Aiden Corvin
Professor Consultant/Head of Discipline, Psychiatry
Professor Consultant/Head of Discipline, Molecular Medicine Ireland

Biography

I completed undergraduate medical training at University College Cork in 1993 and Membership of the Royal College of Psychiatrists (UK) in 1998. I was awarded a Wellcome Trust Research Training Fellowship in Mental Health in 2000 to develop my interest in the genetic etiology of psychosis and founded the Psychosis Research Group (www.medicine.tcd.ie/neuropsychiatric-­‐genetics/psychosis/). I was appointed Senior Lecturer in Psychiatry at TCD (now Professor) and Consultant Psychiatrist at St James's Hospital, Dublin in 2006. Since its inception my research group's goal has been to identify and investigate genetic mechanisms of psychosis, to define molecular etiology, and to use this information to serve patients by improving diagnostics and developing new therapeutic approaches. Through the commitment of more than 3,000 Irish participants we have contributed to substantial research breakthroughs in the field. From identifying molecular overlap between schizophrenia, bipolar disorder, and other psychiatric disorders; to going from finding the first identified risk genes, to the recent confirmation of 108 schizophrenia risk loci. We have identified novel, but rare large genetic effects that may be particularly important in understanding the underlying biology involved. We are increasingly interesting in modeling the risk mechanisms involved and looking at the extent of overlap with other neurological disorders (Brainstorm Project). I am a founder member of the International Schizophrenia Consortium, and lead the Wellcome Trust Case Control Consortium 2-schizophrenia study and Brainstorm (with Ben Neale, Broad Institute MIT/Harvard). I am Associated Editor for Genetics for the Schizophrenia Bulletin. I have authored 190 publications in international peer reviewed journals (Nature, Nature Genetics, Human Molecular Genetics, JAMA Psychiatry) and published 8 book chapters. My group's work has been funded by the Wellcome Trust, NIH, EU, Health Research Board, and Science Foundation Ireland. My h-index (Google Scholar, July 2014)is 43

Publications and Further Research Outputs

Peer-Reviewed Publications

Foley C, Corvin A, Nakagome S, Genetics of Schizophrenia: Ready to Translate?, Current Psychiatry Reports, 19, (9), 2017, p61- Journal Article, 2017 URL DOI

Hibar, D.P., Adams, H.H.H., Jahanshad, N., (...), Thompson, P.M., Ikram, M.A. , Novel genetic loci associated with hippocampal volume, Nature Communications , 8, 2017, p13624 Journal Article, 2017 TARA - Full Text DOI

Marshall, C.R., Howrigan, D.P., Merico, D., (...), Neale, B.M., Sebat, J. , Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects , Nature Genetics, 49, (1), 2017, p27-35 Journal Article, 2017 DOI

McCarthy-Jones S, Smailes D, Corvin A, Gill M, Morris D.W, Dinan T.G, Murphy K.C, Anthony O′Neill F, Waddington J.L, Australian Schizophrenia Research Ban, Donohoe G, Dudley R, Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders, Psychiatry Research, 252, 2017, p154 - 160 Journal Article, 2017 DOI URL

Trampush J.W, Yang M.L.Z, Yu J, Knowles E, Davies G, Liewald D.C, Starr J.M, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, Lundervold A.J, Steen V.M, Espeseth T, RÃ"ikkönen K, Widen E, Palotie A, Eriksson J.G, Giegling I, Konte B, Roussos P, Giakoumaki S, Burdick K.E, Payton A, Ollier W, Horan M, Chiba-Falek O, Attix D.K, Need A.C, Cirulli E.T, Voineskos A.N, Stefanis N.C, Avramopoulos D, Hatzimanolis A, Arking D.E, Smyrnis N, Bilder R.M, Freimer N.A, Cannon T.D, London E, Poldrack R.A, Sabb F.W, Congdon E, Conley E.D, Scult M.A, Dickinson D, Straub R.E, Donohoe G, Morris D, Corvin A, Gill M, Hariri A.R, Weinberger D.R, Pendleton N, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller M.C, Andreassen O.A, Deary I.J, Glahn D.C, Malhotra A.K, Lencz T, GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium, Molecular Psychiatry, 22, (3), 2017, 336-345 Journal Article, 2017 URL TARA - Full Text DOI

Haziza S, Mohan N, Loe-Mie Y, Lepagnol-Bestel A.-M, Massou S, Adam M.-P, Le X.L, Viard J, Plancon C, Daudin R, Koebel P, Dorard E, Rose C, Hsieh F.-J, Wu C.-C, Potier B, Herault Y, Sala C, Corvin A, Allinquant B, Chang H.-C, Treussart F, Simonneau M, Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors, Nature Nanotechnology, 12, (4), 2017, p322 - 328 Journal Article, 2017 URL DOI

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, Project MinE GWAS Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Genetic correlation between amyotrophic lateral sclerosis and schizophrenia., Nature Communications, 2017, p14774 Journal Article, 2017 DOI TARA - Full Text

Walton, E., Hibar, D.P., van Erp, T.G.M., (...), Malmqvist, A., Hedberg, M. , Positive symptoms associate with cortical thinning in the superior temporal gyrus via the ENIGMA Schizophrenia consortium, Acta Psychiatrica Scandinavica, 135, (5), 2017, p439-447 Journal Article, 2017 DOI

O'Reilly, K., O'Connell, P., Corvin, A., (...), Richter, M., Kennedy, H. , Moral cognition and homicide amongst forensic patients with schizophrenia and schizoaffective disorder: A cross-sectional cohort study, Schizophrenia Research, 2017 Journal Article, 2017 DOI TARA - Full Text

Ajetunmobi A, McAllister D, Jain N, Brazil O, Corvin A, Volkov Y, Tropea D, Prina-Mello A, Characterisation of SH-SY5Y Human Neuroblastoma cell growth over glass and SU-8 substrates., Journal of Biomedical Materials Research - Part A, 105, (8), 2017, p2129-2138 Journal Article, 2017 DOI

Schizophrenia in, Genomics, Circuits, and Pathways in Clinical Neuropsychiatry, 2016, 411-428 , [Corvin, A] Book Chapter, 2016

Tulio Guadalupe, Samuel R Mathias, GM Theo, Christopher D Whelan, Marcel P Zwiers, Yoshinari Abe, Lucija Abramovic, Ingrid Agartz, Ole A Andreassen, Alejandro Arias-Vásquez, Benjamin S Aribisala, Nicola J Armstrong, Volker Arolt, Eric Artiges, Rosa Ayesa-Arriola, Vatche G Baboyan, Tobias Banaschewski, Gareth Barker, Mark E Bastin, Bernhard T Baune, John Blangero, Arun LW Bokde, Premika SW Boedhoe, Anushree Bose, Silvia Brem, Henry Brodaty, Uli Bromberg, Samantha Brooks, Christian Büchel, Jan Buitelaar, Vince D Calhoun, Dara M Cannon, Anna Cattrell, Yuqi Cheng, Patricia J Conrod, Annette Conzelmann, Aiden Corvin, Benedicto Crespo-Facorro, Fabrice Crivello, Udo Dannlowski, Greig I De Zubicaray, Sonja MC De Zwarte, Ian J Deary, Sylvane Desrivières, Nhat Trung Doan, Gary Donohoe, Erlend S Dørum, Stefan Ehrlich, Thomas Espeseth, Guillén Fernández, Herta Flor, Jean-Paul Fouche, Vincent Frouin, Masaki Fukunaga, Jürgen Gallinat, Hugh Garavan, Michael Gill, Andrea Gonzalez Suarez, Penny Gowland, Hans J Grabe, Dominik Grotegerd, Oliver Gruber, Saskia Hagenaars, Ryota Hashimoto, Tobias U Hauser, Andreas Heinz, Derrek P Hibar, Pieter J Hoekstra, Martine Hoogman, Fleur M Howells, Hao Hu, Hilleke E Hulshoff Pol, Chaim Huyser, Bernd Ittermann, Neda Jahanshad, Erik G Jönsson, Sarah Jurk, Rene S Kahn, Sinead Kelly, Bernd Kraemer, Harald Kugel, Jun Soo Kwon, Herve Lemaitre, Klaus-Peter Lesch, Christine Lochner, Michelle Luciano, Andre F Marquand, Nicholas G Martin, Ignacio Martínez-Zalacaín, Jean-Luc Martinot, David Mataix-Cols, Karen Mather, Colm Mcdonald, Katie L Mcmahon, Sarah E Medland, José M Menchón, Derek W Morris, Omar Mothersill, Susana Munoz Maniega, Benson Mwangi, Takashi Nakamae, Tomohiro Nakao, Janardhanan C Narayanaswaamy, Frauke Nees, Jan E Nordvik, A Marten H Onnink, Nils Opel, Roel Ophoff, Marie-Laure Paillère Martinot, Dimitri Papadopoulos Orfanos, Paul Pauli, Tomá Paus, Luise Poustka, Janardhan Yc Reddy, Miguel E Renteria, Roberto Roiz-Santiáñez, Annerine Roos, Natalie A Royle, Perminder Sachdev, Pascual Sánchez-Juan, Lianne Schmaal, Gunter Schumann, Elena Shumskaya, Michael N Smolka, Jair C Soares, Carles Soriano-Mas, Dan J Stein, Lachlan T Strike, Roberto Toro, Jessica A Turner, Nathalie Tzourio-Mazoyer, Anne Uhlmann, Maria Valdés Hernández, Odile A Van den Heuvel, Dennis Van Der Meer, Neeltje EM Van Haren, Dick J Veltman, Ganesan Venkatasubramanian, Nora C Vetter, Daniella Vuletic, Susanne Walitza, Henrik Walter, Esther Walton, Zhen Wang, Joanna Wardlaw, Wei Wen, Lars T Westlye, Robert Whelan, Katharina Wittfeld, Thomas Wolfers, Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex, Brain imaging and behavior, 2016, p1 - 18 Journal Article, 2016 TARA - Full Text DOI URL

Coleman C, Quinn E.M, Ryan A.W, Conroy J, Trimble V, Mahmud N, Kennedy N, Corvin A.P, Morris D.W, Donohoe G, O'Morain C, MacMathuna P, Byrnes V, Kiat C, Trynka G, Wijmenga C, Kelleher D, Ennis S, Anney R.J.L, McManus R, Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci, Molecular Psychiatry, 24, 2016, p291 - 297 Journal Article, 2016 URL TARA - Full Text DOI

Hargreaves, A., Mothersill, O., Anderson, M., (...), Corvin, A., Donohoe, G. , Detecting facial emotion recognition deficits in schizophrenia using dynamic stimuli of varying intensities, Neuroscience Letters, 633, 2016, p47-54 Journal Article, 2016 DOI

Tropea D, Mortimer N, Bellini S, Molinos I, Sanfeliu A, Shovlin S, McAllister D, Gill M, Mitchell K, Corvin A, Expression of nuclear Methyl-CpG binding protein 2 (Mecp2) is dependent on neuronal stimulation and application of Insulin-like growth factor 1, Neuroscience Letters, 621, 2016, p111 - 116 Journal Article, 2016 URL DOI

Merikangas, A.K., Segurado, R., Kelleher, E., Hogan, D., Delaney, C., Gill, M., Gallagher, L., Corvin, A.P., and Heron, E.A. , Parental age, birth order and neurodevelopmental disorders, Molecular Psychiatry, 21, 2016, p728-730 Journal Article, 2016 DOI

Corvin, A., O'Donovan, M.C., Psychiatric genetics: What's new in 2015?, The Lancet Psychiatry, 3, (1), 2016, p10-12 Journal Article, 2016

Johnson, E.C., Bjelland, D.W., Howrigan, D.P., (...), Sullivan, P.F., Keller, M.C., No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study, PLoS Genetics, 12, (10), 2016, pe1006343- Journal Article, 2016 TARA - Full Text DOI

Rautanen A, Pirinen M, Mills T.C, Rockett K.A, Strange A, Ndungu A.W, Naranbhai V, Gilchrist J.J, Bellenguez C, Freeman C, Band G, Bumpstead S.J, Edkins S, Giannoulatou E, Gray E, Dronov S, Hunt S.E, Langford C, Pearson R.D, Su Z, Vukcevic D, Macharia A.W, Uyoga S, Ndila C, Mturi N, Njuguna P, Mohammed S, Berkley J.A, Mwangi I, Mwarumba S, Kitsao B.S, Lowe B.S, Morpeth S.C, Khandwalla I, Blackwell J.M, Bramon E, Brown M.A, Casas J.P, Corvin A, Duncanson A, Jankowski J, Markus H.S, Mathew C.G, Palmer C.N.A, Plomin R, Sawcer S.J, Trembath R.C, Viswanathan A.C, Wood N.W, Deloukas P, Peltonen L, Williams T.N, Scott J.A.G, Chapman S.J, Donnelly P, Hill A.V.S, Spencer C.C.A, Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children, American Journal of Human Genetics, 98, (6), 2016, p1092 - 1100 Journal Article, 2016 DOI URL

Corvin A, Sullivan P.F, What next in schizophrenia genetics for the psychiatric genomics consortium?, Schizophrenia Bulletin, 42, (3), 2016, p538 - 541 Journal Article, 2016 URL DOI

McIntosh, A.M., Stewart, R., John, A., (...), Wölbert, E., Porteous, D.J, Data science for mental health: a UK perspective on a global challenge , The Lancet Psychiatry, 3, (10), 2016, p993-998 Journal Article, 2016 DOI

Franke, B., van Hulzen, K.J.E., Arias-Vasquez, A., (...), Thompson, P.M., Medland, S.E., Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept, Nature Neuroscience, 19, (3), 2016, p420-431 Journal Article, 2016 DOI

Bodea, C.A., Neale, B.M., Ripke, S., (...), Devlin, B., Roeder, K., A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies, American Journal of Human Genetics, 98, (5), 2016, p857-868 Journal Article, 2016 DOI

Mothersill O, Tangney N, Morris D.W, McCarthy H, Frodl T, Gill M, Corvin A, Donohoe G, Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia, Schizophrenia Research, 2016 Journal Article, 2016 TARA - Full Text URL DOI

Adams, H.H.H., Hibar, D.P., Chouraki, V., (...), Ikram, M.A., Thompson, P.M., Novel genetic loci underlying human intracranial volume identified through genome-wide association, Nature Neuroscience, 19, (12), 2016, p1569-1582 Journal Article, 2016 DOI

van Erp T.G.M, Hibar D.P, Rasmussen J.M, Glahn D.C, Pearlson G.D, Andreassen O.A, Agartz I, Westlye L.T, Haukvik U.K, Dale A.M, Melle I, Hartberg C.B, Gruber O, Kraemer B, Zilles D, Donohoe G, Kelly S, McDonald C, Morris D.W, Cannon D.M, Corvin A, Machielsen M.W.J, Koenders L, de Haan L, Veltman D.J, Satterthwaite T.D, Wolf D.H, Gur R.C, Gur R.E, Potkin S.G, Mathalon D.H, Mueller B.A, Preda A, Macciardi F, Ehrlich S, Walton E, Hass J, Calhoun V.D, Bockholt H.J, Sponheim S.R, Shoemaker J.M, van Haren N.E.M, Pol H.E.H, Ophoff R.A, Kahn R.S, Roiz-Santiañez R, Crespo-Facorro B, Wang L, Alpert K.I, Jönsson E.G, Dimitrova R, Bois C, Whalley H.C, McIntosh A.M, Lawrie S.M, Hashimoto R, Thompson P.M, Turner J.A, Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium, Molecular Psychiatry, 21, 2016, p547-553 Journal Article, 2016 DOI TARA - Full Text URL

Bigdeli, T.B., Ripke, S., Bacanu, S.-A., (...), Kendler, K.S., Fanous, A.H. , 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, 171, (2), 2016, p276-289 Journal Article, 2016 DOI

Whitton L, Cosgrove D, Clarkson C, Harold D, Kendall K, Richards A, Mantripragada K, Owen M.J, O'Donovan M.C, Walters J, Hartmann A, Konte B, Rujescu D, Gill M, Corvin A, Rea S, Donohoe G, Morris D.W, Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 171, (8), 2016, p1170 - 1179 Journal Article, 2016 URL DOI

Dillon, R., Hargreaves, A., Anderson-Schmidt, H., (...), Robertson, I., Donohoe, G., Adherence to a low-support cognitive remediation training program for psychosis , Journal of Nervous and Mental Disease, 204, (10), 2016, p741-745 Journal Article, 2016 DOI

D.Tropea, I. Molinos, S. Bellini, E. Petit, C. O'Toutaigh, I. Nagakura, K. Mitchell, M. Sur, M. Gill, J. Waddington, A. Corvin, Disrupted in schizophrenia 1 (DISC1) mutants have impaired activity-dependent plasticity in vitro and in vivo, Translational Psychiatry, 6, 2016, p712- Journal Article, 2016 URL TARA - Full Text

Baurecht, H. Hotze, M. Brand, S. Büning, C. Cormican, P. Corvin, A. Ellinghaus, D. Ellinghaus, E. Esparza-Gordillo, J. Fölster-Holst, R. Franke, A. Gieger, C. Hubner, N. Illig, T. Irvine, A.D. Kabesch, M. Lee, Y.A.E. Lieb, W. Marenholz, I. McLean, W.H.I. Morris, D.W. Mrowietz, U. Nair, R. Nöthen, M.M. Novak, N. O'Regan, G.M. Schreiber, S. Smith, C. Strauch, K. Stuart, P.E. Trembath, R. Tsoi, L.C. Weichenthal, M. Barker, J. Elder, J.T. Weidinger, S. Cordell, H.J. Brown, S.J., Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms, American Journal of Human Genetics, 96, (1), 2015, p104 - 120 Journal Article, 2015 URL TARA - Full Text DOI

Patel, V.S., Kelly, S., Wright, C., Gupta, C.N., Arias-Vasquez, A., Perrone-Bizzozero, N., Ehrlich, S., Wang, L., Bustillo, J.R., Morris, D., Corvin, A., Cannon, D.M., McDonald, C., Donohoe, G., Calhoun, V.D., Turner, J.A., MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia, Neuroscience Letters, 602, 2015, p44-49 Journal Article, 2015 TARA - Full Text DOI

Hargreaves A, Dillon R, Anderson-Schmidt H, Corvin A, Fitzmaurice B, Castorina M, Robertson IH, Donohoe G, Computerised working-memory focused cognitive remediation therapy for psychosis - A preliminary study., Schizophrenia research, 2015 Journal Article, 2015

Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L, The phenotypic manifestations of rare genic CNVs in autism spectrum disorder., Molecular psychiatry, 20, (11), 2015, 1366-72 Journal Article, 2015 DOI TARA - Full Text

Hong Lee, S., Byrne, E.M., Hultman, C.M., Kähler, A., Vinkhuyzen, A.A., Ripke, S., Andreassen, O.A., Frisell, T., Gusev, A., Hu, X., Karlsson, R., Mantzioris, V.X., McGrath, J.J., Mehta, D., Stahl, E.A., Zhao, Q., Kendler, K.S., Sullivan, P.F., Price, A.L., O'Donovan, M., Okada, Y., Mowry, B.J., Raychaudhuri, S., Wray, N.R., Agartz, I., Amin, F., Azevedo, M.H., Bass, N., Black, D.W., Blackwood, D.H.R., Bruggeman, R., Buccola, N.G., Choudhury, K., Cloninger, C.R., Corvin, A., Craddock, N., Daly, M.J., Datta, S., Donohoe, G.J., Duan, J., Dudbridge, F., Fanous, A., Freedman, R., Freimer, N.B., Friedl, M., Gill, M., Gurling, H., Haan, L.D., Hamshere, M.L., Hartmann, A.M., Holmans, P.A., Kahn, R.S., Keller, M.C., Kenny, E., Kirov, G.K., Krabbendam, L., Krasucki, R., Lawrence, J., Lencz, T., Levinson, D.F., Lieberman, J.A., Lin, D.-Y., Linszen, D.H., Magnusson, P.K.E., Maier, W., Malhotra, A.K., Mattheisen, M., Mattingsdal, M., McCarroll, S.A., Medeiros, H., Melle, I., Milanova, V., Myin-Germeys, I., Neale, B.M., Ophoff, R.A., Owen, M.J., Pimm, J., Purcell, S.M., Puri, V., Quested, D.J., Rossin, L., Ruderfer, D., Sanders, A.R., Shi, J., Sklar, P., St Clair, D., Scott Stroup, T., Van Os, J., Visscher, P.M., Wiersma, D., Zammit, S., Byerley, W., Cahn, W., Cantor, R.M., Cichon, S., Cormican, P., Curtis, D., Djurovic, S., Escott-Price, V., Gejman, P.V., Georgieva, L., Giegling, I., Hansen, T.F., Ingason, Andrés, Kim, Y., Konte, B., Lee, P.H., McIntosh, A., McQuillin, A., Morris, D.W., Nöthen, M.M., O'Dushlaine, C., Olincy, A., Olsen, L., Pato, C.N., Pato, M.T., Pickard, B.S., Posthuma, D., Rasmussen, H.B., Rietschel, M., Rujescu, D., Schulze, T.G., Silverman, J.M., Thirumalai, S., Werge, T., Louis Bridges, S., Choi, H.K., Coenen, M.J.H., De Vries, N., Dieud, P., Greenberg, J.D., Huizinga, T.W.J., Padyukov, L., Siminovitch, K.A., Tak, P.P., Worthington, J., De Jager, P.L., Denny, J.C., Gregersen, P.K., Klareskog, L., Mariette, X., Plenge, R.M., Van Laar, M., Van Riel, P., New data and an old puzzle: The negative association between schizophrenia and rheumatoid arthritis, International Journal of Epidemiology, 44, (5), 2015, p1706-1721 Journal Article, 2015 DOI TARA - Full Text

Trampush J.W, Lencz T, Knowles E, Davies G, Guha S, Pe'er I, 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, Räikkönen 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, Scult M, Dickinson D, Straub R.E, Donohoe G, Morris D, Corvin A, Gill M, Hariri A, Weinberger D.R, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller M.C, Andreassen O.A, Deary I.J, Glahn D.C, Malhotra A.K, 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, 168, (5), 2015, p363 - 373 Journal Article, 2015 DOI URL

Farrell M.S, Werge T, Sklar P, Owen M.J, Ophoff R.A, O'donovan M.C, Corvin A, Cichon S, Sullivan P.F, Evaluating historical candidate genes for schizophrenia, Molecular Psychiatry, 20, (5), 2015, p555 - 562 Journal Article, 2015 DOI URL

Murray C, Cosgrove D, Corvin A, Gill M, Morris D.W, Donohoe G, Greater number of older siblings is associated with decreased theory of mind ability in psychosis, Schizophrenia Research, 165, (2-3), 2015, p247 - 248 Journal Article, 2015 DOI URL

Baurecht H, Hotze M, Brand S, Büning C, Cormican P, Corvin A, Ellinghaus D, Ellinghaus E, Esparza-Gordillo J, Fölster-Holst R, Franke A, Gieger C, Hubner N, Illig T, Irvine AD, Kabesch M, Lee YA, Lieb W, Marenholz I, McLean WH, Morris DW, Mrowietz U, Nair R, Nöthen 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, Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms., American journal of human genetics, 96, (1), 2015, p104-20 Journal Article, 2015 DOI TARA - Full Text

Hibar, D.P., Stein, J.L., Renteria, M.E., (...), Thompson, P.M., Medland, S.E., Common genetic variants influence human subcortical brain structures, Nature, 520, (7546), 2015, p224-- Journal Article, 2015 DOI

Baurecht H, Hotze M, Brand S, BÌning C, Cormican P, Corvin A, Ellinghaus D, Ellinghaus E, Esparza-Gordillo J, Fölster-Holst R, Franke A, Gieger C, Hubner N, Illig T, Irvine A.D, Kabesch M, Lee Y.A.E, Lieb W, Marenholz I, McLean W.H.I, Morris D.W, Mrowietz U, Nair R, Nöthen M.M, Novak N, O'Regan G.M, Schreiber S, Smith C, Strauch K, Stuart P.E, Trembath R, Tsoi L.C, Weichenthal M, Barker J, Elder J.T, Weidinger S, Cordell H.J, Brown S.J, Erratum: Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms (American Journal of Human Genetics (2015) 96 (104-120)), American Journal of Human Genetics, 97, (6), 2015, p933- Journal Article, 2015 DOI URL

Ruderfer DM, Fanous AH, Ripke S, McQuillin A, Amdur RL, Gejman PV, O'Donovan MC, Andreassen OA, Djurovic S, Hultman CM, Kelsoe JR, Jamain S, Landén M, Leboyer M, Nimgaonkar V, Nurnberger J, Smoller JW, Craddock N, Corvin A, Sullivan PF, Holmans P, Sklar P, Kendler KS, Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia., Molecular psychiatry, 19, (9), 2014, p1017-24 Journal Article, 2014 TARA - Full Text DOI

Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, Pato M, Genovese G, Levinson D, Duan J, Moy W, Göring HH, Morris D, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Craddock N, Sklar P, Hultman C, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Evidence that duplications of 22q11.2 protect against schizophrenia., Molecular psychiatry, 19, (1), 2014, p37-40 Journal Article, 2014 TARA - Full Text DOI

