Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Atrial Fibrillation and RYR2[original query] |
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Common genetic variants in selected Ca²? signaling genes and the risk of appropriate ICD interventions in patients with heart failure. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2013 Dec 38 (3): 169-77. Francia Pietro, Adduci Carmen, Ricotta Agnese, Stanzione Rosita, Sensini Isabella, Uccellini Arianna, Frattari Alessandra, Balla Cristina, Cotugno Maria, Cappato Riccardo, Rubattu Speranza, Volpe Massi |
RyR2 Common Gene Variant G1886S and the Risk of Ventricular Arrhythmias in ICD Patients with Heart Failure. Journal of cardiovascular electrophysiology 2015 Jun 26 (6): 656-61. Francia Pietro, Adduci Carmen, Semprini Lorenzo, Stanzione Rosita, Serdoz Andrea, Caprinozzi Massimo, Santini Daria, Cotugno Maria, Palano Francesca, Musumeci Maria Beatrice, Rubattu Speranza, Volpe Massi |
Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS data. Scientific reports 2016 Nov 6 36630. Husser Daniela, Ueberham Laura, Dinov Borislav, Kosiuk Jedrzej, Kornej Jelena, Hindricks Gerhard, Shoemaker M Benjamin, Roden Dan M, Bollmann Andreas, Büttner Pet |
The 4q25 variant rs13143308T links risk of atrial fibrillation to defective calcium homoeostasis. Cardiovascular research 2018 9 115 (3): 578-589. Herraiz-Martínez Adela, Llach Anna, Tarifa Carmen, Gandía Jorge, Jiménez-Sabado Verónica, Lozano-Velasco Estefanía, Serra Selma A, Vallmitjana Alexander, Vázquez Ruiz de Castroviejo Eduardo, Benítez Raúl, Aranega Amelia, Muñoz-Guijosa Christian, Franco Diego, Cinca Juan, Hove-Madsen Le |
Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.
![]() BMC cardiovascular disorders 2019 Jan 19 (1): 26. Westphal Sabine, Stoppe Christian, Gruenewald Matthias, Bein Berthold, Renner Jochen, Cremer Jochen, Coburn Mark, Schaelte Gereon, Boening Andreas, Niemann Bernd, Kletzin Frank, Roesner Jan, Strouhal Ulrich, Reyher Christian, Laufenberg-Feldmann Rita, Ferner Marion, Brandes Ivo F, Bauer Martin, Kortgen Andreas, Stehr Sebastian N, Wittmann Maria, Baumgarten Georg, Struck Rafael, Meyer-Treschan Tanja, Kienbaum Peter, Heringlake Matthias, Schoen Julika, Sander Michael, Treskatsch Sascha, Smul Thorsten, Wolwender Ewa, Schilling Thomas, Degenhardt Frauke, Franke Andre, Mucha Soeren, Tittmann Lukas, Kohlhaas Madeline, Fuernau Georg, Brosteanu Oana, Hasenclever Dirk, Zacharowski Kai, Meybohm Patrick, |
Association Study of Genetic Variants in Calcium Signaling-Related Genes With Cardiovascular Diseases. Frontiers in cell and developmental biology 2021 12 9 642141. Li Sen, Jia Zhaoqi, Zhang Zhang, Li Yuxin, Yan Meihui, Yu Tingti |
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics. Biomolecules 2024 11 14 (11): . Maria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, Daniele Perrino, Silvia Genovese, Valentina Lanari, Daniela Righi, Federica Calì, Massimo Stefano Silvetti, Elena Falcone, Alessia Bauleo, Fabrizio Drago, Antonio Novelli, Anwar Bab |
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