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Marcus Pembrey

Researcher at University of Bristol

Publications -  154
Citations -  23543

Marcus Pembrey is an academic researcher from University of Bristol. The author has contributed to research in topics: Population & Longitudinal study. The author has an hindex of 48, co-authored 147 publications receiving 22338 citations. Previous affiliations of Marcus Pembrey include UCL Institute of Child Health & University of London.

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Paul Burton, +195 more
- 07 Jun 2007 - 
TL;DR: This study has demonstrated that careful use of a shared control group represents a safe and effective approach to GWA analyses of multiple disease phenotypes; generated a genome-wide genotype database for future studies of common diseases in the British population; and shown that, provided individuals with non-European ancestry are excluded, the extent of population stratification in theBritish population is generally modest.
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ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology.

TL;DR: The comprehensiveness of the ALSPAC approach with a total population sample unselected by disease status, and the availability of parental genotypes, provides an adequate sample for statistical analysis and for avoiding spurious results.
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Paul Burton, +224 more
- 01 Nov 2007 - 
TL;DR: In this paper, the authors report initial association and independent replication in a North American sample of two new loci related to ankylosing spondylitis, ARTS1 and IL23R, and confirm the previously reported association of AITD with TSHR and FCRL3.
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Sex-specific, male-line transgenerational responses in humans.

TL;DR: It is concluded that sex-specific, male-line transgenerational responses exist in humans and hypothesise that these transmissions are mediated by the sex chromosomes, X and Y and add an entirely new dimension to the study of gene–environment interactions in development and health.
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Nicholas John Craddock, +235 more
- 01 Apr 2010 - 
TL;DR: A large, direct genome-wide study of association between CNVs and eight common human diseases concludes that common CNVs that can be typed on existing platforms are unlikely to contribute greatly to the genetic basis ofcommon human diseases.