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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Journal ArticleDOI
Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation
Michael Papadakis,Hariharan Raju,Elijah R. Behr,Sofia V. de Noronha,Nicholas Spath,Alexandros Kouloubinis,Mary N. Sheppard,Sanjay Sharma +7 more
TL;DR: In this article, the authors explored the hypothesis that sudden cardiac deaths represent sudden arrhythmic death syndrome (SADS) and found that a similar proportion of primary arrhythmogenic syndromes to a contemporary series of SADS.
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Drug-induced Brugada syndrome
TL;DR: The cases and evidence of drug-induced Brugada syndrome reported in the literature are reviewed to highlight the growing interest in the mechanisms responsible for this acquired ECG pattern and its clinical significance.
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The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths
Sofia V. de Noronha,Elijah R. Behr,Michael Papadakis,Keiko Ohta-Ogo,Winston Banya,Jemma Wells,Steve Cox,Alison Cox,Sanjay Sharma,Mary N. Sheppard,Mary N. Sheppard +10 more
TL;DR: Expert cardiac pathology improves the accuracy of coronial post-mortem diagnoses in young SCD with fast-track reporting on hearts sent by pathologists in cases of SCD.
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Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.
Yalda Jamshidi,Ilja M. Nolte,Chrysoula Dalageorgou,Dongling Zheng,Toby Johnson,Rachel Bastiaenen,Suzanne Ruddy,Daniel Talbott,Kris Norris,Harold Snieder,Alfred L. George,Vanessa Marshall,Saad A. W. Shakir,Prince J. Kannankeril,Patricia B. Munroe,A. John Camm,Steve Jeffery,Dan M. Roden,Elijah R. Behr +18 more
TL;DR: It is shown that common variations in the NOS1AP gene may have relevance for future pharmacogenomic applications in clinical practice permitting safer prescription of drugs for vulnerable patients, and this results provide the first demonstration that common Variant NOS 1AP gene are associated with a significant increase in the risk of dLQTS.
Journal ArticleDOI
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.
Lia Crotti,Carla Spazzolini,David J. Tester,Alice Ghidoni,Alban-Elouen Baruteau,Alban-Elouen Baruteau,Britt M. Beckmann,Elijah R. Behr,Jeffrey S. Bennett,Connie R. Bezzina,Zahurul A. Bhuiyan,Alpay Celiker,Marina Cerrone,Federica Dagradi,Gaetano M. De Ferrari,Gaetano M. De Ferrari,Susan P. Etheridge,Meena Fatah,Pablo García-Pavía,Saleh Al-Ghamdi,Robert M. Hamilton,Zuhair N. Al-Hassnan,Minoru Horie,Juan Jiménez-Jáimez,Ronald J. Kanter,Juan Pablo Kaski,Maria Christina Kotta,Najim Lahrouchi,Naomasa Makita,Gabrielle Norrish,Hans Henrik Odland,Seiko Ohno,John Papagiannis,Gianfranco Parati,Nicole Sekarski,Kristian Tveten,Matteo Vatta,Gregory Webster,Arthur A.M. Wilde,Julianne Wojciak,Alfred L. George,Michael J. Ackerman,Peter J. Schwartz +42 more
TL;DR: Calmodulinopathies are largely characterized by adrenergically-induced life-threatening arrhythmias, and available therapies are disquietingly insufficient, especially in CALM-LQTS.