Derek Morris

Lecturer Below The Bar BSc, Ph.D

Contact Details

Lecturer Below The Bar
Biomedical Science
Biochemistry
School of Natural Sciences
NUI Galway

E: DEREK.MORRIS@nuigalway.ie
 
researcher

Biography

Derek Morris graduated with a B.Sc. in Biotechnology from the National University of Ireland, Galway in 1998. In 2001, he completed his PhD in molecular genetics at the Department of Psychological Medicine, Cardiff University. He subsequently joined the Neuropsychiatric Genetics Research Group in Trinity College Dublin as a research fellow and was awarded a HRB Postdoctoral Career Development Research Fellowship in 2003. In 2006, Dr. Morris was appointed Lecturer in Molecular Psychiatry within the Discipline of Psychiatry in TCD and in 2013 moved to NUI Galway where he is now Lecturer in Biomedical Science within the Discipline of Biochemistry. Dr. Morris’ research interests are the development of novel methods for mapping genes for complex diseases and the application of high-throughput genomics technologies to the detection of risk genes for schizophrenia and bipolar disorder. He has extensive experience of genome-wide association studies (GWAS) and using SFI funding, set up TrinSeq, the first next-generation sequencing lab in Ireland in 2008. Since moving to NUI Galway in late 2013, Dr. Morris has established, is a PI and leads the genetics studies with the Centre for Neuroimaging and Cognitive Genomics (NICOG). His research activity within NICOG focuses on epigenetic regulation of gene expression as a risk mechanisms for schizophrenia. He also coordinates study design and the management of biosample resources and genetics data used for ongoing studies. Dr. Morris is currently President of the Irish Society of Human Genetics.

Peer Reviewed Journals

  Year Publication
(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 [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 [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'
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, Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C (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 Contributions

