Elijah Behr
Elijah Behr
Professor of Cardiovascular Medicine, St George's University of London
Verified email at sgul.ac.uk - Homepage
Cited by
Cited by
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
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
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
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
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
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
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
Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death
WJ McKenna, ER Behr
Heart 87 (2), 169-176, 2002
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
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
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
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
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
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
Genetic testing for inherited cardiac disease
AAM Wilde, ER Behr
Nature Reviews Cardiology 10 (10), 571-583, 2013
Prevalence and significance of an isolated long QT interval in elite athletes
S Basavarajaiah, M Wilson, G Whyte, A Shah, E Behr, S Sharma
European heart journal 28 (23), 2944-2949, 2007
Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death
ER Behr, A Casey, M Sheppard, M Wright, TJ Bowker, MJ Davies, ...
Heart 93 (5), 601-605, 2007
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
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
A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
S Kääb, DC Crawford, MF Sinner, ER Behr, PJ Kannankeril, AAM Wilde, ...
Circulation: Cardiovascular Genetics 5 (1), 91-99, 2012
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