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Psychiatric Genetics|November 7, 1999
Mapping studies on a pericentric inversion (18) (p11.31 q21.1) in a family with both schizophrenia and learning disabilityR M Hampson, M P Malloy, O Mors, et al.
Molecular Psychiatry|February 10, 2016
Assessing the genetic overlap between BMI and cognitive functionR E Marioni, J Yang, D Dykiert, et al.
Gene Therapy|September 1, 1996
A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correctionJ R Dorin, R Farley, S Webb, et al.
Trends in Genetics : TIG|June 22, 2001
SNP association studies in Alzheimer's disease highlight problems for complex disease analysisT Emahazion, L Feuk, M Jobs, et al.
Nucleic Acids Research|December 11, 1999
HGBASE: a database of SNPs and other variations in and around human genesA J Brookes, H Lehväslaiho, M Siegfried, et al.
Parkinsonism & Related Disorders|March 15, 2001
The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controlsG D. Mellick, D D. Buchanan, N Hattori, et al.
Cancer Research|April 5, 2000
A 700-kb physical map of a region of 16q23.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16DA J Paige, K J Taylor, A Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13D J Porteous, W Bickmore, S Christie, et al.
Molecular Psychiatry|March 5, 2008
Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorderB S Pickard, A Christoforou, P A Thomson, et al.
Molecular and Cellular Biology|June 1, 1986
Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectantsD J Porteous, J E Morten, G Cranston, et al.
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