Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 19 (of 19 Records) |
| Query Trace: Familial Atrial Fibrillation[original query] |
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| KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science (New York, N.Y.) 2003 1 299 (5604): 251-4. Chen Yi-Han, Xu Shi-Jie, Bendahhou Said, Wang Xiao-Liang, Wang Ying, Xu Wen-Yuan, Jin Hong-Wei, Sun Hao, Su Xiao-Yan, Zhuang Qi-Nan, Yang Yi-Qing, Li Yue-Bin, Liu Yi, Xu Hong-Ju, Li Xiao-Fei, Ma Ning, Mou Chun-Ping, Chen Zhu, Barhanin Jacques, Huang W |
| Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation. Journal of human genetics 2009 May 54 (5): 277-83. Yang Yiqing, Li Jun, Lin Xiaoping, Yang Yanzong, Hong Kui, Wang Lei, Liu Jinqiu, Li Li, Yan Dinghong, Liang Dandan, Xiao Junjie, Jin Hongmei, Wu Jie, Zhang Yangyang, Chen Yi-H |
| Novel connexin40 missense mutations in patients with familial atrial fibrillation. 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 Oct 12 (10): 1421-7. Yang Yi-Qing, Liu Xu, Zhang Xian-Ling, Wang Xin-Hua, Tan Hong-Wei, Shi Hai-Feng, Jiang Wei-Feng, Fang Wei- |
| Relationship between -344T/C polymorphism in the aldosterone synthase gene and atrial fibrillation in patients with essential hypertension. Journal of the renin-angiotensin-aldosterone system : JRAAS 2011 Dec 12 (4): 557-63. Sun Xiaojian, Yang Jun, Hou Xiaofei, Li Jun, Shi Yu, Jing Yany |
| GATA4 loss-of-function mutations in familial atrial fibrillation. Clinica chimica acta; international journal of clinical chemistry 2011 Jun . Yang YQ, Wang MY, Zhang XL, Tan HW, Shi HF, Jiang WF, Wang XH, Fang WY, Liu X |
| [KCNQ1 mutation in patients with lone atrial fibrillation]. Zhonghua xin xue guan bing za zhi 2013 Jan 41 (1): 8-12. Feng Ming-jun, Chu Hui-min, Cui Han-bin, He Bin, Liu Jing, Yu Yi-bo, Shen Cai-jie, Chen Xiao-M |
| Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population. TheScientificWorldJournal 2013 2013 373454. Chu Hui-min, Feng Ming-jun, Li Yi-gang, Zhang Yi-xin, Ma Ji-fang, He Bin, Yu Yi-bo, Liu Jing, Chen Xiao-m |
| A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation. International journal of molecular medicine 2013 May 31 (5): 1119-26. Huang Ri-Tai, Xue Song, Xu Ying-Jia, Zhou Min, Yang Yi-Qi |
| A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation. European journal of medical genetics 2014 Jan 57 (1): 25-31. Wang Jun, Zhang Dai-Fu, Sun Yu-Min, Yang Yi-Qi |
| Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation. Clinics (São Paulo, Brazil) 2012 Dec 67 (12): 12. Gu JY, Xu JH, Yu H, Yang YQ |
| 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. Circulation. Cardiovascular genetics 2015 Feb 8 (1): 58-63. Weeke Peter, Denny Joshua C, Basterache Lisa, Shaffer Christian, Bowton Erica, Ingram Christie, Darbar Dawood, Roden Dan |
| NKX2-6 mutation predisposes to familial atrial fibrillation. International journal of molecular medicine 2014 Dec 34 (6): 1581-90. Wang Jun, Zhang Dai-Fu, Sun Yu-Min, Li Ruo-Gu, Qiu Xing-Biao, Qu Xin-Kai, Liu Xu, Fang Wei-Yi, Yang Yi-Qi |
| A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation. European heart journal 2017 01 38 (1): 27-34. Gudbjartsson Daniel F, Holm Hilma, Sulem Patrick, Masson Gisli, Oddsson Asmundur, Magnusson Olafur Th, Saemundsdottir Jona, Helgadottir Hafdis Th, Helgason Hannes, Johannsdottir Hrefna, Gretarsdottir Solveig, Gudjonsson Sigurjon A, Njølstad Inger, Løchen Maja-Lisa, Baum Larry, Ma Ronald C W, Sigfusson Gunnlaugur, Kong Augustine, Thorgeirsson Guðmundur, Sverrisson Jon Th, Thorsteinsdottir Unnur, Stefansson Kari, Arnar David |
| 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 |
| Putative role of Brugada syndrome genes in familial atrial fibrillation. European review for medical and pharmacological sciences 2019 9 23 (17): 7582-7598. Maltese P E, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli |
| Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population. Turkish journal of medical sciences 2019 3 49 (2): 453-457. Amirian Azam, Zafari Zahra, Sharifi Zohreh, Kordafshari Alireza, Karimipoor Morteza, Zeinali Siro |
| ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
| PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation. Journal of the American Heart Association 2021 11 10 (23): e023517. Guo Xiao-Juan, Qiu Xing-Biao, Wang Jun, Guo Yu-Han, Yang Chen-Xi, Li Li, Gao Ri-Feng, Ke Zun-Ping, Di Ruo-Min, Sun Yu-Min, Xu Ying-Jia, Yang Yi-Qi |
| Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation. Frontiers in genetics 2022 2 13 806429. Vad Oliver Bundgaard, Yan Yannan, Denti Federico, Ahlberg Gustav, Refsgaard Lena, Bomholtz Sofia Hammami, Santos Joana Larupa, Rasmussen Simon, Haunsø Stig, Svendsen Jesper Hastrup, Christophersen Ingrid Elizabeth, Schmitt Nicole, Olesen Morten Salling, Bentzen Bo Hjor |
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