David Malcolm St Clair

Professor

    • AB25 2ZD

    • 26172 Citations
    19992019
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    Research Output 1999 2019

    2002
    3 Citations (Scopus)

    Memory and dating of remote events in schizophrenia

    Venneri, A., Bartolo, A., McCrimmon, S. & St Clair, D. M., 2002, In : Journal of the International Neuropsychological Society. 8, p. 861-866 5 p.

    Research output: Contribution to journalArticle

    2001

    Apolipoprotein E e4 allele is a risk factor for late-onset Alzheimer's disease and vascular dementia in Han Chinese

    Zhang, J. G., Yang, J. D., Feng, G. Y., Ma, X. Y., Wang, C. F., Lu, P. F., Song, S. B., Dong, X. Z., Lin, Z. X., Breen, G. D., St Clair, D. M. & He, L., 2001, In : International Journal of Geriatric Psychiatry. 4, p. 217-219 2 p.

    Research output: Contribution to journalArticle

    14 Citations (Scopus)

    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

    69 Citations (Scopus)

    Are the estrogen receptors involved in Alzheimer's disease?

    Lambert, J. C., Harris, J. M., Lemmon, H. A., Cummings, A., Coates, J., Mann, D. & St Clair, D. M., 29 Jun 2001, In : Neuroscience Letters. 306, 3, p. 193-197 4 p.

    Research output: Contribution to journalArticle

    572 Citations (Scopus)

    Co-segregation of schizophrenia and affective disorders with a translocation that ddirectly disrupts brain expressed genes at chromosome 1q42: clinical and P300 findings in a family

    Blackwood, D. H. R., Fordyce, A., Walker, M. T., St Clair, D. M., Porteous, D. J. & Muir, M. J., 2001, In : American Journal of Human Genetics. 69, p. 428-433 5 p.

    Research output: Contribution to journalArticle

    45 Citations (Scopus)

    Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland

    McGinnis, R. E., Fox, H. C., Yates, P., Cameron, L. A., Barnes, M., Gray, I. C., Spurr, N. K., Hurko, O. & St Clair, D. M., Jun 2001, In : Nature Genetics. 28, p. 128-129 1 p.

    Research output: Contribution to journalArticle

    39 Citations (Scopus)

    Lack of association between apolipoprotein E genotype and ischaemic stroke in a Scottish population

    MacLeod, M. J., De Lange, R. P., Breen, G. D., Meiklejohn, D., Lemmon, H. & St Clair, D. M., Jul 2001, In : European Journal of Clinical Investigation. 31, 7, p. 570-573 4 p.

    Research output: Contribution to journalArticle

    2 Citations (Scopus)

    Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of stroke

    De Lange, R. P., Burr, K., Clark, J. S., Negrin, C. D., Brosnan, M. J., St Clair, D. M., Dominiczak, A. F. & Shaw, D. J., 2001, In : Neurogenetics. 3, 2, p. 99-106 7 p.

    Research output: Contribution to journalArticle

    139 Citations (Scopus)

    SNP association studies in Alzheimer's disease highlight problems for complex disease analysis

    Emahazion, T., Feuk, L., Jobs, M., Sawyer, S. L., Fredman, D., St Clair, D., Prince, J. A. & Brookes, A. J., 2001, In : Trends in Genetics. 17, p. 407-413 7 p.

    Research output: Contribution to journalLiterature review

    139 Citations (Scopus)

    Testing multiple SNPs for Alzheimer's disease association highlights problems with this approach to complex disease analysis

    Emahazion, T., Feuk, L., Jobs, M., Sawyer, S., St Clair, D. M., Terwilliger, J. D., Prince, J. A. & Brookes, A. J., 2001, In : Trends in Genetics. 17(7), p. 407-413 6 p.

    Research output: Contribution to journalArticle

    50 Citations (Scopus)

    The -48 CT polymorphism in the presenilin 1 promoter is associated with risk developing Alzheimer's disease and an increased Abeta load in brain

    Lambert, J. C., Mann, D., Harris, J. M., Lemmon, H. A., Chartier-Harlin, M. C., Cummings, A., Coates, J., St Clair, D. M., Iwatsubo, T. & Lendon, C., 2001, In : Journal of Medical Genetics. 38(6), p. 353-355 2 p.

    Research output: Contribution to journalArticle

    2000
    34 Citations (Scopus)
    Apolipoproteins E
    Alzheimer Disease
    Genes
    Genotype
    Alleles
    19 Citations (Scopus)

    Apolipoprotein E is a genetic risk factor for fetal iodine deficiency disorder in China

    Wang, H. Y., Zhang, F. C., Gao, J. J., Fan, J. B., Liu, P., Zheng, Z. J., Xi, H., Sun, Y., Gao, X. C., Huang, T. Z., Ke, Z. J., Guo, G. R., Feng, G. Y., Breen, G., St Clair, D. & He, L., 2000, In : Molecular Psychiatry. 5, p. 363-368 6 p.

    Research output: Contribution to journalArticle

    37 Citations (Scopus)

    Association between angiotensin-converting enzyme gene and late onset Alzheimer's disease in Han Chinese

    Yang, J. D., Feng, G. Y., Zhang, J., Lin, Z. X., Shen, T., Breen, G., St Clair, D. & He, L., 2000, In : Neuroscience Letters. 295, p. 41-44 4 p.

