What's New

Last Posted: Mar 08, 2023

• A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation.
  Mechakra Asma, et al. The American journal of cardiology 2018 0 (5) 787-793
• Putative role of Brugada syndrome genes in familial atrial fibrillation.
  Maltese P E, et al. European review for medical and pharmacological sciences 2019 0 (17) 7582-7598
• Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population.
  Amirian Azam, et al. Turkish journal of medical sciences 2019 0 (2) 453-457
• ISL1 loss-of-function variation causes familial atrial fibrillation.
  Wu Shao-Hui, et al. European journal of medical genetics 2020 0 (11) 104029
• PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
  Guo Xiao-Juan, et al. Journal of the American Heart Association 2021 0 (23) e023517
• KCNQ1 gain-of-function mutation in familial atrial fibrillation.
  Chen Yi-Han, et al. Science (New York, N.Y.) 2003 0 (5604) 251-4
• Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
  Vad Oliver Bundgaard, et al. Frontiers in genetics 2022 0 806429
• The Genetic Puzzle of Familial Atrial Fibrillation.
  Ragab Ahmed A Y et al. Frontiers in cardiovascular medicine 2020 714
• A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
  Gudbjartsson Daniel F, et al. European heart journal 2017 0 (1) 27-34
• A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
  Wang Jun, et al. European journal of medical genetics 2014 1 (1) 25-31
• Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.
  Weeke Peter, et al. Circulation. Cardiovascular genetics 2015 2 (1) 58-63
• NKX2-6 mutation predisposes to familial atrial fibrillation.
  Wang Jun, et al. International journal of molecular medicine 2014 12 (6) 1581-90
• Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.
  Chu Hui-min, et al. TheScientificWorldJournal 2013 0 373454
• [KCNQ1 mutation in patients with lone atrial fibrillation].
  Feng Ming-jun, et al. Zhonghua xin xue guan bing za zhi 2013 1 (1) 8-12
• A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
  Huang Ri-Tai, et al. International journal of molecular medicine 2013 5 (5) 1119-26
• Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.
  Gu JY, et al. Clinics (São Paulo, Brazil) 2012 12 (12) 12
• Relationship between -344T/C polymorphism in the aldosterone synthase gene and atrial fibrillation in patients with essential hypertension.
  Sun Xiaojian, et al. Journal of the renin-angiotensin-aldosterone system : JRAAS 2011 12 (4) 557-63
• GATA4 loss-of-function mutations in familial atrial fibrillation.
  Yang YQ, et al. Clinica chimica acta; international journal of clinical chemistry 2011 6
• Familial atrial fibrillation
  From NCATS Genetic and Rare Diseases Information Center
• Novel connexin40 missense mutations in patients with familial atrial fibrillation.
  Yang Yi-Qing, et al. 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 2010 10 (10) 1421-7
• Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.
  Yang Yiqing, et al. Journal of human genetics 2009 5 (5) 277-83