Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Atrial Fibrillation and HCN4[original query] |
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The rs3807989 G/A polymorphism in CAV1 is associated with the risk of atrial fibrillation in Chinese Han populations. Pacing and clinical electrophysiology : PACE 2015 Feb 38 (2): 164-70. Liu Yaowu, Ni Bixian, Lin Yuan, Chen Xin-Guang, Chen Minglong, Hu Zhibin, Zhang Fengxia |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation. Journal of medical genetics 2015 Jan 52 (1): 28-36. Tsai Chia-Ti, Hsieh Chia-Shan, Chang Sheng-Nan, Chuang Eric Y, Juang Jyh-Ming Jimmy, Lin Lian-Yu, Lai Ling-Ping, Hwang Juey-Jen, Chiang Fu-Tien, Lin Jiunn-L |
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. Journal of the American Heart Association 2015 May 4 (5): . Chen Shanshan, Wang Chuchu, Wang Xiaojing, Xu Chengqi, Wu Manman, Wang Pengxia, Tu Xin, Wang Qing |
Atrial Fibrillation Associated Genetic Variants and Left Atrial Histology: Evaluation for Molecular Sub-Phenotypes. Journal of cardiovascular electrophysiology 2016 Aug . Roberts Jason D, Yang Jingkun, Gladstone Rachel A, Longoria James, Whitman Isaac R, Dewland Thomas A, Miller Caroline, Robles Anatalia, Poon Annie, Seiler Beverly, Laframboise William A, Olgin Jeffrey E, Kwok Pui-Yan, Marcus Gregory |
Gene-gene Interaction Analyses for Atrial Fibrillation. Scientific reports 2016 Nov 6 35371. Lin Honghuang, Mueller-Nurasyid Martina, Smith Albert V, Arking Dan E, Barnard John, Bartz Traci M, Lunetta Kathryn L, Lohman Kurt, Kleber Marcus E, Lubitz Steven A, Geelhoed Bastiaan, Trompet Stella, Niemeijer Maartje N, Kacprowski Tim, Chasman Daniel I, Klarin Derek, Sinner Moritz F, Waldenberger Melanie, Meitinger Thomas, Harris Tamara B, Launer Lenore J, Soliman Elsayed Z, Chen Lin Y, Smith Jonathan D, Van Wagoner David R, Rotter Jerome I, Psaty Bruce M, Xie Zhijun, Hendricks Audrey E, Ding Jingzhong, Delgado Graciela E, Verweij Niek, van der Harst Pim, Macfarlane Peter W, Ford Ian, Hofman Albert, Uitterlinden André, Heeringa Jan, Franco Oscar H, Kors Jan A, Weiss Stefan, Völzke Henry, Rose Lynda M, Natarajan Pradeep, Kathiresan Sekar, Kääb Stefan, Gudnason Vilmundur, Alonso Alvaro, Chung Mina K, Heckbert Susan R, Benjamin Emelia J, Liu Yongmei, März Winfried, Rienstra Michiel, Jukema J Wouter, Stricker Bruno H, Dörr Marcus, Albert Christine M, Ellinor Patrick |
Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction. Heart rhythm 2017 Jan . Ishikawa Taisuke, Ohno Seiko, Murakami Takashi, Yoshida Kentaro, Mishima Hiroyuki, Fukuoka Tetsuya, Kimoto Hiroki, Sakamoto Risa, Ohkusa Takafumi, Aiba Takeshi, Nogami Akihiko, Sumitomo Naokata, Shimizu Wataru, Yoshiura Koh-Ichiro, Horigome Hitoshi, Horie Minoru, Makita Naoma |
HCN4 Gene Polymorphisms Are Associated With Occurrence of Tachycardia-Induced Cardiomyopathy in Patients With Atrial Fibrillation. Circulation. Genomic and precision medicine 2018 Jul 11 (7): e001980. Nakano Yukiko, Ochi Hidenori, Sairaku Akinori, Onohara Yuko, Tokuyama Takehito, Motoda Chikaaki, Matsumura Hiroya, Tomomori Shunsuke, Amioka Michitaka, Hironobe Naoya, Ohkubo Yousaku, Okamura Shou, Makita Naomasa, Yoshida Yukihiko, Chayama Kazuaki, Kihara Yasu |
Correlation between HCN4 gene polymorphisms and lone atrial fibrillation risk. Artificial cells, nanomedicine, and biotechnology 2019 7 47 (1): 2989-2993. Li Xiao-Hong, Hu Ya-Min, Yin Guang-Li, Wu Pi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
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