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Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.
Park J, Lucas AM, Zhang X, Chaudhary K, Cho JH, Nadkarni G, Dobbyn A, Chittoor G, Josyula NS, Katz N, Breeyear JH, Ahmadmehrabi S, Drivas TG, Chavali VRM, Fasolino M, Sawada H, Daugherty A, Li Y, Zhang C, Bradford Y, Weaver J, Verma A, Judy RL, Kember RL, Overton JD, Reid JG, Ferreira MAR, Li AH, Baras A, LeMaire SA, Shen YH, Naji A, Kaestner KH, Vahedi G, Edwards TL, Chen J, Damrauer SM, Justice AE, Do R, Ritchie MD, Rader DJ. Park J, et al. Among authors: ritchie md. Nat Med. 2021 Jan;27(1):66-72. doi: 10.1038/s41591-020-1133-8. Epub 2021 Jan 11. Nat Med. 2021. PMID: 33432171 Free PMC article.
Exploring epistasis in candidate genes for rheumatoid arthritis.
Ritchie MD, Bartlett J, Bush WS, Edwards TL, Motsinger AA, Torstenson ES. Ritchie MD, et al. BMC Proc. 2007;1 Suppl 1(Suppl 1):S70. doi: 10.1186/1753-6561-1-s1-s70. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466572 Free PMC article.
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. Edwards TL, et al. Among authors: ritchie md. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):721-35. doi: 10.1002/ajmg.b.30899. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19105203 Free PMC article.
439 results