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Professor David St Clair

Professor David St Clair

Chair in Applied Medicine

Overview

Contact Details

Telephone
work +44 (0)1224 437965
work +44 (0)1224 557951
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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

    Digital Object Identifier
    https://doi.org/10.1038/s41588-019-0397-8
    Additional Links
    View publication in Scopus
    View publication in Mendeley

  • 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

    Digital Object Identifier
    https://doi.org/10.1080/15622975.2016.1208843
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1080/15622975.2016.1268715
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1186/s13059-016-1041-x
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/9029/1/An_integrated_genetic_epigenetic.pdf
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/npjschz.2016.24
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11526/1/npjschz201624.pdf
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/nn.4267
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/nn.4228

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/tp.2015.151
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11832/1/Expression_analysis_in_a_rat_psychosis_model_identifies_novel.pdf
    Additional Links
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  • 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

    Digital Object Identifier
    https://doi.org/10.1038/srep14613
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11831/1/Bridging_the_translational_divide.pdf
    Additional Links
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  • 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

    Digital Object Identifier
    https://doi.org/10.1038/nature14962
    Additional Links
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  • 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

    Digital Object Identifier
    https://doi.org/10.1159/000438788
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/6052/1/438788.pdf

  • 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

    Digital Object Identifier
    https://doi.org/10.1093/ijnp/pyu054
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1007/s12017-014-8323-9
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/mp.2013.146

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/nature13595
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1016/j.stem.2014.05.003
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1093/hmg/ddu025
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11558/1/ddu025.pdf
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1242/jcs.137604
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/3260/1/Lang_JCS.pdf

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/mp.2013.131
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11278/1/mp2013131.pdf
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  • 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

    Digital Object Identifier
    https://doi.org/10.1016/S0924-9338(14)78383-X

  • 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

    Digital Object Identifier
    https://doi.org/10.1038/ejhg.2012.287
    Additional Links
    View publication in Scopus

  • 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

    Digital Object Identifier
    https://doi.org/10.1001/jamapsychiatry.2013.288
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  • 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

    Digital Object Identifier
    https://doi.org/10.1093/schbul/sbr197
    Additional Links
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  • 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

    Digital Object Identifier
    https://doi.org/10.1371/journal.pone.0059905
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/11469/1/Novel_Loci_Associated_with_Increased_Risk_of_Sudden_Cardiac_Death_in_the_Context_of_Coronary_Artery_Disease.PDF
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  • 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

    Digital Object Identifier
    https://doi.org/10.1016/j.biopsych.2012.04.019

  • 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

    Digital Object Identifier
    https://doi.org/10.1016/j.biopsych.2012.02.040

  • 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

    Digital Object Identifier
    https://doi.org/10.1371/journal.pone.0037852
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/12522/1/Investigation_of_the_Genetic_Association_between.PDF
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  • 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

    Digital Object Identifier
    https://doi.org/10.1371/journal.pgen.1002656
    Open Access
    http://aura.abdn.ac.uk/bitstream/2164/3650/1/Runs_of_Homo.pdf

  • 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

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    https://doi.org/10.1016/j.cell.2011.12.037

  • 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

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    https://doi.org/10.1136/jmedgenet-2011-100397
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  • 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, Ã., Costas, J.

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

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    https://doi.org/10.1016/j.biopsych.2011.09.032

  • 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

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  • 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

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  • 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

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    https://doi.org/10.1038/mp.2010.96
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  • Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Børglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietiläinen, O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N., Tuulio-Henriksson, A., Suvisaari, J., Lönnqvist, J., Paunio, T., Agartz, I., Melle, I., Djurovic, S., Strengman, E., Jürgens, G., Glenthøj, B., Terenius, L., Hougaard, D. M., Ørntoft, T., Wiuf, C., Didriksen, M., Hollegaard, M. V., Nordentoft, M., van Winkel, R., Kenis, G., Abramova, L., Kaleda, V., Arrojo, M., Sanjuán, J., Arango, C., Sperling, S., Rossner, M., Ribolsi, M., Magni, V., Siracusano, A., Christiansen, C., St Clair, D., Irish Schizophrenia Genomics Consortium

    Human Molecular Genetics, vol. 20, no. 20, pp. 4076-4081

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    https://doi.org/10.1093/hmg/ddr325

  • Genome-wide association study identifies five new schizophrenia loci

    Ripke, S., Sanders, A. R., Kendler, K. S., Levinson, D. F., Sklar, P., Holmans, P. A., Lin, D., Duan, J., Ophoff, R. A., Andreassen, O. A., Scolnick, E., Cichon, S., St Clair, D., Corvin, A., Gurling, H., Werge, T., Rujescu, D., Blackwood, D. H. R., Pato, C. N., Malhotra, A. K., Purcell, S., Dudbridge, F., Neale, B. M., Rossin, L., Visscher, P. M., Posthuma, D., Ruderfer, D. M., Fanous, A., Stefansson, H., Steinberg, S., Mowry, B. J., Golimbet, V., De Hert, M., Jönsson, E. G., Bitter, I., Pietiläinen, O. P. H., Collier, D. A., Tosato, S., Agartz, I., Albus, M., Alexander, M., Amdur, R. L., Amin, F., Bass, N., Bergen, S. E., Black, D. W., Børglum, A. D., Brown, M. A., Bruggeman, R., Buccola, N. G., Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium

    Nature Genetics, vol. 43, no. 10, pp. 969-976

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    https://doi.org/10.1038/ng.940

  • Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., Edenberg, H. J., Nurnberger, J. I., Rietschel, M., Blackwood, D., Corvin, A., Flickinger, M., Guan, W., Mattingsdal, M., McQuillin, A., Kwan, P., Wienker, T. F., Daly, M., Dudbridge, F., Holmans, P. A., Lin, D., Burmeister, M., Greenwood, T. A., Hamshere, M. L., Muglia, P., Smith, E. N., Zandi, P. P., Nievergelt, C. M., McKinney, R., Shilling, P. D., Schork, N. J., Bloss, C. S., Foroud, T., Koller, D. L., Gershon, E. S., Liu, C., Badner, J. A., Scheftner, W. A., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W., Rice, J., Byerley, W., McMahon, F. J., Schulze, T. G., Berrettini, W., Li, J., Breen, G., St Clair, D., Psychiatric GWAS Consortium Bipolar Disorder Working Group

    Nature Genetics, vol. 43, no. 10, pp. 977-983

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    https://doi.org/10.1038/ng.943

  • Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia

    Chen, J., Lee, G., Fanous, A. H., Zhao, Z., Jia, P., O'Neill, A., Walsh, D., Kendler, K. S., Chen, X., The International Schizophrenia Consortium (ISC), St Clair, D.

    Schizophrenia Research, vol. 131, no. 1-3, pp. 43-51

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    https://doi.org/10.1016/j.schres.2011.06.023

  • At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia

    Hansen, T., Ingason, A., Djurovic, S., Melle, I., Fenger, M., Gustafsson, O., Jakobsen, K. D., Rasmussen, H. B., Tosato, S., Rietschel, M., Frank, J., Owen, M., Bonetto, C., Suvisaari, J., Thygesen, J. H., Pétursson, H., Lönnqvist, J., Sigurdsson, E., Giegling, I., Craddock, N., O'Donovan, M. C., Ruggeri, M., Cichon, S., Ophoff, R. A., Pietiläinen, O., Peltonen, L., Nöthen, M. M., Rujescu, D., St Clair, D., Collier, D. A., Andreassen, O. A., Werge, T.

    Biological Psychiatry, vol. 70, no. 1, pp. 59-63

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    https://doi.org/10.1016/j.biopsych.2011.01.031

  • DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls

    Green, E. K., Grozeva, D., Sims, R., Raybould, R., Forty, L., Gordon-Smith, K., Russell, E., St. Clair, D., Young, A. H., Ferrier, I. N., Kirov, G., Jones, I., Jones, L., Owen, M. J., O'Donovan, M. C., Craddock, N.

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 156, no. 4, pp. 490-492

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    https://doi.org/10.1002/ajmg.b.31187
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  • Evidence of sex-modulated association of ZNF804A with schizophrenia

    Zhang, F., Chen, Q., Ye, T., Lipska, B. K., Straub, R. E., Vakkalanka, R., Rujescu, D., St Clair, D., Hyde, T. M., Bigelow, L., Kleinman, J. E., Weinberger, D. R.

    Biological Psychiatry, vol. 69, no. 10, pp. 914-917

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    https://doi.org/10.1016/j.biopsych.2011.01.003

  • Genetic classification of populations using supervised learning

    Bridges, M., Heron, E. A., O'Dushlaine, C., Segurado, R., Morris, D., Corvin, A., Gill, M., Pinto, C., Morris, D. W., O'Dushlaine, C., 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., The International Schizophrenia Consortium (ISC)

    PloS ONE, vol. 6, no. 5, pp. 1-12

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    https://doi.org/10.1371/journal.pone.0014802
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  • ADAMTSL3 as a candidate gene for schizophrenia: Gene sequencing and ultra-high density association analysis by imputation

    Dow, D. J., Huxley-Jones, J., Hall, J. M., Francks, C., Maycox, P. R., Kew, J. N., Gloger, I. S., Mehta, N. A., Kelly, F. M., Muglia, P., Breen, G., Jugurnauth, S., Pederoso, I., St.Clair, D., Rujescu, D., Barnes, M. R.

