Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Death and FLNC[original query] |
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Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients. Genetic testing and molecular biomarkers 2016 Nov 20 (11): 674-679. Jaafar Nawel, Gómez Juan, Kammoun Ikram, Zairi Ihsen, Amara Wael Ben, Kachboura Salem, Kraiem Sondes, Hammami Mohamed, Iglesias Sara, Alonso Belén, Coto Eliec |
A novel familial truncating mutation in the filamin C gene associated with cardiac arrhythmias. European journal of medical genetics 2018 8 62 (4): 282-285. Mangum Kevin D, Ferns Sunita |
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy. Molecular genetics & genomic medicine 2018 11 6 (6): 1104-1113. Cui Hao, Wang Jizheng, Zhang Ce, Wu Guixin, Zhu Changsheng, Tang Bing, Zou Yubao, Huang Xiaohong, Hui Rutai, Song Lei, Wang Shuiy |
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death. Circulation. Genomic and precision medicine 2018 08 11 (8): e002151. Sveinbjornsson Gardar, Olafsdottir Eva F, Thorolfsdottir Rosa B, Davidsson Olafur B, Helgadottir Anna, Jonasdottir Adalbjorg, Jonasdottir Aslaug, Bjornsson Eythor, Jensson Brynjar O, Arnadottir Gudny A, Kristinsdottir Hallfridur, Stephensen Sigurdur S, Oskarsson Gylfi, Gudbjartsson Tomas, Sigurdsson Emil L, Andersen Karl, Danielsen Ragnar, Arnar David O, Jonsdottir Ingileif, Thorsteinsdottir Unnur, Sulem Patrick, Thorgeirsson Gudmundur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype. International journal of cardiology 2019 10 307 101-108. Hall Charlotte L, Akhtar Mohammed M, Sabater-Molina Maria, Futema Marta, Asimaki Angeliki, Protonotarios Alexandros, Dalageorgou Chrysoula, Pittman Alan M, Suarez Mari Paz, Aguilera Beatriz, Molina Pilar, Zorio Esther, Hernández Juan Pedro, Pastor Francisco, Gimeno Juan R, Syrris Petros, McKenna William |
Predicting sustained ventricular arrhythmias in dilated cardiomyopathy: a meta-analysis and systematic review. ESC heart failure 2020 4 7 (4): 1430-1441. Sammani Arjan, Kayvanpour Elham, Bosman Laurens P, Sedaghat-Hamedani Farbod, Proctor Tanja, Gi Weng-Tein, Broezel Alicia, Jensen Katrin, Katus Hugo A, Te Riele Anneline S J M, Meder Benjamin, Asselbergs Folkert |
Filamin-C variant-associated cardiomyopathy: A pooled analysis of individual patient data to evaluate the clinical profile and risk of sudden cardiac death. Heart rhythm 2021 Sep . Celeghin Rudy, Cipriani Alberto, Bariani Riccardo, Bueno Marinas Maria, Cason Marco, Bevilacqua Michela, De Gaspari Monica, Rizzo Stefania, Rigato Ilaria, Da Pozzo Stefano, Zorzi Alessandro, Perazzolo Marra Martina, Thiene Gaetano, Iliceto Sabino, Basso Cristina, Corrado Domenico, Pilichou Kalliopi, Bauce Barba |
FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of Cardiomyopathy. International heart journal 2021 1 62 (1): 127-134. Qin Xianyu, Li Ping, Qu Hui-Qi, Liu Yichuan, Xia Yu, Chen Shaoxian, Yang Yongchao, Huang Shufang, Wen Pengju, Zhou Xianwu, Li Xiaofeng, Wang Yonghua, Tian Lifeng, Hakonarson Hakon, Wu Yueheng, Zhuang Ji |
Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes. Journal of the American Heart Association 2022 Sep e025257. Yang Qixin, Berkman Amy M, Ezekian Jordan E, Rosamilia Michael, Rosenfeld Jill A, Liu Pengfei, Landstrom Andrew |
Necroptosis-Related Prognostic Signature and Nomogram Model for Predicting the Overall Survival of Patients with Lung Cancer. Genetics research 2022 2022 4908608. Xuan Yunpeng, Jin Xiangfeng, Wang Mingzhao, Wang Zizo |
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies. Journal of the American College of Cardiology 2022 11 80 (21): 1981-1994. Paldino Alessia, Dal Ferro Matteo, Stolfo Davide, Gandin Ilaria, Medo Kristen, Graw Sharon, Gigli Marta, Gagno Giulia, Zaffalon Denise, Castrichini Matteo, Masè Marco, Cannatà Antonio, Brun Francesca, Storm Garrett, Severini Giovanni Maria, Lenarduzzi Stefania, Girotto Giorgia, Gasparini Paolo, Bortolotti Francesca, Giacca Mauro, Zacchigna Serena, Merlo Marco, Taylor Matthew R G, Mestroni Luisa, Sinagra Gianfran |
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 |
Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathy. American journal of medical genetics. Part A 2023 3 . Gaudreault Nathalie, Ruel Louis-Jacques, Henry Cyndi, Schleit Jennifer, Lagüe Patrick, Champagne Jean, Sénéchal Mario, Sarrazin Jean-François, Philippon François, Bossé Yohan, Steinberg Christi |
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