Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: CASQ2[original query] |
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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 |
Common genetic variants in selected Ca²? signaling genes and the risk of appropriate ICD interventions in patients with heart failure. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2013 Dec 38 (3): 169-77. Francia Pietro, Adduci Carmen, Ricotta Agnese, Stanzione Rosita, Sensini Isabella, Uccellini Arianna, Frattari Alessandra, Balla Cristina, Cotugno Maria, Cappato Riccardo, Rubattu Speranza, Volpe Massi |
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 |
Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Jan 11 (1): 46-52. Weeke Peter, Parvez Babar, Blair Marcia, Short Laura, Ingram Christie, Kucera Gayle, Stubblefield Tanya, Roden Dan M, Darbar Dawo |
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 |
Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling. Cardiovascular research 2015 Aug . Lozano-Velasco Estefanía, Hernández-Torres Francisco, Daimi Houria, Serra Selma A, Herraiz Adela, Hove-Madsen Leif, Aránega Amelia, Franco Die |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
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 |
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovascular research 2015 Jun 106 (3): 520-9. Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, , Jamshidi Yal |
Sequencing of genes involved in the movement of calcium across human skeletal muscle sarcoplasmic reticulum: continuing the search for genes associated with malignant hyperthermia. Anaesthesia and intensive care 2016 Nov 44 (6): 762-768. Bjorksten A R, Gillies R L, Hockey B M, Du Sart |
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 |
Conditional ablation and conditional rescue models for Casq2 elucidate the role of development and of cell-type specific expression of Casq2 in the CPVT2 phenotype. Human molecular genetics 2018 2 27 (9): 1533-1544. Flores Daniel J, Duong ThuyVy, Brandenberger Luke O, Mitra Apratim, Shirali Aditya, Johnson John C, Springer Danielle, Noguchi Audrey, Yu Zu-Xi, Ebert Steven N, Ludwig Andreas, Knollmann Bjorn C, Levin Mark D, Pfeifer Ka |
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
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 |
A novel variant of the CASQ2 gene in a Chinese family with catecholaminergic polymorphic ventricular tachycardia. Cardiology journal 2019 1 25 (6): 756-758. Gao Lu, Cui Lang, Zheng Lihui, Zhao Zhihui, Li Qirui, Yu Xia, Wang Jiahui, Yuan Y |
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 |
Association of T66A polymorphism in CASQ2 with PR interval in a Chinese population. Herz 2020 Apr . Li Xin, Guo Li-Zhu, Liu Nian, Du Xin, Bai Rong, Dong Jian-Zeng, Ma Chang-She |
Association Study of Genetic Variants in Calcium Signaling-Related Genes With Cardiovascular Diseases. Frontiers in cell and developmental biology 2021 12 9 642141. Li Sen, Jia Zhaoqi, Zhang Zhang, Li Yuxin, Yan Meihui, Yu Tingti |
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
European heart journal 2021 8 . Ahlberg Gustav, Andreasen Laura, Ghouse Jonas, Bertelsen Litten, Bundgaard Henning, Haunsø Stig, Svendsen Jesper H, Olesen Morten |
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 |
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