Mothersill O, Morris DW, Kelly S, Rose EJ, Fahey C, O'Brien C, Lyne R, Reilly R, Gill M, Corvin AP, Donohoe G, Effects of MIR137 on fronto-amygdala functional connectivity., NeuroImage, 90, 2014, p189-95 Journal Article, 2014 TARA - Full Text DOI

Li M, Luo XJ, Rietschel M, Lewis CM, Mattheisen M, Müller-Myhsok B, Jamain S, Leboyer M, Landén M, Thompson PM, Cichon S, Nöthen MM, Schulze TG, Sullivan PF, Bergen SE, Donohoe G, Morris DW, Hargreaves A, Gill M, Corvin A, Hultman C, Toga AW, Shi L, Lin Q, Shi H, Gan L, Meyer-Lindenberg A, Czamara D, Henry C, Etain B, Bis JC, Ikram MA, Fornage M, Debette S, Launer LJ, Seshadri S, Erk S, Walter H, Heinz A, Bellivier F, Stein JL, Medland SE, Arias Vasquez A, Hibar DP, Franke B, Martin NG, Wright MJ, Su B, Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility., Molecular psychiatry, 19, (4), 2014, p452-61 Journal Article, 2014 TARA - Full Text DOI

Kenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW, Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders., Molecular psychiatry, 19, 2014, p872-879 Journal Article, 2014 TARA - Full Text DOI

Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, Gill M, Al-Chalabi A, Bradley DG, Hardiman O, Corvin AP, Morris DW, Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample., Neurobiology of aging, 35, (6), 2014, p1510.e1-1510.e5 Journal Article, 2014 TARA - Full Text DOI

Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L., The phenotypic manifestations of rare genic CNVs in autism spectrum disorder., Molecular Psychiatry, 2014, p1-7 Journal Article, 2014 DOI TARA - Full Text

Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1., Human molecular genetics, 23, (6), 2014, 1669-1676 Journal Article, 2014 DOI TARA - Full Text

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, Räikkönen 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, Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)., Molecular psychiatry, 19, (2), 2014, p168-74 Journal Article, 2014 TARA - Full Text DOI

O'Donoghue T, Morris DW, Fahey C, Da Costa A, Moore S, Cummings E, Leicht G, Karch S, Hoerold D, Tropea D, Foxe JJ, Gill M, Corvin A, Donohoe G, Effects of ZNF804A on auditory P300 response in schizophrenia., Translational psychiatry, 4, 2014, pe345 Journal Article, 2014 TARA - Full Text DOI

Ajetunmobi,A. A., Prina-Mello,Adriele A., Volkov,Yuri Y., Corvin,Aiden P. A.P., Tropea,Daniela D., Nanotechnologies for the study of the central nervous system, Progress in Neurobiology, 123, 2014, p18-36 Journal Article, 2014 DOI TARA - Full Text

Davis, O.S.P. Band, G. Pirinen, M. Haworth, C.M.A. Meaburn, E.L. Kovas, Y. Harlaar, N. Docherty, S.J. Hanscombe, K.B. Trzaskowski, M. Curtis, C.J.C. Strange, A. Freeman, C. Bellenguez, C. Su, Z. Pearson, R. Vukcevic, D. Langford, C. Deloukas, P. Hunt, S. Gray, E. Dronov, S. Potter, S.C. Tashakkori-Ghanbaria, A. Edkins, S. Bumpstead, S.J. Blackwell, J.M. Bramon, E. Brown, M.A. Casas, J.P. Corvin, A. Duncanson, A. Jankowski, J.A.Z. Markus, H.S. Mathew, C.G. Palmer, C.N.A. Rautanen, A. Sawcer, S.J. Trembath, R.C. Viswanathan, A.C. Wood, N.W. Barroso, I. Peltonen, L. Dale, P.S. Petrill, S.A. Schalkwyk, L.S. Craig, I.W. Lewis, C.M. Price, T.S. Donnelly, P. Plomin, R. Spencer, C.C.A., The correlation between reading and mathematics ability at age twelve has a substantial genetic component, Nature Communications, 5, 2014, p4204- Journal Article, 2014 TARA - Full Text DOI URL

Rose EJ, Hargreaves A, Morris D, Fahey C, Tropea D, Cummings E, Caltagirone C, Bossù P, Chiapponi C, Piras F, Spalletta G, Gill M, Corvin A, Donohoe G, Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style., The British journal of psychiatry : the journal of mental science, 204, (2), 2014, p115-121 Journal Article, 2014 DOI TARA - Full Text

McCarthy, S.E. McCombie, W.R. Corvin, A., Unlocking the treasure trove: From genes to schizophrenia biology, Schizophrenia Bulletin, 40, (3), 2014, p492 - 496 Journal Article, 2014 DOI TARA - Full Text URL

Corvin A, Morris DW, Genome-wide Association Studies: Findings at the Major Histocompatibility Complex Locus in Psychosis., Biological psychiatry, 75, (4), 2014, p276-83 Journal Article, 2014 DOI

Steinberg, S., De Jong, S., Mattheisen, M., (...), Stefansson, H., Stefansson, K., Common variant at 16p11.2 conferring risk of psychosis, Molecular Psychiatry, 19, (1), 2014, p108-114 Journal Article, 2014 DOI TARA - Full Text

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., No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset, Schizophrenia Research, 154, (1-3), 2014, p79-82 Journal Article, 2014 TARA - Full Text DOI

Rose EJ, Morris DW, Fahey C, Cannon D, McDonald C, Scanlon C, Kelly S, Gill M, Corvin A, Donohoe G., The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals., Am J Med Genet B Neuropsychiatr Genet., 26, 2014, p1209-17 Journal Article, 2014 DOI TARA - Full Text

Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, Strange A, Freeman C, Thiselton DL, Elves RL, Regan R, Ennis S, Dinan TG, McDonald C, Murphy KC, O'Callaghan E, Waddington JL, Walsh D, O'Donovan M, Grozeva D, Craddock N, Stone J, Scolnick E, Purcell S, Sklar P, Coe B, Eichler EE, 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 FA, Kendler KS, Gill M, Riley BP, Spencer CC, Corvin A, An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis., Human molecular genetics, 23, (12), 2014, p3316-26 Journal Article, 2014 DOI TARA - Full Text

McCarthy, S.E., Gillis, J., Kramer, M., (...), McCombie, W.R., Corvin, A. , De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability, Molecular Psychiatry, 19, 2014, p652-658 Journal Article, 2014 DOI TARA - Full Text

Pini G, Scusa MF, Benincasa A, Bottiglioni I, Congiu L, Vadhatpour C, Romanelli AM, Gemo I, Puccetti C, McNamara R, O'Leary S, Corvin A, Gill M, Tropea D, Repeated insulin-like growth factor 1 treatment in a patient with rett syndrome: a single case study., Frontiers in pediatrics, 2, 2014, p52 Journal Article, 2014 TARA - Full Text DOI

Fakiola M, Strange A, Cordell HJ, Miller EN, Pirinen M, Su Z, Mishra A, Mehrotra S, Monteiro GR, Band G, Bellenguez C, Dronov S, Edkins S, Freeman C, Giannoulatou E, Gray E, Hunt SE, Lacerda HG, Langford C, Pearson R, Pontes NN, Rai M, Singh SP, Smith L, Sousa O, Vukcevic D, Bramon E, Brown MA, Casas JP, Corvin A, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Wilson ME, Deloukas P, Peltonen L, Christiansen F, Witt C, Jeronimo SM, Sundar S, Spencer CC, Blackwell JM, Donnelly P, Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis., Nature genetics, 45, (2), 2013, p208-213 Journal Article, 2013 DOI

Cummings E, Donohoe G, Hargreaves A, Moore S, Fahey C, Dinan TG, McDonald C, O'Callaghan E, O'Neill FA, Waddington JL, Murphy KC, Morris DW, Gill M, Corvin A, Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137., Neuroscience Letters, 532, 2013, p33-38 Journal Article, 2013 DOI

Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nöthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Psych D, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G, Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia., JAMA Psychiatry, 70, (3), 2013, p253-60 Journal Article, 2013 TARA - Full Text DOI

Cummings E, Donohoe G, Hargreaves A, Moore S, Fahey C, Dinan TG, McDonald C, O'Callaghan E, O'Neill FA, Waddington JL, Murphy KC, Morris DW, Gill M, Corvin A. , Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137., Neuroscience Letters, 532, 2013, p33-38 Journal Article, 2013 DOI

Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, Blackwood D, Corvin A, Djurovic S, Gurling H, Ophoff R, Pato CN, Pato MT, Riley B, Webb T, Kendler K, O'Donovan M, Craddock N, Kirov G, Owen M, Rujescu D, St Clair D, Werge T, Hultman CM, Delisi LE, Sullivan P, van den Oord EJ, A comprehensive family-based replication study of schizophrenia genes., JAMA psychiatry, 70, (6), 2013, p573-81 Journal Article, 2013

Psychiatric GWAS Consortium Working Group., Combined analysis of 11 genome-wide association studies of bipolar disorder identifies strong evidence for multiple susceptibility loci, Nature Genetics, 2013 Journal Article, 2013

Ruderfer DM, Chambert K, Moran J, Talkowski M, Chen ES, Gigek C, Gusella JF, Blackwood DH, Corvin A, Gurling HM, Hultman CM, Kirov G, Magnusson P, O'Donovan MC, Owen MJ, Pato C, St Clair D, Sullivan PF, Purcell SM, Sklar P, Ernst C, Mosaic copy number variation in schizophrenia., European journal of human genetics : EJHG, 2013 Journal Article, 2013 DOI

Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, Tropea D, Rujescu D, Corvin A, Neuropsychological Effects Of The CSMD1 Genome-Wide Associated Schizophrenia Risk Variant rs10503253., Genes, Brain, and Behavior, 12, (12), 2013, p203- 209 Journal Article, 2013 DOI

Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, Moskvina V, Fernández G, Gill M, Corvin A, O'Donovan MC, Donohoe G, Owen MJ, The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up., The American journal of psychiatry, 170, (8), 2013, p877-85 Journal Article, 2013 DOI

Corvin, A., Schizophrenia at a genetics crossroads: Where to now?, Schizophrenia Bulletin, 39, (3), 2013, p490-495 Journal Article, 2013 DOI TARA - Full Text

Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L. Jones L. Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, Kranz J, The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC), Well Trust Case Control Consortium +(WTCCC+), Welcome Trust Case Control Consortium 2 9WTCCC2), Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC, Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. , Molecular Psychiatry, 18, (2), 2013, p708-12 Journal Article, 2013 DOI

Kenna KP, McLaughlin RL, Byrne S, Elamin M, Heverin M, Kenny EM, Cormican P, Morris DW, Donaghy CG, Bradley DG, Hardiman O, Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing., Journal of medical genetics, 50, (11), 2013, p776-83 Journal Article, 2013 DOI TARA - Full Text

Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT, Levinson DF, Gejman PV, Kendler KS, Laurent C, Mowry BJ, O'Donovan MC, Owen MJ, Pulver AE, Riley BP, Schwab SG, Wildenauer DB, Dudbridge F, Holmans P, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, O'Neill FA, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Lin K, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Powell J, Rujescu D, Van Os J, Walshe M, Weisbrod M, Wiersma D, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Donnelly P, 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, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, Barroso I, Deloukas P, Mathew CG, Blackwell JM, Brown MA, Corvin AP, McCarthy MI, Spencer CC, Bramon E, Corvin AP, O'Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF, Genome-wide association analysis identifies 13 new risk loci for schizophrenia., Nature genetics, 45, (10), 2013, p1150-9 Journal Article, 2013 DOI TARA - Full Text

Hamshere M, Walters JT, Smith R, et al., Genome-wide significant associations in schizophrenia to ITHIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the schizophrenia PGC., Molecular Psychiatry, 18, (6), 2013, p708-712 Journal Article, 2013 DOI

Corvin, A., Cold Spring Harbor Laboratories Lecture. , Cold Spring Harbor Laboratories, 2013 Invited Talk, 2013

Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, Tropea D, Rujescu D, Corvin A, Neuropsychological Effects Of The CSMD1 Genome-Wide Associated Schizophrenia Risk Variant rs10503253, Genes Brain Behaviour, 12, (2), 2013, p203-9 Journal Article, 2013 DOI

Robertson DA, Hargreaves A, Kelleher EB, Morris D, Gill M, Corvin A, Donohoe G, Social dysfunction in schizophrenia: An investigation of the GAF scale's sensitivity to deficits in social cognition., Schizophrenia research, 146, (1-3), 2013, p363-365 Journal Article, 2013 DOI TARA - Full Text

Which aspects of heterogeneity are useful to translational success. in, editor(s)Ernest Strungmann , Forum on Schizophrenia: Evolution and Synthesis, 2013, [Corvin A, Buchanan RW, Carpenter WT Jr, Kennedy JL, Keshavan MS, MacDonald A, Sass L, Wessa M.] Book Chapter, 2013

