Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 45 Records) |
Query Trace: FLNC[original query] |
---|
Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing. Pediatric cardiology 2019 11 41 (1): 165-174. Rojnueangnit Kitiwan, Sirichongkolthong Boonchu, Wongwandee Ratthapon, Khetkham Thanitchet, Noojarern Saisuda, Khongkraparn Arthaporn, Wattanasirichaigoon Duangrurd |
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 |
Genetic Association Between Hypoplastic Left Heart Syndrome and Cardiomyopathies. Circulation. Genomic and precision medicine 2020 12 14 (1): e003126. Theis Jeanne L, Hu Jessie J, Sundsbak Rhianna S, Evans Jared M, Bamlet William R, Qureshi M Yasir, O'Leary Patrick W, Olson Timothy |
Clinical Implications of the Genetic Architecture of Dilated Cardiomyopathy. Current cardiology reports 2020 10 22 (12): 170. Wilsbacher Lisa |
Genetic analysis using targeted next-generation sequencing of sporadic Chinese patients with idiopathic dilated cardiomyopathy. Journal of translational medicine 2021 5 19 (1): 189. Li Mingmin, Xia Shuang, Xu Lan, Tan Hong, Yang Junqing, Wu Zejia, He Xuyu, Li Liw |
Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy. Circulation 2021 4 143 (19): 1852-1862. Goli Rahul, Li Jian, Brandimarto Jeff, Levine Lisa D, Riis Valerie, McAfee Quentin, DePalma Steven, Haghighi Alireza, Seidman J G, Seidman Christine E, Jacoby Daniel, Macones George, Judge Daniel P, Rana Sarosh, Margulies Kenneth B, Cappola Thomas P, Alharethi Rami, Damp Julie, Hsich Eileen, Elkayam Uri, Sheppard Richard, Alexis Jeffrey D, Boehmer John, Kamiya Chizuko, Gustafsson Finn, Damm Peter, Ersbøll Anne S, Goland Sorel, Hilfiker-Kleiner Denise, McNamara Dennis M, , Arany Zo |
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 |
Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency? DNA and cell biology 2021 1 40 (3): 491-498. Januel Louis, Chanavat Valérie, Rollat-Farnier Pierre-Antoine, Bardel Claire, Nony Severine, Millat Gilles, Janin Alexand |
Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's Journey. Journal of neuromuscular diseases 2021 1 8 (2): 261-272. Ten Dam L, de Visser M, Ginjaar Ieke B, van Duyvenvoorde Hermine A, van Koningsbruggen Silvana, van der Kooi Anneke |
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 |
Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics. Circulation. Genomic and precision medicine 2022 9 15 (5): e003675. Nafissi Navid A, Abdulrahim Jawan W, Kwee Lydia Coulter, Coniglio Amanda C, Kraus William E, Piccini Jonathan P, Daubert James P, Sun Albert Y, Shah Svati |
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 |
Loss-of-Function FLNC Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population. Circulation. Genomic and precision medicine 2022 6 15 (4): e003645. Carruth Eric D, Qureshi Maria, Alsaid Amro, Kelly Melissa A, Calkins Hugh, Murray Brittney, Tichnell Crystal, Sturm Amy C, , Baras Aris, Lester Kirchner H, Fornwalt Brandon K, James Cynthia A, Haggerty Christopher |
Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality. JAMA cardiology 2022 5 7 (7): 723-732. Patel Aniruddh P, Dron Jacqueline S, Wang Minxian, Pirruccello James P, Ng Kenney, Natarajan Pradeep, Lebo Matthew, Ellinor Patrick T, Aragam Krishna G, Khera Amit |
TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study. Genetics in medicine : official journal of the American College of Medical Genetics 2022 4 24 (7): 1495-1502. Trachtenberg Barry H, Jimenez Javier, Morris Alanna A, Kransdorf Evan, Owens Anjali, Fishbein Daniel P, Jordan Elizabeth, Kinnamon Daniel D, Mead Jonathan O, Huggins Gordon S, Hershberger Ray E, |
Absence of myofibrillar myopathy in Quarter Horses with a histopathological diagnosis of type 2 polysaccharide storage myopathy and lack of association with commercial genetic tests. Equine veterinary journal 2022 3 55 (2): 230-238. Valberg Stephanie J, Henry Marisa L, Herrick Keely L, Velez-Irizarry Deborah, Finno Carrie J, Petersen Jessica |
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 |