    Research output: Contribution to journalArticle

    20 Citations (Scopus)
    CADASIL
    Complement Factor B
    Electrophoresis, Gel, Two-Dimensional
    Cerebrospinal Fluid
    Mass Spectrometry
    20 Citations (Scopus)

    Diagnosing CADASIL using MRI: evidence from families with known mutations of Notch 3 gene

    Chawda, S. J., De Lange, R. P. J., Hourihan, M. D., Halpin, S. F. S. & St Clair, D., 2000, In : Neuroradiology. 42, p. 249-255 7 p.

    Research output: Contribution to journalArticle

    967 Citations (Scopus)

    Disruption of two novel genes by a translocation co-segregating with schizophrenia

    Millar, J. K., Wilson-Annan, J. C., Anderson, S., Christie, S., Taylor, M. S., Semple, C. A. M., Devon, R. S., St Clair, D. M., Muir, W. J., Blackwood, D. H. R. & Porteous, D. J., 2000, In : Human Molecular Genetics. 9, p. 1415-1423 9 p.

    Research output: Contribution to journalArticle

    15 Citations (Scopus)

    Hereditary vascular dementia linked to notch 3 mutations - CADASIL in British families

    Thomas, N. J., Morris, C. M., Scaravilli, F., Johansson, J., Rossor, M., De Lange, R., St Clair, D., Nicoll, J., Blank, C., Coulthard, A., Bushby, K., Ince, P. G., Burn, D. & Kalaria, R. N., 2000, In : Annals of the New York Academy of Sciences. 903, p. 293-298 6 p.

    Research output: Contribution to journalArticle

    22 Citations (Scopus)

    Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population

    Harris, J. M., Cumming, A. M., Craddock, N., St Clair, D. & Lendon, C. L., 2000, In : Neuroscience Letters. 294, p. 37-40 4 p.

    Research output: Contribution to journalArticle

    7 Citations (Scopus)

    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
    70 Citations (Scopus)

    The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease

    Lambert, J. C., Goumidi, L., Wavrant-De Vrieze, F., Frigard, B., Harris, J. M., Cummings, A., Coates, J., Pasquier, F., Cottel, D., Gaillac, M., St Clair, D., Mann, D. M. A., Hardy, J., Lendon, C. L., Amouyel, P. & Chartier-Harlin, M. C., 2000, In : Human Molecular Genetics. 9, p. 2275-2280 6 p.

    Research output: Contribution to journalArticle

    1999
    41 Citations (Scopus)

    102T/C polymorphism of serotonin receptor type 2A gene is not associated with schizophrenia in either Chinese or British populations

    He, L., Li, T., Melville, C., Liu, S., Feng, G. Y., Gu, N. F., Fox, H., Shaw, D., Breen, G., Liu, X. H., Sham, P., Brown, J., Collier, D. & St Clair, D., 1999, In : American Journal of Medical Genetics. 88, p. 95-98 4 p.

    Research output: Contribution to journalArticle

    58 Citations (Scopus)

    -141 C Del/Ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population

    Breen, G., Brown, J., Maude, S., Fox, H., Collier, D., Li, T., Arranz, M., Shaw, D. & St Clair, D., 1999, In : American Journal of Medical Genetics. 88, p. 407-410 4 p.

    Research output: Contribution to journalArticle

    18 Citations (Scopus)

    Accuracy and sensitivity of DNA pooling with microsatellite repeats using capillary electrophoresis

    Breen, G., Sham, P., Li, T., Shaw, D., Collier, D. A. & St Clair, D., 1999, In : Molecular and Cellular Probes. 13, p. 359-365 7 p.

    Research output: Contribution to journalArticle

    88 Citations (Scopus)

    Association between Alzheimer's disease and the NOS3 gene

    Dahiyat, M., Cumming, A., Harrington, C., Wischik, C., Xuereb, J., Corrigan, F., Breen, G., Shaw, D. & St Clair, D., 1999, In : Annals of Neurology. 46, p. 664-667 4 p.

    Research output: Contribution to journalArticle

    11 Citations (Scopus)

    Association study of the CACN1A4 (SCA6) triplet repeat and schizophrenia

    Breen, G., Fox, H., Glen, I., Collier, D., Shaw, D. & St Clair, D., 1999, In : Psychiatric Genetics. 9, p. 111-113 3 p.

    Research output: Contribution to journalArticle

    52 Citations (Scopus)

    No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke

    MacLeod, M. J., Dahiyat, M. T., Cumming, A., Meiklejohn, D., Shaw, D. & St Clair, D., 1999, In : Neurology. 53, p. 418-420 3 p.

    Research output: Contribution to journalArticle

    3 Citations (Scopus)

    No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects

    Li, T., Breen, G., Brown, J., Liu, X., Murray, R. M., Shaw, D. J., Sham, P. C., St Clair, D. & Collier, D. A., 1999, In : Psychiatric Genetics. 9, p. 123-127 5 p.

    Research output: Contribution to journalArticle

    52 Citations (Scopus)

    Tentative association of the serotonin transporter with schizophrenia and unipolar depression but not with bipolar disorder in Han Chinese

    Liu, W. Q., Gu, N. F., Feng, G. Y., Li, S., Bai, S. C., Zhang, J. G., Shen, T., Xue, H., Breen, G., St Clair, D. & He, L., 1999, In : Pharmacogenetics. 9, p. 491-495 5 p.

    Research output: Contribution to journalArticle