Corvin, A, Forums on Science and Society: Reflections on genetic underpinnings of schizophrenia, Special Seminar Series, European Molecular Biology Laboratory, Heidelberg, Germany, December 5th 2013, 2013 Invited Talk, 2013

Hargreaves, A., Anney, R., O'Dushlaine, C.a, Nicodemus, K.K.a, Gill, M., Corvin, A., Morris, D., Donohoe, G, The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis, Psychological Medicine, 44, (10), 2013, p2177-2187 Journal Article, 2013 TARA - Full Text DOI

Quinn EM, Cormican P, Kenny EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW, Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data., PloS one, 8, (3), 2013, pe58815 Journal Article, 2013 TARA - Full Text DOI

Degenhardt, F Priebe, L Meier, S Lennertz, L Streit, F Witt, SH Hofmann, A Becker, T Mössner, R Maier, W , Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets , Translational Psychiatry , 3 , (11 ), 2013, pe326 - Journal Article, 2013 TARA - Full Text

Mechelli, R., Umeton, R., Policano, C., Annibali, V., Coarelli, G., Ricigliano, V.A.G., Vittori, D., (...), Compston, A, A "Candidate-Interactome" Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis, PLoS ONE 8, 8, (5), 2013, part. no. e63300 Journal Article, 2013 TARA - Full Text DOI

Su Z, Gay LJ, Strange A, Palles C, Band G, Whiteman DC, Lescai F, Langford C, Nanji M, Edkins S, van der Winkel A, Levine D, Sasieni P, Bellenguez C, Howarth K, Freeman C, Trudgill N, Tucker AT, Pirinen M, Peppelenbosch MP, van der Laan LJ, Kuipers EJ, Drenth JP, Peters WH, Reynolds JV, Kelleher DP, McManus R, Grabsch H, Prenen H, Bisschops R, Krishnadath K, Siersema PD, van Baal JW, Middleton M, Petty R, Gillies R, Burch N, Bhandari P, Paterson S, Edwards C, Penman I, Vaidya K, Ang Y, Murray I, Patel P, Ye W, Mullins P, Wu AH, Bird NC, Dallal H, Shaheen NJ, Murray LJ, Koss K, Bernstein L, Romero Y, Hardie LJ, Zhang R, Winter H, Corley DA, Panter S, Risch HA, Reid BJ, Sargeant I, Gammon MD, Smart H, Dhar A, McMurtry H, Ali H, Liu G, Casson AG, Chow WH, Rutter M, Tawil A, Morris D, Nwokolo C, Isaacs P, Rodgers C, Ragunath K, MacDonald C, Haigh C, Monk D, Davies G, Wajed S, Johnston D, Gibbons M, Cullen S, Church N, Langley R, Griffin M, Alderson D, Deloukas P, Hunt SE, Gray E, Dronov S, Potter SC, Tashakkori-Ghanbaria A, Anderson M, Brooks C, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Duncanson A, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood N, Trynka G, Wijmenga C, Cazier JB, Atherfold P, Nicholson AM, Gellatly NL, Glancy D, Cooper SC, Cunningham D, Lind T, Hapeshi J, Ferry D, Rathbone B, Brown J, Love S, Attwood S, MacGregor S, Watson P, Sanders S, Ek W, Harrison RF, Moayyedi P, de Caestecker J, Barr H, Stupka E, Vaughan TL, Peltonen L, Spencer CC, Tomlinson I, Donnelly P, Jankowski JA, Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus., Nature genetics, 44, (10), 2012, p1131-6 Journal Article, 2012 DOI

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, 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, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K, Common variant at 16p11.2 conferring risk of psychosis., Molecular psychiatry, 2012, 1-7 Journal Article, 2012 DOI

Knight J, Spain SL, Capon F, Hayday A, Nestle FO, Clop A, Barker JN, Weale ME, Trembath RC, Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis., Human molecular genetics, 21, (23), 2012, p5185-92 Journal Article, 2012 DOI TARA - Full Text

Corvin, A., Will genomics change the way we manage psychosis?, College of Psychiatry in Ireland, 16th November, 2012 Invited Talk, 2012

Jostins L, Ripke S, Weersma RK, Duerr RH, McGovern DP, Hui KY, Lee JC, Schumm LP, Sharma Y, Anderson CA, Essers J, Mitrovic M, Ning K, Cleynen I, Theatre E, Spain SL, Raychaudhuri S, Goyette P, Wei Z, Abraham C, Achkar JP, Ahmad T, Amininejad L, Ananthakrishnan AN, Andersen V, Andrews JM, Baidoo L, Balschun T, Bampton PA, Bitton A, Boucher G, Brand S, Büning C, Cohain A, Cichon S, D'Amato M, De Jong D, Devaney KL, Dubinsky M, Edwards C, Ellinghaus D, Ferguson LR, Franchimont D, Fransen K, Gearry R, Georges M, Gieger C, Glas J, Haritunians T, Hart A, Hawkey C, Hedl M, Hu X, Karlsen TH, Kupcinskas L, Kugathasan S, Latiano A, Laukens D, Lawrance IC, Lees CW, Louis E, Mahy G, Mansfield J, Morgan AR, Mowat C, Newman W, Palmieri O, Ponsioen CY, Potocnik U, Prescott NJ, Regueiro M, Rotter JI, Russell RK, Sanderson JD, Sans M, Satsangi J, Schreiber S, Simms LA, Sventoraityte J, Targan SR, Taylor KD, Tremelling M, Verspaget HW, De Vos M, Wijmenga C, Wilson DC, Winkelmann J, Xavier RJ, Zeissig S, Zhang B, Zhang CK, Zhao H, Silverberg MS, Annese V, Hakonarson H, Brant SR, Radford-Smith G, Mathew CG, Rioux JD, Schadt EE, Daly MJ, Franke A, Parkes M, Vermeire S, Barrett JC, Cho JH, Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease., Nature, 491, (7422), 2012, p119-124 Journal Article, 2012 DOI

Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Ståhle M, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CC, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Kingo K, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CE, Reis A, Kere J, Nair RP, Franke A, Barker JN, Abecasis GR, Elder JT, Trembath RC, Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity., Nature genetics, 44, (12), 2012, p1341-1348 Journal Article, 2012 DOI

Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR, Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC, Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain., Molecular psychiatry, 17, (2), 2012, p193-201 Journal Article, 2012 URL

Rose EJ, Morris DW, Fahey C, Robertson IH, Greene C, O'Doherty J, Newell FN, Garavan H, McGrath J, Bokde A, Tropea D, Gill M, Corvin AP, Donohoe G., The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function., Twin Research and Human Genetics, 15, (3), 2012, p296 - 303 Journal Article, 2012 TARA - Full Text DOI

Emma J. Rose, Ciara Greene, Sinead Kelly, Derek W. Morris, Ian H. Robertson, Ciara Fahey, Sarah Jacobson, John O'Doherty, Fiona N. Newell, Jane McGrath, Arun Bodke, Hugh Garavan, Thomas Frodl, Michael Gill, Aiden P. Corvin, Gary Donohoe, The NOS1 variant rs6490121 is associated with variation in prefrontal function and gray matter density in healthy individuals, NeuroImage, 60, (1), 2012, p614-622 Journal Article, 2012 TARA - Full Text

Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Büchel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, Guerreiro R, Hernandez DG, Brice A, Ylikotila P, Stefánsson H, Majamaa K, Morris HR, Williams N, Gasser T, Heutink P, Wood NW, Hardy J, Martinez M, Singleton AB, Nalls MA, Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease., Human molecular genetics, 21, (22), 2012, p4996-5009 Journal Article, 2012 DOI TARA - Full Text

Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M, Debette S, Shulman JM, Schmidt H, Srikanth V, Schuur M, Yu L, Choi SH, Sigurdsson S, Verhaaren BF, DeStefano AL, Lambert JC, Jack CR, Struchalin M, Stankovich J, Ibrahim-Verbaas CA, Fleischman D, Zijdenbos A, den Heijer T, Mazoyer B, Coker LH, Enzinger C, Danoy P, Amin N, Arfanakis K, van Buchem MA, de Bruijn RF, Beiser A, Dufouil C, Huang J, Cavalieri M, Thomson R, Niessen WJ, Chibnik LB, Gislason GK, Hofman A, Pikula A, Amouyel P, Freeman KB, Phan TG, Oostra BA, Stein JL, Medland SE, Vasquez AA, Hibar DP, Wright MJ, Franke B, Martin NG, Thompson PM, Nalls MA, Uitterlinden AG, Au R, Elbaz A, Beare RJ, van Swieten JC, Lopez OL, Harris TB, Chouraki V, Breteler MM, De Jager PL, Becker JT, Vernooij MW, Knopman D, Fazekas F, Wolf PA, van der Lugt A, Gudnason V, Longstreth WT, Brown MA, Bennett DA, van Duijn CM, Mosley TH, Schmidt R, Tzourio C, Launer LJ, Ikram MA, Seshadri S, Common variants at 12q14 and 12q24 are associated with hippocampal volume., Nature genetics, 44, (5), 2012, p545-551 Journal Article, 2012 DOI TARA - Full Text

Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M., The Cognitive Genetics of Neuropsychiatric Disorders. , Current Topics in Behavioral Neurosciences, 12, 2012, p579-613 Journal Article, 2012 DOI

Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF, Runs of homozygosity implicate autozygosity as a schizophrenia risk factor., PLoS genetics, 8, (4), 2012, pe1002656 Journal Article, 2012 TARA - Full Text DOI

Collins AL, Kim Y, Sklar P, International Schizophrenia Consortium, O'Donovan MC, Sullivan PF, Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results., Psychological Medicine, 42, 2012, p607 - 616 Journal Article, 2012 URL

Strange A, Riley BP, Spencer CA, 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,15, Bramon E, Brown MA, Casas JP, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CNA, Plomin RP, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Stone J, Scolnick E, Purcell S, Sklar P, SGENE+ Consortium, Ripke S, Walters J, Owen MJ, O'Donovan MC, Schizophrenia Working Group of the Psychiatric GWAS Consortium, Peltonen L, McVean G, Kendler KS, Gill M, Donnelly P, Corvin A for Irish Schizophrenia Genomics Consortium and the Wellcome Trust Case Control Consortium 2, Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia., Biological Psychiatry, 72, (8), 2012, p620-628 Journal Article, 2012 TARA - Full Text DOI

Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Valdés Hernández MC, Van den Heuvel M, van der Wee NJ, Van Haren NE, Veltman JA, Völzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack CR, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW, Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, DeCarli C, Seshadri S, Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, de Zubicaray GI, Deary IJ, Donohoe G, de Geus EJ, Espeseth T, Fernández G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meyer-Lindenberg A, Morris DW, Müller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Sämann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM, Identification of common variants associated with human hippocampal and intracranial volumes., Nature genetics, 44, (5), 2012, p552-561 Journal Article, 2012 DOI TARA - Full Text

O'Donoghue T, Morris DW, Fahey C, Costa AD, Foxe JJ, Hoerold D, Tropea D, Gill M, Corvin A, Donohoe G, A NOS1 variant implicated in cognitive performance influences evoked neural responses during a hight density EEG study of early visual perception. , Human Brain Mapping, 33, (5), 2012, p1202-1211 Journal Article, 2012 DOI

Corvin, A., 'Cognitive genetics and psychosis, Norwegian Neuropsychiatric Association Winter Meeting, November 23rd, 2012 Invited Talk, 2012

Sullivan P,Psychiatric Genetics Investigators. , Don't give up on GWAS., 2012, - 96 Miscellaneous, 2012 DOI

Corvin, A., Schizophrenia Genomics: Progress and Challenges. , Neuroscience Ireland, Annual Meeting, Dublin, 5th September, 2012 Invited Talk, 2012

Delaney C, McGrane J, Cummings E, Morris DW, Tropea D, Gill M, Corvin A, Donohoe G, Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia., Schizophrenia research, 140, (1-3), 2012, p232-6 Journal Article, 2012 DOI

Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman CM, Holmans PA, O'Donovan MC, Purcell SM, Smit AB, Verhage M, Sullivan PF, Visscher PM, Posthuma D, Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia., Molecular Psychiatry, 17, (10), 2012, p996-1006 Journal Article, 2012 DOI TARA - Full Text

Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, Salomon D, Schork NJ, Fanous AH, O'Donovan MC, Niculescu AB, Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction., Molecular psychiatry, 17, (9), 2012, p887-905 Journal Article, 2012 DOI

Gilks WP, Hill M, Gill M, Donohoe G, Corvin AP, Morris DW, Functional investigation of a schizophrenia GWAS signal at the CDC42 gene., World Journal of Biological Psychiatry, 13, (7), 2012, p550-554 Journal Article, 2012 DOI

Corvin, A., Treating Schizophrenia, British Journal of Hospital Medicine Meeting, London UK, 26th April, 2012 Invited Talk, 2012