    Schizophrenia Research, vol. 127, no. 1-3, pp. 28-34

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    https://doi.org/10.1016/j.schres.2010.12.009
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  • Polygenic dissection of the bipolar phenotype

    Hamshere, M. L., O'Donovan, M. C., Jones, I. R., Jones, L., Kirov, G., Green, E. K., Moskvina, V., Grozeva, D., Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Sklar, P., Purcell, S., Holmans, P. A., Owen, M. J., Craddock, N.

    British Journal of Psychiatry, vol. 198, no. 4, pp. 284-288

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    https://doi.org/10.1192/bjp.bp.110.087866
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  • Prevention and schizophrenia: the role of dietary factors

    McGrath, J., Brown, A., St Clair, D.

    Schizophrenia Bulletin, vol. 37, no. 2, pp. 272-283

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    https://doi.org/10.1093/schbul/sbq121

  • Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

    Reilly, M. P., Li, M., He, J., Ferguson, J. F., Stylianou, I. M., Mehta, N. N., Burnett, M. S., Devaney, J. M., Knouff, C. W., Thompson, J. R., Horne, B. D., Stewart, A. F. R., Assimes, T. L., Wild, P. S., Allayee, H., Nitschke, P. L., Patel, R. S., Martinelli, N., Girelli, D., Quyyumi, A. A., Anderson, J. L., Erdmann, J., Hall, A. S., Schunkert, H., Quertermous, T., Blankenberg, S., Hazen, S. L., Roberts, R., Kathiresan, S., Samani, N. J., Epstein, S. E., Rader, D. J., Myocardial Infarction Genetics Consortium, St Clair, D.

    The Lancet, vol. 377, no. 9763, pp. 383-392

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    https://doi.org/10.1016/S0140-6736(10)61996-4

  • Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

    Kähler, A. K., Djurovic, S., Rimol, L. M., Brown, A. A., Athanasiu, L., Jönsson, E. G., Hansen, T., Gústafsson, Ã., Hall, H., Giegling, I., Muglia, P., Cichon, S., Rietschel, M., Pietiläinen, O. P. H., Peltonen, L., Bramon, E., Collier, D., St Clair, D., Sigurdsson, E., Petursson, H., Rujescu, D., Melle, I., Werge, T., Steen, V. M., Dale, A. M., Matthews, R. T., Agartz, I., Andreassen, O. A.

    Biological Psychiatry, vol. 69, no. 1, pp. 90-96

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    https://doi.org/10.1016/j.biopsych.2010.07.035

  • Expanding the range of ZNF804A variants conferring risk of psychosis

    Steinberg, S., Mors, O., Børglum, A. D., Gustafsson, O., Werge, T., Mortensen, P. B., Andreassen, O. A., Sigurdsson, E., Thorgeirsson, T. E., Böttcher, Y., Olason, P., Ophoff, R. A., Cichon, S., Gudjonsdottir, I. H., Pietiläinen, O. P. H., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T., Athanasiu, L., Suvisaari, J., Lonnqvist, J., Paunio, T., Hartmann, A., Jürgens, G., Nordentoft, M., Hougaard, D., Norgaard-Pedersen, B., Breuer, R., Möller, H., Giegling, I., Glenthøj, B., Rasmussen, H. B., Mattheisen, M., Bitter, I., Réthelyi, J. M., Sigmundsson, T., Fossdal, R., Thorsteinsdottir, U., Ruggeri, M., Tosato, S., Strengman, E., Kiemeney, L. A., Melle, I., Djurovic, S., Abramova, L., Kaleda, V., Walshe, M., Bramon, E., Vassos, E., Li, T., Fraser, G., Walker, N., Toulopoulou, T., Yoon, J., Freimer, N. B., Cantor, R. M., Murray, R., Kong, A., Golimbet, V., Jönsson, E. G., Terenius, L., Agartz, I., Petursson, H., Nöthen, M. M., Rietschel, M., Peltonen, L., Rujescu, D., Collier, D. A., Stefansson, H., St Clair, D., Stefansson, K.

