Human Genome Epidemiology Literature Finder
|
Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and CASQ2[original query] |
|---|
| Genetic variability of RyR2 and CASQ2 genes in an Asian population. Forensic science international 2009 Nov 192 (1-3): 53-5. Wong Chang Hua, Koo Seok Hwee, She George Qiongze, Chui Paul, Lee Edmund Jon Deo |
| Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease. Circulation. Cardiovascular genetics 2011 Aug 4 (4): 397-402. Westaway Shawn K, Reinier Kyndaron, Huertas-Vazquez Adriana, Evanado Audrey, Teodorescu Carmen, Navarro Jo, Sinner Moritz F, Gunson Karen, Jui Jonathan, Spooner Peter, Kaab Stefan, Chugh Sumeet |
| Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese. Genetic testing and molecular biomarkers 2013 Jan 17 (1): 25-9. Huang Yi, Lian Jiangfang, Huang R Stephanie, Wang Feiming, Xu Limin, Le Yanping, Yang Xi, Xu Weifeng, Huang Xiaoyan, Ye Meng, Zhou Jianqing, Duan Shiw |
| New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia. Circulation. Cardiovascular genetics 2013 Oct 6 (5): 481-9. Jabbari Javad, Jabbari Reza, Nielsen Morten W, Holst Anders G, Nielsen Jonas B, Haunsø Stig, Tfelt-Hansen Jacob, Svendsen Jesper H, Olesen Morten |
| Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1705-13. Kawamura Mihoko, Ohno Seiko, Naiki Nobu, Nagaoka Iori, Dochi Kenichi, Wang Qi, Hasegawa Kanae, Kimura Hiromi, Miyamoto Akashi, Mizusawa Yuka, Itoh Hideki, Makiyama Takeru, Sumitomo Naokata, Ushinohama Hiroya, Oyama Kotaro, Murakoshi Nobuyuki, Aonuma Kazutaka, Horigome Hitoshi, Honda Takafumi, Yoshinaga Masao, Ito Makoto, Horie Mino |
| Association of CASQ2 polymorphisms with sudden cardiac arrest and heart failure in patients with coronary artery disease. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Apr 11 (4): 646-52. Refaat Marwan M, Aouizerat Bradley E, Pullinger Clive R, Malloy Mary, Kane John, Tseng Zian |
| Common Variants in TRDN and CALM1 Are Associated with Risk of Sudden Cardiac Death in Chronic Heart Failure Patients in Chinese Han Population. PloS one 2015 10 (7): e0132459. Liu Zhouying, Liu Xiaoyan, Yu Haiyun, Pei Juanhui, Zhang Yinhui, Gong Jing, Pu Jiel |
| Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group. Clinica chimica acta; international journal of clinical chemistry 2015 Jun 446 132-40. Glotov Andrey S, Kazakov Sergey V, Zhukova Elena A, Alexandrov Anton V, Glotov Oleg S, Pakin Vladimir S, Danilova Maria M, Poliakova Irina V, Niyazova Svetlana S, Chakova Natalia N, Komissarova Svetlana M, Kurnikova Elena A, Sarana Andrey M, Sherbak Sergey G, Sergushichev Alexey A, Shalyto Anatoly A, Baranov Vladislav |
| Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals. Circulation. Arrhythmia and electrophysiology 2017 Apr 10 (4): . Landstrom Andrew P, Dailey-Schwartz Andrew L, Rosenfeld Jill A, Yang Yaping, McLean Margaret J, Miyake Christina Y, Valdes Santiago O, Fan Yuxin, Allen Hugh D, Penny Daniel J, Kim Jeffrey |
| Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death. The American journal of cardiology 2019 Mar . Tamariz Leonardo, Balda Javier, Pareja Dennise, Palacio Ana, Myerburg Robert J, Conway Douglas, Davis Lea, Goldberger Jeffrey |
| Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung's Disease in Han Chinese Population. Frontiers in genetics 2020 8 11 738. Niu Wei-Bo, Bai Mei-Rong, Song Huan-Lei, Lu Yan-Jiao, Wu Wen-Jie, Gong Yi-Ming, Yu Xian-Xian, Wei Zhi-Liang, Yu Wen-Wen, Gu Bei-Lin, Cai Wei, Chu X |
| Targeted next-generation sequencing for genetic variants of left ventricular mass status among community-based adults in Taiwan. Frontiers in genetics 2023 1 13 1064980. Fan Hsien-Yu, Lin Wan-Yu, Lu Tzu-Pin, Chen Yun-Yu, Hsu Justin BoKai, Yu Sung-Liang, Su Ta-Chen, Lin Hung-Ju, Chen Yang-Ching, Chien Kuo-Lio |
- Page last reviewed:Feb 1, 2024
- Content source: