Showing 346 - 360 of 611 results
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Epperla N, Brilliant MH, Vidaillet HJ. (2014 February). Topical timolol for treatment of epistaxis in hereditary haemorrhagic telangiectasia associated with bradycardia: a look at CYP2D6 metabolising variants. BMJ Case Rep. 2014 :pii: bcr2013203056.
PubMed ID: 24518395
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Hebbring S. (2014 February). The Challenges, Advantages, and Future of Phenome-Wide Association Studies. IMMUNOLOGY. 141(2):157-65.
PubMed ID: 24147732
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Loomis S, Kang J, Weinreb R, Yaspan B, Cooke Bailey J, Gaasterland D,...Wiggs J [including Brilliant MH.] (2014 February). Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss. OPHTHALMOLOGY. 121(2):508-16.
PubMed ID: 24572674
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Hall M, Dudek S, Goodloe R, Crawford D, Pendergrass S, Peissig PL,...Ritchie MD [including Brilliant MH.] (2014). Environment-wide association study (ewas) for type 2 diabetes in the marshfield personalized medicine research project biobank. Pac Symp Biocomput. 19 :200-11.
PubMed ID: 24297547
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McCarty CA, Berg RL, Rottscheit CM, Waudby CJ, Kitchner TE, Brilliant MH. (2014 January). Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies. BMC Med Genomics. 7(1):3.
PubMed ID: 24423110
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Mahnke A, Plasek JM, Hoffman DG, Partridge NS, Foth WS, Waudby CJ,...McCarty CA [including McManus V.] (2014 January). A rural community's involvement in the design and usability testing of a computer-based informed consent process for the personalized medicine research project. American Journal of Medical Genetics Part A. 164(1):129-40.
PubMed ID: 24273095
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Shameer K, Denny J, Ding K, Jouni H, Crosslin D, De Andrade M,...Kullo IJ [including Peissig PL.] (2014 January). A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. HUMAN GENETICS. 133(1):95-109.
PubMed ID: 24026423
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Kimmel SE, French B, Kasner SE, Johnson JA, Anderson JL, Gage BF,...Mazza, JJ [including Caldwell MD, Schmelzer, J.] (2013 December 12). A pharmacogenetic versus a clinical algorithm for warfarin dosing. N Engl J Med. 369(24):2283-93.
PubMed ID: 24251361
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Margolis KL, Davis BR, Baimbridge C, Ciocon JO, Cuyjet AB, Dart RA,...Williamson JD. (2013 December). Author response to lipid-lowering in African Americans in ALLHAT-optimism bias? J Clin Hypertens (Greenwich). 15(12):941.
PubMed ID: 24299695
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Liu J, Page D, Nassif H, Peissig PL, McCarty CA, Onitilo AA, Burnside E. Genetic variants improve breast cancer risk prediction on mammograms. AMIA Annu Symp Proc. 2013 November; 2013(eCollection 2013):876-85.
PubMed ID: 24551380
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McCarty CA, Berg RL, Rottscheit CM, Dart RA. (2013 November). The use of dietary supplements and their association with blood pressure in a large Midwestern cohort. BMC Complement Altern Med. 13 :339.
PubMed ID: 24283381
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Denny J, Bastarache L, Ritchie MD, Carroll R, Zink R, Mosley J,...Roden DM [including Peissig PL, Brilliant MH.] (2013 November). Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. NATURE BIOTECHNOLOGY. 31(12):1102-1111.
PubMed ID: 24270849
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Gottesman O, Kuivaniemi H, Tromp G, Faucett W, Li R, Manolio T,...Peissig P [including Brilliant MH.] (2013 October). The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. GENETICS IN MEDICINE. 15(10):761-71.
PubMed ID: 23743551
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McPherson EW, Cold CJ. (2013 October). Severe Pallister-Hall syndrome with persistent urogenital sinus, renal agenesis, imperforate anus, bilateral hypothalamic hamartomas, and severe skeletal anomalies. American Journal of Medical Genetics Part A. 161(10):2666-9.
PubMed ID: 23950073
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Chute CG, Ullman-Cullere M, Wood G, Lin S, He M, Pathak J. (2013 October). Some experiences and opportunities for big data in translational research. GENETICS IN MEDICINE. 15(10):802-809.
PubMed ID: 24008998
