Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Arrhythmia and PKP2[original query] |
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Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population. Annals of medicine 2013 Jun 45 (4): 328-35. Lahtinen Annukka M, Havulinna Aki S, Noseworthy Peter A, Jula Antti, Karhunen Pekka J, Perola Markus, Newton-Cheh Christopher, Salomaa Veikko, Kontula Kim |
Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (6): 1534-42. Ohno Seiko, Nagaoka Iori, Fukuyama Megumi, Kimura Hiromi, Itoh Hideki, Makiyama Takeru, Shimizu Akihiko, Horie Mino |
Correlation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy. Circulation. Cardiovascular genetics 2013 Dec 6 (6): 552-6. Bao Jingru, Wang Jizheng, Yao Yan, Wang Yilu, Fan Xiaohan, Sun Kai, He Ding Sheng, Marcus Frank I, Zhang Shu, Hui Rutai, Song L |
Arrhythmogenic Right Ventricular Cardiomyopathy - 4 Swedish families with an associated PKP2 c.2146-1G>C variant. American journal of cardiovascular disease 2016 6 (2): 55-65. Svensson Anneli, Åström-Aneq Meriam, Widlund Kjerstin Ferm, Fluur Christina, Green Anna, Rehnberg Malin, Gunnarsson Cecil |
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature genetics 2018 Jul . Nielsen Jonas B, Thorolfsdottir Rosa B, Fritsche Lars G, Zhou Wei, Skov Morten W, Graham Sarah E, Herron Todd J, McCarthy Shane, Schmidt Ellen M, Sveinbjornsson Gardar, Surakka Ida, Mathis Michael R, Yamazaki Masatoshi, Crawford Ryan D, Gabrielsen Maiken E, Skogholt Anne Heidi, Holmen Oddgeir L, Lin Maoxuan, Wolford Brooke N, Dey Rounak, Dalen Håvard, Sulem Patrick, Chung Jonathan H, Backman Joshua D, Arnar David O, Thorsteinsdottir Unnur, Baras Aris, O'Dushlaine Colm, Holst Anders G, Wen Xiaoquan, Hornsby Whitney, Dewey Frederick E, Boehnke Michael, Kheterpal Sachin, Mukherjee Bhramar, Lee Seunggeun, Kang Hyun M, Holm Hilma, Kitzman Jacob, Shavit Jordan A, Jalife José, Brummett Chad M, Teslovich Tanya M, Carey David J, Gudbjartsson Daniel F, Stefansson Kari, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
Putative role of Brugada syndrome genes in familial atrial fibrillation. European review for medical and pharmacological sciences 2019 9 23 (17): 7582-7598. Maltese P E, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli |
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia. European journal of heart failure 2019 Feb . Hermida Alexis, Fressart Véronique, Hidden-Lucet Francoise, Donal Erwan, Probst Vincent, Deharo Jean-Claude, Chevalier Philippe, Klug Didier, Mansencal Nicolas, Delacretaz Etienne, Cosnay Pierre, Scanu Patrice, Extramiana Fabrice, Keller Dagmar I, Rouanet Stephanie, Charron Philippe, Gandjbakhch Estel |
"Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest. International journal of cardiology 2020 9 324 96-101. Isbister Julia C, Nowak Natalie, Butters Alexandra, Yeates Laura, Gray Belinda, Sy Raymond W, Ingles Jodie, Bagnall Richard D, Semsarian Christoph |
Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy. Circulation 2020 5 141 (23): 1872-1884. Smith Eric D, Lakdawala Neal K, Papoutsidakis Nikolaos, Aubert Gregory, Mazzanti Andrea, McCanta Anthony C, Agarwal Prachi P, Arscott Patricia, Dellefave-Castillo Lisa M, Vorovich Esther E, Nutakki Kavitha, Wilsbacher Lisa D, Priori Silvia G, Jacoby Daniel L, McNally Elizabeth M, Helms Adam |
Genetic Variant Score and Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Plakophilin-2 Mutation Carriers. Cardiology 2021 9 146 (6): 763-771. Svensson Anneli, Platonov Pyotr G, Haugaa Kristina H, Zareba Wojciech, Jensen Henrik Kjærulf, Bundgaard Henning, Gilljam Thomas, Madsen Trine, Hansen Jim, Dejgaard Lars A, Karlsson Lars O, Gréen Anna, Polonsky Bronislava, Edvardsen Thor, Svendsen Jesper Hastrup, Gunnarsson Cecil |
Genotype-phenotype correlation in arrhythmogenic right ventricular cardiomyopathy-risk of arrhythmias and heart failure. Journal of medical genetics 2021 8 59 (9): 858-864. Christensen Alex Hørby, Platonov Pyotr G, Jensen Henrik Kjærulf, Chivulescu Monica, Svensson Anneli, Dahlberg Pia, Madsen Trine, Frederiksen Tanja Charlotte, Heliö Tiina, Lie Øyvind Haugen, Haugaa Kristina H, Hastrup Svendsen Jesper, Bundgaard Henni |
Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. International journal of molecular sciences 2021 7 22 (13): . Treat Jacqueline A, Pfeiffer Ryan, Barajas-Martinez Hector, Goodrow Robert J, Bot Corina, Haedo Rodolfo J, Knox Ronald, Cordeiro Jonathan |
Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator. European heart journal 2022 6 43 (32): 3053-3067. Protonotarios Alexandros, Bariani Riccardo, Cappelletto Chiara, Pavlou Menelaos, García-García Alba, Cipriani Alberto, Protonotarios Ioannis, Rivas Adrian, Wittenberg Regitze, Graziosi Maddalena, Xylouri Zafeirenia, Larrañaga-Moreira José M, de Luca Antonio, Celeghin Rudy, Pilichou Kalliopi, Bakalakos Athanasios, Lopes Luis Rocha, Savvatis Konstantinos, Stolfo Davide, Dal Ferro Matteo, Merlo Marco, Basso Cristina, Freire Javier Limeres, Rodriguez-Palomares Jose F, Kubo Toru, Ripoll-Vera Tomas, Barriales-Villa Roberto, Antoniades Loizos, Mogensen Jens, Garcia-Pavia Pablo, Wahbi Karim, Biagini Elena, Anastasakis Aris, Tsatsopoulou Adalena, Zorio Esther, Gimeno Juan R, Garcia-Pinilla Jose Manuel, Syrris Petros, Sinagra Gianfranco, Bauce Barbara, Elliott Perry |
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2023 7 31 (7-8): 315-323. Thomas A Bos, Sebastiaan R D Piers, Marja W Wessels, Arjan C Houweling, Regina Bökenkamp, Marianne Bootsma, Laurens P Bosman, Reinder Evertz, Debby M E I Hellebrekers, Yvonne M Hoedemaekers, Jeroen Knijnenburg, Ronald Lekanne Deprez, Anneke M van Mil, Anneline S J M Te Riele, Marjon A van Slegtenhorst, Arthur A M Wilde, Sing-Chien Yap, Dennis Dooijes, Tamara T Koopmann, J Peter van Tintelen, Daniela Q C M Barge-Schaapveld, |
Population-Level Prevalence of Rare Variants Associated With Atrial Fibrillation and its Impact on Patient Outcomes. JACC. Clinical electrophysiology 2023 1 . Kandola Manjinder S, Kulm Scott, Kim Luke K, Markowitz Steven M, Liu Christopher F, Thomas George, Ip James E, Lerman Bruce B, Elemento Olivier, Cheung Jim |
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