Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 467 Records) |
Query Trace: Sudden cardiac death[original query] |
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Mitral annular disjunction and Pickelhaube sign in children with mitral valve prolapse: A prospective cohort study. Archives of cardiovascular diseases 2023 9 . Guy Vaksmann, Ivan Bouzguenda, Marie-Paule Guillaume, Pauline Gras, Valentina Silvestri, Adélaïde Richa |
TCAP gene is not a common cause of cardiomyopathy in Iranian patients. European journal of medical research 2023 9 28 (1): 376. Zahra Alaei, Nasrin Zamani, Bahareh Rabbani, Nejat Mahdi |
Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series. Pacing and clinical electrophysiology : PACE 2023 9 . Deepanjan Bhattacharya, Narayanan Namboodiri, Madhusoodanan Pillai Sreelekshmi, Mukund A Prabhu, Abhilash Sreevilasam Pushpangadhan, Sabarinath Menon, Baiju S Dharan, Ajitkumar Valaparamb |
Clinical and Genetic Features of Korean Inherited Arrhythmia Probands. Korean circulation journal 2023 9 . Joo Hee Jeong, Suk-Kyu Oh, Yun Gi Kim, Yun Young Choi, Hyoung Seok Lee, Jaemin Shim, Yae Min Park, Jun-Hyung Kim, Yong-Seog Oh, Nam-Ho Kim, Hui-Nam Pak, Young Keun On, Hyung Wook Park, Gyo-Seung Hwang, Dae-Kyeong Kim, Young-Ah Park, Hyoung-Seob Park, Yongkeun Cho, Seil Oh, Jong-Il Choi, Young-Hoon K |
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 |
Phenotypic Variability of Filamin C-related Cardiomyopathy: Insights from a Novel Dutch Founder Variant. Heart rhythm 2023 8 . Stephan A C Schoonvelde, Claudine W B Ruijmbeek, Alexander Hirsch, Marjon A van Slegtenhorst, Marja W Wessels, Jan H von der Thusen, Annette F Baas, Sophie L V M Stroeks, Job A J Verdonschot, Paul A van der Zwaag, Judith M A Verhagen, Michelle Miche |
Genetic Variations Within METTL16 and Susceptibility to Sudden Cardiac Death in Chinese Populations With Coronary Artery Disease. The American journal of cardiology 2023 7 202 90-99. Xiaoyuan Zhen, Wenfeng Zhao, Jiawen Wang, Lijuan Li, Yan He, Jianhua Zhang, Chengtao Li, Suhua Zhang, Jiang Huang, Bin Luo, Yuzhen G |
MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2023 7 . Luisa Marsili, Freyja H M van Lint, Francesco Russo, Karin Y van Spaendonck-Zwarts, Flavie Ader, Marie-Line Bichon, Laurence Faivre, Arjan C Houweling, Bertrand Isidor, Ronald H Lekanne Deprez, Moniek G P J Cox, Arthur A M Wilde, Benoit Mazel, Sandra Mercier, Dennis Dooijes, Gilles Millat, Karine Nguyen, Jan G Post, Pascale Richard, Irma van de Beek, Alexa M C Vermeer, Ludolf Boven, Jan D H Jongbloed, J Peter van Tintelen, |
Deep learning-derived 12-lead electrocardiogram-based genotype prediction for hypertrophic cardiomyopathy: a pilot study. Annals of medicine 2023 7 55 (1): 2235564. LaiTe Chen, GuoSheng Fu, ChenYang Jia |
Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland. Journal of the American Heart Association 2023 7 12 (14): e029845. Gardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, Kristjan Norland, Olafur B Davidsson, Rosa B Thorolfsdottir, Vinicius Tragante, Gudny A Arnadottir, Brynjar O Jensson, Hildigunnur Katrinardottir, Run Fridriksdottir, Hallbera Gudmundsdottir, Hildur M Aegisdottir, Brynjar Fridriksson, Gudmundur Thorgeirsson, Vidar Magnusson, Asmundur Oddsson, Patrick Sulem, Daniel F Gudbjartsson, Hilma Holm, David O Arnar, Kari Stefanss |
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 |
Principal components analysis to evaluate complex association of polymorphisms in ACE and ACTN3 genes and the extent of cardiovascular adaptive changes in elite athletes. The Journal of sports medicine and physical fitness 2023 12 . Tijana Petrovic, Marina Djelic, Marija Zdravkovic, Tamara Gavrilovic, Nikola Atanasijevic, Oliver Stojkov |
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern. Journal of cardiovascular medicine (Hagerstown, Md.) 2023 11 24 (12): 864-870. Laura Tonelli, Cristina Balla, Marianna Farnè, Alice Margutti, Eugenia Tiziana Maniscalchi, Gaetano De Feo, Assunta Di Domenico, Martina De Raffele, Antonio Percesepe, Vera Uliana, Valeria Barili, Walter Serra, Biagio Sassone, Santo Virzì, Elia De Maria, Giulia Parmeggiani, Gabriele Egidy Assenza, Elena Biagini, Vanda Parisi, Mauro Biffi, Valeria Carinci, Enrica Perugini, Paola Imbrici, Alessandra Ferlini, Matteo Bertini, Rita Selvatici, Francesca Gualan |
Genetic QT Score and Sleep Apnea as Predictors of Sudden Cardiac Death in the UK Biobank. medRxiv : the preprint server for health sciences 2023 11 . Amit Arora, Wojciech Zareba, Raymond L Woosley, Yann C Klimentidis, Imran Y Patel, Stuart F Quan, Christopher Wendel, Fadi Shamoun, Stefano Guerra, Sairam Parthasarathy, Salma I Pat |
Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients. Orphanet journal of rare diseases 2023 11 18 (1): 356. Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-Ze Zheng, Liang-Liang Qiu, Zhi-Xian Ye, Hai-Zhu Chen, Min-Ting Lin, Ning Wang, Zhi-Qiang Wa |
Role of genetic polymorphisms in clopidogrel response variability: a systematic review. Open heart 2023 11 10 (2): . Jose Lopez, Justin Mark, Gustavo J Duarte, Mohammed Shaban, Franklin Sosa, Rishabh Mishra, Swati Jain, An Tran, Asma Khizar, Daniel Karpel, Giancarlo Acosta, Miguel Rodriguez-Guer |
Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information. Clinical research in cardiology : official journal of the German Cardiac Society 2023 10 . Ali Amr, Jan Koelemen, Christoph Reich, Farbod Sedaghat-Hamedani, Elham Kayvanpour, Jan Haas, Karen Frese, David Lehmann, Hugo A Katus, Norbert Frey, Benjamin Med |
Clinical Heterogeneity in Patients with Long QT Syndrome and Segregation of Single Nucleotide Variants and Clinical Symptoms in 17 Affected Families. Molecular syndromology 2023 10 14 (5): 363-374. Elcin Bora, Ayca Y?ld?z Bulut, Tufan Cankaya, Tayfun Cinleti, Halise Zeynep Genç, Emin Evren Ozcan, Ebru Ozpelit, Ayfer Ulgenalp, Ahmet Okay Caglay |
RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndrome. Molecular genetics & genomic medicine 2023 10 e2290. Jingjing Zheng, Longyun Peng, Ruofei Cheng, Zhiyan Li, Jianjie Xie, Erwen Huang, Jianding Cheng, Qianhao Zh |
Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review. The Indian journal of medical research 2023 10 158 (2): 119-135. Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, M Madhuma, Y Vysakh, L R Lakshmikanth, Sivadasanpillai Harikrishn |
THE ROLE OF LEFT VENTRICULAR HYPERTROPHY, RS1801253 AND RS1801252 ALLELIC POLYMORPHISMS OF ADRB1 IN ASSESSING THE RISK OF SUDDEN CARDIAC DEATH IN PATIENTS WITH ARTERIAL HYPERTENSION. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2023 10 76 (9): 2054-2060. Olexandr N Grytsay, Boris M Todurov, Yaroslav V Skybchyk, Dina V Shorikova, Eugene I Shorik |
