Human Genome Epidemiology Literature Finder
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Query Trace: Atrial Fibrillation and GJA5[original query] |
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A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation. Circulation. Arrhythmia and electrophysiology 2011 Feb 4 (1): 87-93. Wirka Robert C, Gore Shamone, Van Wagoner David R, Arking Dan E, Lubitz Steven A, Lunetta Kathryn L, Benjamin Emelia J, Alonso Alvaro, Ellinor Patrick T, Barnard John, Chung Mina K, Smith Jonathan |
Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis. Journal of internal medicine 2012 Dec 272 (6): 573-82. Smith J G, Almgren P, Engström G, Hedblad B, Platonov P G, Newton-Cheh C, Melander |
Low prevalence of connexin-40 gene variants in atrial tissues and blood from atrial fibrillation subjects. BMC medical genetics 2012 13 102. Tchou Gregory D, Wirka Robert C, Van Wagoner David R, Barnard John, Chung Mina K, Smith Jonathan |
Rare variants in GJA5 are associated with early-onset lone atrial fibrillation. The Canadian journal of cardiology 2013 Jan 29 (1): 111-6. Christophersen Ingrid E, Holmegard Haya N, Jabbari Javad, Sajadieh Ahmad, Haunsø Stig, Tveit Arnljot, Svendsen Jesper H, Olesen Morten |
Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Feb 11 (2): 246-51. Olesen Morten S, Andreasen Laura, Jabbari Javad, Refsgaard Lena, Haunsø Stig, Olesen Søren-Peter, Nielsen Jonas B, Schmitt Nicole, Svendsen Jesper |
Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation. Molecular medicine reports 2012 Dec . Shi HF, Yang JF, Wang Q, Li RG, Xu YJ, Qu XK, Fang WY, Liu X, Yang YQ |
Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication. Human mutation 2013 Jan . Sun Y, Yang YQ, Gong XQ, Wang XH, Li RG, Tan HW, Liu X, Fang WY, Bai D |
A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation. The American journal of cardiology 2018 12 123 (5): 787-793. Mechakra Asma, Footz Tim, Walter Michael, Aránega Amelia, Hernández-Torres Francisco, Morel Elodie, Millat Gilles, Yang Yi-Qing, Chahine Mohamed, Chevalier Philippe, Christé Georg |
The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. Molecular genetics & genomic medicine 2019 Jul e835. Liu Xiumin, Li Yujie, Zhang Huan, Ji Yuqiang, Zhao Zhao, Wang Chang |
- Page last reviewed:Feb 1, 2024
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