Showing 1 - 15 of 190 results
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Jeffrey J. VanWormer, Casper G. Bendixsen, Sanjay K. Shukla. Dairy Farm Work and Protection from Gastrointestinal Illness. [published online ahead of print 2023 May 2]. Journal of Agromedicine. doi: 10.1080/1059924x.2023.2209091.
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Hellwege JN, Stallings S, Torstenson ES, Carroll R, Borthwick KM, Brilliant MH,...Edwards TL [including Peissig PL.] Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network. Sci Rep. 2019 April 15; 9(1):6077. PMCID: PMC6465359.
PubMed ID: 30988330
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Weichelt B, Pena AA, Joyce J, Keifer M. Economic Evaluation and Systematic Review of Publicly Available Workers' Compensation Practice Details and Mod Rate Calculators Applied to Upper Midwest Agriculture. [published online ahead of print 2019 April 2]. J Agromedicine. :1-13. doi: 30940000.
PubMed ID: 30940000
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Guo S, Jiang S, Epperla N, Ma Y, Maadooliat M, Ye Z,...Schrodi SJ [including Kitchner T, Joyce J, Strenn R, Meece JK, Knecht JE.] A gene-based recessive diplotype exome scan discovers FGF6, a novel hepcidin-regulating iron metabolism gene. [published online ahead of print 2019 February 27]. BLOOD.
PubMed ID: 30814063
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Mosley JD, Benson MD, Smith JG, Melander O, Ngo D, Shaffer CM,...Wang TJ [including McCarty CA, Peissig PL, Brilliant MH, Kitchner TE, Linneman JG.] Probing the Virtual Proteome to Identify Novel Disease Biomarkers. Circulation. 2018 November 27; 138(22):2469-2481.
PubMed ID: 30571344
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Brilliant MH, Cohen-Barak O, Hagiwara N, King RA, Newton JM, Gardner JM, Davisson MT. Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. AMERICAN JOURNAL OF HUMAN GENETICS. 2018 November; 69(5):981-8.
PubMed ID: 11574907
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Lee DJ, Woertz EN, Visotcky A, Wilk MA, Heitkotter H, Linderman RE,...Carroll J [including Brilliant MH.] The Henle Fiber Layer in Albinism: Comparison to Normal and Relationship to Outer Nuclear Layer Thickness and Foveal Cone Density. Invest. Ophthalmol. Vis. Sci.. 2018 November 1; 59(13):5336-5348.
PubMed ID: 30398625
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Antommaria AHM, Brothers KB, Myers JA, Feygin YB, Aufox SA, Brilliant MH,...Holm IA [including McCarty CA.] Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey. [published online ahead of print 2018 September 21]. AJOB Empir Bioeth. 9(3):128-142.
PubMed ID: 30240342
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Bishop-Fitzpatrick L, Movaghar A, Greenberg JS, Page D, DaWalt LS, Brilliant MH, Mailick MR. Using machine learning to identify patterns of lifetime health problems in decedents with autism spectrum disorder. Autism Res. 2018 August; 11(8):1120-1128.
PubMed ID: 29734508
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Brilliant MH, Garrison NA, Cohen-Barak O, Yi Z, Karafet TM, King RA,...Hammer MF. A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population. AMERICAN JOURNAL OF HUMAN GENETICS. 2018 January; 72(1):62-72.
PubMed ID: 12469324
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Huang X, Elston RC, Rosa GJ, Mayer J, Ye Z, Kitchner T,...Hebbring SJ [including Brilliant MH.] (2017 September 14). Applying Family Analyses to Electronic Health Records to Facilitate Genetic Research. BIOINFORMATICS.
PubMed ID: 28968884
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Almoguera B, Vazquez L, Mentch F, Connolly J, Pacheco JA, Sundaresan AS,...Hakonarson H [including Brilliant M.] Identification of Four Novel Loci in Asthma in European American and African American Populations. Am J Sports Med. 2017 February 15; 195(5):456-463.
PubMed ID: 27611488
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Jonathan D. Mosley, Sara L. van Driest, Quinn S. Wells, Christian M. Shaffer, Todd L. Edwards, Lisa Bastarache,...Dan M. Roden [including Peggy L. Peissig, Murray H. Brilliant.] (2016 December). Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical DataCLINICAL PERSPECTIVE. Circulation: Cardiovascular Genetics. 9(6):521-530.
PubMed ID: 27780847
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Verma SS, Cooke Bailey JN, Lucas A, Bradford Y, Linneman JG, Hauser MA,...Ritchie MD [including Peissig PL, Brilliant MH.] (2016 September). Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. PLoS Genet.. 12(9):e1006186.
PubMed ID: 27623284
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Anurag Verma, Shefali S. Verma, Sarah A. Pendergrass, Dana C. Crawford, David R. Crosslin, Helena Kuivaniemi,...Gerard Tromp [including Peggy Peissig, Scott Hebbring.] (2016 August). eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. BMC Medical Genomics. 9
