HuGE Literature Finder
Records 1-6
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Whole-Exome Sequencing to Identify Rare Variants and Gene Networks that Increase Susceptibility to Scleroderma in African Americans.
Arthritis & rheumatology (Hoboken, N.J.) 2018 May . Gourh Pravitt, Remmers Elaine F, Boyden Steven E, Alexander Theresa, Morgan Nadia D, Shah Ami A, Mayes Maureen D, Doumatey Ayo, Bentley Amy R, Shriner Daniel, Domsic Robyn T, Medsger Thomas A, Steen Virginia D, Ramos Paula S, Silver Richard M, Korman Benjamin, Varga John, Schiopu Elena, Khanna Dinesh, Hsu Vivien, Gordon Jessica K, Saketkoo Lesley Ann, Gladue Heather, Kron Brynn, Criswell Lindsey A, Derk Chris T, Bridges S Louis, Shanmugam Victoria K, Kolstad Kathleen D, Chung Lorinda, Jan Reem, Bernstein Elana J, Goldberg Avram, Trojanowski Marcin, Kafaja Suzanne, Maksimowicz-McKinnon Kathleen M, Mullikin James C, , Adeyemo Adebowale, Rotimi Charles, Boin Francesco, Kastner Daniel L, Wigley Fredrick |
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African genetic ancestry interacts with body mass index to modify risk for uterine fibroids.
PLoS genetics 2017 Jul 13 (7): e1006871. Giri Ayush, Edwards Todd L, Hartmann Katherine E, Torstenson Eric S, Wellons Melissa, Schreiner Pamela J, Velez Edwards Digna |
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Whole Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis.
Arthritis & rheumatology (Hoboken, N.J.) 2016 Apr . Mak Angel Cy, Tang Paul Lf, Cleveland Clare, Smith Melanie H, Connolly M Kari, Katsumoto Tamiko R, Wolters Paul J, Kwok Pui-Yan, Criswell Lindsey |
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Copy number variation in patients with cervical artery dissection.
European journal of human genetics : EJHG 2012 Dec 20 (12): 1295-9. Grond-Ginsbach Caspar, Chen Bowang, Pjontek Rastislav, Wiest Tina, Jiang Yanxiang, Burwinkel Barbara, Tchatchou Sandrine, Krawczak Michael, Schreiber Stefan, Brandt Tobias, Kloss Manja, Arnold Marie-Luise, Hemminki Kari, Lichy Christoph, Lyrer Philippe A, Hausser Ingrid, Engelter Stefan |
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Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads.
BMC medical genetics 2011 12 (1): 174. Myking Solveig, Myhre Ronny, Gjessing Håkon K, Morken Nils-Halvdan, Sengpiel Verena, Williams Scott M, Ryckman Kelli K, Magnus Per, Jacobsson |
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Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.
Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
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- Page last updated:Jan 15, 2021
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