Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 38 Records) |
Query Trace: Death and RYR2[original query] |
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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 |
Neuronal Na+ channel blockade suppresses arrhythmogenic diastolic Ca2+ release. Cardiovascular research 2015 Apr 106 (1): 143-52. Radwa?ski Przemys?aw B, Brunello Lucia, Veeraraghavan Rengasayee, Ho Hsiang-Ting, Lou Qing, Makara Michael A, Belevych Andriy E, Anghelescu Mircea, Priori Silvia G, Volpe Pompeo, Hund Thomas J, Janssen Paul M L, Mohler Peter J, Bridge John H B, Poelzing Steven, Györke Sánd |
Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. European journal of human genetics : EJHG 2015 Sep . Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie |
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 |
Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients. PloS one 2015 10 (6): e0131517. Ohno Seiko, Hasegawa Kanae, Horie Mino |
RyR2 Common Gene Variant G1886S and the Risk of Ventricular Arrhythmias in ICD Patients with Heart Failure. Journal of cardiovascular electrophysiology 2015 Jun 26 (6): 656-61. Francia Pietro, Adduci Carmen, Semprini Lorenzo, Stanzione Rosita, Serdoz Andrea, Caprinozzi Massimo, Santini Daria, Cotugno Maria, Palano Francesca, Musumeci Maria Beatrice, Rubattu Speranza, Volpe Massi |
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 |
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 |
Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors. Journal of human genetics 2017 Jun 62 (6): 615-620. Song Ju Sun, Kang Jong-Sun, Kim Young-Eun, Park Seung-Jung, Park Kyoung-Min, Huh June, Kim June Soo, Cho Hana, Ki Chang-Seok, On Young Ke |
Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death. Journal of electrocardiology 2017 11 51 (2): 309-315. Lin Yubi, He Siqi, Liao Zili, Feng Ruiling, Liu Ruilin, Peng Yongzheng, Yu Nan, Qi Hang, Chen Jia, Huang Zifeng, Lei Heping, Liu Yang, Rao Fang, Deng Chunyu, Xue Yumei, Zhang Guolin, Zhang Bin, Yao Hua, Wu Shul |
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 |
Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis. Medicine 2018 Sep 97 (38): e12428. Liu Xiaoli, Shi Jianli, Xiao Peil |
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome. Journal of the American College of Cardiology 2018 Mar 71 (11): 1217-1227. Tester David J, Wong Leonie C H, Chanana Pritha, Jaye Amie, Evans Jared M, FitzPatrick David R, Evans Margaret J, Fleming Peter, Jeffrey Iona, Cohen Marta C, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael |
Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia. Indian pacing and electrophysiology journal 2018 2 18 (3): 91-94. Rangaraju Advithi, Krishnan Shuba, Aparna G, Sankaran Satish, Mannan Ashraf U, Rao B Hygr |
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 |
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 |
Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. PloS one 2020 12 15 (12): e0243649. Koponen Mikael, Marjamaa Annukka, Tuiskula Annukka M, Viitasalo Matti, Nallinmaa-Luoto Terhi, Leinonen Jaakko T, Widen Elisabeth, Toivonen Lauri, Kontula Kimmo, Swan Heik |
Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction. Frontiers in cardiovascular medicine 2021 6 8 635141. Leone Maria Pia, Palumbo Pietro, Saenen Johan, Mastroianno Sandra, Castellana Stefano, Amico Cesare, Mazza Tommaso, Potenza Domenico Rosario, Petracca Antonio, Castori Marco, Carella Massimo, Di Stolfo Giusep |
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 |
An International Multicenter Cohort Study on ?-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation 2021 12 145 (5): 333-344. Peltenburg Puck J, Kallas Dania, Bos Johan M, Lieve Krystien V V, Franciosi Sonia, Roston Thomas M, Denjoy Isabelle, Sorensen Katrina B, Ohno Seiko, Roses-Noguer Ferran, Aiba Takeshi, Maltret Alice, LaPage Martin J, Atallah Joseph, Giudicessi John R, Clur Sally-Ann B, Blom Nico A, Tanck Michael, Extramiana Fabrice, Kato Koichi, Barc Julien, Borggrefe Martin, Behr Elijah R, Sarquella-Brugada Georgia, Tfelt-Hansen Jacob, Zorio Esther, Swan Heikki, Kammeraad Janneke A E, Krahn Andrew D, Davis Andrew, Sacher Frederic, Schwartz Peter J, Roberts Jason D, Skinner Jonathan R, van den Berg Maarten P, Kannankeril Prince J, Drago Fabrizio, Robyns Tomas, Haugaa Kristina, Tavacova Terezia, Semsarian Christopher, Till Jan, Probst Vincent, Brugada Ramon, Shimizu Wataru, Horie Minoru, Leenhardt Antoine, Ackerman Michael J, Sanatani Shubhayan, van der Werf Christian, Wilde Arthur A |
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 |
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca regulation. Proceedings of the National Academy of Sciences of the United States of America 2021 12 118 (52): . Halvorsen Matthew, Gould Laura, Wang Xiaohan, Grant Gariel, Moya Raquel, Rabin Rachel, Ackerman Michael J, Tester David J, Lin Peter T, Pappas John G, Maurano Matthew T, Goldstein David B, Tsien Richard W, Devinsky Orr |
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome. Heart rhythm O2 2021 10 2 (5): 431-438. Giudicessi John R, Maleszewski Joseph J, Tester David J, Ackerman Michael |
Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With ?-Blockers. JAMA cardiology 2022 3 7 (5): 504-512. Mazzanti Andrea, Kukavica Deni, Trancuccio Alessandro, Memmi Mirella, Bloise Raffaella, Gambelli Patrick, Marino Maira, Ortíz-Genga Martín, Morini Massimo, Monteforte Nicola, Giordano Umberto, Keegan Roberto, Tomasi Luca, Anastasakis Aristides, Davis Andrew M, Shimizu Wataru, Blom Nico A, Santiago Demetrio Julián, Napolitano Carlo, Monserrat Lorenzo, Priori Silvia |
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 |
Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis. Frontiers in cardiovascular medicine 2021 8 755062. Vähätalo Juha H, Holmström Lauri T A, Pylkäs Katri, Skarp Sini, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kerkelä Risto, Huikuri Heikki V, Myerburg Robert J, Junttila M Juha |
An artificial intelligence prediction model based on extracellular matrix proteins for the prognostic prediction and immunotherapeutic evaluation of ovarian serous adenocarcinoma. Frontiers in molecular biosciences 2023 6 10 1200354. Tianxiang Geng, Mengxue Zheng, Yongfeng Wang, Janne Elin Reseland, Athina Sama |
Non?synonymous polymorphisms in the HRC and ADRB1 genes may be associated with all?cause death in patients with non?ischemic heart failure. Experimental and therapeutic medicine 2023 12 27 (1): 48. Tanise Machado Telles, Bruna Miers May, Mauricio Pimentel, Bruna Letícia Da Silva Pereira, Michael Andrades, Luis Eduardo Rohde, Kátia Gonçalves Dos Sant |
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- Page last updated:Apr 22, 2024
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