Showing 211 - 225 of 589 results
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Hoh BL, Gong Y, McDonough CW, Waters MF, Royster AJ, Sheehan TO,...Johnson JA [including Brilliant MH, Kitchner TE, Linneman JG.] (2016 June). CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic disease. J Neurosurg. 124(6):1746-51.
PubMed ID: 26587656
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Mosley JD, Shaffer CM, Van Driest SL, Weeke PE, Wells QS, Karnes JH,...Roden DM [including Linneman JG, Brilliant MH.] (2016 June). A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. Pharmacogenomics J.. 16(3):231-7.
PubMed ID: 26169577
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Howley MM, Carter TC, Browne ML, Romitti PA, Cunniff CM, Druschel CM. (2016 May 27). Fluconazole use and birth defects in the National Birth Defects Prevention Study. Am J Obstet Gynecol. 214(5):657.
PubMed ID: 26640069
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Aswani V, Mau B, Shukla SK. (2016 May 12). Complete Genome Sequence of Staphylococcus aureus MCRF184, a Necrotizing Fasciitis-Causing Methicillin-Sensitive Sequence Type 45 Staphylococcus Strain. Genome Announc.. 4(3)
PubMed ID: 27174283
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Li R, Dudek SM, Kim D, Hall MA, Bradford Y, Peissig PL,...Ritchie MD [including Brilliant MH, Linneman JG.] (2016 May 10). Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network. BioData Min. 9 :18.
PubMed ID: 27168765
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McPherson E. (2016 May). Recurrence of stillbirth and second trimester pregnancy loss. Am J Med Genet A. 170(5):1174-80.
PubMed ID: 26945668
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Mosley JD, Witte JS, Larkin EK, Bastarache L, Shaffer CM, Karnes JH,...Denny JC [including Hebbring SJ, Brilliant MH, Mayer J, Ye Z.] (2016 April 25). Identifying genetically driven clinical phenotypes using linear mixed models. Nat Commun. 7 :11433.
PubMed ID: 27109359
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Heatherly R, Rasmussen LV, Peissig PL, Pacheco JA, Harris P, Denny JC, Malin BA. (2016 April 13). A multi-institution evaluation of clinical profile anonymization. J Am Med Inform Assoc. 23(e1):e131-7..
PubMed ID: 26567325
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Carter TC, He MM. Challenges of Identifying Clinically Actionable Genetic Variants for Precision Medicine. J Healthc Eng. 2016 April 6; 2016 doi: 10.1155/2016/3617572 . PMCID: PMC4955563 .
PubMed ID: 27195526
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VanderMeer JE, Carter TC, Pangilinan F, Mitchell A, Kurnat-Thoma E, Kirke PN,...Brody LC. (2016 April). Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. Am J Med Genet A. 170A(4):1007-16.
PubMed ID: 26789141
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Kirby JC, Speltz P, Rasmussen LV, Basford M, Gottesman O, Peissig PL,...Denny JC. (2016 March 28). PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability. J Am Med Inform Assoc.
PubMed ID: 27026615
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Shimpi N, Schroeder D, Kilsdonk J, Chyou PH, Glurich I, Penniman E, Acharya A. Medical Providers' Oral Health Knowledgeability, Attitudes, and Practice Behaviors: An Opportunity for Interprofessional Collaboration. J Evid Based Dent Pract. 2016 March; 16(1):19-29.
PubMed ID: 27132552
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Brilliant MH, Vaziri K, Connor TB, Schwartz SG, Carroll JJ, McCarty CA,...McKay BS [including Schrodi SJ, Hebbring SJ.] (2016 Mar). Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration. Am J Med. 129(3):292-8.
PubMed ID: 26524704
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Wu Y, Abbey CK, Liu J, Peissig P, Onitilo AA, Fan J,...Burnside ES. Discriminatory power of common genetic variants in personalized breast cancer diagnosis. Proc SPIE Int Soc Opt Eng. 2016 February 27; 9787
PubMed ID: 27279675
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Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL,...Heid IM [including Hebbring SJ, Kitchner TE, Brilliant MH.] A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nat Genet. 2016 February 21; 48(2):134-43.. doi: 10.1038/ng.3448. PMCID: PMC4745342 .
PubMed ID: 26691988