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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Sclerosis and ATP8B4[original query]
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
Arthritis & rheumatology (Hoboken, N.J.) 2015 Oct .
Gao Li, Emond Mary J, Louie Tin, Cheadle Chris, Berger Alan E, Rafaels Nicholas, Vergara Candelaria, Kim Yoonhee, Taub Margaret A, Ruczinski Ingo, Mathai Stephen C, Rich Stephen S, Nickerson Deborah A, Hummers Laura K, Bamshad Michael J, Hassoun Paul M, Mathias Rasika A, , Barnes Kathleen
Brief Report: 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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