Benjamin S. Pickard
Department of Medical Genetics
Molecular Medicine Centre
University of Edinburgh
Western General Hospital
UK
Name/email consistency: high
- Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder. Pickard, B.S., Christoforou, A., Thomson, P.A., Fawkes, A., Evans, K.L., Morris, S.W., Porteous, D.J., Blackwood, D.H., Muir, W.J. Mol. Psychiatry (2009)
- A common variant in the 3'UTR of the GRIK4 glutamate receptor gene affects transcript abundance and protects against bipolar disorder. Pickard, B.S., Knight, H.M., Hamilton, R.S., Soares, D.C., Walker, R., Boyd, J.K., Machell, J., Maclean, A., McGhee, K.A., Condie, A., Porteous, D.J., St Clair, D., Davis, I., Blackwood, D.H., Muir, W.J. Proc. Natl. Acad. Sci. U.S.A. (2008)
- The PDE4B gene confers sex-specific protection against schizophrenia. Pickard, B.S., Thomson, P.A., Christoforou, A., Evans, K.L., Morris, S.W., Porteous, D.J., Blackwood, D.H., Muir, W.J. Psychiatr. Genet. (2007)
- Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, GRIK4, in schizophrenia and bipolar disorder. Pickard, B.S., Malloy, M.P., Christoforou, A., Thomson, P.A., Evans, K.L., Morris, S.W., Hampson, M., Porteous, D.J., Blackwood, D.H., Muir, W.J. Mol. Psychiatry (2006)
- The NPAS3 gene--emerging evidence for a role in psychiatric illness. Pickard, B.S., Pieper, A.A., Porteous, D.J., Blackwood, D.H., Muir, W.J. Ann. Med. (2006)
- Cytogenetics and gene discovery in psychiatric disorders. Pickard, B.S., Millar, J.K., Porteous, D.J., Muir, W.J., Blackwood, D.H. Pharmacogenomics J. (2005)
- Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18. Pickard, B.S., Malloy, M.P., Clark, L., Lehellard, S., Ewald, H.L., Mors, O., Porteous, D.J., Blackwood, D.H., Muir, W.J. Psychiatr. Genet. (2005)
- Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia and learning disability. Pickard, B.S., Malloy, M.P., Porteous, D.J., Blackwood, D.H., Muir, W.J. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2005)
- A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation. Pickard, B.S., Hollox, E.J., Malloy, M.P., Porteous, D.J., Blackwood, D.H., Armour, J.A., Muir, W.J. BMC Med. Genet. (2004)