    Molecular Psychiatry, vol. 16, no. 1, pp. 59-66

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    https://doi.org/10.1038/mp.2009.149

  • Copy number variations of chromosome 16p13.1 region associated with schizophrenia

    Ingason, A., Rujescu, D., Cichon, S., Sigurdsson, E., Sigmundsson, T., Pietiläinen, O. P. H., Buizer-Voskamp, J. E., Strengman, E., Francks, C., Muglia, P., Gylfason, A., Gustafsson, O., Olason, P. I., Steinberg, S., Hansen, T., Jakobsen, K. D., Rasmussen, H. B., Giegling, I., Möller, H., Hartmann, A., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Bramon, E., Kiemeney, L. A., Franke, B., Murray, R., Vassos, E., Toulopoulou, T., Mühleisen, T. W., Tosato, S., Ruggeri, M., Djurovic, S., Andreassen, O. A., Zhang, Z., Werge, T., Ophoff, R. A., Rietschel, M., Nöthen, M. M., Petursson, H., Stefansson, H., Peltonen, L., Collier, D., Stefansson, K., St Clair, D. M., GROUP Investigators

    Molecular Psychiatry, vol. 16, no. 1, pp. 17-25

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    https://doi.org/10.1038/mp.2009.101

  • Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

    O'Dushlaine, C., Kenny, E., Heron, E., Donohoe, G., Gill, M., Morris, D., Corvin, A., O'Dushlaine, C. T., Quinn, E. M., 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., Van Beck, M., Wray, N. R., Visscher, P. M., The International Schizophrenia Consortium (ISC)

    Molecular Psychiatry, vol. 16, no. 3, pp. 286-292

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

    Thorleifsson, G., Walters, G. B., Hewitt, A. W., Masson, G., Helgason, A., Dewan, A., Sigurdsson, A., Jonasdottir, A., Gudjonsson, S. A., Magnusson, K. P., Stefansson, H., Lam, D. S., Tam, P. O., Gudmundsdottir, G. J., Southgate, L., Burdon, K. P., Gottfredsdottir, M. S., Aldred, M. A., Mitchell, P., St Clair, D., Collier, D. A., Tang, N., Sveinsson, O., MacGregor, S., Martin, N. G., Cree, A. J., Gibson, J., MacLeod, A., Jacob, A., Ennis, S., Young, T. L., Chan, J. C., Karwatowski, W. S., Hammond, C. J., Thordarson, K., Zhang, M., Wadelius, C., Lotery, A. J., Trembath, R. C., Pang, C. P., Hoh, J., Craig, J. E., Kong, A., MacKey, D. A., Jonasson, F., Thorsteinsdottir, U., Stefansson, K.

    Nature Genetics, vol. 42, no. 10, pp. 906-909

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    https://doi.org/10.1038/ng.661
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  • Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets

    Xu, M., St Clair, D. M., He, L.

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

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    https://doi.org/10.1002/ajmg.b.31096

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

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

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 153, no. 7, pp. 1347-1349

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    https://doi.org/10.1002/ajmg.b.31108
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  • Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

    Raychaudhuri, S., Korn, J. M., McCarroll, S. A., The International Schizophrenia Consortium (ISC), Altshuler, D., Sklar, P., Purcell, S., Daly, M. J., St Clair, D. M.

    PLoS Genetics, vol. 6, no. 9, e1001097

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    https://doi.org/10.1371/journal.pgen.1001097
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    http://aura.abdn.ac.uk/bitstream/2164/3644/1/Accurately_assessing.pdf

  • Penetrance for copy number variants associated with schizophrenia

    Vassos, E., Collier, D. A., Holden, S., Patch, C., Rujescu, D., St Clair, D. M., Lewis, C. M.

    Human Molecular Genetics, vol. 19, no. 17, pp. 3477-3481

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    Digital Object Identifier
    https://doi.org/10.1093/hmg/ddq259

  • Perseverative eye movements in obsessive-compulsive disorder and schizophrenia

    Shephard, E., Beedie, S. A., Kuriakose, J., Benson, P. J., St Clair, D. M.

    Perception, vol. 39, no. ECVP Abstract Supplement, pp. 37

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    https://doi.org/10.1177/03010066100390S101

  • Scanpaths as a generalised deficit in schizophrenia

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

    Perception, vol. 39, no. ECVP Abstract Supplement, pp. 34

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

    Xu, M., Xing, Q., Li, S., Zheng, Y., Wu, S., Gao, R., Yu, L., Guo, T., Yang, Y., Liu, J., Zhang, A., Zhao, X., He, G., Zhou, J., Wang, L., Xuan, J., Du, J., Li, X., Feng, G., Lin, Z., Xu, Y., St Clair, D. M., Lin, Z., He, L.

    Progress in Neuro -Psychopharmacology & Biological Psychiatry, vol. 34, no. 6, pp. 1026-1032

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

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

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

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

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  • 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

    Digital Object Identifier
    https://doi.org/10.1038/nature05911
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