Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Abnormalities and KCNH2[original query] |
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Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circulation. Arrhythmia and electrophysiology 2010 Jun 3 (3): 222-9. Albert Christine M, MacRae Calum A, Chasman Daniel I, VanDenburgh Martin, Buring Julie E, Manson JoAnn E, Cook Nancy R, Newton-Cheh Christoph |
Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation. Circulation. Arrhythmia and electrophysiology 2015 Jun . Hayashi Kenshi, Konno Tetsuo, Tada Hayato, Tani Satoyuki, Liu Li, Fujino Noboru, Nohara Atsushi, Hodatsu Akihiko, Tsuda Toyonobu, Tanaka Yoshihiro, Kawashiri Masa-Aki, Ino Hidekazu, Makita Naomasa, Yamagishi Masaka |
High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance. Scientific reports 2015 5 10009. Steffensen Annette Buur, Refaat Marwan M, David Jens-Peter, Mujezinovic Amer, Calloe Kirstine, Wojciak Julianne, Nussbaum Robert L, Scheinman Melvin M, Schmitt Nico |
Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases. International journal of legal medicine 2016 Feb . Neubauer Jacqueline, Haas Cordula, Bartsch Christine, Domingo-Medeiros Argelia, Berger Wolfga |
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
Genetic biomarkers for the risk of seizures in long QT syndrome. Neurology 2016 Oct 87 (16): 1660-1668. Auerbach David S, McNitt Scott, Gross Robert A, Zareba Wojciech, Dirksen Robert T, Moss Arthur |
Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families. Journal of applied genetics 2018 9 59 (4): 463-469. Szperl Ma?gorzata, Kozicka Urszula, Kosiec Agnieszka, Kukla Piotr, Roszczynko Marta, Biernacka El?bieta Katarzy |
Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use. Scientific reports 2018 May 8 (1): 8443. Nagasawa Sayaka, Saitoh Hisako, Kasahara Shiori, Chiba Fumiko, Torimitsu Suguru, Abe Hiroko, Yajima Daisuke, Iwase Hirota |
Genetic Profile and Clinical Characteristics of Brugada Syndrome in the Chinese Population. Journal of cardiovascular development and disease 2022 11 9 (11): . Wang Lin-Lin, Chen Yang-Hui, Sun Yang, Huang Man, Wei Hao-Ran, Liu Hao, Xu Ke, Song Xiu-Li, Chen Peng, Tan Lun, Huang Jin, Li Zong-Zhe, Li Rui, Yu Ting, Ma Fei, Ding Hu, Wang Yan, Wang Dao-Wen, Wang Hong, Zhao Chun-X |
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- Page last updated:Apr 16, 2024
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