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation 2023 10 . Auke T Bergeman, Krystien V V Lieve, Dania Kallas, Johan M Bos, Ferran Roses Y Noguer, Isabelle Denjoy, Esther Zorio, Janneke A E Kammeraad, P J Peltenburg, Katie Tobert, Takeshi Aiba, Joseph Atallah, Fabrizio Drago, Anjan S Batra, Ramon Brugada, Martin Borggrefe, Sally-Ann B Clur, Moniek G P J Cox, Andrew Davis, Santokh Dhillon, Susan P Etheridge, Peter Fischbach, Sonia Franciosi, Kristina Haugaa, Minoru Horie, Christopher Johnsrude, Austin M Kane, Ulrich Krause, Sit-Yee Kwok, Martin J LaPage, Seiko Ohno, Vincent Probst, Jason D Roberts, Tomas Robyns, Frederic Sacher, Christopher Semsarian, Jonathan R Skinner, Heikki Swan, Terezia Tavacova, Svjetlana Tisma-Dupanovic, Jacob Tfelt-Hansen, Sing-Chien Yap, Prince J Kannankeril, Antoine Leenhardt, Janice Till, Shubhayan Sanatani, Michael W T Tanck, Michael J Ackerman, Arthur A M Wilde, Christian van der We |
Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives. Journal of the American College of Cardiology 2023 10 82 (18): 1751-1761. Søren K Nielsen, Frederikke G Hansen, Torsten B Rasmussen, Thomas Fischer, Jens F Lassen, Trine Madsen, Dorthe S Møller, Ib C Klausen, John B Brodersen, Morten S K Jensen, Jens Mogens |
Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population. Forensic science international. Genetics 2024 4 71 103051. Qianhao Zhao, Nan Zhou, Qiuping Wu, Kai Zhang, Jiacheng Yue, Da Zheng, Yunyi Wang, Yuxi Xiao, Rui Li, Ruofei Cheng, Li Quan, Erwen Huang, Bingjie Hu, Jiangding Che |
Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening. Biochemistry. Biokhimiia 2024 4 89 (3): 543-552. Denis Abramochkin, Bowen Li, Han Zhang, Ekaterina Kravchuk, Tatiana Nesterova, Grigory Glukhov, Anna Shestak, Elena Zaklyazminskaya, Olga S Sokolo |
Genetic and functional variants of the TBX20 gene promoter in dilated cardiomyopathy. Molecular genetics & genomic medicine 2024 1 12 (1): e2355. Xue Gao, Shuchao Pang, Liangcai Ding, Han Yan, Yinghua Cui, Bo Y |
Characterization of cardiac involvement in patients with LMNA splice-site mutation-related dilated cardiomyopathy and sudden cardiac death. Frontiers in genetics 2024 1 14 1291411. Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Lia |
A missense variant in MYOF is associated with ARVC and sudden cardiac death. Gene 2024 1 902 148193. Jiao Xiao, Yi Dong, Jieyuan Jin, Zhuangzhuang Yuan, Chenyu Wang, Rong Xiang, Yadong G |
Natural history and outcomes in paediatric RASopathy-associated hypertrophic cardiomyopathy. ESC heart failure 2024 1 . Olga Boleti, Gabrielle Norrish, Ella Field, Kathleen Dady, Kim Summers, Gauri Nepali, Vinay Bhole, Orhan Uzun, Amos Wong, Piers E F Daubeney, Graham Stuart, Precylia Fernandes, Karen McLeod, Maria Ilina, Muhammad Najih Liaqath Ali, Tara Bharucha, Grazia Delle Donne, Elspeth Brown, Katie Linter, Caroline B Jones, Jonathan Searle, William Regan, Sujeev Mathur, Nicola Boyd, Zdenka Reinhardt, Sophie Duignan, Terence Prendiville, Satish Adwani, Juan Pablo Kas |
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- Page last updated:May 06, 2024
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