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David StClair

University of Aberdeen

11

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311

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A Genome Wide Survey Supports the Involvement of Large Copy Number Variants in Schizophrenia With and Without Intellectual Disability

2013 American Journal of Medical Genetics
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Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

2010 Neuroscience Letters
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Genetic Differences between Five European Populations

2010 Human Heredity
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Genetic association between schizophrenia and the DISC1 gene in the Scottish population

2006 American Journal of Medical Genetics
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Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations

2005 American Journal of Medical Genetics
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The -48 C/T polymorphism in the presenilin 1 promoter is associated with an increased risk of developing Alzheimer's disease and an increased Abeta load in brain.

2001 Journal of Medical Genetics
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Linkage disequilibrium mapping of chromosome 8, 13 and 22 linkage regions in schizophrenia using DNA pooling on Chinese and Scottish populations

1999 Molecular Psychiatry
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A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12

1998 Schizophrenia Research
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MICRODISSECTION AND MICROCLONING OF THE TRANSLOCATION BREAKPOINT T(1-11)(Q42.2-Q21) ASSOCIATED WITH MAJOR MENTAL-ILLNESS

1993 American Journal of Human Genetics
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