Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Arrhythmia and RYR2[original query] |
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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 |
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population. Annals of medicine 2013 Jun 45 (4): 328-35. Lahtinen Annukka M, Havulinna Aki S, Noseworthy Peter A, Jula Antti, Karhunen Pekka J, Perola Markus, Newton-Cheh Christopher, Salomaa Veikko, Kontula Kim |
RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort. PloS one 2014 9 (6): e101059. Akilzhanova Ainur, Guelly Christian, Nuralinov Omirbek, Nurkina Zhannur, Nazhat Dinara, Smagulov Shalkhar, Tursunbekov Azat, Alzhanova Anar, Rashbayeva Gulzhaina, Abdrakhmanov Ayan, Dosmagambet Sholpan, Trajanoski Slave, Zhumadilov Zhaxybay, Sharman Almaz, Bekbosynova Mahabb |
A novel human R25C-phospholamban mutation is associated with super-inhibition of calcium cycling and ventricular arrhythmia. Cardiovascular research 2015 Jul 107 (1): 164-74. Liu Guan-Sheng, Morales Ana, Vafiadaki Elizabeth, Lam Chi Keung, Cai Wen-Feng, Haghighi Kobra, Adly George, Hershberger Ray E, Kranias Evangelia |
An insertion/deletion polymorphism within 3'UTR of RYR2 modulates sudden unexplained death risk in Chinese populations. Forensic science international 2017 Jan 270 165-172. Wang Shouyu, Zhang Zhixiang, Yang Ya, Wang Chaoqun, Tao Ruiyang, Hu Shuxiang, Yin Zhixia, Zhang Qing, Li Lijuan, He Yan, Zhu Shaohua, Li Chengtao, Zhang Suhua, Zhang Jianhua, Sheng Lihui, Wu Fangyu, Luo Bin, Gao Yuzh |
A type 2 ryanodine receptor variant associated with reduced Ca release and short-coupled torsades de pointes ventricular arrhythmia. Heart rhythm : the official journal of the Heart Rhythm Society 2016 Oct . Fujii Yusuke, Itoh Hideki, Ohno Seiko, Murayama Takashi, Kurebayashi Nagomi, Aoki Hisaaki, Blancard Malorie, Nakagawa Yoshihisa, Yamamoto Satoshi, Matsui Yumie, Ichikawa Mari, Sonoda Keiko, Ozawa Tomoya, Ohkubo Kimie, Watanabe Ichiro, Guicheney Pascale, Horie Mino |
The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia? International journal of cardiology 2017 10 250 139-145. Leinonen Jaakko T, Crotti Lia, Djupsjöbacka Aurora, Castelletti Silvia, Junna Nella, Ghidoni Alice, Tuiskula Annukka M, Spazzolini Carla, Dagradi Federica, Viitasalo Matti, Kontula Kimmo, Kotta Maria-Christina, Widén Elisabeth, Swan Heikki, Schwartz Peter |
Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1?- Modified Schwartz Score. Circulation journal : official journal of the Japanese Circulation Society 2018 6 82 (9): 2269-2276. Ozawa Junichi, Ohno Seiko, Fujii Yusuke, Makiyama Takeru, Suzuki Hiroshi, Saitoh Akihiko, Horie Mino |
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy. BMC cardiovascular disorders 2019 Jul 19 (1): 174. Raju Hariharan, Ware James S, Skinner Jonathan R, Hedley Paula L, Arno Gavin, Love Donald R, van der Werf Christian, Tfelt-Hansen Jacob, Winkel Bo Gregers, Cohen Marta C, Li Xinzhong, John Shibu, Sharma Sanjay, Jeffery Steve, Wilde Arthur A M, Christiansen Michael, Sheppard Mary N, Behr Elijah |
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia. Frontiers in neuroscience 2021 4 15 629610. Ma Mei-Gang, Liu Xiao-Rong, Wu Yuan, Wang Jie, Li Bing-Mei, Shi Yi-Wu, Su Tao, Li Bin, Liu De-Tian, Yi Yong-Hong, Liao Wei-Pi |
Provocation Testing and Therapeutic Response in a Newly Described Channelopathy: RyR2 Calcium Release Deficiency Syndrome. Circulation. Genomic and precision medicine 2021 12 15 (1): e003589. Ormerod Julian O M, Ormondroyd Elizabeth, Li Yanhui, Taylor John, Wei Jinhong, Guo Wenting, Wang Ruiwu, Sarton Caroline N S, McGuire Karen, Dreau Helene M P, Taylor Jenny C, Ginks Matthew R, Rajappan Kim, Chen S R Wayne, Watkins Hu |
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jan . Mazzarotto Francesco, Hawley Megan H, Beltrami Matteo, Beekman Leander, de Marvao Antonio, McGurk Kathryn A, Statton Ben, Boschi Beatrice, Girolami Francesca, Roberts Angharad M, Lodder Elisabeth M, Allouba Mona, Romeih Soha, Aguib Yasmine, Baksi A John, Pantazis Antonis, Prasad Sanjay K, Cerbai Elisabetta, Yacoub Magdi H, O'Regan Declan P, Cook Stuart A, Ware James S, Funke Birgit, Olivotto Iacopo, Bezzina Connie R, Barton Paul J R, Walsh Rod |
Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program. Journal of community genetics 2022 10 13 (6): 629-639. Siskind Tamar, Williams Nori, Sebastin Monisha, Marion Robert, McDonald Thomas V, Walsh Christine, Sampson Barbara, Tang Yingying, Clark Bradley |
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- Page last updated:Apr 16, 2024
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