Showing 196 - 210 of 580 results
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Liu Y, Bailey JC, Helwa I, Dismuke WM, Cai J, Drewry M,...Wiggs JL [including Brilliant MH.] (2016 August 1). A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium. Invest Ophthalmol Vis Sci. 57(10):3974-81.
PubMed ID: 27537254
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Kuang Z, Thomson J, Caldwell M, Peissig P, Stewart R, Page D. (2016 August). Computational Drug Repositioning Using Continuous Self-Controlled Case Series. KDD. 2016 :491-500.
PubMed ID: 28316874
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Bush WS, Crosslin DR, Owusu-Obeng A, Wallace J, Almoguera B, Basford MA,...Ritchie MD [including Kitchner T, Brilliant MH.] (2016 August). Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network. Clin Pharmacol Ther. 100(2):160-9.
PubMed ID: 26857349
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van 't Hof FN, Ruigrok YM, Lee CH, Ripke S, Anderson G, de Andrade M,...de Bakker PI [including Peissig PL.] (2016 July 14). Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. J Am Heart Assoc. 5(7)
PubMed ID: 27418160
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Kuang Z, Thomson J, Caldwell M, Peissig P, Stewart R, Page D. (2016 July). Baseline Regularization for Computational Drug Repositioning with Longitudinal Observational Data. IJCAI (U S). 2016 :2521-2528.
PubMed ID: 28392671
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Hernandez NB, Sharma C, Okorie U, McPherson E. (2016 Jul). Catecholaminergic Polymorphic Ventricular Tachycardia Due to Ryanodine Receptor (RYRS) Gene Mutation Presenting as Recurrent Apparent Life-Threatening Event Followed by Sudden Death. Congenital Cardiology Today. 14(7):1-4.
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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
