Elijah Behr
Elijah Behr
Professor of Cardiovascular Medicine, St George's University of London
Verified email at sgul.ac.uk - Homepage
TitleCited byYear
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
11832013
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
4872013
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
3922008
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, 2013
3142013
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
2742003
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
2622012
Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death
WJ McKenna, ER Behr
Heart 87 (2), 169-176, 2002
2522002
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
1942016
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
1932008
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
1822015
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, 2014
1782014
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
1752003
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
1602009
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
1402007
Genetic testing for inherited cardiac disease
AAM Wilde, ER Behr
Nature Reviews Cardiology 10 (10), 571, 2013
1362013
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
1362007
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
1312012
Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height
MB Lanktree, Y Guo, M Murtaza, JT Glessner, SD Bailey, ...
The American Journal of Human Genetics 88 (1), 6-18, 2011
1252011
Drug-induced Brugada syndrome
YG Yap, ER Behr, AJ Camm
Europace 11 (8), 989-994, 2009
1182009
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
1092014
The system can't perform the operation now. Try again later.
Articles 1–20