Sarah Collier
Last active: 4/7/2017

  1. Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note. Weeke P, Denny JC, Basterache L, Shaffer C, Bowton E, Ingram C, Darbar D, Roden DM (2015) Circ Cardiovasc Genet 8(1): 58-63
    › Primary publication · 25410959 (PubMed) · PMC4334677 (PubMed Central)
  2. Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies. Jeff JM, Brown-Gentry K, Goodloe R, Ritchie MD, Denny JC, Kho AN, Armstrong LL, McClellan B, Mayo P, Allen M, Jin H, Gillani NB, Schnetz-Boutaud N, Dilks HH, Basford MA, Pacheco JA, Jarvik GP, Chisholm RL, Roden DM, Hayes MG, Crawford DC (2014) Evol Comput Mach Learn Data Min Bioinform : 939-951
    › Primary publication · 25590050 (PubMed) · PMC4290789 (PubMed Central)
  3. Regulation of the Th1 genomic locus from Ifng through Tmevpg1 by T-bet. Collier SP, Henderson MA, Tossberg JT, Aune TM (2014) J Immunol 193(8): 3959-65
    › Primary publication · 25225667 (PubMed) · PMC4185266 (PubMed Central)
  4. Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium. Lim U, Kocarnik JM, Bush WS, Matise TC, Caberto C, Park SL, Carlson CS, Deelman E, Duggan D, Fesinmeyer M, Haiman CA, Henderson BE, Hindorff LA, Kolonel LN, Peters U, Stram DO, Tiirikainen M, Wilkens LR, Wu C, Kooperberg C, Le Marchand L (2014) PLoS One 9(3): e89791
    › Primary publication · 24598796 (PubMed) · PMC3943855 (PubMed Central)
  5. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Cronin RM, Field JR, Bradford Y, Shaffer CM, Carroll RJ, Mosley JD, Bastarache L, Edwards TL, Hebbring SJ, Lin S, Hindorff LA, Crane PK, Pendergrass SA, Ritchie MD, Crawford DC, Pathak J, Bielinski SJ, Carrell DS, Crosslin DR, Ledbetter DH, Carey DJ, Tromp G, Williams MS, Larson EB, Jarvik GP, Peissig PL, Brilliant MH, McCarty CA, Chute CG, Kullo IJ, Bottinger E, Chisholm R, Smith ME, Roden DM, Denny JC (2014) Front Genet : 250
    › Primary publication · 25177340 (PubMed) · PMC4134007 (PubMed Central)
  6. Mitochondrial haplogroups are associated with severity of diabetic retinopathy. Estopinal CB, Chocron IM, Parks MB, Wade EA, Roberson RM, Burgess LG, Brantley MA, Samuels DC (2014) Invest Ophthalmol Vis Sci 55(9): 5589-95
    › Primary publication · 25118268 (PubMed) · PMC4160073 (PubMed Central)
  7. Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. Mitchell SL, Hall JB, Goodloe RJ, Boston J, Farber-Eger E, Pendergrass SA, Bush WS, Crawford DC (2014) BioData Min : 6
    › Primary publication · 24731735 (PubMed) · PMC4021623 (PubMed Central)
  8. Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. Mosley JD, Van Driest SL, Weeke PE, Delaney JT, Wells QS, Bastarache L, Roden DM, Denny JC (2014) PLoS One 9(6): e100322
    › Primary publication · 24949630 (PubMed) · PMC4065041 (PubMed Central)
  9. Genotype and risk of major bleeding during warfarin treatment. Kawai VK, Cunningham A, Vear SI, Van Driest SL, Oginni A, Xu H, Jiang M, Li C, Denny JC, Shaffer C, Bowton E, Gage BF, Ray WA, Roden DM, Stein CM (2014) Pharmacogenomics 15(16): 1973-83
    › Primary publication · 25521356 (PubMed) · PMC4304738 (PubMed Central)
  10. Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting. Iwuchukwu OF, Feng Q, Wei WQ, Jiang L, Jiang M, Xu H, Denny JC, Wilke RA, Krauss RM, Roden DM, Stein CM (2014) Pharmacogenomics 15(14): 1739-1747
    › Primary publication · 25493567 (PubMed) · PMC4292894 (PubMed Central)