Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and HCN4[original query] |
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| 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 |
| HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy. European journal of medical genetics 2015 Sep 58 (9): 439-42. Millat Gilles, Janin Alexandre, de Tauriac Olivier, Roux Antoine, Dauphin Clai |
| hERG potassium channel blockade by the HCN channel inhibitor bradycardic agent ivabradine. Journal of the American Heart Association 2015 Apr 4 (4): . Melgari Dario, Brack Kieran E, Zhang Chuan, Zhang Yihong, El Harchi Aziza, Mitcheson John S, Dempsey Christopher E, Ng G André, Hancox Jules |
| 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 |
| Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. Clinical genetics 2018 11 95 (3): 356-367. Richard Pascale, Ader Flavie, Roux Maguelonne, Donal Erwan, Eicher Jean-Christophe, Aoutil Nadia, Huttin Olivier, Selton-Suty Christine, Coisne Damien, Jondeau Guillaume, Damy Thibaud, Mansencal Nicolas, Casalta Anne-Claire, Michel Nicolas, Haentjens Julie, Faivre Laurence, Lavoute Cecile, Nguyen Karine, Tregouët David-Alexandre, Habib Gilbert, Charron Philip |
| Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations. Epilepsia open 2024 10 . Peiwei Zhao, Hongbo Xiong, Gunagtao Kuang, Chen Sun, Xiankai Zhang, Yufeng Huang, Sukun Luo, Lei Zhang, Jun Jiang, Xuelian |
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