Professor Aiden Corvin

Professor Aiden Corvin

Professor Consultant, Psychiatry

Deputy Director

3531896 2467http://people.tcd.ie/acorvin

Biography

Professor Aiden Corvin (MB, PhD, MRCPsych, FTCD) is a Professor in the Discipline of Psychiatry TCD (formerly Head of Discipline 2016-2022) and Clinical Director of the St. James"s Hospital Mental Health Service. He leads the Neuropsychiatric Genetics Research Group at TCD. Over more than twenty years he has investigated the genetic basis of psychiatric disorders, in particular schizophrenia and bipolar disorder. His work is driven by the clinical imperatives of being able to answer the questions of patients and their families; to improve understanding of disease biology; and to develop better patient care. He has significantly contributed to a revolution in understanding of the genetic basis of psychiatric disorders. He was lead investigator for schizophrenia with the Wellcome Trust Case Control Consortium (WTCCCC) and is Chair of the Pedigree Sequencing Working Group of the Psychiatric Genomics Consortium (PGC), an international collaborative research project that includes more than 800 scientists. He has published in journals such as Science, Nature, Nature Genetics, JAMA Psychiatry, and the British Journal of Psychiatry. His work has been funded by the National Institute of Health (US), Wellcome, Science Foundation Ireland, and the Health Research Board, Ireland. He is consistently one of the most cited Irish biomedical scientists and has published more than 320 peer reviewed journal articles (h-index 100 and >65,000 citations as of October 2023).

Publications and Further Research Outputs

  • Mothersill O, Morris DW, Kelly S, Rose EJ, Bokde A, Reilly R, Gill M, Corvin AP, Donohoe G, Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients, Schizophrenia research, 157, 2014, p225 - 230Journal Article, 2014, 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, 20, (11), 2015, 1366-72Journal Article, 2015, DOI , TARA - Full Text
  • Nicodemus KK, Hargreaves A, Morris D, Anney R, Gill M, Corvin A, Donohoe G, Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway., JAMA psychiatry, 71, (7), 2014, p778-85Journal Article, 2014, DOI , TARA - Full Text
  • 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, p776-83Journal Article, 2013, DOI , TARA - Full Text
  • Kelly,Sinéad S., Morris,Derek W. D.W., Mothersill,Omar O., Rose,Emma Jane E.J., Fahey,Ciara A. C.A., O'Brien,Carol H. C.H., O'Hanlon,Erik E., Gill,Michael M., Corvin,Aiden P. A.P., Donohoe,Gary J. G.J., Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants, Neuroscience Letters, 574, 2014, p6-10Journal Article, 2014, DOI , TARA - Full Text
  • Merikangas AK, Segurado R, Cormican P, Heron EA, Anney RJ, Moore S, Kelleher E, Hargreaves A, Anderson-Schmidt H, Gill M, Gallagher L, Corvin A., The phenotypic manifestations of rare CNVs in schizophrenia., Schizophrenia Research, 158, (1-3), 2014, p255 - 260Journal Article, 2014, 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, p1-7Journal Article, 2014, DOI , 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 - 120Journal Article, 2015, DOI , URL , 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, DOI , URL , 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 - 496Journal Article, 2014, DOI , URL , TARA - Full Text
  • 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, p1209-17Journal Article, 2014, DOI , TARA - Full Text
  • Schizophrenia Working Group of the Psychiatric Genomics Consortium , Biological insights from 108 schizophrenia-associated genetic loci., Nature, 511, (7510), 2014, p421-7Journal Article, 2014, DOI , TARA - Full Text
  • 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, p547-553Journal Article, 2016, DOI , URL , TARA - Full Text
  • 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, European Journal of Human Genetics, 24, 2016, p291 - 297Journal Article, 2016, DOI , URL , 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 - 373Journal 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 - 562Journal 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 - 248Journal Article, 2015, DOI , URL
  • 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, 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, p104-20Journal Article, 2015, DOI , TARA - Full Text
  • 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, 2015Journal Article, 2015
  • 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, p452-61Journal Article, 2014, DOI , TARA - Full Text
  • 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, p1017-24Journal 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, p52Journal Article, 2014, DOI , TARA - Full Text
  • Corvin, A., O'Donovan, M.C., Psychiatric genetics: What's new in 2015?, The Lancet Psychiatry, 3, (1), 2016, p10-12Journal Article, 2016
  • 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, p1706-1721Journal Article, 2015, DOI , TARA - Full Text
  • 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, p44-49Journal Article, 2015, DOI , TARA - Full Text
  • 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
  • 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 - 1100Journal Article, 2016, DOI , URL
  • 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 - 116Journal 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 - 541Journal Article, 2016, DOI , URL
  • Baurecht H, Hotze M, Brand S, BÃŒning 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
