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Year Number of Results
1999 1
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2008 2
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2020 2
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PubMed for id: 1519243937

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Page 1
ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.
Hartmann S, Yasmeen S, Jacobs BM, Denaxas S, Pirmohamed M, Gamazon ER, Caulfield MJ; Genes & Health Research Team; Hemingway H, Pietzner M, Langenberg C. Hartmann S, et al. Nat Commun. 2023 Oct 12;14(1):6156. doi: 10.1038/s41467-023-41876-5. Nat Commun. 2023. PMID: 37828025 Free PMC article.
Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.
Trynka G, Zhernakova A, Romanos J, Franke L, Hunt KA, Turner G, Bruinenberg M, Heap GA, Platteel M, Ryan AW, de Kovel C, Holmes GK, Howdle PD, Walters JR, Sanders DS, Mulder CJ, Mearin ML, Verbeek WH, Trimble V, Stevens FM, Kelleher D, Barisani D, Bardella MT, McManus R, van Heel DA, Wijmenga C. Trynka G, et al. Gut. 2009 Aug;58(8):1078-83. doi: 10.1136/gut.2008.169052. Epub 2009 Feb 24. Gut. 2009. PMID: 19240061
A genome-wide scan maps a novel high myopia locus to 5p15.
Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS. Lam CY, et al. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3768-78. doi: 10.1167/iovs.07-1126. Epub 2008 Apr 17. Invest Ophthalmol Vis Sci. 2008. PMID: 18421076