Bellenguez C, Bevan S, Gschwendtner A, Spencer CC, Burgess AI, Pirinen M, Jackson CA, Traylor M, Strange A, Su Z, Band G, Syme PD, Malik R, Pera J, Norrving B, Lemmens R, Freeman C, Schanz R, James T, Poole D, Murphy L, Segal H, Cortellini L, Cheng YC, Woo D, Nalls MA, Müller-Myhsok B, Meisinger C, Seedorf U, Ross-Adams H, Boonen S, Wloch-Kopec D, Valant V, Slark J, Furie K, Delavaran H, Langford C, Deloukas P, Edkins S, Hunt S, Gray E, Dronov S, Peltonen L, Gretarsdottir S, Thorleifsson G, Thorsteinsdottir U, Stefansson K, Boncoraglio GB, Parati EA, Attia J, Holliday E, Levi C, Franzosi MG, Goel A, Helgadottir A, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Duncanson A, Jankowski J, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Worrall BB, Kittner SJ, Mitchell BD, Kissela B, Meschia JF, Thijs V, Lindgren A, Macleod MJ, Slowik A, Walters M, Rosand J, Sharma P, Farrall M, Sudlow CL, Rothwell PM, Dichgans M, Donnelly P, Markus HS, Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke., Nature genetics, 44, (3), 2012, p328-33 Journal Article, 2012 TARA - Full Text DOI

Jia P, Wang L, Fanous AH, Pato CN, Edwards TL, Zhao Z, Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia., PLoS computational biology, 8, (7), 2012, pe1002587 Journal Article, 2012 DOI TARA - Full Text

Jablensky A, Angelicheva D, Donohoe GJ, Cruickshank M, Azmanov DN, Morris DW, McRae A, Weickert CS, Carter KW, Chandler D, Alexandrov B, Usheva A, Morar B, Verbrugghe PL, Filipovska A, Rackham O, Bishop AR, Rasmussen KO, Dragovic M, Cooper M, Phillips M, Badcock J, Bramon-Bosch E, Almeida OP, Flicker L, Gill M, Corvin A, Macgregor S, Kalaydjieva L, Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia., Molecular psychiatry, 17, (12), 2012, p1328-1339 Journal Article, 2012 DOI

Donohoe G, Duignan A, Hargreaves A, Morris DW, Rose E, Robertson D, Cummings E, Moore S, Gill M, Corvin A, Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits., Bipolar Disorders, 14, (7), 2012, p743-748 Journal Article, 2012 DOI

Derks EM, Vorstman JA, Ripke S, Kahn RS, Schizophrenia Psychiatric Genomic Consortium, Ophoff RA, Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis., PloS one, 7, (6), 2012, pe37852 Journal Article, 2012 TARA - Full Text DOI

Corvin AP, Molinos I, Little G, Donohoe G, Gill M, Morris DW, Tropea D, 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., Neuroscience letters, 520, (1), 2012, p51-56 Journal Article, 2012 DOI

Hill MJ, Kenny E, Roche S, Morris DW, Corvin A, Hawi Z, Gill M, Anney RJ, Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation., Psychiatric genetics, 21, (6), 2011, p281-286 Journal Article, 2011 DOI

Zhou, K., Bellenguez, C., Spencer, C.C.A., Bennett, A.J., Coleman, R.L., Tavendale, R., Hawley, S.A., (...), Pearson, E.R., Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes, Nature Genetics , 43, (2), 2011, p117-120 Journal Article, 2011 DOI TARA - Full Text

Runker AE, O'Tuathaight C, Dunleavy M, Morris DW, Little GE, Corvin AP, Gill M, Henshall DC, Waddington JL, Mitchell KJ. , Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychpathology, PLoS ONE , 6, 2011, pe26488 Journal Article, 2011 DOI TARA - Full Text

O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D, Consortium IS, Corvin A, Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility., Molecular Psychiatry, 16, (3), 2011, p286-292 Journal Article, 2011 DOI TARA - Full Text

Donohoe G, Walters J, Morris DW, Da Costa A, Rose E, Hargreaves A, Maher K, Hayes E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Moskvina V, Owen MJ, O'Donovan MC, Gill M, Corvin A, Rujescu D, A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809, Schizophrenia Research, 125, (2-3), 2011, p304-306 Journal Article, 2011 DOI

Kenny EM, Cormican P, Gilks WP, Gates AS, O'Dushlaine CT, Pinto C, Corvin AP, Gill M, Morris DW, Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection., DNA research : an international journal for rapid publication of reports on genes and genomes, 18, (1), 2011, p31-38 Journal Article, 2011 DOI TARA - Full Text

Annette E. Rünker, Colm O'Tuathaigh, Mark Dunleavy,Derek W. Morris, Graham E. Little, Aiden P. Corvin,Michael Gill, David C. Henshall, John L. Waddington, Kevin J. Mitchell, Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychopathology, PLoS ONE , 6, (11, ), 2011, pe26488 Journal Article, 2011 TARA - Full Text

Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jönsson EG, Bitter I, Pietiläinen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger CR, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegling I, Gill M, Glenthøj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jürgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer FB, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nöthen MM, O'Dushlaine CT, Olincy A, Olsen L, O'Neill FA, Orntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Réthelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV, Genome-wide association study identifies five new schizophrenia loci., Nature genetics, 43, (10), 2011, p969-976 Journal Article, 2011 DOI TARA - Full Text

Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, Lichtenstein P, Thiselton D, Maher BS; Molecular Genetics of Schizophrenia Collaboration (MGS) International Schizophrenia Consortium (ISC), SGENE-plus, GROUP, Malhotra AK, Riley B, Kendler KS, Gill M, Sullivan P, Sklar P, Purcell S, Nimgaonkar VL, Kirov G, Holmans P, Corvin A, Rujescu D, Craddock N, Owen MJ, O'Donovan MC, Fine mapping of ZNF804A and genomime-wide significant evidence for it's involvement in Schizophrenia and bipolar disorder. , Molecular Psychiatry, 16, (4), 2011, p429-441 Journal Article, 2011 DOI TARA - Full Text

Hargreaves A, Morris DW, Rose E, Fahey C, Moore S, Cummings E, Tropea D, Gill M, Corvin A, Donohoe G, ZNF804A and social cognition in patients with schizophrenia and healthy controls., Molecular psychiatry, 17, (2), 2011, p118 - 119 Journal Article, 2011 DOI

Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, Craig D, Kelsoe JR, Gershon ES, Leal SM, Dell Aquila M, Morris DW, Gill M, Corvin A, Insel PA, McClellan J, King MC, Karayiorgou M, Levy DL, DeLisi LE, Sebat J, Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia., Nature, 471, (7339), 2011, p499-503 Journal Article, 2011 TARA - Full Text DOI

Corvin AP, Two patients walk into a clinic...a genomics perspective on the future of schizophrenia., BMC Biology, 9, (77), 2011 Journal Article, 2011 DOI URL TARA - Full Text

Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, Kwan P, Wienker TF, Daly M, Dudbridge F, Holmans PA, Lin D, Burmeister M, Greenwood TA, Hamshere ML, Muglia P, Smith EN, Zandi PP, Nievergelt CM, McKinney R, Shilling PD, Schork NJ, Bloss CS, Foroud T, Koller DL, Gershon ES, Liu C, Badner JA, Scheftner WA, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon FJ, Schulze TG, Berrettini W, Lohoff FW, Potash JB, Mahon PB, McInnis MG, Zöllner S, Zhang P, Craig DW, Szelinger S, Barrett TB, Breuer R, Meier S, Strohmaier J, Witt SH, Tozzi F, Farmer A, McGuffin P, Strauss J, Xu W, Kennedy JL, Vincent JB, Matthews K, Day R, Ferreira MA, O'Dushlaine C, Perlis R, Raychaudhuri S, Ruderfer D, Hyoun PL, Smoller JW, Li J, Absher D, Thompson RC, Meng FG, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Watson SJ, Myers RM, Akil H, Boehnke M, Chambert K, Moran J, Scolnick E, Djurovic S, Melle I, Morken G, Gill M, Morris D, Quinn E, Mühleisen TW, Degenhardt FA, Mattheisen M, Schumacher J, Maier W, Steffens M, Propping P, Nöthen MM, Anjorin A, Bass N, Gurling H, Kandaswamy R, Lawrence J, McGhee K, McIntosh A, McLean AW, Muir WJ, Pickard BS, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Jones IR, Kirov G, Moskvina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Williamson R, Young AH, Ferrier IN, Stefansson K, Stefansson H, Thornorgeirsson T, Steinberg S, Gustafsson O, Bergen SE, Nimgaonkar V, Hultman C, Landén M, Lichtenstein P, Sullivan P, Schalling M, Osby U, Backlund L, Frisén L, Langstrom N, Jamain S, Leboyer M, Etain B, Bellivier F, Petursson H, Sigur Sson E, Müller-Mysok B, Lucae S, Schwarz M, Schofield PR, Martin N, Montgomery GW, Lathrop M, Oskarsson H, Bauer M, Wright A, Mitchell PB, Hautzinger M, Reif A, Kelsoe JR, Purcell SM, Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4., Nature Genetics, 43, (10), 2011, p977-83 Journal Article, 2011 DOI

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., Aquila, M.D., 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., Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia (Nature (2011) 471 (499-501)), 2011, - 114 Miscellaneous, 2011 DOI

Bridges M, Heron E, O'Dushlaine, Segurado R, The International Schizophrenia Consortium (ISC), Morris DW, Corvin A, Gill M, Pinto C. , Genetic Classification of Populations using Supervised Learning., PLos One, 6, (5), 2011, pe14802 Journal Article, 2011 DOI TARA - Full Text

Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S, Cichon S, Corvin A, Gary S, Gershon ES, Gill M, Karayiorgou M, Kelsoe JR, Krastoshevsky O, Krause V, Leibenluft E, Levy DL, Makarov V, Bhandari A, Malhotra AK, McMahon FJ, Nöthen MM, Potash JB, Rietschel M, Schulze TG, Sebat J, High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia, Neuron, 72, (6), 2011, p951 - 963 Journal Article, 2011 TARA - Full Text DOI

Moore, Susan; Kelleher, Eric; Corvin, Aiden, The Shock of the New: Progress in Schizophrenia Genomics , Current Genomics, 12, (7), 2011, p516-524 Journal Article, 2011

Evans DM, Spencer CC, Pointon JJ, Su Z, Harvey D, Kochan G, Oppermann U, Opperman U, Dilthey A, Pirinen M, Stone MA, Appleton L, Moutsianas L, Moutsianis L, Leslie S, Wordsworth T, Kenna TJ, Karaderi T, Thomas GP, Ward MM, Weisman MH, Farrar C, Bradbury LA, Danoy P, Inman RD, Maksymowych W, Gladman D, Rahman P, Morgan A, Marzo-Ortega H, Bowness P, Gaffney K, Gaston JS, Smith M, Bruges-Armas J, Couto AR, Sorrentino R, Paladini F, Ferreira MA, Xu H, Liu Y, Jiang L, Lopez-Larrea C, Díaz-Peña R, López-Vázquez A, Zayats T, Band G, Bellenguez C, Blackburn H, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Corvin A, Craddock N, Deloukas P, Dronov S, Duncanson A, Edkins S, Freeman C, Gillman M, Gray E, Gwilliam R, Hammond N, Hunt SE, Jankowski J, Jayakumar A, Langford C, Liddle J, Markus HS, Mathew CG, McCann OT, McCarthy MI, Palmer CN, Peltonen L, Plomin R, Potter SC, Rautanen A, Ravindrarajah R, Ricketts M, Samani N, Sawcer SJ, Strange A, Trembath RC, Viswanathan AC, Waller M, Weston P, Whittaker P, Widaa S, Wood NW, McVean G, Reveille JD, Wordsworth BP, Brown MA, Donnelly P, Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility., Nature genetics, 43, (8), 2011, p761-767 Journal Article, 2011 DOI

Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, Potter SC, Goris A, Band G, Oturai AB, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B, Gwilliam R, Zipp F, Jayakumar A, Martin R, Leslie S, Hawkins S, Giannoulatou E, D'alfonso S, Blackburn H, Martinelli Boneschi F, Liddle J, Harbo HF, Perez ML, Spurkland A, Waller MJ, Mycko MP, Ricketts M, Comabella M, Hammond N, Kockum I, McCann OT, Ban M, Whittaker P, Kemppinen A, Weston P, Hawkins C, Widaa S, Zajicek J, Dronov S, Robertson N, Bumpstead SJ, Barcellos LF, Ravindrarajah R, Abraham R, Alfredsson L, Ardlie K, Aubin C, Baker A, Baker K, Baranzini SE, Bergamaschi L, Bergamaschi R, Bernstein A, Berthele A, Boggild M, Bradfield JP, Brassat D, Broadley SA, Buck D, Butzkueven H, Capra R, Carroll WM, Cavalla P, Celius EG, Cepok S, Chiavacci R, Clerget-Darpoux F, Clysters K, Comi G, Cossburn M, Cournu-Rebeix I, Cox MB, Cozen W, Cree BA, Cross AH, Cusi D, Daly MJ, Davis E, de Bakker PI, Debouverie M, D'hooghe MB, Dixon K, Dobosi R, Dubois B, Ellinghaus D, Elovaara I, Esposito F, Fontenille C, Foote S, Franke A, Galimberti D, Ghezzi A, Glessner J, Gomez R, Gout O, Graham C, Grant SF, Guerini FR, Hakonarson H, Hall P, Hamsten A, Hartung HP, Heard RN, Heath S, Hobart J, Hoshi M, Infante-Duarte C, Ingram G, Ingram W, Islam T, Jagodic M, Kabesch M, Kermode AG, Kilpatrick TJ, Kim C, Klopp N, Koivisto K, Larsson M, Lathrop M, Lechner-Scott JS, Leone MA, Leppä V, Liljedahl U, Bomfim IL, Lincoln RR, Link J, Liu J, Lorentzen AR, Lupoli S, Macciardi F, Mack T, Marriott M, Martinelli V, Mason D, McCauley JL, Mentch F, Mero IL, Mihalova T, Montalban X, Mottershead J, Myhr KM, Naldi P, Ollier W, Page A, Palotie A, Pelletier J, Piccio L, Pickersgill T, Piehl F, Pobywajlo S, Quach HL, Ramsay PP, Reunanen M, Reynolds R, Rioux JD, Rodegher M, Roesner S, Rubio JP, Rückert IM, Salvetti M, Salvi E, Santaniello A, Schaefer CA, Schreiber S, Schulze C, Scott RJ, Sellebjerg F, Selmaj KW, Sexton D, Shen L, Simms-Acuna B, Skidmore S, Sleiman PM, Smestad C, Sørensen PS, Søndergaard HB, Stankovich J, Strange RC, Sulonen AM, Sundqvist E, Syvänen AC, Taddeo F, Taylor B, Blackwell JM, Tienari P, Bramon E, Tourbah A, Brown MA, Tronczynska E, Casas JP, Tubridy N, Corvin A, Vickery J, Jankowski J, Villoslada P, Markus HS, Wang K, Mathew CG, Wason J, Palmer CN, Wichmann HE, Plomin R, Willoughby E, Rautanen A, Winkelmann J, Wittig M, Trembath RC, Yaouanq J, Viswanathan AC, Zhang H, Wood NW, Zuvich R, Deloukas P, Langford C, Duncanson A, Oksenberg JR, Pericak-Vance MA, Haines JL, Olsson T, Hillert J, Ivinson AJ, De Jager PL, Peltonen L, Stewart GJ, Hafler DA, Hauser SL, McVean G, Donnelly P, Compston A, Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis., Nature, 476, (7359), 2011, p214-9 Journal Article, 2011 TARA - Full Text DOI

Quinn EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW, Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression., Bipolar disorders, 12, (4), 2010, p440-445 Journal Article, 2010 DOI

Corvin A, Craddock N, Sullivan PF., Genome-wide association studies: a primer., Psychological Medicine, 40, (7), 2010, p1063-1077 Journal Article, 2010 TARA - Full Text

Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva , Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N. O'Donovan MC, Owen MJ. , Evidence for rate and common genetic risk variants for schizophrenia at a protein kinase C, alpha, Molecular Psychiatry, 15, (11), 2010, p1101-1111 Journal Article, 2010 DOI

Cummings E, Donohoe G, Morris DW, Gill M, Corvin A. , Clinical symptomatology and the psychosis risk gene, ZNF804A, Schizophrenia Research, 122, (1-3), 2010, p273-275 Journal Article, 2010 TARA - Full Text

Donohoe G, Frodl T, Morris D, Spoletini I, Cannon DM, Cherubini A, Caltagirone C, Bossù P, McDonald C, Gill M, Corvin AP, Spalletta G, Reduced Occipital and Prefrontal Brain Volumes in Dysbindin-Associated Schizophrenia, Neuropsychopharmacology, 35, (2), 2010, p368 - 373 Journal Article, 2010 DOI

UK Parkinson's Disease Consortium; Wellcome Trust Case Control Consortium 2, Spencer CC, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, Markus HS, Mathew CG, McCarthy MI, Morrison KE, Palmer CN, Pearson JP, Peltonen L, Pirinen M, Plomin R, Potter S, Rautanen A, Sawcer SJ, Su Z, Trembath RC, Viswanathan AC, Williams NW, Morris HR, Donnelly P, Wood NW., Dissection of the genetics of Parkinsons disease identifies an additional association 5'of SNCA and multiple associated haplotypes at 17 q 21, Human Molecular Genetics, 20, (2), 2010, p345-353 Journal Article, 2010 DOI

Donohoe G, Morris DW, Corvin A, The Psychosis Susceptibility gene ZNF804A: associations, functions and phenotypes, Schizophrenia Bulletin, 36, (5), 2010, p904-909 Review Article, 2010 URL TARA - Full Text DOI

Spalletta G, Morris DW, Angelucci F, Rubino IA, Spoletini I, Bria P, Martinotti G, Siracusano A, Bonaviri G, Bernadini S, Caltagirone C, Bossu P, Donohoe G, Gill M, Corvin AP. , BDNF Val66 Met polymorphism is associated with aggressive behaviour in schizophrenia. , European Psychiatry, 25, (6), 2010, p311-313 Journal Article, 2010 DOI

Strange A, Capon F, Spencer CC, Knight J, Weale ME, Allen MH, Barton A, Band G, Bellenguez C, Bergboer JG, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Cork MJ, Corvin A, Deloukas P, Dilthey A, Duncanson A, Edkins S, Estivill X, Fitzgerald O, Freeman C, Giardina E, Gray E, Hofer A, Hüffmeier U, Hunt SE, Irvine AD, Jankowski J, Kirby B, Langford C, Lascorz J, Leman J, Leslie S, Mallbris L, Markus HS, Mathew CG, McLean WH, McManus R, Mössner R, Moutsianas L, Naluai AT, Nestle FO, Novelli G, Onoufriadis A, Palmer CN, Perricone C, Pirinen M, Plomin R, Potter SC, Pujol RM, Rautanen A, Riveira-Munoz E, Ryan AW, Salmhofer W, Samuelsson L, Sawcer SJ, Schalkwijk J, Smith CH, Ståhle M, Su Z, Tazi-Ahnini R, Traupe H, Viswanathan AC, Warren RB, Weger W, Wolk K, Wood N, Worthington J, Young HS, Zeeuwen PL, Hayday A, Burden AD, Griffiths CE, Kere J, Reis A, McVean G, Evans DM, Brown MA, Barker JN, Peltonen L, Donnelly P, Trembath RC, A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1., Nature genetics, 42, (11), 2010, p985-990 Journal Article, 2010 DOI

Cognitive intermediate phenotypes in schizophrenia genetics in, Cognitive Genomics, US., MIT Press,, 2010, [Donohoe G, Goldberg T, Corvin A.] Book Chapter, 2010

O'Dushlaine C, McQuillan R, Weale ME, Crouch DJ, Johansson A, Aulchenko Y, Franklin CS, Pola"ek O, Fuchsberger C, Corvin A, Hicks AA, Vitart V, Hayward C, Wild SH, Meitinger T, van Duijn CM, Gyllensten U, Wright AF, Campbell H, Pramstaller PP, Rudan I, Wilson JF, Genes predict village of origin in rural Europe., European Journal of Human Genetics, 18, 2010, p1269-1270 Journal Article, 2010 TARA - Full Text DOI

International Stroke Genetics Consortium & Wellcome Trust Case Control Consortium 2, Failure to validate association between 12p13 variants and ischaemic stroke, New England Journal of Medicine, 362, (16), 2010, p1547-1550 Journal Article, 2010 URL TARA - Full Text

Gill, M., Donohoe, G., Corvin, A, What have the genomics ever done for the psychoses?, Psychological Medicine, 40, (4), 2010, p529-540 Journal Article, 2010 TARA - Full Text

Psychiatric Genetics in, Wright, Stern, Phelan , Core Psychiatry, Elsevier Saunders, 2010, [Corvin A, Gill M.] Book Chapter, 2010

James T. R. Walters; Aiden Corvin; Michael J. Owen; Hywel Williams; Milan Dragovic; Emma M. Quinn; Róisín Judge;Daniel J. Smith; Nadine Norton; Ina Giegling; Annette M. Hartmann; Hans-Jürgen Möller; Pierandrea Muglia; Valentina Moskvina; Sarah Dwyer;Therese O'Donoghue; Bharti Morar; Matthew Cooper; David Chandler; Assen Jablensky; Michael Gill; Luba Kaladjieva;Derek W. Morris; Michael C. O'Donovan; Dan Rujescu; Gary Donohoe, Psychosis Susceptibility Gene ZNF804A and Cognitive Performance in Schizophrenia, 67, 7, 2010 Journal Article, 2010 TARA - Full Text URL

Corvin A. , Neuronal cell adhesion genes: key players in risk for schizophrenia, bipolar disorder and other neurodevelopmental brain disorders? , Cell Adhesion & Migration, 4, (4), 2010, p1-13 Journal Article, 2010 TARA - Full Text

Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS, GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia., Molecular Psychiatry, 153B, (8), 2010, p1417 - 1424 Journal Article, 2010 DOI TARA - Full Text

Haq F, Behan C, McGlade N, Mulkerrin U, O'Callaghan E, Kinsella A, Corvin A, Donohoe G, Gill M. , The clinical and demographic factors that influence attitudes to antipsychotic medication among people with schizophrenia and schizoaffective disorder, Irish Journal of Psychological Medicine, 2010 Journal Article, 2010

Walters J, Corvin A, Williams H, Dragovic M, Quinn E, Judge R, Smith D, Norton N, Giegline I, Hartmann A, Moller HJ, Muglia P, Moskvina V, O'Donoghue T, Morar B, Cooper M, Chandler D, Jablensky A, Gill M, Owen MJ, Kaladjieva L, Morris D, O'Donovan MC, Rujescu D, Donohoe G., Variation in memory function associated with the psychosis susceptibility gene ZNF804A. , Archives of General Psychiatry, 67, (7), 2010, p692 - 700 Journal Article, 2010 URL

O'Dushlaine CT, Morris DW, Moskvina V, Kirov G, International Schizophrenia Consortium, Gill M, Corvin A, Wilson JF, Cavalleri GL. , Population structure and genome-wide patters of variation in Ireland and Britain. , European Journal of Human Genetics, 18, (11), 2010, p1248-1254 Journal Article, 2010 TARA - Full Text DOI

Gilks WP, Allott EH, Donohoe G, Cummings E, Consortium IS, Gill M, Corvin AP, Morris DW, Replicated genetic evidence supports a role for HOMER2 in schizophrenia., Neuroscience Letters, 468, (3), 2010, p229 - 233 Journal Article, 2010 DOI

Gary Donohoe, Emma Rose, Thomas Frodl, Derek Morris, Ilaria Spoletini, Fulvia Adriano, Sergio Bernardini, CarloCaltagirone, Paola Bossù, Michael Gill, Aiden P. Corvin and Gianfranco Spalletta, ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia, NeuroImage, 54, (3), 2010, p2132-2137 Journal Article, 2010 TARA - Full Text

Murtagh A, Hurley AL, Kinsella A, Corvin A, Donohoe G, Gill M, O'Callaghan E, Murphy KC. , The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness , European Psychiatry, 25, (2), 2010, p101-104 Journal Article, 2010 DOI

Donohoe G, Morris DW, Corvin A, The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypes., Schizophrenia bulletin, 36, (5), 2010, p904-9 Review Article, 2010 DOI TARA - Full Text

Moskvina V, Smith M, Ivanov D, Blackwood D, St. Clair D, Hultman C, Toncheva D, Gill M, Corvin A, O'Dushlaine C, Morris DW, Wray N, Sullivan P, Pato C, Pato M, Sklar Pm Purcell S, Holmans P, O'Donovan M, Owen M, Kirov, G, International Schizophrenia Consortium. , Genetic Differences between five european populations. , Human Heredity, 70, 2010, p141 - 149 Journal Article, 2010 DOI

Raychaudhuri S, Korn JM, McCarroll SA, International Schizophrenia Consortium, Altshuler D, Sklar P, Purcell S, Daly MJ, Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function., PLoS genetics, 6, (9, e1001097), 2010 Journal Article, 2010 DOI TARA - Full Text

