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29 results
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Deconstructing the relationship between genetics and race.
Bamshad M, Wooding S, Salisbury BA, Stephens JC. Bamshad M, et al. Among authors: salisbury ba. Nat Rev Genet. 2004 Aug;5(8):598-609. doi: 10.1038/nrg1401. Nat Rev Genet. 2004. PMID: 15266342 Review. No abstract available.
SNP and haplotype variation in the human genome.
Salisbury BA, Pungliya M, Choi JY, Jiang R, Sun XJ, Stephens JC. Salisbury BA, et al. Mutat Res. 2003 May 15;526(1-2):53-61. doi: 10.1016/s0027-5107(03)00014-9. Mutat Res. 2003. PMID: 12714183 Review.
The SLCO1B1*5 genetic variant is associated with statin-induced side effects.
Voora D, Shah SH, Spasojevic I, Ali S, Reed CR, Salisbury BA, Ginsburg GS. Voora D, et al. Among authors: salisbury ba. J Am Coll Cardiol. 2009 Oct 20;54(17):1609-16. doi: 10.1016/j.jacc.2009.04.053. J Am Coll Cardiol. 2009. PMID: 19833260 Free PMC article. Clinical Trial.
How many SNPs does a genome-wide haplotype map require?
Judson R, Salisbury B, Schneider J, Windemuth A, Stephens JC. Judson R, et al. Pharmacogenomics. 2002 May;3(3):379-91. doi: 10.1517/14622416.3.3.379. Pharmacogenomics. 2002. PMID: 12052145 Review.
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Kapplinger JD, Tester DJ, Alders M, Benito B, Berthet M, Brugada J, Brugada P, Fressart V, Guerchicoff A, Harris-Kerr C, Kamakura S, Kyndt F, Koopmann TT, Miyamoto Y, Pfeiffer R, Pollevick GD, Probst V, Zumhagen S, Vatta M, Towbin JA, Shimizu W, Schulze-Bahr E, Antzelevitch C, Salisbury BA, Guicheney P, Wilde AA, Brugada R, Schott JJ, Ackerman MJ. Kapplinger JD, et al. Among authors: salisbury ba. Heart Rhythm. 2010 Jan;7(1):33-46. doi: 10.1016/j.hrthm.2009.09.069. Epub 2009 Oct 8. Heart Rhythm. 2010. PMID: 20129283 Free PMC article.
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