Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: 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 |
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. American journal of human genetics 2012 Sep 91 (3): 489-501. Soemedi Rachel, Wilson Ian J, Bentham Jamie, Darlay Rebecca, Töpf Ana, Zelenika Diana, Cosgrove Catherine, Setchfield Kerry, Thornborough Chris, Granados-Riveron Javier, Blue Gillian M, Breckpot Jeroen, Hellens Stephen, Zwolinkski Simon, Glen Elise, Mamasoula Chrysovalanto, Rahman Thahira J, Hall Darroch, Rauch Anita, Devriendt Koenraad, Gewillig Marc, O' Sullivan John, Winlaw David S, Bu'Lock Frances, Brook J David, Bhattacharya Shoumo, Lathrop Mark, Santibanez-Koref Mauro, Cordell Heather J, Goodship Judith A, Keavney Bernard |
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot. European journal of human genetics : EJHG 2013 Jan 21 (1): 69-75. Guida Valentina, Ferese Rosangela, Rocchetti Marcella, Bonetti Monica, Sarkozy Anna, Cecchetti Serena, Gelmetti Vania, Lepri Francesca, Copetti Massimiliano, Lamorte Giuseppe, Cristina Digilio Maria, Marino Bruno, Zaza Antonio, den Hertog Jeroen, Dallapiccola Bruno, De Luca Alessand |
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 |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
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 |
Two polymorphisms in the Cx40 promoter are associated with hypertension and left ventricular hypertrophy preferentially in men. Clinical and experimental hypertension (New York, N.Y. : 1993) 2015 Aug 1-7. Schmidt Kjestine, Kaiser Frank J, Erdmann Jeanette, Wit Cor |
Genotypic and phenotypic predictors of complete heart block and recovery of conduction after surgical repair of congenital heart disease. Heart rhythm : the official journal of the Heart Rhythm Society 2016 Nov . Murray Laura, Smith Andrew H, Flack English C, Crum Kim, Owen Jill, Kannankeril Prince |
Association of Polymorphism in SCN5A, GJA5, and KCNN3 Gene with Sudden Cardiac Death. Bulletin of experimental biology and medicine 2017 Jun . Ivanova A A, Maksimov V N, Ivanoshchuk D E, Orlov P S, Novoselov V P, Savchenko S V, Voevoda M |
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 |
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death. The American journal of cardiology 2019 Mar . Tamariz Leonardo, Balda Javier, Pareja Dennise, Palacio Ana, Myerburg Robert J, Conway Douglas, Davis Lea, Goldberger Jeffrey |
Role of genetic testing in young patients with idiopathic atrioventricular conduction disease. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 11 25 (2): 643-650. Auricchio Angelo, Demarchi Andrea, Özkartal Tardu, Campanale Daniela, Caputo Maria Luce, di Valentino Marcello, Menafoglio Andrea, Regoli Francois, Facchini Marco, Del Bufalo Alessandro, Foglia Pietro, Ferrari Nicola, Bomio Fulvio, Medeiros-Domingo Argelia, Moccetti Tiziano, Pedrazzini Giovanni B, Klersy Catherine, Conte Giul |
Genome-wide Analysis of Motor Progression in Parkinson Disease. Neurology. Genetics 2023 8 9 (5): e200092. Alejandro Martínez Carrasco, Raquel Real, Michael Lawton, Regina Hertfelder Reynolds, Manuela Tan, Lesley Wu, Nigel Williams, Camille Carroll, Jean-Christophe Corvol, Michele Hu, Donald Grosset, John Hardy, Mina Ryten, Yoav Ben-Shlomo, Maryam Shoai, Huw R Morr |
A novel GJA5 variant associated with increased risk of essential hypertension. American journal of translational research 2023 3 15 (2): 1259-1270. Wang Juan, Wang Xue-Cheng, Gu Zhao-Hua, Ren Guang-Wei, Zhao Xiao-Hong, Qu Xin-Kai, Xu Ying-Jia, Yang Yi-Qi |
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