Professor David St Clair

Professor David St Clair

Chair in Applied Medicine

Overview

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Research

Research Overview

Psychiatric Genetics, particularly of schizophrenia.

Publications

Publications 

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  • Genome-wide association study identifies 30 loci associated with bipolar disorder

    Stahl, E. A., Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V., Mattheisen, M., Wang, Y., Coleman, J. R., Gaspar, H. A., de Leeuw, C. A., Steinberg, S., Pavlides, J. M., Trzaskowski, M., Byrne, E. M., Pers, T. H., Holmans, P. A., Richards, A. L., Abbott, L., Agerbo, E., Akil, H., Albani, D., Alliey-Rodriguez, N., Als, T. D., Anjorin, A., Antilla, V., Awasthi, S., Badner, J. A., Bækvad-Hansen, M., Barchas, J. D., Bass, N., Bauer, M., Belliveau, R., Bergen, S. E., Pedersen, C. B., Bøen, E., Boks, M. P., Boocock, J., Budde, M., Bunney, W., Burmeister, M., Bybjerg-Grauholm, J., Byerley, W., Casas, M., Cerrato, F., Cervantes, P., Chambert, K., Charney, A. W., Chen, D., St Clair, D., eQTLGen Consortium, BIOS Consortium, the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium

    Nature Genetics, vol. 51, pp. 793-803

    Contributions to Journals: Articles

  • Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response

    Fabbri, C., Hosak, L., Mössner, R., Giegling, I., Mandelli, L., Bellivier, F., Claes, S., Collier, D. A., Corrales, A., Delisi, L. E., Gallo, C., Gill, M., Kennedy, J. L., Leboyer, M., Lisoway, A., Maier, W., Marquez, M., Massat, I., Mors, O., Muglia, P., Nöthen, M. M., O’Donovan, M. C., Ospina-Duque, J., Propping, P., Shi, Y., St Clair, D., Thibaut, F., Cichon, S., Mendlewicz, J., Rujescu, D., Serretti, A.

    World Journal of Biological Psychiatry, vol. 18, no. 1, pp. 5-28

    Contributions to Journals: Review articles

  • Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

    Giegling, I., Hosak, L., Mössner, R., Serretti, A., Bellivier, F., Claes, S., Collier, D. A., Corrales, A., DeLisi, L. E., Gallo, C., Gill, M., Kennedy, J. L., Leboyer, M., Maier, W., Marquez, M., Massat, I., Mors, O., Muglia, P., Nöthen, M. M., Ospina-Duque, J., Owen, M. J., Propping, P., Shi, Y. Y., St Clair, D., Thibaut, F., Cichon, S., Mendlewicz, J., O'Donovan, M. C., Rujescu, D.

    World Journal of Biological Psychiatry, vol. 18, no. 7, pp. 492-505

    Contributions to Journals: Articles

  • An integrated genetic-epigenetic analysis of schizophrenia: Evidence for co-localization of genetic associations and differential DNA methylation

    Hannon, E., Dempster, E., Viana, J., Burrage, J., Smith, A. R., Macdonald, R., St Clair, D., Mustard, C., Breen, G., Therman, S., Kaprio, J., Toulopoulou, T., Pol, H. E., Bohlken, M. M., Kahn, R. S., Nenadic, I., Hultman, C. M., Murray, R. M., Collier, D. A., Bass, N., Gurling, H., McQuillin, A., Schalkwyk, L., Mill, J.

    Genome Biology, vol. 17, 176

    Contributions to Journals: Articles

  • Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function

    Thomson, P. A., Duff, B., Blackwood, D. H., Romaniuk, L., Watson, A., Whalley, H. C., Li, X., Dauvermann, M. R., Moorhead, T. W. J., Bois, C., Ryan, N. M., Redpath, H., Hall, L., Morris, S. W., Van Beek, E. J., Roberts, N., Porteous, D. J., St Clair, D., Whitcher, B., Dunlop, J., Brandon, N. J., Hughes, Z. A., Hall, J., McIntosh, A., Lawrie, S. M.

    npj Schizophrenia, vol. 2, 16024

    Contributions to Journals: Articles

  • Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

    Singh, T., Kurki, M. I., Curtis, D., Purcell, S. M., Crooks, L., McRae, J., Suvisaari, J., Chheda, H., Blackwood, D., Breen, G., Pietilinen, O., Gerety, S. S., Ayub, M., Blyth, M., Cole, T., Collier, D., Coomber, E. L., Craddock, N., Daly, M. J., Danesh, J., DiForti, M., Foster, A., Freimer, N. B., Geschwind, D., Johnstone, M., Joss, S., Kirov, G., Körkkö, J., Kuismin, O., Holmans, P., Hultman, C. M., Iyegbe, C., Lönnqvist, J., Mnnikkö, M., McCarroll, S. A., McGuffin, P., McIntosh, A. M., McQuillin, A., Moilanen, J. S., Moore, C., Murray, R. M., Newbury-Ecob, R., Ouwehand, W., Paunio, T., Prigmore, E., Rees, E., Roberts, D., Sambrook, J., Sklar, P., St Clair, D., Veijola, J., Walters, J. T., Williams, H., Sullivan, P. F., Hurles, M. E., O'Donovan, M. C., Palotie, A., Owen, M. J., Barrett, J. C.

