, E. M.,Schulze, T. G.,Iwata, N.,Ikeda, M.,Darvasi, A.,Shifman, S.,He, L.,Duan, J.,Sanders, A. R.,Levinson, D. F.,Adolfsson, R.,Osby, U.,Terenius, L.,Jonsson, E. G.,Cichon, S.,Nothen, M. M.,Gill, M.,Corvin, A. P.,Rujescu, D.,Gejman, P. V.,Kirov, G.,Craddock, N.,Williams, N. M.,Owen, M. J. (2009) 'Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2'. Molecular Psychiatry, 14 (11):30-6 [Details]
(2009) 'Common polygenic variation contributes to risk of schizophrenia and bipolar disorder'
International Schizophrenia Consortium (2009) 'Common polygenic variation contributes to risk of schizophrenia and bipolar disorder'. Nature, 460 (72567256):748-52 [Details]
(2008) 'A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis'
Corvin, A.,Donohoe, G.,Nangle, J. M.,Schwaiger, S.,Morris, D.,Gill, M. (2008) 'A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis'. Neuroscience Letters, 431 (22):146-9 [Details]
(2008) 'Rare chromosomal deletions and duplications increase risk of schizophrenia'
International Schizophrenia Consortium (2008) 'Rare chromosomal deletions and duplications increase risk of schizophrenia'. Nature, 455 (72107210):237-41 [Details]
(2008) 'Dysbindin (DTNBP1) and the biogenesis of lysosome-related organelles complex 1 (BLOC-1): main and epistatic gene effects are potential contributors to schizophrenia susceptibility'
Morris DW, Murphy K, Kenny N, Purcell SM, McGhee KA, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, Gill M, Corvin AP (2008) 'Dysbindin (DTNBP1) and the biogenesis of lysosome-related organelles complex 1 (BLOC-1): main and epistatic gene effects are potential contributors to schizophrenia susceptibility'. Biological Psychiatry, 63 (1):24-31 [DOI] [Details]
(2008) 'An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases'
O'Dushlaine CT, Dolan C, Weale ME, Stanton A, Croke DT, Kalviainen R, Eriksson K, Kantanen AM, Gibson RA, Hosford D, Sisodiya SM, Gill M, Corvin AP, Morris DW, Delanty N, Cavalleri GL (2008) 'An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases'. European Journal Of Human Genetics, 16 (2):176-183 [DOI] [Details]
(2008) 'Early visual processing deficits in dysbindin-associated schizophrenia'
Donohoe G, Morris DW, De Sanctis P, Magno E, Montesi JL, Garavan HP, Robertson IH, Javitt DC, Gill M, Corvin AP, Foxe JJ (2008) 'Early visual processing deficits in dysbindin-associated schizophrenia'. Biological Psychiatry, 63 (5):484-489 [DOI] [Details]
(2008) 'Identification of loci associated with schizophrenia by genome-wide association and follow-up'
O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV, Cichon S, Nöthen MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR (2008) 'Identification of loci associated with schizophrenia by genome-wide association and follow-up'. Nature Genetics, 40 (9):1053-1055 [DOI] [Details]
(2008) 'Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies'
Anney RJ, Kenny E, O'Dushlaine CT, Lasky-Su J, Franke B, Morris DW, Neale BM, Asherson P, Faraone SV, Gill M (2008) 'Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B (8):1379-1386 [DOI] [Details]
(2008) 'Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism'
Yang MS, Morris DW, Donohoe G, Kenny E, O'Dushalaine CT, Schwaiger S, Nangle JM, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, Gill M, Corvin A (2008) 'Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism'. Biological Psychiatry, 64 (2):98-103 [DOI] [Details]
(2008) 'Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder'
Ferreira, M. A.,O'Donovan, M. C.,Meng, Y. A.,Jones, I. R.,Ruderfer, D. M.,Jones, L.,Fan, J.,Kirov, G.,Perlis, R. H.,Green, E. K.,Smoller, J. W.,Grozeva, D.,Stone, J.,Nikolov, I.,Chambert, K.,Hamshere, M. L.,Nimgaonkar, V. L.,Moskvina, V.,Thase, M. E.,Caesar, S.,Sachs, G. S.,Franklin, J.,Gordon-Smith, K.,Ardlie, K. G.,Gabriel, S. B.,Fraser, C.,Blumenstiel, B.,Defelice, M.,Breen, G.,Gill, M.,Morris, D. W.,Elkin, A.,Muir, W. J.,McGhee, K. A.,Williamson, R.,MacIntyre, D. J.,MacLean, A. W.,St, C. D.,Robinson, M.,Van Beck, M.,Pereira, A. C.,Kandaswamy, R.,McQuillin, A.,Collier, D. A.,Bass, N. J.,Young, A. H.,Lawrence, J.,Ferrier, I. N.,Anjorin, A.,Farmer, A.,Curtis, D.,Scolnick, E. M.,McGuffin, P.,Daly, M. J.,Corvin, A. P.,Holmans, P. A.,Blackwood, D. H.,Gurling, H. M.,Owen, M. J.,Purcell, S. M. (2008) 'Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder'. Nature Genetics, 40 (99):1056-8 [Details]
(2007) 'Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma'
Maynadié M, Cocco PL, Boffetta P, Brennan P, Chanock SJ, Browne PV, Lawler M, Hayden PJ, Tewari P, Morris DW, Staines A, Crowley D, Nieters A, Becker N, de Sanjosé S, Foretova L (2007) 'Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma'. Human Molecular Genetics, 16 (24):3117-3127 [DOI] [Details]
(2007) 'DAOA ARG30LYS and verbal memory function in schizophrenia'
Donohoe G, Morris DW, Robertson IH, McGhee KA, Murphy K, Kenny N, Clarke S, Gill M, Corvin AP (2007) 'DAOA ARG30LYS and verbal memory function in schizophrenia'. Molecular Psychiatry, 12 (9):795-796 [DOI] [Details]
(2007) 'Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample'
Corvin A, McGhee KA, Murphy K, Donohoe G, Nangle JM, Schwaiger S, Kenny N, Clarke S, Meagher D, Quinn J, Scully P, Baldwin P, Browne D, Walsh C, Waddington JL, Morris DW, Gill M (2007) 'Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B (7):949-953 [DOI] [Details]
(2007) 'Variance in facial recognition performance associated with BDNF in schizophrenia'
