Showing 346 - 360 of 589 results
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Pasquale L, Loomis S, Weinreb R, Kang J, Yaspan B, Bailey J,...Wiggs J [including Brilliant MH.] (2013 July). Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. MOLECULAR VISION. 19 :1471-81.
PubMed ID: 23869166
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Martignetti JA, Tian L, Li D, Ramirez MC, Camacho-Vanegas O, Camacho SC,...Hakonarson H [including McPherson EW.] (2013 June 6). Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet. 92(6):1001-7.
PubMed ID: 23731542
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Newton KM, Peissig PL, Kho A, Bielinski S, Berg RL, Choudhary V,...Denny J. (2013 June). Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION. 20(e1):e147-54.
PubMed ID: 23531748
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McDavid A, Crane P, Newton KM, Crosslin D, McCormick W, Weston N,...Carlson C [including Rottscheit CM, Peissig PL, Stefanski EL.] (2013 June). Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. PLoS One. 8(6):e63481.
PubMed ID: 23762230
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Vinitsky A, Zaleski CA, Sajjad SM, McPherson EW. (2013 May). Intestinal Ganglioneuromatosis: Unusual Presentation of Cowden Syndrome Resulting in Delayed Diagnosis. American Journal of Medical Genetics Part A. 161(5):1085-90.
PubMed ID: 23512313
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McPherson EW. (2013 April). Discovering the cause of stillbirth. CURRENT OPINION IN OBSTETRICS & GYNECOLOGY. 25(2):152-6.
PubMed ID: 23354074
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Hebbring S, Schrodi SJ, Ye Z, Zhou Z, Page D, Brilliant MH. (2013 April). A PheWAS approach in studying HLA-DRB1*1501 GENES AND IMMUNITY. 14(3):187-91.
PubMed ID: 23392276
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Manolio T, Chisholm R, Ozenberger B, Roden DM, Williams M, Wilson R,...Ginsburg G [including Brilliant MH.] (2013 April). Implementing genomic medicine in the clinic: the future is here. GENETICS IN MEDICINE. 15(4):258-67.
PubMed ID: 23306799
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Haas DM, Dantzer J, Lehmann AS, Philips S, Skaar TC, McCormick CL,...Li L [including Hebbring SJ.] (2013 March). The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease after antenatal betamethasone administration. Am J Obstet Gynecol. 208(3):215.e1-6.
PubMed ID: 23295978
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Ellsworth KA, Moon I, Eckloff BW, Fridley BL, Jenkins GD, Batzler A,...Wang L [including Hebbring S.] (2013 March). FKBP5 genetic variation: association with selective serotonin reuptake inhibitor treatment outcomes in major depressive disorder. Pharmacogenet Genomics. 23(3):156-66.
PubMed ID: 23324805
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Pan N, Frome WL, Dart RA, Tewksbury DA, Luo J. (2013 February). Expression of the renin-angiotensin system in a human placental cell line. Clinical Medicine & Research. 11(1):1-6.
PubMed ID: 22997355
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Pendergrass S, Verma S, Holzinger E, Moore C, Wallace J, Dudek S,...Ritchie MD [including Kitchner TE, Berg RL.] (2013). Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit. Pac Symp Biocomput. :147-58.
PubMed ID: 23424120
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Meyer JD, Light AR, Shukla SK, Clevidence D, Yale SH, Stegner AJ, Cook DB. (2013). Post-exertion malaise in chronic fatigue syndrome: symptoms and gene expression Fatigue: Biomedicine, Health & Behavior. 1(4):190-209.
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Davis JG, Santos Costa V, Peissig PL, Caldwell MD, Page D. (2013 January). A preliminary investigation into predictive models for adverse drug events. Expanding the Boundaries of Health Informations Using Artificial Intelligence: Papers from the AAAI . :8-11.
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Hebbring S, Slager S, Epperla N, Mazza JJ, Ye Z, Zhou Z,...Schrodi SJ [including Vasco DA, Brilliant MH.] (2013 January). Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia. BLOOD. 121(1):237-8.
PubMed ID: 23287625