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John Bowes

Researcher at University of Manchester

Publications -  132
Citations -  11574

John Bowes is an academic researcher from University of Manchester. The author has contributed to research in topics: Genome-wide association study & Single-nucleotide polymorphism. The author has an hindex of 42, co-authored 105 publications receiving 10341 citations. Previous affiliations of John Bowes include Royal National Hospital for Rheumatic Diseases & National Health Service.

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Journal ArticleDOI

Genetics of rheumatoid arthritis contributes to biology and drug discovery

Yukinori Okada, +115 more
- 20 Feb 2014 - 
TL;DR: A genome-wide association study meta-analysis in a total of >100,000 subjects of European and Asian ancestries provides empirical evidence that the genetics of RA can provide important information for drug discovery, and sheds light on fundamental genes, pathways and cell types that contribute to RA pathogenesis.
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Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

Eli A. Stahl, +74 more
- 01 Jun 2010 - 
TL;DR: Seven new rheumatoid arthritis risk alleles were identified at genome-wide significance (P < 5 × 10−8) in an analysis of all 41,282 samples, and an additional 11 SNPs replicated at P < 0.05, suggesting that most represent genuine rhearatoid arthritisrisk alleles.
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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.
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High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

TL;DR: This study illustrates the advantages of dense SNP mapping analysis to inform subsequent functional investigations and refined the peak of association to a single gene for 19 loci, identified secondary independent effects at 6 loci and identified association to low-frequency variants at 4 loci.