Donohoe G, Morris DW, Robertson IH, Clarke S, McGhee KA, Schwaiger S, Nangle JM, Gill M, Corvin A (2007) 'Variance in facial recognition performance associated with BDNF in schizophrenia'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B (4):578-579 [DOI] [Details]
(2007) 'D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia'
Corvin, A.,Donohoe, G.,McGhee, K.,Murphy, K.,Kenny, N.,Schwaiger, S.,Nangle, J. M.,Morris, D.,Gill, M. (2007) 'D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia'. Neuroscience Letters, 426 (22):97-100 [Details]
(2007) 'Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: a preliminary study'
Donohoe G, Morris DW, Clarke S, McGhee KA, Schwaiger S, Nangle JM, Garavan H, Robertson IH, Gill M, Corvin A (2007) 'Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: a preliminary study'. Neuropsychologia, 45 (2):454-458 [DOI] [Details]
(2006) 'Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia'
Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer S, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, Corvin AP, Owen MJ, O'Donovan MC (2006) 'Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 141B (1):96-101 [DOI] [Details]
(2006) 'Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples'
Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, Levitt P, Lewis DA, Li T, Mirnics K, Morris DW, Norton N, O'Donovan MC, Owen MJ, Richard C, Semwal P, Sobell JL, St Clair D, Straub RE, Thelma BK, Vallada H, Weinberger DR, Williams NM, Wood J, Zhang F, Devlin B, Nimgaonkar VL (2006) 'Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples'. Biological Psychiatry, 60 (2):152-162 [DOI] [Details]
(2006) 'Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders'
Nangle JM, Clarke S, Morris DW, Schwaiger S, McGhee KA, Kenny N, Murphy K, Gill M, Corvin A, Donohoe G (2006) 'Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders'. Schizophrenia Research, 85 (1-3):196-200 [DOI] [Details]
(2006) 'Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia'
Mutsuddi M, Morris DW, Waggoner SG, Daly MJ, Scolnick EM, Sklar P (2006) 'Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia'. American Journal Of Human Genetics, 79 (5):903-909 [DOI] [Details]
(2006) 'Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function?'
Donohoe, G.,Reilly, R.,Clarke, S.,Meredith, S.,Green, B.,Morris, D.,Gill, M.,Corvin, A.,Garavan, H.,Robertson, I. H. (2006) 'Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function?'. Journal Of The International Neuropsychological Society, 12 (66):901-6 [Details]
(2006) 'Are deficits in executive sub-processes simply reflecting more general cognitive decline in schizophrenia?'
Donohoe, G.,Clarke, S.,Morris, D.,Nangle, J. M.,Schwaiger, S.,Gill, M.,Corvin, A.,Robertson, I. H. (2006) 'Are deficits in executive sub-processes simply reflecting more general cognitive decline in schizophrenia?'. Schizophrenia Research, 85 (1-31-3):168-73 [Details]
(2005) 'Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs'
McGhee KA, Morris DW, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Meagher D, Quinn J, Scully P, Waddington JL, Gill M, Corvin A (2005) 'Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs'. Schizophrenia Research, 76 (2-3):231-238 [DOI] [Details]
(2004) 'Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability'
Morris DW, Ivanov D, Robinson L, Williams N, Stevenson J, Owen MJ, Williams J, O'Donovan MC (2004) 'Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 129B (1):97-103 [DOI] [Details]
(2004) 'Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus'
Corvin AP, Morris DW, McGhee K, Schwaiger S, Scully P, Quinn J, Meagher D, Clair DS, Waddington JL, Gill M (2004) 'Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus'. Molecular Psychiatry, 9 (2):208-213 [DOI] [Details]
(2004) 'Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1)'
Williams NM, Preece A, Morris DW, Spurlock G, Bray NJ, Stephens M, Norton N, Williams H, Clement M, Dwyer S, Curran C, Wilkinson J, Moskvina V, Waddington JL, Gill M, Corvin AP, Zammit S, Kirov G, Owen MJ, O'Donovan MC (2004) 'Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1)'. Archives Of General Psychiatry, 61 (4):336-344 [DOI] [Details]
(2004) 'Confirming RGS4 as a susceptibility gene for schizophrenia'
Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP (2004) 'Confirming RGS4 as a susceptibility gene for schizophrenia'. American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, 125B (1):50-53 [DOI] [Details]
(2003) 'Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22'
Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J (2003) 'Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22'. Molecular Psychiatry, 8 (2):176-185 [DOI] [Details]
(2003) 'No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study'
Morris DW, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP (2003) 'No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study'. Schizophrenia Research, 60 (2-3):167-172 [Details]
(2002) 'Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools'
Norton N, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, Hoogendoorn B, Owen MJ, O'Donovan MC (2002) 'Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools'. Human Genetics, 110 (5):471-478 [DOI] [Details]
(2000) 'Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q'
Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, Hopkin E, Pound K, Fernando S, Easton M, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. (2000) 'Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q'. Human Molecular Genetics, 9 (5):843-848 [Details]

