P
P. W. Teague
Researcher at Western General Hospital
Publications - 17
Citations - 1829
P. W. Teague is an academic researcher from Western General Hospital. The author has contributed to research in topics: Population & Locus (genetics). The author has an hindex of 13, co-authored 17 publications receiving 1772 citations. Previous affiliations of P. W. Teague include University of Edinburgh.
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Journal ArticleDOI
Differences in the localization and morphology of chromosomes in the human nucleus
TL;DR: It is demonstrated that the distribution of genomic sequences between chromosomes has implications for nuclear structure and the findings are discussed in relation to a model of the human nucleus that is functionally compartmentalized.
Journal ArticleDOI
Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder.
Rebecca S. Devon,Susan Anderson,P. W. Teague,Paul Burgess,Tiina Kipari,Colin A. Semple,J. K. Millar,Walter J. Muir,V. Murray,Anthony J. Pelosi,Douglas Blackwood,David J. Porteous +11 more
TL;DR: It is argued that an even greater density of informative markers is required to test rigorously for association in this genomic region, because it could not detect linkage disequilibrium between all these markers in the control population.
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Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
Elspeth A. Bruford,Ruth Riise,P. W. Teague,K. Porter,K. L. Thomson,Anthony T. Moore,Marcelle Jay,M. Warburg,Albert Schinzel,Niels Tommerup,Kristina Tornqvist,Thomas Rosenberg,Michael A. Patton,D. C. Mansfield,A F Wright +14 more
TL;DR: Three consanguineous BBS families are homozygous for three adjacent chromosome 15 markers, consistent with identity by descent for this region, and a fourth group of families, estimated at 8%, are unlinked to all three of the above loci, showing that at least one other BBS locus remains to be found.
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Presence of Multiple Functional Polyadenylation Signals and a Single Nucleotide Polymorphism in the 3′ Untranslated Region of the Human Serotonin Transporter Gene
Sharon Battersby,Alan D. Ogilvie,Douglas Blackwood,Sanbing Shen,Miratul M. K. Muqit,Walter J. Muir,P. W. Teague,G M Goodwin,A J Harmar +8 more
TL;DR: This single nucleotide polymorphism in the 3′ untranslated region of the hSert gene should provide a useful genetic marker in the evaluation of hSERT as a candidate gene influencing susceptibility to mood disorders.
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Influences of chromosome size, gene density and nuclear position on the frequency of constitutional translocations in the human population
Wendy A. Bickmore,P. W. Teague +1 more
TL;DR: In this article, the authors examined factors that might influence the occurrence of constitutional translocations in the population and identified chromosome size as the major determinant of translocation frequency, which probably reflects the large target size for double-strand breakage and repair presented by the largest chromosomes.