Late gadolinium enhancement distribution patterns in non-ischemic dilated cardiomyopathy: Genotype-phenotype correlation. European heart journal. Cardiovascular Imaging 2023 8 . Fernando de Frutos, Juan Pablo Ochoa, Ana Isabel Fernández, María Gallego-Delgado, Marina Navarro-Peñalver, Guillem Casas, María Teresa Basurte, José María Larrañaga-Moreira, María Victoria Mogollón, Ainhoa Robles-Mezcua, Pablo Elpidio García-Granja, Vicente Climent, Julián Palomino-Doza, Ana García-Álvarez, María Brion, Ramón Brugada, Juan Jiménez-Jáimez, Antoni Bayes-Genis, Tomas Ripoll-Vera, María Luisa Peña-Peña, José F Rodríguez-Palomares, Josefa Gonzalez-Carrillo, Eduardo Villacorta, Maria Angeles Espinosa, Pablo Garcia-Pavia, Jesus G Mirel |
Cardiac fludeoxyglucose-18 positron emission tomography in genotype-positive arrhythmogenic cardiomyopathy. International journal of cardiology 2023 7 131173. Raquel Neves, Andrew S Tseng, Ramin Garmany, Angela L Fink, Christopher J McLeod, Leslie T Cooper, Ciorsti J MacIntyre, Andrew C Homb, Andrew N Rosenbaum, John P Bois, Omar F Abou Ezzeddine, Konstantinos C Siontis, Naveen L Pereira, Michael J Ackerman, John R Giudices |
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum. medRxiv : the preprint server for health sciences 2023 7 . David S M Lee, John S DePaolo, Krishna G Aragam, Kiran Biddinger, Mitchell Conery, Ozan Dilitikas, Lily Hoffman-Andrews, Renae L Judy, Atlas Khan, Iftikhar Kulo, Mugan J Puckelwartz, Nosheen Reza, Benjamin A Satterfield, Pankhuri Singhal, , Zoltan P Arany, Thomas P Cappola, Eric Carruth, Sharlene M Day, Ron Do, Christopher M Haggarty, Jacob Joseph, Elizabeth McNally, Girish Nadkarni, Anjali T Owens, Daniel J Rader, Marylyn D Ritchie, Yan Sun, Benjamin F Voight, Michael G Levin, Scott M Damrau |
The Definition of Sarcomeric and Non-Sarcomeric Gene Mutations in Hypertrophic Cardiomyopathy Patients: A Multicenter Diagnostic Study Across Türkiye. Anatolian journal of cardiology 2023 7 . Veysel Oktay, Omaç Tüfekçio?lu, Dilek Çicek Y?lmaz, Ersel Onrat, Dilay Karabulut, Murat Çelik, Akif Serhat Balc?o?lu, Mehmet Murat Sucu, Güllü Özdemir, Hakk? Kaya, Mehmet K??, Bar?? Güven, Oktay Ba?dato?lu, Fatma Nihan Turhan Ça?lar, Uygar Ça?da? Yüksel, ?rfan Veysel Düzen, Ahmet Barutçu, Özgüç Semih ?im?ir, ?brahim Ba?ar?c?, Af?in Parspur, Onur Dalg?ç, Fatma Özlem Ar?can Özlük, Mert Evlice, Saim Sa?, Muhammed Furkan Deniz, Arslan Öcal, Emine Gazi, Taner ?en, Osman Özdabako?lu, Nermin Bayar Çak?c?, Eren Ozan Bak?r, Ay?egül Ülgen Kunak, Gizem Çayl?, Aybike Gül Ta?delen, Ercan Ak?it, ?efika Uslu Çil, Hüseyin On |
Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing. Journal of translational medicine 2023 7 21 (1): 476. Hong Lian, Shen Song, Wenzheng Chen, Anteng Shi, Haobin Jiang, Shengshou |
Clinical Outcomes and Genetic Analyses of Restrictive Cardiomyopathy in Children. Circulation. Genomic and precision medicine 2023 6 e004054. Hidekazu Ishida, Jun Narita, Ryo Ishii, Hidehiro Suginobe, Hirofumi Tsuru, Renjie Wang, Chika Yoshihara, Atsuko Ueyama, Kazutoshi Ueda, Masaki Hirose, Kazuhisa Hashimoto, Hiroki Nagano, Shigetoyo Kogaki, Yuki Kuramoto, Yohei Miyashita, Yoshihiro Asano, Keiichi Ozo |
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI. European journal of human genetics : EJHG 2023 4 . Jacobs Johanna, Van Aelst Lucas, Breckpot Jeroen, Corveleyn Anniek, Kuiperi Cuno, Dupont Matthias, Heggermont Ward, De Vadder Katrien, Willems Rik, Van Cleemput Johan, Bogaert Jan G, Robyns Tom |
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 |
[Genetic testing and clinical analysis of a patient with Dilated cardiomyopathy due to variant of FLNC gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 11 40 (12): 1551-1555. Yanlong Ren, Yahui Zhang, Xiaoping Zhang, Yueli Wang, Xuxia Liu, Jin Sheng, Shangqiu Ning, Wenxian Liu, Xiaoyan |
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2023 11 . Lisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, Bart A Mulder, Imke Christiaans, Gijs F L Kapel, Marco Alings, Marianne Bootsma, Daniela Q C M Barge-Schaapveld, Jippe C Balt, Sing-Chien Yap, Ingrid P C Krapels, Rachel M A Ter Bekke, Paul G A Volders, Saskia N van der Crabben, Pieter G Postema, Arthur A M Wilde, Dennis Dooijes, Annette F Baas, Rutger J Hassi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: