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S. W. Brouilette

Researcher at University of Leicester

Publications -  12
Citations -  1903

S. W. Brouilette is an academic researcher from University of Leicester. The author has contributed to research in topics: Offspring & Telomere. The author has an hindex of 10, co-authored 12 publications receiving 1808 citations.

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Telomere length, risk of coronary heart disease, and statin treatment in the West of Scotland Primary Prevention Study: a nested case-control study

TL;DR: In this article, the authors investigated whether mean leucocyte telomere length is a predictor of the development of coronary heart disease and found that individuals in the middle and lowest tertiles of telomeres were more at risk of developing a heart disease event than those in the highest tertile.
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White Cell Telomere Length and Risk of Premature Myocardial Infarction

TL;DR: The findings support the concept that biological age may play a role in the etiology of coronary heart disease and have potentially important implications for the understanding of its genetic etiology, pathogenesis, and variable age of onset.
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Mapping of a Major Locus that Determines Telomere Length in Humans

TL;DR: Mapping of the first locus that determines mean telomere length in humans is reported, and preliminary analysis of a strong candidate gene in the region, the DNA helicase DDX11, is presented.
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Telomere length is shorter in healthy offspring of subjects with coronary artery disease: support for the telomere hypothesis

TL;DR: In this article, the authors investigated whether shorter telomeres are a primary abnormality or secondary to coronary artery disease in healthy young adults with contrasting familial risk of CAD and found a decrease in mean telomere restriction fragment (TRF) length in DNA from circulating leucocytes.
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A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans

TL;DR: A genome-wide linkage analysis of mean leukocyte telomere length and fine-mapping identified a 51 kb region of association within intron 1 of the Bicaudal-D homolog 1 (BICD 1, MIM 602204) gene, indicating that BICD1 plays a similar role in humans.