Merikangas AK, Corvin A, Gallagher L., Promises and challenges of copy number variants in Neuropsychiatric Disorders. , Trends in Genetics , 25, (12), 2009, p536-544 Journal Article, 2009 DOI

O'Dushlaine C., Kenny E., Heron E.A., Segurado R., Gill M,, Morris D.W., Corvin A. , The SNP ratio test: pathway analysis of genome-wide association datasets., Bioinformatics, 25, (20), 2009, p2762 - 2763 Journal Article, 2009 DOI

O'Gráda C, Barry S, McGlade N, Behan C, Haq F, Hay, Does the ability to sustain attention underlie symptom severity in schizophrenia? , Schizophrenia Research, 107, (2-3), 2009, p319 - 323 Journal Article, 2009 DOI URL

Cognitive intermediate phenotypes in schizophrenia genetics in, The Genetics of Cognitive Neuroscience , US. , MIT Press, 2009, [Donohoe G, Goldberg T, Corvin A] Book Chapter, 2009

Donohoe G, Hayden J, McGlade N, O'Gráda C, Burke T, Barry S, Behan C, Dinan TG, O'Callaghan E, Gill M, Corvin AP, Is "clinical" insight the same as "cognitive" insight in schizophrenia?, Journal of the International Neuropsychological Society : JINS, 15, (3), 2009, p471-5 Journal Article, 2009 TARA - Full Text DOI

Barrett JC, Lee JC, Lees CW, Prescott NJ, Anderson CA, Phillips A, Wesley E, Parnell K, Zhang H, Drummond H, Nimmo ER, Massey D, Blaszczyk K, Elliott T, Cotterill L, Dallal H, Lobo AJ, Mowat C, Sanderson JD, Jewell DP, Newman WG, Edwards C, Ahmad T, Mansfield JC, Satsangi J, Parkes M, Mathew CG, Donnelly P, Peltonen L, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Craddock N, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, McCarthy MI, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Samani N, Trembath RC, Viswanathan AC, Wood N, Spencer CC, Barrett JC, Bellenguez C, Davison D, Freeman C, Strange A, Donnelly P, 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, Perez ML, Potter SC, Ravindrarajah R, Ricketts M, Waller M, Weston P, Widaa S, Whittaker P, Deloukas P, Peltonen L, Mathew CG, Blackwell JM, Brown MA, Corvin A, McCarthy MI, Spencer CC, Attwood AP, Stephens J, Sambrook J, Ouwehand WH, McArdle WL, Ring SM, Strachan DP, Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region., Nature Genetics, 41, (12), 2009, p1330-1334 Journal Article, 2009 DOI TARA - Full Text

International Schizophrenia Consortium, Common polygenic variation contributes to risk of schizophrenia and bipolar disorder., Nature, 460, (7256), 2009, p748-752 Journal Article, 2009 DOI

Cichon, S, Craddock, N, Daly, M, Faraone, SV, Gejman, PV, Kelsoe, J, Lehner, T, Levinson, DF, Moran, A, Sklar, P, Sullivan, PF, Genomewide association studies: history, rationale, and prospects for psychiatric disorders., The American journal of Psychiatry, 166, (5), 2009, p540-556 Journal Article, 2009 DOI

O'Donovan MC, 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, Giegling I, 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, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Adolfsson R, Osby U, Terenius L, Jönsson EG, Cichon S, Nöthen MM, Gill M, Corvin AP, Rujescu D, Gejman PV, Kirov G, Craddock N, Williams NM, Owen MJ., Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2., Molecular Psychiatry, 14, (1), 2009, p30 - 36 Journal Article, 2009 TARA - Full Text URL DOI

Kirov G, Grozeva D, Norton N, Ivanov D, Mantripragada KK, Holmans P; International Schizophrenia Consortium; Wellcome Trust Case Control Consortium, Craddock N, Owen MJ, O'Donovan MC, Support for the involvement of large copy number variants in the pathogenesis of schizophrenia., Human Molecular Genetics, 18, (8), 2009, p1497 - 1503 Journal Article, 2009 DOI

Merikangas AK, Corvin AP, Gallagher L, Copy-number variants in neurodevelopmental disorders: promises and challenges., Trends in genetics : TIG, 25, (12), 2009, p536-44 Journal Article, 2009 DOI

Donohoe G, Hayden J, McGlade N, O'Grada C, Burke T, Barry S, Behan C, DInan T, O'Callaghan E, Gill M, Corvin A. , Is 'Clinical' insight the same as 'Cognitive' insight in schizophrenia?, Journal of the International Neuropsychological Society, 15, (3), 2009, p471-475 Journal Article, 2009 TARA - Full Text DOI

Raychaudhuri S, Plenge RM, Rossin EJ, Ng AC; International Schizophrenia Consortium, Purcell SM, Sklar P, Scolnick EM, Xavier RJ, Altshuler D, Daly MJ, Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions., PLoS Genetics, 5, (6), 2009, pe1000534- Journal Article, 2009 TARA - Full Text

Donohoe G, Walters J, Morris DW, Quinn EM, Judge R, Norton N, Giegling I, Hartmann AM, Möller HJ, Muglia P, Williams H, Moskvina V, Peel R, O'Donoghue T, Owen MJ, O'Donovan MC, Gill M, Rujescu D, Corvin A, Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects., Archives of General Psychiatry, 66, (10), 2009, p1045-54 Journal Article, 2009 TARA - Full Text URL DOI

Hamshere ML, Schulze TG, Schumacher J, Corvin A, Owen JM, Jamra RA, Propping Pm Maier W. Orozco y Diaz G, Mayoral F, Rivas F. Jones I, Jones L, Kirov G, Gill M, Holmans PA, Nothen MM, Cichon S, Rietschel M, Craddock N, Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis show genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31., Bipolar Disorders, 11, (6), 2009, p610 - 620 Journal Article, 2009 DOI

Corvin A, Donohoe G, Nangle JM, Schwaiger S, Morris D, Gill M., A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis., Neuroscience Letters, 431, (2), 2008, p146 - 149 Journal Article, 2008 DOI URL URL

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; Molecular Genetics of Schizophrenia Collaboration, Gejman PV, Sanders AR, Duan J, Levinson DF, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR, Cichon S, Nöthen MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ., Identification of loci associated with schizophrenia by genome-wide association and follow-up., Nature Genetics, 40, (9), 2008, p1053 - 1055 Journal Article, 2008 URL DOI

Donohoe G, Morris D.W., De Sanctis P, Magno E, Montesi J, Garavan H, Robertson I, Javitt D, Gill M, Corvin A, Fox J. , Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia, Biological Psychiatry, 63, (5), 2008, p484 - 489 Journal Article, 2008 TARA - Full Text

Yang MS, Morris DW, 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, Chitinase-3-Like1 (CHI3L1) Gene and Schizophrenia: Genetic Association and a Potential functional Mechanism. , Biological Psychaitry, 64, (2), 2008, p98 - 103 Journal Article, 2008 URL URL DOI

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, Dysbindin (DTNBP1) and the BLOC-1 protein complex: main and epistatic gene effects are potential contributors to schizophrenia susceptibility, Biological Psychiatry, 63, (1), 2008, p24 - 31 Journal Article, 2008 URL DOI URL

Neuregulin-1-induced cell migration: a neurodevelopmental mechanism for schizophrenia susceptibility? in, Cell Science , 2008, [Corvin A. ] Book Chapter, 2008

Nicola McGlade, Caragh Behan, Judy Hayden, Therese O'Donoghue, Rosie Peel, Farhan Haq, Michael Gill, Aiden Corvin, Eadbhard O'Callaghan, Gary Donohoe, Mental state decoding v. mental state reasoning as a mediator between cognitive and social function in psychosis , British Journal of Psychiatry, 193, (1), 2008, p77-78 Journal Article, 2008 TARA - Full Text DOI

Barnett KJ, Newell FN, Finucane C, Corvin AP, Mitchell KJ., Familial patterns and the origins of individual differences in synaesthesia, Cognition, 106, (2), 2008, p871 - 893 Journal Article, 2008 DOI

Behan C, McGlade N, Haq F, Kinsella A, Gill M, Corvin A, O'Callaghan E. , Physical health and attendance at primary care in people with schizophrenia., Irish Journal of Psychological Medicine, 25, 2008, p57 - 60 Journal Article, 2008 URL

Ferreira MA, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L, Fan J, Kirov G, Perlis RH, Green EK, Smoller JW, Grozeva D, Stone J, Nikolov I, Chambert K, Hamshere ML, Nimgaonkar VL, Moskvina V, Thase ME, Caesar S, Sachs GS, Franklin J, Gordon-Smith K, Ardlie KG, Gabriel SB, Fraser C, Blumenstiel B, Defelice M, Breen G, Gill M, Morris DW, Elkin A, Muir WJ, McGhee KA, Williamson R, Macintyre DJ, Maclean AW, St Clair D, Robinson M, Van Beck M, Pereira AC, Kandaswamy R, McQuillin A, Collier DA, Bass NJ, Young AH, Lawrence J, Nicol Ferrier I, Anjorin A, Farmer A, Curtis D, Scolnick EM, McGuffin P, Daly MJ, Corvin AP, Holmans PA, Blackwood DH; Wellcome Trust Case Control Consortium, Gurling HM, Owen MJ, Purcell SM, Sklar P, Craddock N., Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder., Nature Genetics, 40, (9), 2008, p1056 - 1058 Journal Article, 2008 TARA - Full Text DOI

Morris, D.W. , Murphy, K. , Kenny, N. , Purcell, S.M. , McGhee, K.A. , Schwaiger, S., Nangle, J.-M. , Donohoe, G. , Clarke, S. , Scully, P. , Quinn, J. , Meagher, D. , Baldwin, P. , Crumlish, N. , O'Callaghan, E., Waddington, J.L. , Gill, M. , Corvin, A.P., 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), 2008, p24-31 Journal Article, 2008 URL DOI

O'Dushlaine, C. T., Dolan, C., Weale, M. E., Stanton, A., Croke, D. T., Kalviainen, R., Eriksson, K., Kantanen, A. M., Gibson, R. A., Hosford, D., Sisodiya, S. M., Gill, M., Corvin, A. P., Morris, D. W., Delanty, N., Cavalleri, G. L., An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases, Eur J Hum Genet, 16, (2), 2008, p176 - 183 Journal Article, 2008 DOI TARA - Full Text

International Schizophrenia Consortium, Greater burden of rare copy number variants in schizophrenia, Nature, 7210, (455), 2008, p237 - 241 Journal Article, 2008 URL DOI

Barnett, KJ, Finucane, C, Asher, JE, Bargary, G, Corvin, AP, Newell, FN, Mitchell, KJ, Familial patterns and the origins of individual differences in synaesthesia., Cognition, 106, (2), 2008, p871-893 Journal Article, 2008 DOI

Donohoe G, Spoletini I, McGlade N, Behan C, Hayden J, O'Donoghue T, Peel R, Haq F, Walker C, O'Callaghan E, Spalletta G, Gill M, Corvin A , Are relational style and neuropsychological performance predictors of social attributions in chronic schizophrenia?, Psychiatric Research, 161, (1), 2008, p19-27 Journal Article, 2008 URL DOI

International Schizophrenia Consortium, Rare chromosomal deletions and duplications increase risk of schizophrenia., Nature, 455, (7210), 2008, p237 - 241 Journal Article, 2008 DOI TARA - Full Text

Donohoe G, Behan C, Hayden J, O'Donoghue T, Peel R, Haq F, Gill M, Corvin A, O'Callaghan E. , Mental state decoding versus mental state reasoning as a mediator between cognitive and social function in psychosis., British Journal of Psychiatry, 193, (1), 2008, p77 - 78 Journal Article, 2008 DOI

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, 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, 144, (7), 2007, p949 - 953 Journal Article, 2007 DOI URL URL

Donohoe G, Morris DW, Clarke S, McGhee K, Schwaiger S, Nangle JM, Garavan H, Robertson I, Gill M, Corvin A., Variance in neurocognitive performance is associated with Dysbindin-1 in schizophrenia: a preliminary study., Neuropsychologia, 45, (2), 2007, p454 - 458 Journal Article, 2007 URL URL DOI

Donohoe G, Morris D, Clarke S, McGhee K, Schwaiger S, Nangle JM, Robertson I, Gill M, Corvin A. , Variance in facial recognition performance associated with BDNF in schizophrenia., American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B, 2007, p578 - 579 Journal Article, 2007 URL DOI URL

Donohoe G, Morris DW, Robertson IH, McGhee KA, Murphy K, Kenny N, Clarke S, Gill M, Corvin AP., DAOA ARG30LYS and verbal memory function in schizophrenia., Molecular Psychiatry, 12, (9), 2007, p795 - 796 Journal Article, 2007 DOI URL URL