  • Anxiety Disorders in, editor(s)Wright, Stern, Phelan , Core Psychiatry, UK, Elsevier Saunders , 2005, pp193 - 204, [Corvin A, Lucey JV]Book Chapter, 2005
  • 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 - 32Journal Article, 2006, DOI , URL
  • 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 - 32Journal Article, 2006, 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, 336-345Journal Article, 2017, DOI , URL , TARA - Full Text
  • 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 - 1179Journal Article, 2016, DOI , URL
  • Luo X.-J, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, Cichon S, Collier D.A, Tosato S, Suvisaari J, Rujescu D, Golimbet V, Silagadze T, Durmishi N, Milovancevic M.P, Stefansson H, Schulze T.G, Nöthen M.M, Chen C, Lyne R, Morris D.W, Gill M, Corvin A, Zhang D, Dong Q, Moyzis R.K, Stefansson K, Sigurdsson E, Hu F, SCZ Consortium3, Su B, Gan L, Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene, Molecular Psychiatry, 19, (7), 2014, p774 - 783Journal Article, 2014, DOI , URL
  • 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, 2016Journal Article, 2016, DOI , URL , TARA - Full Text
  • 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 - 18Journal Article, 2016, DOI , URL , TARA - Full Text
  • 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 - 356Journal Article, 2005, DOI , 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 - 61Journal Article, 2002, DOI , URL
  • 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 - 38Journal Article, 2001, 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 - 125Journal Article, 2001, URL
  • Corvin A, O'Mahony E , Trainees access to computers and computer software, Psychiatric Bulletin , 25, (4), 2001, p155 - 155Journal Article, 2001, URL
  • Corvin A, Fitzgerald M, Evidence-Based Medicine: Psychoanalysis and Psychotherapy. , Psychoanalytic Psychotherapy , 14, (2), 2000, p143 - 151Journal Article, 2000, DOI , URL
  • 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, p14774Journal 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, p2129-2138Journal 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 - 160Journal Article, 2017, DOI , URL
  • 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 - 328Journal Article, 2017, DOI , URL
  • Foley C, Corvin A, Nakagome S, Genetics of Schizophrenia: Ready to Translate?, Current Psychiatry Reports, 19, (9), 2017, p61-Journal Article, 2017, DOI , URL
  • 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, p439-447Journal Article, 2017, 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, p13624Journal Article, 2017, DOI , TARA - Full Text
  • 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, 193, 2018, p468-469Journal Article, 2018, DOI , TARA - Full Text
  • 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, p27-35Journal Article, 2017, 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, p1569-1582Journal Article, 2016, 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, p47-54Journal Article, 2016, 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, p741-745Journal Article, 2016, 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, p993-998Journal Article, 2016, DOI
  • 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, DOI , TARA - Full Text
  • Schizophrenia in, Genomics, Circuits, and Pathways in Clinical Neuropsychiatry, 2016, 411-428 , [Corvin, A]Book Chapter, 2016
  • 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, p857-868Journal Article, 2016, DOI
  • 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, p276-289Journal 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, p420-431Journal Article, 2016, DOI
  • Donohoe, G. and Dillon, R. and Hargreaves, A. and Mothersill, O. and Castorina, M. and Furey, E. and Fagan, A.J. and Meaney, J.F. and Fitzmaurice, B. and Hallahan, B. and McDonald, C. and Wykes, T. and Corvin, A. and Robertson, I.H., Effectiveness of a low support, remotely accessible, cognitive remediation training programme for chronic psychosis: cognitive, functional and cortical outcomes from a single blind randomised controlled trial, Psychological Medicine, 48, (5), 2018, p751-764Journal Article, 2018, DOI , URL
  • Blokland, G.A.M. and del Re, E.C. and Mesholam-Gately, R.I. and Jovicich, J. and Trampush, J.W. and Keshavan, M.S. and DeLisi, L.E. and Walters, J.T.R. and Turner, J.A. and Malhotra, A.K. and Lencz, T. and Shenton, M.E. and Voineskos, A.N. and Rujescu, D. and Giegling, I. and Kahn, R.S. and Roffman, J.L. and Holt, D.J. and Ehrlich, S. and Kikinis, Z. and Dazzan, P. and Murray, R.M. and Di Forti, M. and Lee, J. and Sim, K. and Lam, M. and Wolthusen, R.P.F. and de Zwarte, S.M.C. and Walton, E. and Cosgrove, D. and Kelly, S. and Maleki, N. and Osiecki, L. and Picchioni, M.M. and Bramon, E. and Russo, M. and David, A.S. and Mondelli, V. and Reinders, A.A.T.S. and Falcone, M.A. and Hartmann, A.M. and Konte, B. and Morris, D.W. and Gill, M. and Corvin, A.P. and Cahn, W. and Ho, N.F. and Liu, J.J. and Keefe, R.S.E. and Gollub, R.L. and Manoach, D.S. and Calhoun, V.D. and Schulz, S.C. and Sponheim, S.R. and Goff, D.C. and Buka, S.L. and Cherkerzian, S. and Thermenos, H.W. and Kubicki, M. and Nestor, P.G. and Dickie, E.W. and Vassos, E. and Ciufolini, S. and Reis Marques, T. and Crossley, N.A. and Purcell, S.M. and Smoller, J.W. and van Haren, N.E.M. and Toulopoulou, T. and Donohoe, G. and Goldstein, J.M. and Seidman, L.J. and McCarley, R.W. and Petryshen, T.L., The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project, Schizophrenia Research, 195, 2018, p306-317Journal Article, 2018, DOI , URL , TARA - Full Text
  • Van Erp, T.G.M. and Hibar, D.P. and Rasmussen, J.M. and Glahn, D.C. and Pearlson, G.D. and Andreassen, O.A. and Agartz, I. and Westlye, L.T. and Haukvik, U.K. and Dale, A.M. and Melle, I. and Hartberg, C.B. and Gruber, O. and Kraemer, B. and Zilles, D. and Donohoe, G. and Kelly, S. and Mcdonald, C. and Morris, D.W. and Cannon, D.M. and Corvin, A. and Machielsen, M.W.J. and Koenders, L. and De Haan, L. and Veltman, D.J. and Satterthwaite, T.D. and Wolf, D.H. and Gur, R.C. and Gur, R.E. and Potkin, S.G. and Mathalon, D.H. and Mueller, B.A. and Preda, A. and Macciardi, F. and Ehrlich, S. and Walton, E. and Hass, J. and Calhoun, V.D. and Bockholt, H.J. and Sponheim, S.R. and Shoemaker, J.M. and Van Haren, N.E.M. and Pol, H.E.H. and Ophoff, R.A. and Kahn, R.S. and Roiz-Santiañez, R. and Crespo-Facorro, B. and Wang, L. and Alpert, K.I. and Jönsson, E.G. and Dimitrova, R. and Bois, C. and Whalley, H.C. and Mcintosh, A.M. and Lawrie, S.M. and Hashimoto, R. and Thompson, P.M. and Turner, J.A., Erratum: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium (Molecular Psychiatry (2015) DOI:10.1038/mp.2015.63), 2016, - 585Miscellaneous, 2016, DOI , URL
  • Donohoe, G. and Holland, J. and Mothersill, D. and McCarthy-Jones, S. and Cosgrove, D. and Harold, D. and Richards, A. and Mantripragada, K. and Owen, M.J. and O'Donovan, M.C. and Wtccc2 and Gill, M. and Corvin, A. and Morris, D.W., Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation, Psychological Medicine, 2018, p1-10Journal Article, 2018, DOI , URL
  • Walton, E. and Hibar, D.P. and Van Erp, T.G.M. and Potkin, S.G. and Roiz-Santiañez, R. and Crespo-Facorro, B. and Suarez-Pinilla, P. and Van Haren, N.E.M. and De Zwarte, S.M.C. and Kahn, R.S. and Cahn, W. and Doan, N.T. and Jorgensen, K.N. and Gurholt, T.P. and Agartz, I. and Andreassen, O.A. and Westlye, L.T. and Melle, I. and Berg, A.O. and Morch-Johnsen, L. and FÊrden, A. and Flyckt, L. and Fatouros-Bergman, H. and Jönsson, E.G. and Hashimoto, R. and Yamamori, H. and Fukunaga, M. and Jahanshad, N. and De Rossi, P. and Piras, F. and Banaj, N. and Spalletta, G. and Gur, R.E. and Gur, R.C. and Wolf, D.H. and Satterthwaite, T.D. and Beard, L.M. and Sommer, I.E. and Koops, S. and Gruber, O. and Richter, A. and KrÀmer, B. and Kelly, S. and Donohoe, G. and McDonald, C. and Cannon, D.M. and Corvin, A. and Gill, M. and Di Giorgio, A. and Bertolino, A. and Lawrie, S. and Nickson, T. and Whalley, H.C. and Neilson, E. and Calhoun, V.D. and Thompson, P.M. and Turner, J.A. and Ehrlich, S., Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium, Psychological Medicine, 48, (1), 2018, p82-94Journal Article, 2018, DOI , URL , TARA - Full Text
  • Lam, M. and Trampush, J.W. and Yu, J. and Knowles, E. and Davies, G. and Liewald, D.C. and Starr, J.M. and Djurovic, S. and Melle, I. and Sundet, K. and Christoforou, A. and Reinvang, I. and DeRosse, P. and Lundervold, A.J. and Steen, V.M. and Espeseth, T. and RÀikkönen, K. and Widen, E. and Palotie, A. and Eriksson, J.G. and Giegling, I. and Konte, B. and Roussos, P. and Giakoumaki, S. and Burdick, K.E. and Payton, A. and Ollier, W. and Chiba-Falek, O. and Attix, D.K. and Need, A.C. and Cirulli, E.T. and Voineskos, A.N. and Stefanis, N.C. and Avramopoulos, D. and Hatzimanolis, A. and Arking, D.E. and Smyrnis, N. and Bilder, R.M. and Freimer, N.A. and Cannon, T.D. and London, E. and Poldrack, R.A. and Sabb, F.W. and Congdon, E. and Conley, E.D. and Scult, M.A. and Dickinson, D. and Straub, R.E. and Donohoe, G. and Morris, D. and Corvin, A. and Gill, M. and Hariri, A.R. and Weinberger, D.R. and Pendleton, N. and Bitsios, P. and Rujescu, D. and Lahti, J. and Le Hellard, S. and Keller, M.C. and Andreassen, O.A. and Deary, I.J. and Glahn, D.C. and Malhotra, A.K. and Lencz, T., Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets, Cell Reports, 21, (9), 2017, p2597-2613Journal Article, 2017, DOI , URL
  • Cosgrove, D. and Harold, D. and Mothersill, O. and Anney, R. and Hill, M.J. and Bray, N.J. and Blokland, G. and Petryshen, T. and Richards, A. and Mantripragada, K. and Owen, M. and O'Donovan, M.C. and Gill, M. and Corvin, A. and Morris, D.W. and Donohoe, G., MiR-137-derived polygenic risk: Effects on cognitive performance in patients with schizophrenia and controls, Translational Psychiatry, 7, (1), 2017, pe1012-Journal Article, 2017, DOI , URL , TARA - Full Text
  • Iglesias, A.I. and Mishra, A. and Vitart, V. and Bykhovskaya, Y. and Höhn, R. and Springelkamp, H. and Cuellar-Partida, G. and Gharahkhani, P. and Bailey, J.N.C. and Willoughby, C.E. and Li, X. and Yazar, S. and Nag, A. and Khawaja, A.P. and PolaÅ¡ek, O. and Siscovick, D. and Mitchell, P. and Tham, Y.C. and Haines, J.L. and Kearns, L.S. and Hayward, C. and Shi, Y. and Van Leeuwen, E.M. and Taylor, K.D. and Wang, J.J. and Rochtchina, E. and Attia, J. and Scott, R. and Holliday, E.G. and Baird, P.N. and Xie, J. and Inouye, M. and Viswanathan, A. and Sim, X. and Bonnemaijer, P. and Rotter, J.I. and Martin, N.G. and Zeller, T. and Mills, R.A. and Staffieri, S.E. and Jonas, J.B. and Schmidtmann, I. and Boutin, T. and Kang, J.H. and Lucas, S.E.M. and Wong, T.Y. and Beutel, M.E. and Wilson, J.F. and Allingham, R.R. and Brilliant, M.H. and Budenz, D.L. and Christen, W.G. and Fingert, J. and Friedman, D.S. and Gaasterland, D. and Gaasterland, T. and Hauser, M.A. and Kraft, P. and Lee, R.K. and Lichter, P.R. and Liu, Y. and Loomis, S.J. and Moroi, S.E. and Pericak-Vance, M.A. and Realini, A. and Richards, J.E. and Schuman, J.S. and Scott, W.K. and Singh, K. and Sit, A.J. and Vollrath, D. and Weinreb, R.N. and Wollstein, G. and Zack, D.J. and Zhang, K. and Donnelly, P. and Barroso, I. and Blackwell, J.M. and Bramon, E. and Brown, M.A. and Casas, J.P. and Corvin, A. and Deloukas, P. and Duncanson, A. and Jankowski, J. and Markus, H.S. and Mathew, C.G. and Palmer, C.N.A. and Plomin, R. and Rautanen, A. and Sawcer, S.J. and Trembath, R.C. and Wood, N.W. and Spencer, C.C.A. and Band, G. and Bellenguez, C. and Freeman, C. and Hellenthal, G. and Giannoulatou, E. and Pirinen, M. and Pearson, R. and Strange, A. and Su, Z. and Vukcevic, D. and Langford, C. and Hunt, S.E. and Edkins, S. and Gwilliam, R. and Blackburn, H. and Bumpstead, S.J. and Dronov, S. and Gillman, M. and Gray, E. and Hammond, N. and Jayakumar, A. and McCann, O.T. and Liddle, J. and Potter, S.C. and Ravindrarajah, R. and Ricketts, M. and Waller, M. and Weston, P. and Widaa, S. and Whittaker, P. and Uitterlinden, A.G. and Vithana, E.N. and Foster, P.J. and Hysi, P.G. and Hewitt, A.W. and Khor, C.C. and Pasquale, L.R. and Montgomery, G.W. and Klaver, C.C.W. and Aung, T. and Pfeiffer, N. and MacKey, D.A. and Hammond, C.J. and Cheng, C.-Y. and Craig, J.E. and Rabinowitz, Y.S. and Wiggs, J.L. and Burdon, K.P. and Van Duijn, C.M. and MacGregor, S., Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases, Nature Communications, 9, (1), 2018, p1864-Journal Article, 2018, DOI , URL , TARA - Full Text
  • Cosgrove, D. and Mothersill, D.O. and Whitton, L. and Harold, D. and Kelly, S. and Holleran, L. and Holland, J. and Anney, R. and Richards, A. and Mantripragada, K. and Owen, M. and O'Donovan, M.C. and Gill, M. and Corvin, A. and Morris, D.W. and Donohoe, G., Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 177, (3), 2018, p369-376Journal Article, 2018, DOI , URL
  • Ni, G. and Moser, G. and Ripke, S. and Neale, B.M. and Corvin, A. and Walters, J.T.R. and Farh, K.-H. and Holmans, P.A. and Lee, P. and Bulik-Sullivan, B. and Collier, D.A. and Huang, H. and Pers, T.H. and Agartz, I. and Agerbo, E. and Albus, M. and Alexander, M. and Amin, F. and Bacanu, S.A. and Begemann, M. and Belliveau, R.A. and Bene, J. and Bergen, S.E. and Bevilacqua, E. and Bigdeli, T.B. and Black, D.W. and Bruggeman, R. and Buccola, N.G. and Buckner, R.L. and Byerley, W. and Cahn, W. and Cai, G. and Campion, D. and Cantor, R.M. and Carr, V.J. and Carrera, N. and Catts, S.V. and Chambert, K.D. and Chan, R.C.K. and Chen, R.Y.L. and Chen, E.Y.H. and Cheng, W. and Cheung, E.F.C. and Chong, S.A. and Cloninger, C.R. and Cohen, D. and Cohen, N. and Cormican, P. and Craddock, N. and Crowley, J.J. and Curtis, D. and Davidson, M. and Davis, K.L. and Degenhardt, F. and Del Favero, J. and Demontis, D. and Dikeos, D. and Dinan, T. and Djurovic, S. and Donohoe, G. and Drapeau, E. and Duan, J. and Dudbridge, F. and Durmishi, N. and Eichhammer, P. and Eriksson, J. and Escott-Price, V. and Essioux, L. and Fanous, A.H. and Farrell, M.S. and Frank, J. and Franke, L. and Freedman, R. and Freimer, N.B. and Friedl, M. and Friedman, J.I. and Fromer, M. and Genovese, G. and Georgieva, L. and Giegling, I. and Giusti-Rodríguez, P. and Godard, S. and Goldstein, J.I. and Golimbet, V. and Gopal, S. and Gratten, J. and de Haan, L. and Hammer, C. and Hamshere, M.L. and Hansen, M. and Hansen, T. and Haroutunian, V. and Hartmann, A.M. and Henskens, F.A. and Herms, S. and Hirschhorn, J.N. and Hoffmann, P. and Hofman, A. and Hollegaard, M.V. and Hougaard, D.M. and Ikeda, M. and Joa, I. and Juliá, A. and Kahn, R.S. and Kalaydjieva, L. and Karachanak-Yankova, S. and Karjalainen, J. and Kavanagh, D. and Keller, M.C. and Kennedy, J.L. and Khrunin, A. and Kim, Y. and Klovins, J. and Knowles, J.A. and Konte, B. and Kucinskas, V. and Kucinskiene, Z.A. and Kuzelova-Ptackova, H. and KÃ"hler, A.K. and Laurent, C. and Keong, J.L.C. and Legge, S.E. and Lerer, B. and Li, M. and Li, T. and Liang, K.-Y. and Lieberman, J. and Limborska, S. and Loughland, C.M. and Lubinski, J. and Lönnqvist, J. and Macek, M. and Magnusson, P.K.E. and Maher, B.S. and Maier, W. and Mallet, J. and Marsal, S. and Mattheisen, M. and Mattingsda, M. and McCarley, R.W. and McDonald, C. and McIntosh, A.M. and Meier, S. and Meijer, C.J. and Melegh, B. and Melle, I. and Mesholam-Gately, R.I. and Metspalu, A. and Michie, P.T. and Milani, L. and Milanova, V. and Mokrab, Y. and Morris, D.W. and Mors, O. and Murphy, K.C. and Murray, R.M. and Myin-Germeys, I. and MÃ"ller-Myhsok, B. and Nelis, M. and Nenadic, I. and Nertney, D.A. and Nestadt, G. and Nicodemus, K.K. and Nikitina-Zake, L. and Nisenbaum, L. and Nordin, A. and O'Callaghan, E. and O'Dushlaine, C. and O'Neill, F.A. and Oh, S.-Y. and Olinc, A. and Olsen, L. and Van Os, J. and Pantelis, C. and Papadimitriou, G.N. and Papio, S. and Parkhomenko, E. and Pato, M.T. and Paunio, T. and Pejovic-Milovancevic, M. and Perkins, D.O. and PietilÃ"inenl, O. and Pimm, J. and Pocklington, A.J. and Powell, J. and Price, A. and Pulver, A.E. and Purcell, S.M. and Quested, D. and Rasmussen, H.B. and Reichenberg, A. and Reimers, M.A. and Richards, A.L. and Roffman, J.L. and Roussos, P. and Ruderfer, D.M. and Salomaa, Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood, American Journal of Human Genetics, 102, (6), 2018, p1185-1194Journal Article, 2018, DOI , URL , TARA - Full Text
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  • Richter MS, O'Reilly K, O'Sullivan D, O'Flynn P, Corvin A, Donohoe G, Coyle C, Davoren M, Higgins C, Byrne O, Nutley T, Nulty A, Sharma K, O'Connell P, Kennedy HG, Prospective observational cohort study of 'treatment as usual' over four years for patients with schizophrenia in a national forensic hospital., BMC psychiatry, 8, (1), 2018, p289-Journal Article, 2018, DOI , TARA - Full Text
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  • 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, p77-83Journal Article, 2000, URL
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  • Springelkamp, H., Höhn, R., Mishra, A., Hysi, P.G., Khor, C.-C., Loomis, S.J., Bailey, J.N.C., Gibson, J., Thorleifsson, G., Janssen, S.F., Luo, X., Ramdas, W.D., Vithana, E., Nongpiur, M.E., Montgomery, G.W., Xu, L., Mountain, J.E., Gharahkhani, P., Lu, Y., Amin, N., Karssen, L.C., Sim, K.-S., Van Leeuwen, E.M., Iglesias, A.I., Verhoeven, V.J.M., Hauser, M.A., Loon, S.-C., Despriet, D.D.G., Nag, A., Venturini, C., Sanfilippo, P.G., Schillert, A., Kang, J.H., Landers, J., Jonasson, F., Cree, A.J., Van Koolwijk, L.M.E., Rivadeneira, F., Souzeau, E., Jonsson, V., Menon, G., Mitchell, P., Wang, J.J., Rochtchina, E., Attia, J., Scott, R., Holliday, E.G., Baird, P.N., Xie, J., Inouye, M., Viswanathan, A., Sim, X., Weinreb, R.N., De Jong, P.T.V.M., Oostra, B.A., Uitterlinden, A.G., Hofman, A., Ennis, S., Thorsteinsdottir, U., Burdon, K.P., Allingham, R.R., Brilliant, M.H., Budenz, D.L., Christen, W.G., Fingert, J., Friedman, D.S., Gaasterland, D., Gaasterland, T., Haines, J.L., Kang, J.H., Kraft, P., Lee, R.K., Lichter, P.R., Liu, Y., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Vollrath, D., Wollstein, G., Zack, D.J., Zhang, K., Barroso, I., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H.S., Mathew, C.G., Palmer, C.N.A., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Viswanathan, A.C., Wood, N.W., Spencer, C.C.A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S.E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S.J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O.T., Liddle, J., Potter, S.C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Spector, T.D., Mirshahi, A., Saw, S.-M., Vingerling, J.R., Teo, Y.-Y., Wolfs, R.C.W., Lemij, H.G., Tai, E.-S., Jansonius, N.M., Jonas, J.B., Cheng, C.-Y., Aung, T., Klaver, C.C.W., Craig, J.E., MacGregor, S., MacKey, D.A., Lotery, A.J., Stefansson, K., Bergen, A.A.B., Young, T.L., Wiggs, J.L., Pfeiffer, N., Wong, T.-Y., Pasquale, L.R., Hewitt, A.W., Van Duijn, C.M., Hammond, C.J., Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process, Nature Communications, 5, 2014Journal Article, 2014
  • Postmus, I., Trompet, S., Deshmukh, H.A., Barnes, M.R., Li, X., Warren, H.R., Chasman, D.I., Zhou, K., Arsenault, B.J., Donnelly, L.A., Wiggins, K.L., Avery, C.L., Griffin, P., Feng, Q., Taylor, K.D., Li, G., Evans, D.S., Smith, A.V., De Keyser, C.E., Johnson, A.D., De Craen, A.J.M., Stott, D.J., Buckley, B.M., Ford, I., Westendorp, R.G.J., Slagboom, P.E., Sattar, N., Munroe, P.B., Sever, P., Poulter, N., Stanton, A., Shields, D.C., O'Brien, E., Shaw-Hawkins, S., Ida Chen, Y.-D., Nickerson, D.A., Smith, J.D., Dubé, M.P., Boekholdt, S.M., Hovingh, G.K., Kastelein, J.J.P., McKeigue, P.M., Betteridge, J., Neil, A., Durrington, P.N., Doney, A., Carr, F., Morris, A., McCarthy, M.I., Groop, L., Ahlqvist, E., Barroso, I., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H.S., Mathew, C.G., Palmer, C.N.A., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Viswanathan, A.C., Wood, N.W., Spencer, C.C.A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S.E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S.J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O.T., Liddle, J., Potter, S.C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Bis, J.C., Rice, K., Smith, N.L., Lumley, T., Whitsel, E.A., Stürmer, T., Boerwinkle, E., Ngwa, J.S., O'Donnell, C.J., Vasan, R.S., Wei, W.-Q., Wilke, R.A., Liu, C.-T., Sun, F., Guo, X., Heckbert, S.R., Post, W., Sotoodehnia, N., Arnold, A.M., Stafford, J.M., Ding, J., Herrington, D.M., Kritchevsky, S.B., Eiriksdottir, G., Launer, L.J., Harris, T.B., Chu, A.Y., Giulianini, F., MacFadyen, J.G., Barratt, B.J., Nyberg, F., Stricker, B.H., Uitterlinden, A.G., Hofman, A., Rivadeneira, F., Emilsson, V., Franco, O.H., Ridker, P.M., Gudnason, V., Liu, Y., Denny, J.C., Ballantyne, C.M., Rotter, J.I., Cupples, L.A., Psaty, B.M., Tardif, J.-C., Colhoun, H.M., Hitman, G., Krauss, R.M., Jukema, J.W., Caulfield, M.J., Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins, Nature Communications, 5, 2014Journal Article, 2014
  • Ormond C., Ryan N.M., Heron E.A., Gill M., Byerley W., Corvin A., Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia, Biological Psychiatry Global Open Science, 3, (4), 2023, p797 - 802, p797-802Journal Article, 2023, DOI
  • King S., Mothersill D., Holleran L., Patlola S.R., Burke T., McManus R., Kenyon M., McDonald C., Hallahan B., Corvin A., Morris D.W., Kelly J.P., McKernan D.P., Donohoe G., Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia, Translational Psychiatry, 13, (1), 2023Journal Article, 2023, 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 - 893Journal Article, 2008, DOI
