E
Elijah R. Behr
Researcher at St George’s University Hospitals NHS Foundation Trust
Publications - 314
Citations - 14605
Elijah R. Behr is an academic researcher from St George’s University Hospitals NHS Foundation Trust. The author has contributed to research in topics: Brugada syndrome & Sudden cardiac death. The author has an hindex of 52, co-authored 274 publications receiving 11337 citations. Previous affiliations of Elijah R. Behr include University of London & St. George's University.
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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 May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G. Priori,Arthur A.M. Wilde,Minoru Horie,Yongkeun Cho,Elijah R. Behr,Charles I. Berul,Nico A. Blom,Josep Brugada,Chern En Chiang,Heikki V. Huikuri,Prince J. Kannankeril,Andrew D. Krahn,Antoine Leenhardt,Arthur J. Moss,Peter J. Schwartz,Wataru Shimizu,Gordon F. Tomaselli,Cynthia M. Tracy +17 more
TL;DR: Developed in partnership with the Heart Rhythm Society (HRS), the European Heart Rhythm Association (EHRA), a registered branch of the European Society of Cardiology, and the Asia Pacific Heart Rhythm society (APHRS).
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Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
Silvia G. Priori,Arthur A.M. Wilde,Minoru Horie,Yongkeun Cho,Elijah R. Behr,Charles I. Berul,Nico A. Blom,Josep Brugada,Chern En Chiang,Heikki V. Huikuri,Prince J. Kannankeril,Andrew D. Krahn,Antoine Leenhardt,Arthur J. Moss,Peter J. Schwartz,Wataru Shimizu,Gordon F. Tomaselli,Cynthia M. Tracy,Michael J. Ackerman,Bernard Belhassen,N.A. Mark Estes,Diane Fatkin,Jonathan M. Kalman,Elizabeth S. Kaufman,Paulus Kirchhof,Eric Schulze-Bahr,Christian Wolpert,Jitendra K. Vohra,Marwan M. Refaat,Susan P. Etheridge,Robert M. Campbell,Edward T. Martin,Swee Chye Quek +32 more
TL;DR: This international consensus statement is the collaborative effort of three medical societies representing electrophysiology in North America, Europe, and Asian-Pacific area and summarizes the opinion of the international writing group members based on their own experience and on a general review of the literature.
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Connie R. Bezzina,Julien Barc,Yuka Mizusawa,Carol Ann Remme,Jean-Baptiste Gourraud,Floriane Simonet,Floriane Simonet,Floriane Simonet,Arie O. Verkerk,Peter J. Schwartz,Lia Crotti,Federica Dagradi,Pascale Guicheney,Pascale Guicheney,Véronique Fressart,Véronique Fressart,Antoine Leenhardt,Antoine Leenhardt,Charles Antzelevitch,Susan Bartkowiak,Martin Borggrefe,Rainer Schimpf,Eric Schulze-Bahr,Sven Zumhagen,Elijah R. Behr,Rachel Bastiaenen,Jacob Tfelt-Hansen,Jacob Tfelt-Hansen,Morten S. Olesen,Morten S. Olesen,Stefan Kääb,Britt M. Beckmann,Peter Weeke,Hiroshi Watanabe,Naoto Endo,Tohru Minamino,Minoru Horie,Seiko Ohno,Kanae Hasegawa,Naomasa Makita,Akihiko Nogami,Wataru Shimizu,Takeshi Aiba,Philippe Froguel,Philippe Froguel,Philippe Froguel,Beverley Balkau,Beverley Balkau,Olivier Lantieri,Margherita Torchio,Cornelia Wiese,David Weber,Rianne Wolswinkel,Ruben Coronel,Bas J. Boukens,Stéphane Bézieau,Eric Charpentier,Eric Charpentier,Eric Charpentier,Stéphanie Chatel,Aurore Despres,Françoise Gros,Françoise Gros,Françoise Gros,Florence Kyndt,Simon Lecointe,Pierre Lindenbaum,Vincent Portero,Vincent Portero,Vincent Portero,Jade Violleau,Manfred Gessler,Hanno L. Tan,Dan M. Roden,Vincent M. Christoffels,Hervé Le Marec,Arthur A.M. Wilde,Vincent Probst,Jean-Jacques Schott,Christian Dina,Richard Redon +80 more
TL;DR: The association signals at SCN5A-SCN10A demonstrate that genetic polymorphisms modulating cardiac conduction can also influence susceptibility to cardiac arrhythmia and indicate that common genetic variation can have a strong impact on the predisposition to rare diseases.
Journal ArticleDOI
Hypertrophic Cardiomyopathy
TL;DR: In this paper, the authors evaluated the Mendelian autosomal-dominant inheritance with an electrocardiogram (ECG) and echocardiogram and found that the risk of atrial fibrillation (AF) or left atrial enlargement carries a significant risk of thromboembolism.
Journal ArticleDOI
Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.
Elijah R. Behr,Chrysoula Dalageorgou,Michael Christiansen,Petros Syrris,S. Hughes,Maria Teresa Tome Esteban,Edward Rowland,Steve Jeffery,William J. McKenna +8 more
TL;DR: Over half of SADS deaths were likely to be due to inherited heart disease; accurate identification is vital for appropriate prophylaxis amongst relatives who should undergo comprehensive cardiological evaluation, guided and confirmed by mutation analysis.