• 34781 Citations
19972020

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Letter
2014

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., 1 Jan 2014, In : Molecular Psychiatry. 19, 8, p. 857-858 2 p.

Research output: Contribution to journalLetter

Open Access
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17 Citations (Scopus)
6 Downloads (Pure)
2012

Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder

Pickard, B. S., Van Den Bossche, M. J. A., Malloy, M. P., Johnstone, M., Lenaerts, A. S., Nordin, A., Goossens, D., St Clair, D., Muir, W. J., Nilsson, L. G., Sabbe, B., Adolfsson, R., Blackwood, D. H. R. & Del-Favero, J., Oct 2012, In : Psychiatric Genetics. 22, 5, p. 269-270 2 p.

Research output: Contribution to journalLetter

6 Citations (Scopus)
2009

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

St Clair, D. M., Purcell, M., Wray, N. R., Stone, J., Visscher, P. M., O'Donovan, M. C., Sullivan, P. F., Sklar, P. & The International Schizophrenia Consortium (ISC), 6 Aug 2009, In : Nature. 460, 7256, p. 748-752 5 p.

Research output: Contribution to journalLetter

2902 Citations (Scopus)

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. & 31 others, Hartmann, A., Fink-Jensen, A., Nordentoft, M., Hougaard, D., Norgaard-Pedersen, B., Böttcher, Y., Olesen, J., Breuer, R., Möller, H-J., 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), 6 Aug 2009, In : Nature. 460, 7256, p. 744-747 4 p.

Research output: Contribution to journalLetter

1226 Citations (Scopus)
2008

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. & 31 others, 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), 11 Sep 2008, In : Nature. 455, 7210, p. 237-241 5 p.

Research output: Contribution to journalLetter

1159 Citations (Scopus)
2006

Bipolar 1 disorder is not associated with the RGS4, PRODH, COMT and GRK3 genes

Prata, D. P., Breen, G., Munro, J., Sinclair, M., Osborne, S., Li, T., Kerwin, R., St. Clair, D. & Collier, D. A., Dec 2006, In : Psychiatric Genetics. 16, 6, p. 229-230 2 p.

Research output: Contribution to journalLetter

17 Citations (Scopus)
2004

Candidate gene association studies of the alpha4 (CHRNA4) and beta2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease

Cook, L. J., Horrobin, L. W., Taylor, A. E., Brayne, C., Evans, J. G., Xuereb, J., Cairns, N. J., Pritchard, A., Lemmon, H. A., Mann, D., St Clair, D. M., Turic, D., Hollingworth, P., Moore, P. J., Jehu, L., Archer, N., Walter, S., Foy, C., Edmondson, A. & Powell, J., 2004, In : Neuroscience Letters. 358, p. 142-146 4 p.

Research output: Contribution to journalLetter

35 Citations (Scopus)
2003

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

Fan, J. B., Ma, J., Zhang, C. S., Tang, J. X., Gu, N. F., Feng, G. Y., St Clair, D. M. & He, L., 2003, In : Neuroscience Letters. 338(3), p. 252-254 2 p.

Research output: Contribution to journalLetter

32 Citations (Scopus)

Apolipoprotein-491 promoter polymorphism is an independent risk factor for Alzheimer's disease

Yang, J. D., Feng, G. Y., Zhang, J., Cheung, J., St Clair, D. M., He, L. & Ichimura, K., 2003, In : Neuroscience Letters. p. 215-216 1 p.

Research output: Contribution to journalLetter

7 Citations (Scopus)
2001

Apolipoprotein E ε4 allele is a risk factor for late-onset Alzheimer's disease and vascular dementia in Han Chinese

Zhang, J. G., Yang, J. G., Lin, Z. X., He, L., Feng, G. Y., Ma, X. Y., Wang, C. F., Lu, P. F., Song, S. B., Dong, X. Z., St Clair, D. & Breen, G., Apr 2001, In : International Journal of Geriatric Psychiatry. 16, 4, p. 438-439 2 p.

Research output: Contribution to journalLetter

14 Citations (Scopus)
2000

Screening British CADASIL families for mutations in the NOTCH3 gene

De Lange, R. P. J., Bolt, J., Reid, E., Da Silva, R., Shaw, D. J. & St Clair, D. M., 18 May 2000, In : Journal of Medical Genetics. 37, 3, p. 224-225 2 p.

Research output: Contribution to journalLetter

Open Access
8 Citations (Scopus)