  • 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 - 841Journal Article, 2005, DOI , 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 - 238Journal Article, 2005, DOI , URL
  • 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 - 1088Journal Article, 2005, URL
  • 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 - 101Journal Article, 2006, DOI
  • Morris DW, Nangle JM, Kiely B, Corvin A, Gill M. , The molecular basis of schizophrenia: a complex genetic disorder. , Irish Psychiatrist, 5, 2004, p134 - 137Journal Article, 2004
  • 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 - 162Journal Article, 2006, DOI , URL , TARA - Full Text
  • Corvin A, Gill M , Psychiatric Genetics in the post genome age, British Journal of Psychiatry, 182, 2003, p95 - 96Journal Article, 2003, URL , TARA - Full Text
  • 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 - 6Journal Article, 2007, 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 - 200Journal Article, 2006, DOI , 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 - 458Journal Article, 2007, DOI , URL
  • 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 - 579Journal Article, 2007, DOI , URL
  • 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 - 808Journal Article, 2005, URL
  • 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 - 31Journal Article, 2008, DOI , URL
  • 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 - 953Journal Article, 2007, DOI , URL
  • 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 - 906Journal Article, 2006, DOI , URL , TARA - Full Text
  • 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 - 200Journal Article, 2006, DOI , 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 - 200Journal Article, 2006, 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 - 796Journal Article, 2007, DOI , URL
  • 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 - 489Journal Article, 2008, DOI , URL , TARA - Full Text
  • 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 - 399Journal Article, 2007, URL
  • 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 - 100Journal Article, 2007, DOI , URL
  • 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 - 103Journal Article, 2008, DOI , URL
  • 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 - 149Journal Article, 2008, DOI , URL
  • 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 - 183Journal 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 - 78Journal Article, 2008, DOI , TARA - Full Text
  • 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 - 1055Journal Article, 2008, DOI , 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 - 1058Journal Article, 2008, DOI , TARA - Full Text
  • 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 - 323Journal Article, 2009, DOI , URL
  • 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 - 36Journal Article, 2009, DOI , URL , TARA - Full Text
  • International Schizophrenia Consortium, Greater burden of rare copy number variants in schizophrenia, Nature, 7210, (455), 2008, p237 - 241Journal Article, 2008, DOI , URL
  • 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 - 60Journal Article, 2008, URL
  • 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, 2010Journal Article, 2010
  • 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 - 53Journal Article, 2004, DOI , URL
  • 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 - 213Journal Article, 2004, DOI , URL
  • International Schizophrenia Consortium, Rare chromosomal deletions and duplications increase risk of schizophrenia., Nature, 455, (7210), 2008, p237 - 241Journal Article, 2008, DOI , TARA - Full Text
  • 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, p24-31Journal Article, 2008, DOI , URL
  • 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, p471-475Journal Article, 2009, DOI , TARA - Full Text
  • Donohoe G, Morris D, Robertson IH, Gill M, Foxe J, Corvin A, Dysbindin and Cognition In An Irish Sample., Biological Psychiatry , 59, (8), 2006, pp623Meeting Abstract, 2006
  • 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, pp129Meeting Abstract, 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, pp353Meeting Abstract, 2005
  • 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, p77-78Journal Article, 2008, DOI , TARA - Full Text
  • 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, p19-27Journal Article, 2008, DOI , URL
  • 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, p871-893Journal Article, 2008, DOI
  • International Schizophrenia Consortium, Common polygenic variation contributes to risk of schizophrenia and bipolar disorder., Nature, 460, (7256), 2009, p748-752Journal Article, 2009, DOI
  • Neuropsychiatric Genetics in, editor(s)Lawlor , Revision Psychiatry, MedMedia , 2001, [Corvin A, Gill M. ]Book Chapter, 2001
  • Anxiety Disorders in, Wright, Stern , Core Psychiatry, Elsevier Saunders, 2005, pp193-204 , [Corvin A, Lucey JV]Book Chapter, 2005
  • Psychiatric Genetics in, editor(s)Wright, Stern , Core Psychiatry, Phelan, Elsevier Saunders, 2005, pp35-54 , [Corvin A, Gill M.]Book Chapter, 2005
  • Neuregulin-1-induced cell migration: a neurodevelopmental mechanism for schizophrenia susceptibility? in, Cell Science , 2008, [Corvin A. ]Book Chapter, 2008
  • Cognitive intermediate phenotypes in schizophrenia genetics in, Cognitive Genomics, US., MIT Press,, 2010, [Donohoe G, Goldberg T, Corvin A.]Book Chapter, 2010
