HuGE Literature Finder
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| Genetic Determinants of Sudden Unexpected Death in Pediatrics. Genetics in medicine : official journal of the American College of Medical Genetics 2022 1 24 (4): 839-850. Koh Hyun Yong, Haghighi Alireza, Keywan Christine, Alexandrescu Sanda, Plews-Ogan Erin, Haas Elisabeth A, Brownstein Catherine A, Vargas Sara O, Haynes Robin L, Berry Gerard T, Holm Ingrid A, Poduri Annapurna H, Goldstein Richard |
| Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST). Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2021 Jun . Te Rijdt W P, Hoorntje E T, de Brouwer R, Oomen A, Amin A, van der Heijden J F, Karper J C, Westenbrink B D, Silljé H H W, Te Riele A S J M, Wiesfeld A C P, van Gelder I C, Willems T P, van der Zwaag P A, van Tintelen J P, Hillege J H, Tan H L, van Veldhuisen D J, Asselbergs F W, de Boer R A, Wilde A A M, van den Berg M |
| Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction. Frontiers in cardiovascular medicine 2021 6 8 635141. Leone Maria Pia, Palumbo Pietro, Saenen Johan, Mastroianno Sandra, Castellana Stefano, Amico Cesare, Mazza Tommaso, Potenza Domenico Rosario, Petracca Antonio, Castori Marco, Carella Massimo, Di Stolfo Giusep |
| 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 |
| Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC). Journal of cardiovascular electrophysiology 2018 Apr . Murray Brittney, Hoorntje Edgar T, Te Riele Anneline S J M, Tichnell Crystal, van der Heijden Jeroen F, Tandri Harikrishna, van den Berg Maarten P, Jongbloed Jan D H, Wilde Arthur A M, Hauer Richard N W, Calkins Hugh, Judge Daniel P, James Cynthia A, van Tintelen J Peter, Dooijes Denn |
| Effect of GWAS-Identified Genetic Variants on Maximum QT Interval in Patients With Schizophrenia Receiving Antipsychotic Agents: A 24-Hour Holter ECG Study. Journal of clinical psychopharmacology 2017 Jun . Watanabe Junzo, Fukui Naoki, Suzuki Yutaro, Sugai Takuro, Ono Shin, Tsuneyama Nobuto, Saito Mami, Tajiri Misuzu, Someya Toshiyu |
| High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation. PloS one 2017 12 12 (12): e0189489. Klauke Baerbel, Gaertner-Rommel Anna, Schulz Uwe, Kassner Astrid, Zu Knyphausen Edzard, Laser Thorsten, Kececioglu Deniz, Paluszkiewicz Lech, Blanz Ute, Sandica Eugen, van den Bogaerdt Antoon J, van Tintelen J Peter, Gummert Jan, Milting Hendr |
| Sudden Cardiac Arrest and Rare Genetic Variants in the Community. Circulation. Cardiovascular genetics 2016 Jan . Milano Annalisa, Blom Marieke T, Lodder Elisabeth M, van Hoeijen Daniel A, Barc Julien, Koopmann Tamara T, Bardai Abdennasser, Beekman Leander, Lichtner Peter, van den Berg Maarten P, Wilde Arthur A M, Bezzina Connie R, Tan Hanno |
| Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovascular research 2015 Jun 106 (3): 520-9. Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, , Jamshidi Yal |
| Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2013 Jun 21 (6): 286-93. van der Zwaag P A, van Rijsingen I A W, de Ruiter R, Nannenberg E A, Groeneweg J A, Post J G, Hauer R N W, van Gelder I C, van den Berg M P, van der Harst P, Wilde A A M, van Tintelen J |
| Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. European journal of heart failure 2013 Jan . van Spaendonck-Zwarts KY, van Rijsingen IA, van den Berg MP, Lekanne Deprez RH, Post JG, van Mil AM, Asselbergs FW, Christiaans I, van Langen IM, Wilde AA, de Boer RA, Jongbloed JD, Pinto YM, van Tintelen JP |
Impact of ancestry and common genetic variants on QT interval in African Americans.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 647-55. Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, |
| PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: summary of the literature and implications for genetic testing. American heart journal 2011 Jan 161 (1): 165-71. Landstrom Andrew P, Adekola Babatunde A, Bos J Martijn, Ommen Steve R, Ackerman Michael |
| Common variants at ten loci influence QT interval duration in the QTGEN Study.
Nature genetics 2009 Apr 41 (4): 4. Newton-Cheh C, Eijgelsheim M, Rice KM, de Bakker PI, Yin X, Estrada K, Bis JC, Marciante K, Rivadeneira F, Noseworthy PA, Sotoodehnia N, Smith NL, Rotter JI, Kors JA, Witteman JC, Hofman A, Heckbert SR, O'Donnell CJ, Uitterlinden AG, Psaty BM, Lumley T, Larson MG, Stricker BH |
| Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nature genetics 2009 Apr 41 (4): 4. Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A |
| Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.
PloS one 2009 4 (7): e6138. Nolte Ilja M, Wallace Chris, Newhouse Stephen J, Waggott Daryl, Fu Jingyuan, Soranzo Nicole, Gwilliam Rhian, Deloukas Panos, Savelieva Irina, Zheng Dongling, Dalageorgou Chrysoula, Farrall Martin, Samani Nilesh J, Connell John, Brown Morris, Dominiczak Anna, Lathrop Mark, Zeggini Eleftheria, Wain Louise V, , , Newton-Cheh Christopher, Eijgelsheim Mark, Rice Kenneth, de Bakker Paul I W, , Pfeufer Arne, Sanna Serena, Arking Dan E, , Asselbergs Folkert W, Spector Tim D, Carter Nicholas D, Jeffery Steve, Tobin Martin, Caulfield Mark, Snieder Harold, Paterson Andrew D, Munroe Patricia B, Jamshidi Yal |
| No evidence for an association between the -36A>C phospholamban gene polymorphism and a worse prognosis in heart failure. BMC cardiovascular disorders 2009 9 (1): 33. Santos Diogo G B, Medeiros Alessandra, Brum Patrícia C, Mill José G, Mansur Alfredo J, Krieger José E, Pereira Alexandre |
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