    Nature Neuroscience, vol. 19, no. 4, pp. 571-577

    Contributions to Journals: Articles

  • Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

    Franke, B., Stein, J. L., Ripke, S., Anttila, V., Hibar, D. P., van Hulzen, K. J. E., Arias-Vasquez, A., Smoller, J. W., Nichols, T. E., Neale, M. C., McIntosh, A. M., Lee, P., McMahon, F. J., Meyer-Lindenberg, A., Mattheisen, M., Andreassen, O. A., Gruber, O., Sachdev, P. S., Roiz-Santianez, R., Saykin, A. J., Ehrlich, S., Mather, K. A., Turner, J. A., Wright, M. J., O'Donovan, M. C., Thompson, P. M., Neale, B. M., Medland, S. E., Sullivan, P. F., Psychiat Genomics Consortium, ENIGMA Consortium, St Clair, D. M., Pike, G. B.

    Nature Neuroscience, vol. 19, no. 3, pp. 420-431

    Contributions to Journals: Articles

  • Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia

    Ingason, A., Giegling, I., Hartmann, A. M., Genius, J., Konte, B., Friedl, M., Ripke, S., Sullivan, P. F., St Clair, D., Collier, D. A., O'Donovan, M. C., Mirnics, K., Rujescu, D.

    Translational Psychiatry, vol. 5, e656

    Contributions to Journals: Articles

  • Bridging the translational divide: Identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene

    Nithianantharajah, J., McKechanie, A. G., Stewart, T. J., Johnstone, M., Blackwood, D. H., St Clair, D., Grant, S. G., Bussey, T. J., Saksida, L. M.

    Scientific Reports, vol. 5, 14613

    Contributions to Journals: Articles

  • The UK10K project identifies rare variants in health and disease

    Walter, K., Min, J. L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J. R., Xu, C., Futema, M., Lawson, D., Iotchkova, V., Schiffels, S., Hendricks, A. E., Danecek, P., Li, R., Floyd, J., Wain, L. V., Barroso, I., Humphries, S. E., Hurles, M. E., Zeggini, E., Barrett, J. C., Plagnol, V., Richards, J. B., Greenwood, C. M., Timpson, N. J., Durbin, R., Bala, S., Clapham, P., Coates, G., Cox, T., Daly, A., Du, Y., Edkins, S., Ellis, P., Flicek, P., Guo, X., Guo, X., Huang, L., Jackson, D. K., Joyce, C., Keane, T., Kolb-Kokocinski, A., Langford, C., Li, Y., Liang, J., Lin, H., Liu, R., Breen, G., St Clair, D., UK10K Consortium

    Nature, vol. 526, no. 7571, pp. 82-89

    Contributions to Journals: Articles

  • Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

    Johnstone, M., Maclean, A., Heyrman, L., Lenaerts, A., Nordin, A., Nilsson, L., De Rijk, P., Goossens, D., Adolfsson, R., St Clair, D. M., Hall, J., Lawrie, S. M., McIntosh, A. M., Del-Favero, J., Blackwood, D. H. R., Pickard, B. S.

    Journal of Neuropsychiatry and Clinical Neurosciences, vol. 1, no. 3, pp. 175-190

    Contributions to Journals: Articles

  • Prenatal Nutritional Deficiency Reprogrammed Postnatal Gene Expression in Mammal Brains: Implications for Schizophrenia

    Xu, J., He, G., Zhu, J., Zhou, X., Clair, D. S., Wang, T., Xiang, Y., Zhao, Q., Xing, Q., Liu, Y., Wang, L., Li, Q., He, L., Zhao, X.

    International Journal of Neuropsychopharmacology, vol. 18, no. 4, pyu054

    Contributions to Journals: Articles

  • No Association Between NRG1 and ErbB4 Genes and Psychopathological Symptoms of Schizophrenia

    Tosato, S., Zanoni, M., Bonetto, C., Tozzi, F., Francks, C., Ira, E., Tomassi, S., Bertani, M., Rujescu, D., Giegling, I., St Clair, D., Tansella, M., Ruggeri, M., Muglia, P.

    NeuroMolecular Medicine, vol. 16, no. 4, pp. 742-751

    Contributions to Journals: Articles

  • Common genetic variants on 1p13.2 associate with risk of autism

    Xia, K., Guo, H., Xun, G., Zuo, L., Peng, Y., He, Y., Xiong, Z., Sun, L., Pan, Q., Long, Z., Zou, X., Lu, L., Liu, Y., Tian, D., Long, L., Liu, Y., Peng, H., Luo, X., Su, W., Liang, D., Dai, H., Yan, X., Feng, Y., Tang, B., Miedzybrodzka, Z., Xia, J., Zhang, Z., Luo, X., Zhang, X., St Clair, D., Zhao, J., Zhang, F.

    Molecular Psychiatry, vol. 19, no. 11, pp. 1212-1219

    Contributions to Journals: Articles

  • Biological insights from 108 schizophrenia-associated genetic loci

    Ripke, S., Neale, B. M., Corvin, A., Walters, J. T., Farh, K. H., Holmans, P. A., Lee, P., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C., Chen, R. Y., Chen, E. Y., Cheng, W., Cheung, E. F., Chong, S. A., Cloninger, C. R., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., St Clair, D., Schizophrenia Working Group of the Psychiatric Genomics Consortium

    Nature, vol. 511, no. 7510, pp. 421-427

    Contributions to Journals: Articles

  • Modeling a genetic risk for schizophrenia in iPSCs and Mice reveals neural stem cell deficits associated with adherens junctions and polarity

    Yoon, K. J., Nguyen, H. N., Ursini, G., Zhang, F., Kim, N. S., Wen, Z., Makri, G., Nauen, D., Shin, J. H., Park, Y., Chung, R., Pekle, E., Zhang, C., Towe, M., Hussaini, S. M. Q., Lee, Y., Rujescu, D., St. Clair, D., Kleinman, J. E., Hyde, T. M., Krauss, G., Christian, K. M., Rapoport, J. L., Weinberger, D. R., Song, H., Ming, G. L.

    Cell Stem Cell, vol. 15, no. 1, pp. 79-91

    Contributions to Journals: Articles

  • An inherited duplication at the gene p21 protein-activated Kinase 7 (PAK7) is a risk factor for psychosis

    Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L. P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., Kelleher, E., Fahey, C., Molinos, I., Bellini, S., Pirinen, M., Strange, A., Freeman, C., Thiselton, D. L., Elves, R. L., Regan, R., Ennis, S., Dinan, T. G., McDonald, C., Murphy, K. C., O'Callaghan, E., Waddington, J. L., Walsh, D., O'Donovan, M., Grozeva, D., Craddock, N., Stone, J., Scolnick, E., Purcell, S., Sklar, P., Coe, B., Eichler, E. E., Ophoff, R., Buizer, J., Szatkiewicz, J., Hultman, C., Sullivan, P., Gurling, H., Mcquillin, A., St Clair, D., Rees, E., Kirov, G., Walters, J., Blackwood, D., Johnstone, M., Donohoe, G., The International Schizophrenia Consortium (ISC), SGENE+ Consortium, O'Neill, F. A., The Wellcome Trust Case Control Consortium 2 (WTCCC2), Kendler, K. S., Gill, M., Riley, B. P., Spencer, C. C. A., Corvin, A.

    Human Molecular Genetics, vol. 23, no. 12, pp. 3316-3326

    Contributions to Journals: Articles

  • Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility

    Lang, B., Pu, J., Hunter, I., Liu, M., Martin-Granados, C., Reilly, T. J., Gao, G., Guan, Z., Li, W., Shi, Y., He, G., He, L., Stefansson, H., St Clair, D., Blackwood, D. H., McCaig, C. D., Shen, S.

    Journal of Cell Science, vol. 127, no. 3, pp. 630-640

    Contributions to Journals: Articles

  • A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing

    Hu, X., Zhang, B., Liu, W., Paciga, S., He, W., Lanz, T. A., Kleiman, R., Dougherty, B., Hall, S. K., Mcintosh, A. M., Lawrie, S. M., Power, A., John, S. L., Blackwood, D., St Clair, D., Brandon, N. J.

    Molecular Psychiatry, vol. 19, no. 8, pp. 857-858

    Contributions to Journals: Letters

  • Can eye movements be used as a marker for major depression?

    Nouzova, E., Beedie, S. A., Bheemaraddi, S., Kuriakose, J., Kulkarni, M., Shand, A. J., Walker, N., St Clair, D., Benson, P. J.

    European Psychiatry, vol. 29, no. supplement 1, EPA-112

    Contributions to Journals: Abstracts

  • Mosaic copy number variation in schizophrenia

    Ruderfer, D. M., Chambert, K., Moran, J., Talkowski, M., Chen, E. S., Gigek, C., Gusella, J. F., Blackwood, D. H., Corvin, A., Gurling, H. M., Hultman, C. M., Kirov, G., Magnusson, P., O'Donovan, M. C., Owen, M. J., Pato, C., St Clair, D., Sullivan, P. F., Purcell, S. M., Sklar, P., Ernst, C.

    EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 21, no. 9, pp. 1007-1011

    Contributions to Journals: Articles

  • A comprehensive family-based replication study of schizophrenia genes

    Aberg, K. A., Liu, Y., Bukszár, J., McClay, J. L., Khachane, A. N., Andreassen, O. A., Blackwood, D., Corvin, A., Djurovic, S., Gurling, H., Ophoff, R., Pato, C. N., Pato, M. T., Riley, B., Webb, T., Kendler, K., O'Donovan, M., Craddock, N., Kirov, G., Owen, M., Rujescu, D., St Clair, D., Werge, T., Hultman, C. M., Delisi, L. E., Sullivan, P., Van Den Oord, E. J.

    JAMA Psychiatry, vol. 70, no. 6, pp. 573-581

    Contributions to Journals: Articles

  • Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population

    Zhao, Q., Li, T., Zhao, X., Huang, K., Wang, T., Li, Z., Ji, J., Zeng, Z., Zhang, Z., Li, K., Feng, G., St Clair, D., He, L., Shi, Y.

    Schizophrenia Bulletin, vol. 39, no. 3, pp. 712-719

    Contributions to Journals: Articles

  • Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease

    Huertas-Vazquez, A., Nelson, C. P., Guo, X., Reinier, K., Uy-Evanado, A., Teodorescu, C., Ayala, J., Jerger, K., Chugh, H., Braund, P. S., Deloukas, P., Hall, A. S., Balmforth, A. J., Jones, M., Taylor, K. D., Pulit, S. L., Newton-Cheh, C., Gunson, K., Jui, J., Rotter, J. I., Albert, C. M., Samani, N. J., Chugh, S. S., Aerts, J., Ahmad, T., Arbury, H., Attwood, A., Auton, A., Ball, S. G., Balmforth, A. J., Barnes, C., Barrett, J. C., Barroso, I., Barton, A., Bennett, A. J., Bhaskar, S., Blaszczyk, K., Bowes, J., Brand, O. J., Braund, P. S., Bredin, F., Breen, G., Brown, M. J., Bruce, I. N., Bull, J., Burren, O. S., Burton, J., Hocking, L., Reid, D. M., St Clair, D., WTCCC+

    PloS ONE, vol. 8, no. 4, e59905

    Contributions to Journals: Articles

  • Simple viewing tests can detect eye movement abnormalities that distinguish schizophrenia cases from controls with exceptional accuracy

    Benson, P. J., Beedie, S. A., Shephard, E., Giegling, I., Rujescu, D., St Clair, D.

    Biological Psychiatry, vol. 72, no. 9, pp. 716-724

    Contributions to Journals: Articles

  • Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

    Vassos, E., Steinberg, S., Cichon, S., Breen, G., Sigurdsson, E., Andreassen, O. A., Djurovic, S., Morken, G., Grigoroiu-Serbanescu, M., Diaconu, C. C., Czerski, P. M., Hauser, J., Babadjanova, G., Abramova, L. I., Mühleisen, T. W., Nöthen, M. M., Rietschel, M., McGuffin, P., Clair, D. S., Gustafsson, O., Melle, I., Pietiläinen, O. P. H., Ruggeri, M., Tosato, S., Werge, T., Ophoff, R. A., Rujescu, D., Børglum, A. D., Mors, O., Mortensen, P. B., Demontis, D., Hollegaard, M. V., van Winkel, R., Kenis, G., De Hert, M., Réthelyi, J. M., Bitter, I., Rubino, I. A., Golimbet, V., Kiemeney, L. A., van den Berg, L. H., Franke, B., Jönsson, E. G., Farmer, A., Stefansson, H., Stefansson, K., Collier, D. A., GROUP Consortium

    Biological Psychiatry, vol. 72, no. 8, pp. 645-650

    Contributions to Journals: Articles

  • Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: A polygenic risk score analysis

    Derks, E. M., Vorstman, J. A., Ripke, S., Kahn, R. S., Ophoff, R. A., O'Donovan, M. C., Craddock, N., Holmans, P. A., Hamshere, M., Williams, H. J., Moskvina, V., Dwyer, S., Georgieva, L., Zammit, S., Owen, M. J., Sullivan, P. F., Lin, D. Y., van den Oord, E., Kim, Y., Scott Stroup, T., Lieberman, J. A., St Clair, D., Kirov, G. K., Nikolov, I., Toncheva, D., Milanova, V., Morris, D. W., O'Dushlaine, C. T., Kenny, E., Quinn, E. M., Gill, M., Corvin, A., Blackwood, D. H., McGhee, K. A., Pickard, B., Malloy, P., Maclean, A. W., McIntosh, A., McQuillin, A., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Gurling, H., Pato, M. T., The Schizophrenia Psychiatric Genomic Consortium

    PloS ONE, vol. 7, no. 6, e37852

    Contributions to Journals: Articles

  • Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

    Keller, M. C., Simonson, M. A., Ripke, S., Neale, B. M., Gejman, P. V., Howrigan, D. P., Lee, S. H., Lencz, T., Levinson, D. F., Sullivan, P. F., Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, St Clair, D. M.

    PLoS Genetics, vol. 8, no. 4, e1002656

    Contributions to Journals: Articles

  • Interplay between DISC1 and GABA signaling regulates neurogenesis in mice and risk for schizophrenia

    Kim, J. Y., Liu, C. Y., Zhang, F., Duan, X., Wen, Z., Song, J., Feighery, E., Lu, B., Rujescu, D., St Clair, D., Christian, K., Callicott, J. H., Weinberger, D. R., Song, H., Ming, G.

    Cell, vol. 148, no. 5, pp. 1051-1064

    Contributions to Journals: Articles

  • A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

    Jia, P., Wang, L., Fanous, A. H., Chen, X., Kendler, K. S., Zhao, Z., Morris, D. W., O'Dushlaine, C. T., Kenny, E., Quinn, E. M., Gill, M., Corvin, A., O'Donovan, M. C., Kirov, G. K., Craddock, N. J., Holmans, P. A., Williams, N. M., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Toncheva, D., Milanova, V., Owen, M. J., Hultman, C. M., Lichtenstein, P., Thelander, E. F., Sullivan, P., McQuillin, A., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Gurling, H., Crombie, C., Fraser, G., Kuan, S. L., Walker, N., St Clair, D., Blackwood, D. H., Muir, W. J., McGhee, K. A., Pickard, B., Malloy, P., Maclean, A. W., The International Schizophrenia Consortium (ISC)

    Journal of Medical Genetics, vol. 49, no. 2, pp. 96-103

    Contributions to Journals: Articles

  • Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

    Carrera, N., Arrojo, M., Sanjuán, J., Ramos-Ríos, R., Paz, E., Suárez-Rama, J. J., Páramo, M., Agra, S., Brenlla, J., Martínez, S., Rivero, O., Collier, D. A., Palotie, A., Cichon, S., Nöthen, M. M., Rietschel, M., Rujescu, D., Stefansson, H., Steinberg, S., Sigurdsson, E., St Clair, D., Tosato, S., Werge, T., Stefansson, K., González, J. C., Valero, J., Gutiérrez-Zotes, A., Labad, A., Martorell, L., Vilella, E., Carracedo, ., Costas, J.

    Biological Psychiatry, vol. 71, no. 2, pp. 169-177

    Contributions to Journals: Articles

  • HDAC9 is implicated in schizophrenia and expressed specifically in post-mitotic neurons but not in adult neural stem cells

    Lang, B., Alrahbeni, T. M. A., St Clair, D., Blackwood, D. H., McCaig, C. D., Shen, S.

    American Journal of Stem Cells, vol. 1, no. 1, pp. 31-41

    Contributions to Journals: Articles

  • Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

    Shi, Y., Li, Z., Xu, Q., Wang, T., Li, T., Shen, J., Zhang, F., Chen, J., Zhou, G., Ji, W., Li, B., Xu, Y., Liu, D., Wang, P., Yang, P., Liu, B., Sun, W., Wan, C., Qin, S., He, G., Steinberg, S., Cichon, S., Werge, T., Sigurdsson, E., Tosato, S., Palotie, A., Nöthen, M. M., Rietschel, M., Ophoff, R. A., Collier, D. A., Rujescu, D., St Clair, D., Stefansson, H., Stefansson, K., Ji, J., Wang, Q., Li, W., Zheng, L., Zhang, H., Feng, G., He, L.

    Nature Genetics, vol. 43, pp. 1224-1227

    Contributions to Journals: Articles

  • GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

    Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., Van Den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, M. J., Craddock, N. J., O'Donovan, M. C., Blackman, J., Lewis, D., Kirov, G. K., Qin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D., Bronstein, M., Darvasi, A., Lencz, T., Malhotra, A. K., Rujescu, D., Giegling, I., Werge, T., Hansen, T., Ingason, A., Nöethen, M. M., Rietschel, M., Cichon, S., Djurovic, S., Andreassen, O. A., Cantor, R. M., Ophoff, R., Corvin, A., St Clair, D., Crombie, C., Fraser, G., Kuan, S. L., St Clair, D., Genetic Risk and Outcome in Psychosis (GROUP), The International Schizophrenia Consortium (ISC)

    Molecular Psychiatry, vol. 16, no. 11, pp. 1117-1129

    Contributions to Journals: Articles

  • Common variants at VRK2 and TCF4 conferring risk of schizophrenia

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  • Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

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  • Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets

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    American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, vol. 153B, no. 7, pp. 1266-1275

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  • Variation at the GABAA receptor gene, rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder

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  • Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

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  • Penetrance for copy number variants associated with schizophrenia

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  • Perseverative eye movements in obsessive-compulsive disorder and schizophrenia

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  • Scanpaths as a generalised deficit in schizophrenia

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  • Pharacogenetic effects of dopamine transporter gene polymorphisms on response to chlorpromazine and clozapine and on extrapyramidal syndrome in schizophrenia

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  • A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia

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  • Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging

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    Grozeva, D., Kirov, G., Ivanov, D., Jones, I. R., Jones, L., Green, E. K., St Clair, D. M., Young, A. H., Ferrier, N., Farmer, A. E., McGuffin, P., Holmans, P. A., Owen, M. J., O'Donovan, M. C., Craddock, N., Wellcome Trust Case Control Consortium

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  • A classification model of schizophrenia using a multivariate eye movement phenotype

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    European Psychiatry, vol. 25, no. S1, pp. 611

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  • Frontal brain function and visual exploration of natural scenes in schizophrenia

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    European Psychiatry, vol. 25, no. S1, pp. 1104

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  • A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

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  • Deregulation of EIF4E: a novel mechanism for autism

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  • Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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  • Common variants conferring risk of schizophrenia

    Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Cichon, S., Rujescu, D., Werge, T., Pietiläinen, O. P. H., Mors, O., Mortensen, P. B., Sigurdsson, E., Gustafsson, O., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T., Suvisaari, J., Lonnqvist, J., Paunio, T., Børglum, A. D., Hartmann, A., Fink-Jensen, A., Nordentoft, M., Hougaard, D., Norgaard-Pedersen, B., Böttcher, Y., Olesen, J., Breuer, R., Möller, H., Giegling, I., Rasmussen, H. B., Timm, S., Mattheisen, M., Bitter, I., Réthelyi, J. M., Magnusdottir, B. B., Sigmundsson, T., Olason, P., Masson, G., Gulcher, J. R., Haraldsson, M., Fossdal, R., Thorgeirsson, T. E., Thorsteinsdottir, U., Ruggeri, M., Tosato, S., Franke, B., Strengman, E., Walker, N., St Clair, D., Genetic Risk and Outcome in Psychosis (GROUP)

    Nature, vol. 460, no. 7256, pp. 744-747

    Contributions to Journals: Letters

  • Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

    Hamshere, M. L., Green, E. K., Jones, I. R., Jones, L., Moskvina, V., Kirov, G., Grozeva, D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, P. A., Owen, M. J., O'Donovan, M. C., Craddock, N.

    British Journal of Psychiatry, vol. 195, no. 1, pp. 23-29

    Contributions to Journals: Articles

  • Identifying relationships among genomic disease regions: Predicting genes at pathogenic SNP associations and rare deletions

    Raychaudhuri, S., Plenge, R. M., Rossin, E. J., Ng, A. C., Purcell, S. M., Sklar, P., Scolnick, E. M., Xavier, R. J., Altshuler, D., Daly, M. J., Ardlie, K., Azevedo, M. H., Bass, N., Blackwood, D. H., Carvalho, C., Chambert, K., Choudhury, K., Conti, D., Corvin, A., Craddock, N. J., Crombie, C., Curtis, D., Datta, S., Gabrie, S. B., Gates, C., Georgieva, L., Gill, M., Gurling, H., Holmans, P. A., Hultman, C. M., Fanous, A., Fraser, G., Kenny, E., Kirov, G. K., Knowles, J. A., Krasucki, R., Korn, J., Soh, L. K., Lawrence, J., Lichtenstein, P., Macedo, A., Macgregor, S., Maclean, A. W., Mahon, S., Malloy, P., McGhee, K. A., McQuillin, A., Medeiros, H., Middleton, F., St. Clair, D., The International Schizophrenia Consortium (ISC)

    PLoS Genetics, vol. 5, no. 6, e1000534

    Contributions to Journals: Articles

  • An association study of the neuregulin 1 gene, bipolar affective disorder and psychosis

    Prata, D. P., Breen, G., Osborne, S., Munro, J., St. Clair, D., Collier, D.

    Psychiatric Genetics, vol. 19, no. 3, pp. 113-116

    Contributions to Journals: Articles

  • Prenatal malnutrition and adult schizophrenia: Further evidence from the 1959-1961 Chinese famine

    Xu, M., Sun, W., Liu, B., Feng, G., Yu, L., Yang, L., He, G., Sham, P., Susser, E., St Clair, D., He, L.

    Schizophrenia Bulletin, vol. 35, no. 3, pp. 568-576

    Contributions to Journals: Articles

  • A genome-wide investigation of SNPs and CNVs in schizophrenia

    Need, A. C., Ge, D., Weale, M. E., Maia, J., Feng, S., Heinzen, E. L., Shianna, K. V., Yoon, W., Kasperaviciute, D., Gennarelli, M., Strittmatter, W. J., Bonvicini, C., Rossi, G., Jayathilake, K., Cola, P. A., McEvoy, J. P., Keefe, R. S. E., Fisher, E. M. C., St Jean, P. L., Giegling, I., Hartmann, A. M., Möller, H., Ruppert, A., Fraser, G., Crombie, C., Middleton, L. T., St Clair, D., Roses, A. D., Muglia, P., Francks, C., Rujescu, D., Meltzer, H. Y., Goldstein, D. B.

    PLoS Genetics, vol. 5, no. 2, e1000373

    Contributions to Journals: Articles

  • Copy number variation and schizophrenia

    St Clair, D.

    Schizophrenia Bulletin, vol. 35, no. 1, pp. 9-12

    Contributions to Journals: Articles

  • Disruption of the neurexin 1 gene is associated with schizophrenia

    Rujescu, D., Ingason, A., Cichon, S., Pietiläinen, O. P. H., Barnes, M. R., Toulopoulou, T., Picchioni, M., Vassos, E., Ettinger, U., Bramon, E., Murray, R., Ruggeri, M., Tosato, S., Bonetto, C., Steinberg, S., Sigurdsson, E., Sigmundsson, T., Petursson, H., Gylfason, A., Olason, P. I., Hardarsson, G., Jonsdottir, G. A., Gustafsson, O., Fossdal, R., Giegling, I., Möller, H., Hartmann, A. M., Hoffmann, P., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Djurovic, S., Melle, I., Andreassen, O. A., Hansen, T., Werge, T., Kiemeney, L. A., Franke, B., Veltman, J., Buizer-Voskamp, J. E., Sabatti, C., Ophoff, R. A., Rietschel, M., Nöthen, M. M., Stefansson, K., Peltonen, L., St Clair, D., GROUP Investigators

    Human Molecular Genetics, vol. 18, no. 5, pp. 988-996

    Contributions to Journals: Articles

  • Treatment and Diagnosis of Behavioural Disorders

    Miedzybrodzka, Z. H., St Clair, D. M., Muller, B. M., Neves-Pereira, M. D. L., Massie, D.

    Patents: Patents

  • Schizophrenia-related neural and behavioral phenotypes in transgenic mice expressing truncated Disc1

    Shen, S., Lang, B., Nakamoto, C., Zhang, F., Pu, J., Kuan, S., Chatzi, C., He, S., Mackie, I., Brandon, N. J., Marquis, K. L., Day, M., Hurko, O., McCaig, C. D., Riedel, G., St Clair, D.

    Journal of Neuroscience, vol. 28, no. 43, pp. 10893-10904

    Contributions to Journals: Articles

  • Rare chromosomal deletions and duplications increase risk of schizophrenia

    Stone, J. L., O'Donovan, M. C., Gurling, H., Kirov, G. K., Blackwood, D. H. R., Corvin, A., Craddock, N. J., Gill, M., Hultman, C. M., Lichtenstein, P., McQuillin, A., Pato, C. N., Ruderfer, D. M., Owen, M. J., St Clair, D., Sullivan, P. F., Sklar, P., Purcell, S. M., Scolnick, E. M., Holmans, P. A., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Williams, N. M., Toncheva, D., Milanova, V., Thelander, E. F., Morris, D. W., O'Dushlaine, C. T., Kenny, E., Waddington, J. L., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Curtis, D., Crombie, C., Fraser, G., Kwan, S. L., Muir, W. J., McGhee, K. A., Pickard, B., Malloy, P., Maclean, A. W., The International Schizophrenia Consortium (ISC)

    Nature, vol. 455, no. 7210, pp. 237-241

    Contributions to Journals: Letters

  • Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder

    Prata, D., Breen, G. D., Osborne, S., Munro, J., St Clair, D. M., Collier, D.

    American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, vol. 147B, no. 6, pp. 914-917

    Contributions to Journals: Articles

  • Association study of a (TG)n dinucleotide repeat at chromosome 15q13.3 and schizophrenia in the Chinese population

    Ma, J., Fan, J., Bian, L., Zhang, C., Li, X., Gu, N., Feng, G., St Clair, D. M., He, L.

    Psychiatry Research, vol. 159, no. 1-2, pp. 245-249

    Contributions to Journals: Articles

  • Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

    Nejentsev, S., Howson, J. M., Walker, N. M., Szeszko, J., Field, S. F., Stevens, H. E., Reynolds, P., Hardy, M., King, E., Masters, J., Hulme, J., Maier, L. M., Smyth, D., Bailey, R., Cooper, J. D., Ribas, G., Campbell, R. D., Clayton, D. G., Todd, J. A., Burton, P. R., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., Ouwehand, W. H., Samani, N. J., Donnelly, P., Barrett, J. C., Davison, D., Easton, D., Evans, D., Leung, H. T., Marchini, J. L., Morris, A. P., Spencer, C. C., Tobin, M. D., Attwood, A. P., Boorman, J. P., Cant, B., Everson, U., Hussey, J. M., Jolley, J. D., Knight, A. S., Koch, K., Meech, E., Nutland, S., Prowse, C. V., Taylor, N. C., Walters, G. R., Watkins, N. A., Winzer, T., Jones, R. W., McArdle, W. L., Ring, S. M., Strachan, D. P., Pembrey, M., Breen, G., St Clair, D., Caesar, S., Gordon-Smith, K., Jones, L., Fraser, C., Green, E. K., Grozeva, D., Hamshere, M. L., Holmans, P. A., Jones, I. R., Kirov, G., Moskvina, V., Nikolov, I., O'Donovan, M. C., Owen, M. J., Collier, D. A., Elkin, A., Farmer, A., Williamson, R., McGuffin, P., Young, A. H., Ferrier, I. N., Ball, S. G., Balmforth, A. J., Barrett, J. H., Bishop, D. T., Iles, M. M., Maqbool, A., Yuldasheva, N., Hall, A. S., Braund, P. S., Dixon, R. J., Mangino, M., Stevens, S., Thompson, J. R., Bredin, F., Tremelling, M., Parkes, M., Drummond, H., Lees, C. W., Nimmo, E. R., Satsangi, J., Fisher, S. A., Forbes, A., Lewis, C. M., Onnie, C. M., Prescott, N. J., Sanderson, J., Mathew, C. G., Barbour, J., Mohiuddin, M. K., Todhunter, C. E., Mansfield, J. C., Tariq, A., Cummings, F. R., Jewell, D. P., Webster, J., Brown, M. J., Lathrop, G. M., Connell, J., Dominiczak, A., Braga Marcano, C. A., Burke, B., Dobson, R., Gungadoo, J., Lee, K. L., Munroe, P. B., Newhouse, S. J., Onipinla, A., Wallace, C., Xue, M., Caulfield, M., Farrall, M., Barton, A., Bruce, I. N., Donovan, H., Eyre, S., Gilbert, P. D., Hider, S. L., Hinks, A. M., John, S. L., Potter, C., Silman, A. J., Symmons, D. P., Thomson, W., Worthington, J., Dunger, D. B., Widmer, B., Frayling, T. M., Freathy, R. M., Lango, H., Perry, J. R., Shields, B. M., Weedon, M. N., Hattersley, A. T., Hitman, G. A., Walker, M., Elliott, K. S., Groves, C. J., Lindgren, C. M., Rayner, N. W., Timpson, N. J., Zeggini, E., Newport, M., Sirugo, G., Lyons, E., Vannberg, F., Hill, A. V., Bradbury, L. A., Farrar, C., Pointon, J. J., Wordsworth, P., Brown, M. A., Franklyn, J. A., Heward, J. M., Simmonds, M. J., Gough, S. C., Seal, S., Stratton, M. R., Rahman, N., Ban, M., Goris, A., Sawcer, S. J., Compston, A., Conway, D., Jallow, M., Rockett, K. A., Bryan, C., Bumpstead, S. J., Chaney, A., Downes, K., Ghori, J., Gwilliam, R., Hunt, S. E., Inouye, M., Keniry, A., King, E., McGinnis, R., Potter, S., Ravindrarajah, R., Whittaker, P., Withers, D., Cardin, N. J., Ferreira, T., Pereira-Gale, J., Hallgrimsdóttir, I. B., Howie, B. N., Su, Z., Yik, Y. T., Vukcevic, D., Bentley, D., Compston, A.

