Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: Tachycardia and SCN5A[original query] |
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Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. Circulation 2005 Aug 112 (6): 798-802. Burke Allen, Creighton Wendy, Mont Erik, Li Ling, Hogan Susan, Kutys Robert, Fowler David, Virmani Re |
The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genetics in medicine : official journal of the American College of Medical Genetics 2006 Mar 8 (3): 143-55. Modell Stephen M, Lehmann Michael |
Polymorphisms in multiple genes are associated with resting heart rate in a stepwise allele-dependent manner. Heart rhythm : the official journal of the Heart Rhythm Society 2008 May 5 (5): 694-700. Wilton Stephen B, Anderson Todd J, Parboosingh Jillian, Bridge Peter J, Exner Derek V, Forrest Dana, Duff Henry |
The electrocardiographic abnormalities in highly trained athletes compared to the genetic study related to causes of unexpected sudden cardiac death. Journal of medicine and life 0 2 (4): 361-72. Macarie C, Stoian Ioana, Dermengiu D, Barbarii Ligia, Piser Ileana Tepes, Chioncel O, Carp A, Stoian |
SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. Journal of the American College of Cardiology 2011 May 57 (21): 2160-8. McNair William P, Sinagra Gianfranco, Taylor Matthew R G, Di Lenarda Andrea, Ferguson Debra A, Salcedo Ernesto E, Slavov Dobromir, Zhu Xiao, Caldwell John H, Mestroni Luisa, |
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction. Circulation. Cardiovascular genetics 2011 Apr 4 (2): 163-8. Sun Albert Y, Koontz Jason I, Shah Svati H, Piccini Jonathan P, Nilsson Kent R, Craig Damian, Haynes Carol, Gregory Simon G, Hranitzky Patrick M, Pitt Geoffrey |
Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing. Mayo Clinic proceedings 2012 Jun 87 (6): 524-39. Tester David J, Medeiros-Domingo Argelia, Will Melissa L, Haglund Carla M, Ackerman Michael |
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC cardiovascular disorders 2012 12 (1): 95. Stattin Eva-Lena, Boström Ida Maria, Winbo Annika, Cederquist Kristina, Jonasson Jenni, Jonsson Björn-Anders, Diamant Ulla-Britt, Jensen Steen M, Rydberg Annika, Norberg An |
Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia. Journal of Korean medical science 2013 Jul 28 (7): 1021-6. Son Myoung Kyun, Ki Chang-Seok, Park Seung-Jung, Huh June, Kim June Soo, On Young Ke |
Sudden cardiac arrest associated with use of a non-cardiac drug that reduces cardiac excitability: evidence from bench, bedside, and community. European heart journal 2013 May 34 (20): 1506-16. Bardai Abdennasser, Amin Ahmad S, Blom Marieke T, Bezzina Connie R, Berdowski Jocelyn, Langendijk Pim N J, Beekman Leander, Klemens Christine A, Souverein Patrick C, Koster Rudolph W, de Boer Anthonius, Tan Hanno |
Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2015 Jun . Jagodzi?ska Michalina, Szperl Ma?gorzata, Poni?ska Joanna, Kosiec Agnieszka, Gajda Robert, Kukla Piotr, Biernacka El?bieta Katarzy |
Influence of Pregnancy in Patients With Congenital Long QT Syndrome. Cardiology in review 2016 Mar . Garg Lohit, Garg Jalaj, Krishnamoorthy Parasuram, Ahnert Amy, Shah Neeraj, Dusaj Raman S, Bozorgnia Bab |
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 |
Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. Annals of laboratory medicine 2017 10 38 (1): 54-58. Seo Soo Hyun, Kim So Yeon, Cho Sung Im, Park Hyunwoong, Lee Seungjun, Choi Jong Moon, Kim Man Jin, Lee Jee Soo, Ahn Kyung Jin, Song Mi Kyoung, Bae Eun Jung, Park Sung Sup, Seong Moon W |
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience. Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349. Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C |
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 |
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype. Frontiers in genetics 2019 6 10 547. Micaglio Emanuele, Monasky Michelle M, Ciconte Giuseppe, Vicedomini Gabriele, Conti Manuel, Mecarocci Valerio, Giannelli Luigi, Giordano Federica, Pollina Alberto, Saviano Massimo, Pozzi Paolo R, Di Resta Chiara, Benedetti Sara, Ferrari Maurizio, Santinelli Vincenzo, Pappone Car |
Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population. Cardiology 2019 Nov 1-8. Wang Feng, Liu Yang, Liao Hongtao, Xue Yumei, Zhan Xianzhang, Fang Xianhong, Liang Yuanhong, Wei Wei, Rao Fang, Zhang Qianhuan, Deng Hai, Lin Yubi, Liu Fangzhou, Lin Weidong, Zhang Bin, Wu Shul |
Prevalence and Prognostic Impact of Pathogenic Variants in Patients With Dilated Cardiomyopathy Referred for Ventricular Tachycardia Ablation. JACC. Clinical electrophysiology 2020 9 6 (9): 1103-1114. Ebert Micaela, Wijnmaalen Adrianus P, de Riva Marta, Trines Serge A, Androulakis Alexander F A, Glashan Claire A, Schalij Martin J, Peter van Tintelen J, Jongbloed Jan D H, Zeppenfeld Kat |
Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong. Frontiers in physiology 2020 11 574590. Tse Gary, Lee Sharen, Liu Tong, Yuen Ho Chuen, Wong Ian Chi Kei, Mak Chloe, Mok Ngai Shing, Wong Wing T |
Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent. NPJ genomic medicine 2021 6 6 (1): 51. Lacaze Paul, Sebra Robert, Riaz Moeen, Ingles Jodie, Tiller Jane, Thompson Bryony A, James Paul A, Fatkin Diane, Semsarian Christopher, Reid Christopher M, Tonkin Andrew M, Winship Ingrid, Schadt Eric, McNeil John |
Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome. Frontiers in pharmacology 2022 9 13 984299. Zaklyazminskaya Elena, Shestak Anna, Podolyak Dmitry, Komoliatova Vera, Makarov Leonid, Novitskaya Anna, Revishvili Amir |
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome. Molecular genetics & genomic medicine 2023 8 e2263. Hung Manh Pham, Duy Phuong Nguyen, Thanh Dat Ta, Thi Phuong Le, Phong Hai Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tr |
Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China. BMC genomics 2023 2 24 (1): 57. Wei Si-Jie, Du Jin-Liang, Wang Yue-Bing, Qu Peng-Fei, Ma Lin, Sun Zhong-Chun, Tang Xue, Liu Kai, Xi Yan-Mei, Nie Sheng-Jie, Jia Peng-Lin, Long Wu, Qu Yong-Qiang, Li Yu-Hua, Lei Pu-Pi |
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