| HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in … SG Priori, AA Wilde, M Horie, Y Cho, ER Behr, C Berul, N Blom, ... Heart rhythm 10 (12), 1932-1963, 2013 | 2063 | 2013 |
| 2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed by the task force for the management of … K Zeppenfeld, J Tfelt-Hansen, M De Riva, BG Winkel, ER Behr, NA Blom, ... European heart journal 43 (40), 3997-4126, 2022 | 1053 | 2022 |
| Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes SG Priori, AA Wilde, M Horie, Y Cho, ER Behr, C Berul, N Blom, ... Europace 15 (10), 1389-1406, 2013 | 786 | 2013 |
| Etiology of sudden death in sports: insights from a United Kingdom regional registry G Finocchiaro, M Papadakis, JL Robertus, H Dhutia, AK Steriotis, M Tome, ... Journal of the American college of cardiology 67 (18), 2108-2115, 2016 | 612 | 2016 |
| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013 | 537 | 2013 |
| Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families ER Behr, C Dalageorgou, M Christiansen, P Syrris, S Hughes, ... European heart journal 29 (13), 1670-1680, 2008 | 511 | 2008 |
| Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death M Nyegaard, MT Overgaard, MT Søndergaard, M Vranas, ER Behr, ... The American Journal of Human Genetics 91 (4), 703-712, 2012 | 448 | 2012 |
| Fibrosis, connexin-43, and conduction abnormalities in the Brugada syndrome K Nademanee, H Raju, SV De Noronha, M Papadakis, L Robinson, ... Journal of the American College of Cardiology 66 (18), 1976-1986, 2015 | 359 | 2015 |
| Subcutaneous or transvenous defibrillator therapy RE Knops, LRA Olde Nordkamp, PPHM Delnoy, LVA Boersma, J Kuschyk, ... New England Journal of Medicine 383 (6), 526-536, 2020 | 353 | 2020 |
| Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome E Behr, DA Wood, M Wright, P Syrris, MN Sheppard, A Casey, MJ Davies, ... The Lancet 362 (9394), 1457-1459, 2003 | 324 | 2003 |
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ... Nature genetics 46 (8), 826-836, 2014 | 319 | 2014 |
| Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death WJ McKenna, ER Behr Heart 87 (2), 169-176, 2002 | 304 | 2002 |
| The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome N Makita, E Behr, W Shimizu, M Horie, A Sunami, L Crotti, E Schulze-Bahr, ... The Journal of clinical investigation 118 (6), 2219-2229, 2008 | 268 | 2008 |
| Utility of post-mortem genetic testing in cases of sudden arrhythmic death syndrome N Lahrouchi, H Raju, EM Lodder, E Papatheodorou, JS Ware, ... Journal of the American College of Cardiology 69 (17), 2134-2145, 2017 | 263 | 2017 |
| SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes CI Wu, PG Postema, E Arbelo, ER Behr, CR Bezzina, C Napolitano, ... Heart rhythm 17 (9), 1456-1462, 2020 | 261 | 2020 |
| heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus statement on the state of genetic testing for … AAM Wilde, C Semsarian, MF Márquez, A Sepehri Shamloo, ... Europace 24 (8), 1307-1367, 2022 | 236 | 2022 |
| 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families MK Stiles, AAM Wilde, DJ Abrams, MJ Ackerman, CM Albert, ER Behr, ... Heart Rhythm 18 (1), e1-e50, 2021 | 215 | 2021 |
| PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome MR Donaldson, JL Jensen, M Tristani–Firouzi, R Tawil, S Bendahhou, ... Neurology 60 (11), 1811-1816, 2003 | 213 | 2003 |
| Novel calmodulin mutations associated with congenital arrhythmia susceptibility N Makita, N Yagihara, L Crotti, CN Johnson, BM Beckmann, MS Roh, ... Circulation: Cardiovascular Genetics 7 (4), 466-474, 2014 | 209 | 2014 |
| The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales M Papadakis, S Sharma, S Cox, MN Sheppard, VF Panoulas, ER Behr Europace 11 (10), 1353-1358, 2009 | 208 | 2009 |
