Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and GJA5[original query] |
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| 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 |
| 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 |
| 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 |
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