Jones I, Hanshere M L, Nangle J M, Bennett P, Middle F, Heron J, Segurado R, Lambert D, Williams H, Corvin A, Owen J J, Jones L, Gill M Craddock N, Bipolar affective puerperal psychosis- genome-wide significant evidence for linkage to chromosome 16., American Journal of Psychiatry , 164, (7), 2007, p1 - 6 Journal Article, 2007 DOI TARA - Full Text

Corvin A, Donohoe G, McGhee K, Murphy K, Kenny N, Schwaiger S, Nangle JM, Morris D, Gill M., D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia., Neuroscience Letters, 426, (2), 2007, p97 - 100 Journal Article, 2007 URL URL DOI

Waddington JL, Corvin A, Donohoe G, O'Tuathaigh C, Mitchell K, Gill M., Functional genomics and schizophrenia; endophenotypes and mutant models., Psychiatric Clinics of North America, 30, (3), 2007, p365 - 399 Journal Article, 2007 URL

Donohoe G, Clarke S, Morris D, Nangle JM, Schwaiger S, Gill M, Corvin A, Robertson I., Are Deficits in Executive Sub-processes simply reflecting more general cognitive decline in Schizophrenia?, Schizophrenia Research, 85, (1-3), 2006, p196 - 200 Journal Article, 2006 URL DOI

Donohoe G, Corvin A, Robertson IH. , Evidence that specific executive functions predict symptom variance among patients with a predominately negative symptom profile of schizophrenia. , Cognitive Neuropsychiatry, 11, (1), 2006, p13 - 32 Journal Article, 2006 URL DOI

Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer SL, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, Corvin AP, Owen MJ, O?Donovan MC. , 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), 2006, p96 - 101 Journal Article, 2006 DOI

Donohoe G, Morris D, Robertson IH, Gill M, Foxe J, Corvin A, Dysbindin and Cognition In An Irish Sample., Biological Psychiatry , 59, (8), 2006, pp623 Meeting Abstract, 2006

Donohoe G, Reilly R, Clarke S, Meredith S, Greene B, Morris D, Gill M, Corvin A, Garavan H, Robertson I. , Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function?, Journal of the International Neuropsychological Society, 12, (6), 2006, p901 - 906 Journal Article, 2006 URL DOI TARA - Full Text

Nangle JM, Clarke S, Morris DW, Schwaiger S, McGhee KA, Kenny N, Murphy K, Gill M, Corvin A, Donohoe G., Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders., Schizophrenia Research, 85, (1-3), 2006, p196 - 200 Journal Article, 2006 DOI URL URL

Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande S, Egan MF, Ferrell RE, Gill M, Kendler KS, Kirov G, Levitt P, Lewis DA, Li T, Mirnics K, Morris DW, O?Donovan MC, Owen MJ, Sobell JL, Thelma BK, Vallada H, Weinberger DR, Williams NM, Wood J, Devlin B, and Nimgaonkar VL. , Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples , Biological Psychiatry, 60, (2), 2006, p152 - 162 Journal Article, 2006 URL TARA - Full Text DOI URL

Nangle JM, Clarke S, Donohoe G, Schwaiger S, Morris DW, McGhee KA, Kenny N, Murphy K, Gill M, Corvin A. , Neurocognition and Suicidal Behaviour in an Irish population with Major Psychotic Disorders., Schizophrenia Research, 85, (1-3), 2006, p196 - 200 Journal Article, 2006 DOI URL

Donohoe G, Corvin A, Robertson I. , Evidence That Specific Executive Functions Predict Symptom Variance Among Patients With A Predominantly Negative Symptom Profile. , Cognitive Neuropsychiatry, 11, (1), 2006, p13 - 32 Journal Article, 2006 DOI URL

Psychiatric Genetics in, editor(s)Wright, Stern , Core Psychiatry, Phelan, Elsevier Saunders, 2005, pp35-54 , [Corvin A, Gill M.] Book Chapter, 2005

Clarke S, Donohoe G, Morris D, Nangle JM, Schwaiger S, McGhee K, Gill M, Garavan H, Robertson IH, Corvin A. , Evidence Of independence between antisaccade performance and working memory task performance in schizophrenia, Schizophrenia Bulletin , 31, (2), 2005, pp353 Meeting Abstract, 2005

Donohoe G, Corvin A, Robertson IH, Are the cognitive deficits associated with impaired insight in schizophrenia specific to executive task performance?, Journal of Nervous and Mental Disease, 193, (12), 2005, p803 - 808 Journal Article, 2005 URL

McGhee KA, Morris DW, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Meagher D, QuinnJ, Scully P, Waddington JL, Gill M, Corvin A, 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), 2005, p231 - 238 Journal Article, 2005 URL URL DOI

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 Corvin AP., Association analyses of the BLOC-1 genes suggest the involvement of BLOC-1 in schizophrenia etiology, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 138B, 2005, pp129 Meeting Abstract, 2005

Hamshere M, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan M, Owen M, Craddock N., Genome-wide linkage scan in schizoaffective disorder: Significant evidence for linkage (LOD=3.54) at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19q13., Archives of General Psychiatry, 62, (10), 2005, p1081 - 1088 Journal Article, 2005 URL

Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, O'Mahony E, Mulcahy T, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M and Craddock N, Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. , Molecular Psychiatry, 10, (9), 2005, p831 - 841 Journal Article, 2005 URL DOI

Murtagh A, McTigue O, Hegarty AM, Stallings RL, Green AJ, Ramsay L and Corvin A. , Interstitial deletion of chromosome 21 and schizophrenia., Schizophrenia Research, 78, (2-3), 2005, p353 - 356 Journal Article, 2005 URL DOI

Anxiety Disorders in, editor(s)Wright, Stern, Phelan , Core Psychiatry, UK, Elsevier Saunders , 2005, pp193 - 204, [Corvin A, Lucey JV] Book Chapter, 2005

Anxiety Disorders in, Wright, Stern , Core Psychiatry, Elsevier Saunders, 2005, pp193-204 , [Corvin A, Lucey JV] Book Chapter, 2005

Morris DW, Nangle JM, Kiely B, Corvin A, Gill M. , The molecular basis of schizophrenia: a complex genetic disorder. , Irish Psychiatrist, 5, 2004, p134 - 137 Journal Article, 2004

Corvin AP, Morris DW, McGhee K, Schwaiger S, Scully P, Quinn J, Meagher D, Clair DS, Waddington JL, Gill M, 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), 2004, p208 - 213 Journal Article, 2004 URL URL DOI

N. M. Williams, A. Preece, D. W. Morris, G. Spurlock, N. J. Bray, M. Stephens, N. Norton, H. Williams, M. Clement, S. Dwyer, C. Curran, J. Wilkinson, V. Moskvina, J. L. Waddington, M. Gill, A. P. Corvin, S. Zammit, G. Kirov, M. J. Owen and M. C. O'Donovan, Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1), Archives of General Psychiatry, 61, (4), 2004, p336 - 344 Journal Article, 2004 URL

Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP, Confirming RGS4 as a susceptibility gene for schizophrenia., American Journal of Medical Genetics (Part B: Neuropsychiatric Genetics), 125B, (1), 2004, p50 - 53 Journal Article, 2004 URL DOI URL

D. W. Morris, K. A. McGhee, S. Schwaiger, P. Scully, J. Quinn, D. Meagher, J. L. Waddington, M. Gill and A. P. Corvin, No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study, Schizophrenia research, 60, (2-3), 2003, p167-72 Journal Article, 2003 URL URL DOI

Corvin A, Gill M , Psychiatric Genetics in the post genome age, British Journal of Psychiatry, 182, 2003, p95 - 96 Journal Article, 2003 TARA - Full Text URL

O'Mahony E, Corvin A, Comerford C, O'Connell R, Larsen B, Jones IR, Mc Candless F, Kirov G, Cardno A, Craddock N, and Gill M. , Sibling pairs with affective disorders: resemblance of demographic and clinical features, Psychological Medicine, 32 , (1), 2002, p55 - 61 Journal Article, 2002 URL DOI

P. Bennett, R. Segurado, I. Jones, S. Bort, F. McCandless, D. Lambert, J. Heron, C. Comerford, F. Middle, A. Corvin, G. Pelios, G. Kirov, B. Larsen, T. Mulcahy, N. Williams, R. O'Connell, E. O'Mahony, A. Payne, M. Owen, P. Holmans, N. Craddock and M. Gill, The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report, Molecular Psychiatry, 7, (2), 2002, p189-200 Journal Article, 2002 TARA - Full Text DOI

A. Corvin, Schizophrenia and velocardio-facial syndrome, Lancet, 360, (9334), 2002, p721-2; Journal Article, 2002 URL DOI URL

Fitzgerald M. & Corvin A., Diagnosis and differential diagnosis of Asperger's Syndrome., Advances in Psychiatric Treatment , 7, (4), 2001, p310 - 318 Journal Article, 2001 URL URL

O'Mahony E, Corvin A. , The attitudes of Irish trainees to their training and its supervision: a five-year follow up study, Irish Journal of Psychological Medicine, 18, 2001, p120 - 125 Journal Article, 2001 URL

A. Corvin, E. O'Mahony, M. O'Regan, C. Comerford, R. O'Connell, N. Craddock and M. Gill, Cigarette smoking and psychotic symptoms in bipolar affective disorder, The British Journal of Psychiatry , 179, 2001, p35-38 Journal Article, 2001 URL TARA - Full Text

Corvin A, O'Mahony E, O'Regan M, Comerford C, O'Connell R, Craddock N, Gill M., Cigarette smoking predicts psychosis in bipolar affective disorder., British Journal of Psychiatry, 179, 2001, p35 - 38 Journal Article, 2001 URL

Neuropsychiatric Genetics in, editor(s)Lawlor , Revision Psychiatry, MedMedia , 2001, [Corvin A, Gill M. ] Book Chapter, 2001

Corvin A, O'Mahony E , Trainees access to computers and computer software, Psychiatric Bulletin , 25, (4), 2001, p155 - 155 Journal Article, 2001 URL

Corvin A, Fitzgerald M, Evidence-Based Medicine: Psychoanalysis and Psychotherapy. , Psychoanalytic Psychotherapy , 14, (2), 2000, p143 - 151 Journal Article, 2000 DOI URL

Corvin A. , Psychosis: a genetic perspective., Irish Journal of Psychological Medicine, 12, (supp), 2000, p3-6 Journal Article, 2000

M. Garland, D. Hickey, A. Corvin, J. Golden, P. Fitzpatrick, S. Cunningham and N. Walsh, Total serum cholesterol in relation to psychological correlates in parasuicide, The British journal of psychiatry; the journal of mental science, 177, (468), 2000, p77-83 Journal Article, 2000 URL URL

Non-Peer-Reviewed Publications

Robinson, P.C., Leo, P.J., Pointon, J.J., (...), Duncan, E.L., Wordsworth, B.P., The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis, Genes and Immunity, 17, (1), 2016, p46-51 Journal Article, 2016 DOI

Corvin, A., Symposium Organizer, Schizophrenia International Research Society,, April 16th, In:Schizophrenia International Research Society,, 2012, Florence, Italy Meetings /Conferences Organised, 2012

Corvin, A., Schizophrenia: Evolution and Synthesis: A think tank to accelerate treatment development and prevention efforts. , Ernst Strungman Forum, Frankfurt, Germany, 20-28th July, 2012 Invited Talk, 2012

Corvin A. , The changing faces of schizophrenia. The Big Idea. , 2012, - Miscellaneous, 2012

Corvin AP, McGhee K, Murphy K, Walsh C, Kenny N, Nangle J, Schwaiger S, Baldwin P, Scully P, Quinn J, Crumlish N, O'Callaghan E, Waddington J, Morris D, Gill M, Evidence for association and interaction between G72 and DAAO markers in an Irish case-control schizophrenia sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, SEP 5, 138B, (1), 2005, pp25 - 25 Meeting Abstract, 2005

Research Expertise

Description

I am interested in applying genomics methods to improving understanding of heritable major mental disorders and cognitive processes. Specifically, my research involves the identification and characterization of genes/molecular pathways contributing to disorders such as schizophrenia and bipolar disorder. I have headed the Psychosis Research Group at the Neuropsychiatric Genetics Laboratory since 1999. The group's research activities span from the genome to clinical symptoms (including genomics, biostatistics, bioinformatics, clinical phenotyping, neuropsychology, electrophysiology and neuroimaging). We collaborate with local researchers at the Institute of Molecular Medicine, Department of Genetics and TCIN. We are members of the International Schizophrenia Consortium and collaborate with researchers in the UK, Italy, Australia and US. I am also involved in projects relating to the genetics of cognition and synaesthesia.

Keywords

Aetiology of mental illness; Cognitive dysfunction in psychotic disorders; Neurodegenerative diseases including schizophrenia & Alzheimer's disease; Neurogenetics; Psychiatric genetics; Schizophrenia