  Year Publication
(2012) Cognitive Neuroscience Society,
Rose, E.J., Hargreaves, A., Morris, D.W., Fahey, C., Gill, M., Corvin, A., and Donohoe, G. (2012) The novel psychosis risk variant rs7914558 at CNNM2 is associated with variability in social cognitive function and gray matter volume. [Conference Paper], Cognitive Neuroscience Society, Chicago, IL, USA , 31-MAR-12 - 04-APR-12. [Details]
(2011) Organization for Human Brain Mapping,
Rose, E.J., Greene, C., Morris, D.W., Fahey, C., Robertson, I., Garavan, H., Gill, M., Corvin, A.P., and Donohoe, G. (2011) The NOS1 polymorphism rs6490121 is associated with variation in prefrontal function and gray matter density in healthy individuals. [Conference Paper], Organization for Human Brain Mapping, Quebec, Canada , 26-JUN-11 - 30-JUN-11. [Details]
(2011) Wiring the Brain,
Rose, E.J., Mothersill, O., Greene, C., Kelly, S., Morris, D.W., Fahey, C., Robertson, I., Garavan, H., Gill, M., Corvin, A.P., and Donohoe, G. (2011) The putative NOS1 schizophrenia risk variant rs6490121 is associated with prefrontal function and gray matter density in healthy individuals. [Conference Paper], Wiring the Brain, Ireland , 12-APR-11 - 15-APR-11. [Details]
(2010) Organization for Human Brain Mapping,
Rose, E.J., Donohoe, G., Frodl, T., Morris, D.W., Spoletini, I., Cherubini, A., Adriano, F., Caltagirone, C., Bossu, P., Gill, M., Corvin, A.P., and Spalletta, G. (2010) ZNF804A risk allele is associated with relatively intact hippocampal grey matter volume in schizophrenia. [Poster Presentation], Organization for Human Brain Mapping, Barcelona, Spain , 06-JUN-10 - 10-JUN-10. [Details]
(2010) 2nd Conference Of The Schizophrenia International Research Society (SIRS),
Donohoe, G; Walters, J; Rose, E; Morris, D; Frodl, T; Spolletini, I; Gill, M; O'donovan, M; Owen, M; Spalletta, G; Rujescu, D; Corvin, A (2010) Znf804a Delineates A Schizophrenia Subtype Characterised By Relatively Spared Cognitive Performance And Brain Volume. [Chaired Session], 2nd Conference Of The Schizophrenia International Research Society (SIRS), Florence, Italy , 10-APR-10 - 14-APR-10. [Details]
(2007) 62nd Annual Scientific Meeting Of The Society Of Biological Psychiatry,
Morris, DW; Donohoe, G; Runker, A; O'Tuathaigh, CMP; Dunleavy, M; Gilks, WR; Allott, EH; Hakansson, K; Suto, F; Fujisawa, H; Manabe, T; Henshall, DC; Gill, M; Waddington, JL; Corvin, AP and Mitchell, KJ (2007) Animal Knockout Studies In Mice And Human Studies Of Clinical And Neurocognitive Phenotypes Identify A Role For SEMA6A And PLXNA2 In Schizophrenia. [Conference Paper], 62nd Annual Scientific Meeting Of The Society Of Biological Psychiatry, San Diego, CA, USA , 17-MAY-07 - 19-MAY-07. [Details]
(2007) 62nd Annual Scientific Meeting Of The Society Of Biological Psychiatry,
Donohoe, G; Morris, DW; Allot, E; Clarke, S; Quinn, EM; Robertson, IH; Waddington, JL; Gill, M. and Corvin, AP (2007) Olig-2 And CNP Are Associated With Schizophrenia Risk And Variance In General Cognition And Memory Function In An Irish Sample. [Conference Paper], 62nd Annual Scientific Meeting Of The Society Of Biological Psychiatry, San Diego, CA, USA , 17-MAY-07 - 19-MAY-07. [Details]
(2006) 14th World Congress Of Psychiatric Genetics,
Donohoe, G; Morris, DW; Robertson, IH; Clarke, S; Nangle, JM; Schwaiger, S; Magno, E; Desanctis, P; Montesi, J; Garavan, H; Javitt, DC; Gill, M; Foxe, J and Corvin, A (2006) A Characterisation Of Dysbindin Positive Schizophrenia Using Clinical, Cognitive, And Neurophysiological Measures. [Conference Paper], 14th World Congress Of Psychiatric Genetics, Cagliari, Italy , 28-OCT-06 - 01-NOV-06. [Details]
(2005) 13th World Congress Of Psychiatric Genetics,
Donohoe, G; Morris, D; Clarke, S; Robertson, IH; Gill, M. and Corvin, A. (2005) Evidence That G72 And DAAO Influence Neurocognitive Performance In Patients With Schizophrenia. [Conference Paper], 13th World Congress Of Psychiatric Genetics, Boston, MA, USA , 04-SEP-05 - 08-SEP-05. [Details]
(2005) 13th World Congress Of Psychiatric Genetics,
Morris, DW; Murphy, K; Kenny, N; Williams, NM; McGhee, KA; Schwaiger, S; Nangle, J; Donohoe, G; Clarke, S; Owen, MJ; O'Donovan, MC; Waddington, JL; Gill, M. and Corvin, AP (2005) Association Analyses Of The BLOC-1 Genes Suggest The Involvement Of BLOC-1 In Schizophrenia. [Conference Paper], 13th World Congress Of Psychiatric Genetics, Boston, MA, USA , 04-SEP-05 - 08-SEP-05. [Details]
(2005) 20th International Congress On Schizophrenia Research,
Nangle, JE; Clarke, S; Donohoe, G; Schwaiger, S; Morris, D; McGee, K; Gill, M. and Corvin, A. (2005) Neurocognition And Suicidal Behaviour In An Irish Population With Major Psychotic Disorders. [Conference Paper], 20th International Congress On Schizophrenia Research, Savannah, GA, USA , 02-APR-05 - 06-APR-05. [Details]
(2005) 13th World Congress Of Psychiatric Genetics,
McGhee, KA; Morris, DW; Schwaiger, S; Nangle, J; Murphy, K; Kenny, N; Donohoe, G; Clarke, S; Meagher, D; Quinn, J; Scully, P; Waddington, JL; Gill, M. and Corvin, AP (2005) Association Study Of Three Oxidative Stress Genes Putatively Involved In The Pathogenesis Of Schizophrenia. [Conference Paper], 13th World Congress Of Psychiatric Genetics, Boston, MA, USA , 04-SEP-05 - 08-SEP-05. [Details]
(2005) 20th International Congress On Schizophrenia Research,
Clarke, S; Donohoe, G; Corvin, A; Reilly, R; Garavan, H; Gill, M; Morris, D; McGee, K; Nangle, JM; Schwaiger, S; Greene, B; Meredith, S. and Robertson, IH (2005) Evidence Of Independence Between Antisaccade And Working Memory Task Performance In Schizophrenia. [Conference Paper], 20th International Congress On Schizophrenia Research, Savannah, GA, USA , 02-APR-05 - 06-APR-05. [Details]
(2005) 13th World Congress Of Psychiatric Genetics,
Donohoe, G; Morris, D; McGhee, K; Clarke, S; Nangle, J; Schwaiger, S; Garavan, H; Robertson, IH; Gill, M. and Corvin, A. (2005) Evidence That Dysbindin-1 Is Associated With Poorer Spatial Working Memory Performance In Schizophrenia. [Conference Paper], 13th World Congress Of Psychiatric Genetics, Boston, MA, USA , 04-SEP-05 - 08-SEP-05. [Details]
(2004) 12th World Congress Of Psychiatric Genetics,
Morris, D; McGhee, K; Schwaiger, S; Nangle, J; Murphy, K; Donohoe, G; Clarke, S; Baldwin, P; Scully, P; Quinn, J; Meagher, D; Waddington, JL; Gill, M. and Corvin, AP (2004) An Update On Association Studies Of DTNBP1, NRG-1, RGS4 And MRDS1 In An Extended Irish Schizophrenia Case-Control Sample. [Conference Paper], 12th World Congress Of Psychiatric Genetics, Dublin, Ireland , 09-OCT-04 - 13-OCT-04. [Details]
(2004) 12th World Congress Of Psychiatric Genetics,
McGhee, KA; Morris, DW; Murphy, K; Schwaiger, S; Naugle, J; Donohoe, G; Clarke, S; Scully, P; Quinn, J; Meagher, D; Baldwin, P; Waddington, JL; Gill, M. and Corvin, AP (2004) Positive Association Of G72-G30 And DAAO With Schizophrenia In An Irish Case-Control Sample. [Conference Paper], 12th World Congress Of Psychiatric Genetics, Dublin, Ireland , 09-OCT-04 - 13-OCT-04. [Details]
(2004) 12th World Congress Of Psychiatric Genetics,
McGhee, KA; Morris, DW; Schwaiger, S; Nangle, J; Murphy, K; Donohoe, G; Clarke, S; Baldwin, P; Scully, P; Quinn, J; Meagher, D; Waddington, JL; Gill, M. and Corvin, AP (2004) Association Analysis In A Large Irish Case-Control Sample Of HSPA8 And GSTM3, Two Genes Putatively Involved In Schizophrenia. [Conference Paper], 12th World Congress Of Psychiatric Genetics, Dublin, Ireland , 09-OCT-04 - 13-OCT-04. [Details]