  • Corvin A. , Psychosis: a genetic perspective., Irish Journal of Psychological Medicine, 12, (supp), 2000, p3-6Journal Article, 2000
  • Fitzgerald M. & Corvin A., Diagnosis and differential diagnosis of Asperger's Syndrome., Advances in Psychiatric Treatment , 7, (4), 2001, p310 - 318Journal Article, 2001, URL
  • 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 - 620Journal 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, p540-556Journal 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 - 2763Journal Article, 2009, DOI , 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, p1101-1111Journal Article, 2010, 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 - 233Journal Article, 2010, DOI
  • 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 - 373Journal Article, 2010, DOI
  • 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, p286-292Journal Article, 2011, DOI , URL , TARA - Full Text
  • 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 - 1503Journal Article, 2009, 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, DOI , URL , TARA - Full Text
  • 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 - 700Journal Article, 2010, URL
  • Merikangas AK, Corvin A, Gallagher L., Promises and challenges of copy number variants in Neuropsychiatric Disorders. , Trends in Genetics , 25, (12), 2009, p536-544Journal Article, 2009, DOI
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  • 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, p101-104Journal Article, 2010, DOI
  • 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, p429-441Journal Article, 2011, DOI , 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, p1045-54Journal Article, 2009, DOI , URL , TARA - Full Text
  • 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, p311-313Journal Article, 2010, DOI
  • 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, p1248-1254Journal Article, 2010, DOI , TARA - Full Text
  • Cummings E, Donohoe G, Morris DW, Gill M, Corvin A. , Clinical symptomatology and the psychosis risk gene, ZNF804A, Schizophrenia Research, 122, (1-3), 2010, p273-275Journal Article, 2010, DOI , URL , TARA - Full Text
  • 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, p1-13Journal Article, 2010, DOI , URL , TARA - Full Text
  • 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, p1547-1550Journal Article, 2010, URL , TARA - Full Text
  • 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, p1269-1270Journal Article, 2010, DOI , URL , TARA - Full Text
  • 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, p1330-1334Journal Article, 2009, DOI , TARA - Full Text
  • 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, 2010Journal Article, 2010, URL , TARA - Full Text
  • Donohoe G, Morris DW, Corvin A, The Psychosis Susceptibility gene ZNF804A: associations, functions and phenotypes, Schizophrenia Bulletin, 36, (5), 2010, p904-909Review Article, 2010, DOI , URL , TARA - Full Text
  • 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, p440-445Journal Article, 2010, DOI
  • 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 - 149Journal 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, p2132-2137Journal Article, 2010, DOI , URL , TARA - Full Text
  • Gill, M., Donohoe, G., Corvin, A, What have the genomics ever done for the psychoses?, Psychological Medicine, 40, (4), 2010, p529-540Journal Article, 2010, DOI , URL , 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, p304-306Journal Article, 2011, 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), 2010Journal Article, 2010, DOI , URL , 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 - 1424Journal Article, 2010, DOI , TARA - Full Text
  • 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, p31-38Journal Article, 2011, DOI , URL , 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, p1202-1211Journal Article, 2012, DOI , URL , TARA - Full Text
  • 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, pe14802Journal Article, 2011, DOI , URL , TARA - Full Text
  • 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, p471-5Journal Article, 2009, DOI , URL , TARA - Full Text
  • 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, - 114Miscellaneous, 2011, DOI
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  • 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, p345-353Journal Article, 2010, DOI , TARA - Full Text
  • 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, p499-503Journal Article, 2011, DOI , TARA - Full Text
  • Donohoe G, Morris DW, Corvin A, The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypes., Schizophrenia bulletin, 36, (5), 2010, p904-9Review Article, 2010, 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 - 119Journal Article, 2011, DOI
  • 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, p977-83Journal Article, 2011, DOI
  • 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, p1328-1339Journal Article, 2012, DOI
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  • Corvin AP, Two patients walk into a clinic...a genomics perspective on the future of schizophrenia., BMC Biology, 9, (77), 2011Journal Article, 2011, DOI , URL , TARA - Full Text
  • 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, p996-1006Journal Article, 2012, DOI , URL , 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, pe26488Journal Article, 2011, DOI , URL , 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, pe26488Journal Article, 2011, DOI , TARA - Full Text