    Nature, vol. 450, no. 7171, pp. 887-892

    Contributions to Journals: Articles

  • LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells

    Francks, C., Maegawa, S., Laurén, J., Abrahams, B. S., Velayos-Baeza, A., Medland, S. E., Colella, S., Groszer, M., McAuley, E. Z., Caffrey, T. M., Timmusk, T., Pruunsild, P., Koppel, I., Lind, P. A., Matsumoto-Itaba, N., Nicod, J., Xiong, L., Joober, R., Enard, W., Krinsky, B., Nanba, E., Richardson, A. J., Riley, B. P., Martin, N. G., Strittmatter, S. M., Möller, H. J., Rujescu, D., St. Clair, D., Muglia, P., Roos, J. L., Fisher, S. E., Wade-Martins, R., Rouleau, G. A., Stein, J. F., Karayiorgou, M., Geschwind, D. H., Ragoussis, J., Kendler, K. S., Airaksinen, M. S., Oshimura, M., Delisi, L. E., Monaco, A. P.

    Molecular Psychiatry, vol. 12, 1057

    Contributions to Journals: Articles

  • LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

    Francks, C., Maegawa, S., Laurén, J., Abrahams, B. S., Velayos-Baeza, A., Medland, S. E., Colella, S., Groszer, M., McAuley, E. Z., Caffrey, T. M., Timmusk, T., Pruunsild, P., Koppel, I., Lind, P. A., Matsumoto-Itaba, N., Nicod, J., Xiong, L., Joober, R., Enard, W., Krinsky, B., Nanba, E., Richardson, A. J., Riley, B. P., Martin, N. G., Strittmatter, S. M., Möller, H., Rujescu, D., St Clair, D., Muglia, P., Roos, J. L., Fisher, S. E., Wade-Martins, R., Rouleau, G. A., Stein, J. F., Karayiorgou, M., Geschwind, D. H., Ragoussis, J., Kendler, K. S., Airaksinen, M. S., Oshimura, M., DeLisi, L. E., Monaco, A. P.

    Molecular Psychiatry, vol. 12, no. 12, pp. 1129-1139

    Contributions to Journals: Articles

  • Visual scan paths in first-episode schizophrenia and cannabis-induced psychosis

    Benson, P. J., Leonards, U., Lothian, R. M., St Clair, D. M., Merlo, M. C. G.

    Journal of Psychiatry and Neuroscience, vol. 32, no. 4, pp. 267-274

    Contributions to Journals: Articles

  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

    Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., Ouwehand, W. H., Samani, N. J., Todd, J. A., Donnelly, P., Barrett, J. C., Davison, D., Easton, D., Evans, D., Leung, H., Marchini, J. L., Morris, A. P., Spencer, C. C. A., Tobin, M. D., Attwood, A. P., Boorman, J. P., Cant, B., Everson, U., Hussey, J. M., Jolley, J. D., Knight, A. S., Koch, K., Meech, E., Nutland, S., Prowse, C. V., Stevens, H. E., Taylor, N. C., Walters, G. R., Walker, N. M., Watkins, N. A., Winzer, T., Jones, R. W., McArdle, W. L., Ring, S. M., Strachan, D. P., Pembrey, M., Breen, G., St Clair, D., Caesar, S., Gordon-Smith, K., Jones, L., Fraser, C., Green, E. K., Biol RA Genet & Genom Study Syndicate, Wellcome Trust Case Control Consortium, Breast Canc Susceptib Collaborat

    Nature, vol. 447, no. 7145, pp. 661-678

    Contributions to Journals: Literature Reviews

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