Conference Publications

  Year Publication
(2018) SIRS
Holland, J,Dauvermann, M,Morris, D,Zammit, S,Khandaker, G,Donohoe, G (2018) EFFECTS OF EARLY LIFE ADVERSITY ON IMMUNE FUNCTION AND COGNITIVE PERFORMANCE IN YOUTHS WITH AND WITHOUT EXPERIENCE OF PSYCHOTIC SYMPTOMS SIRS , pp.325-325 [Details]
(2020) European Neuropsychopharmacology
33. Costello L, Nabulsi L, McPhilemy G, O’Donoghue S, Kilmartin L, Kakodkar P, Neo WX, Dauvermann MR, Mothersill D, Rokita KI, Holleran L, Kane R, Hallahan B, Corvin A, Morris D, McKernan DP, Kelly J, McDonald C, Donohoe G, Cannon DM (2020) Childhood trauma does not explain altered brain network integration or segregation detected in schizophrenia European Neuropsychopharmacology , pp.S65-S66 [Details]

Abstract

  Year Publication
(2019) GENE-SET ANALYSIS OF GWAS DATA IDENTIFIES A ROLE FOR SATB2 AND THE NURD COMPLEX IN SCHIZOPHRENIA AND EDUCATIONAL ATTAINMENT.
Whitton, L,Apostolova, G,Donohoe, G,Morris, D (2019) GENE-SET ANALYSIS OF GWAS DATA IDENTIFIES A ROLE FOR SATB2 AND THE NURD COMPLEX IN SCHIZOPHRENIA AND EDUCATIONAL ATTAINMENT. Abstract [DOI] [Details]

ANET/COS

  Year Publication
(2019) A MOLECULAR ANALYSIS OF SDCCAG8, A SCHIZOPHRENIA RISK GENE THAT IS REQUIRED FOR EFFICIENT PRIMARY CILIOGENESIS.
Flynn, M,Whitton, L,Corvin, A,Gill, M,Donohoe, G,Morrison, C,Morris, D (2019) A MOLECULAR ANALYSIS OF SDCCAG8, A SCHIZOPHRENIA RISK GENE THAT IS REQUIRED FOR EFFICIENT PRIMARY CILIOGENESIS. ANET/COS [DOI] [Details]

Book Review

  Year Publication
(2019) A molecular analysis of SDCCAG8, a schizophrenia risk gene that functions in the centrosome.
Flynn, M,Whitton, L,Donohoe, G,Morrison, C,Morris, D (2019) A molecular analysis of SDCCAG8, a schizophrenia risk gene that functions in the centrosome. Book Review [Details]

Reviews

  Year Publication
(2020) Cognitive Genomics: Recent Advances and Current Challenges.
Fitzgerald, J;Morris, DW;Donohoe, G (2020) Cognitive Genomics: Recent Advances and Current Challenges. NEW YORK: Reviews [DOI] [Details]
(2015) Greater number of older siblings is associated with decreased theory of mind ability in psychosis.
Murray, C,Cosgrove, D,Corvin, A,Gill, M,Morris, DW,Donohoe, G (2015) Greater number of older siblings is associated with decreased theory of mind ability in psychosis. Reviews [DOI] [Details]