  • 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, p614-622Journal Article, 2012, DOI , URL , 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 - 963Journal Article, 2011, DOI , TARA - Full Text
  • 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 - 616Journal Article, 2012, URL
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  • Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M., The Cognitive Genetics of Neuropsychiatric Disorders. , Current Topics in Behavioral Neurosciences, 12, 2012, p579-613Journal Article, 2012, DOI
  • 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, p328-33Journal Article, 2012, DOI , TARA - Full Text
  • 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, p214-9Journal Article, 2011, DOI , TARA - Full Text
  • 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, 2013Journal Article, 2013
  • Sullivan P,Psychiatric Genetics Investigators. , Don't give up on GWAS., 2012, - 96Miscellaneous, 2012, DOI
  • 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, p761-767Journal Article, 2011, DOI
  • 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
  • Psychiatric Genetics in, Wright, Stern, Phelan , Core Psychiatry, Elsevier Saunders, 2010, [Corvin A, Gill M.]Book Chapter, 2010
  • 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
  • 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, 2013Invited Talk, 2013
  • Corvin, A., Cold Spring Harbor Laboratories Lecture. , Cold Spring Harbor Laboratories, 2013Invited Talk, 2013
  • Corvin, A., 'Cognitive genetics and psychosis, Norwegian Neuropsychiatric Association Winter Meeting, November 23rd, 2012Invited Talk, 2012
  • Corvin, A., Will genomics change the way we manage psychosis?, College of Psychiatry in Ireland, 16th November, 2012Invited Talk, 2012
  • Corvin, A., Schizophrenia Genomics: Progress and Challenges. , Neuroscience Ireland, Annual Meeting, Dublin, 5th September, 2012Invited Talk, 2012
  • Corvin, A., Treating Schizophrenia, British Journal of Hospital Medicine Meeting, London UK, 26th April, 2012Invited Talk, 2012
  • 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, pe58815Journal 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, p708-12Journal Article, 2013, DOI
  • 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. e63300Journal Article, 2013, DOI , TARA - Full Text
  • Corvin, A., Schizophrenia at a genetics crossroads: Where to now?, Schizophrenia Bulletin, 39, (3), 2013, p490-495Journal Article, 2013, DOI , TARA - Full Text
  • 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.e5Journal Article, 2014, DOI , TARA - Full Text
  • 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, p189-95Journal Article, 2014, DOI , TARA - Full Text
  • 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, p115-121Journal Article, 2014, DOI , TARA - Full Text
  • Corvin A, Morris DW, Genome-wide Association Studies: Findings at the Major Histocompatibility Complex Locus in Psychosis., Biological psychiatry, 75, (4), 2014, p276-83Journal Article, 2014, DOI
  • 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, 1669-1676Journal Article, 2014, 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, p1150-9Journal Article, 2013, DOI , TARA - Full Text
  • 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, p877-85Journal 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, p573-81Journal Article, 2013
  • 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, pe345Journal Article, 2014, DOI , TARA - Full Text
  • 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, p872-879Journal 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, p79-82Journal Article, 2014, DOI , TARA - Full Text
  • 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, p108-114Journal 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, p652-658Journal 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, p168-74Journal Article, 2014, DOI , TARA - Full Text
  • 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, p37-40Journal Article, 2014, DOI , TARA - Full Text
  • 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, p2177-2187Journal Article, 2013, 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, p3316-26Journal Article, 2014, DOI , TARA - Full Text
  • 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
  • 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, p18-36Journal Article, 2014, DOI , TARA - Full Text
  • 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, 1826, 2016, -Miscellaneous, DOI
  • 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, p46-51Journal Article, DOI
  • 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 - 25Meeting Abstract
  • Corvin A. , The changing faces of schizophrenia. The Big Idea. , 2012, -Miscellaneous
  • Corvin, A., Schizophrenia: Evolution and Synthesis: A think tank to accelerate treatment development and prevention efforts. , Ernst Strungman Forum, Frankfurt, Germany, 20-28th July, 2012Invited Talk
  • Corvin, A., Symposium Organizer, Schizophrenia International Research Society,, April 16th, In:Schizophrenia International Research Society,, 2012, Florence, ItalyMeetings /Conferences Organised

Research Expertise

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.

Mental Health (including Psychiatry and Clinical Psychology), Genetics and Genomics, Population Health, Public & Environment Health, Neuroscience and clinical neurology,