Drug-induced arrhythmia: pharmacogenomic prescribing?

Por Behr, Elijah R., Roden, Dan
Publicado em 2013

Sudden Unexplained Death – Treating the Family

Por Mellor, Greg, Behr, Elijah R
Publicado no Arrhythm Electrophysiol Rev (2014)

QRS–ST–T triangulation with repolarization shortening as a precursor of sustained ventricular tachycardia during acute myocardial ischemia

Por Batchvarov, Velislav N., Behr, Elijah R.
Publicado no J Arrhythm (2015)

Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death

Por McKenna, William J, Behr, Elijah R
Publicado em 2002

The genetics of pro-arrhythmic adverse drug reactions

Por Petropoulou, Evmorfia, Jamshidi, Yalda, Behr, Elijah R
Publicado em 2014

Pharmacological treatment of acquired QT prolongation and torsades de pointes

Por Thomas, Simon H. L., Behr, Elijah R.
Publicado no Br J Clin Pharmacol (2015)

Electrocardiographic methods for diagnosis and risk stratification in the Brugada syndrome

Por Naseef, Abdulrahman, Behr, Elijah R., Batchvarov, Velislav N.
Publicado no J Saudi Heart Assoc (2015)

Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases

Por Lahrouchi, Najim, Behr, Elijah R., Bezzina, Connie R.
Publicado no Front Cardiovasc Med (2016)

Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

Por Goldman, Alica M., Behr, Elijah R., Semsarian, Christopher, Bagnall, Richard D., Sisodiya, Sanjay, Cooper, Paul N.
Publicado no Epilepsia (2016)

Antipsychotics and Torsadogenic Risk: Signals Emerging from the US FDA Adverse Event Reporting System Database

Por Poluzzi, Elisabetta, Raschi, Emanuel, Koci, Ariola, Moretti, Ugo, Spina, Edoardo, Behr, Elijah R., Sturkenboom, Miriam, De Ponti, Fabrizio
Publicado em 2013

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome

Por Hedley, Paula L., Carlsen, Anting L., Christiansen, Kasper M., Kanters, Jørgen K., Behr, Elijah R., Corfield, Valerie A., Christiansen, Michael
Publicado em 2014

Next Generation Diagnostics in Inherited Arrhythmia Syndromes: A Comparison of Two Approaches

Por Ware, James S., John, Shibu, Roberts, Angharad M., Buchan, Rachel, Gong, Sungsam, Peters, Nicholas S., Robinson, David O., Lucassen, Anneke, Behr, Elijah R., Cook, Stuart A.
Publicado em 2012

The International Serious Adverse Events Consortium (iSAEC) phenotype standardization project for drug-induced torsades de pointes

Por Behr, Elijah R., January, Craig, Schulze-Bahr, Eric, Grace, Andrew A., Kääb, Stefan, Fiszman, Monica, Gathers, Shaniece, Buckman, ShaAvhrée, Youssef, Ashraf, Pirmohamed, Munir, Roden, Dan
Publicado em 2013

A Common Genetic Variant Risk Score Is Associated with Drug-Induced QT Prolongation and Torsade de Pointes Risk: a Pilot Study

Por Strauss, David G., Vicente, Jose, Johannesen, Lars, Blinova, Ksenia, Mason, Jay W., Weeke, Peter, Behr, Elijah R., Roden, Dan, Woosley, Ray, Kosova, Gulum, Rosenberg, Michael A., Newton-Cheh, Christopher
Publicado no Circulation (2017)

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

Por Nyegaard, Mette, Overgaard, Michael T., Søndergaard, Mads T., Vranas, Marta, Behr, Elijah R., Hildebrandt, Lasse L., Lund, Jacob, Hedley, Paula L., Camm, A. John, Wettrell, Göran, Fosdal, Inger, Christiansen, Michael, Børglum, Anders D.
Publicado em 2012

A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation

Por Bartos, Daniel C., Anderson, Jeffrey B., Bastiaenen, Rachel, Johnson, Jonathan N., Gollob, Michael H, Tester, David J., Burgess, Don E., Homfray, Tessa, Behr, Elijah R., Ackerman, Michael J., Guicheney, Pascale, Delisle, Brian P.
Publicado em 2013

Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome

Por Nademanee, Koonlawee, Raju, Hariharan, de Noronha, Sofia V., Papadakis, Michael, Robinson, Laurence, Rothery, Stephen, Makita, Naomasa, Kowase, Shinya, Boonmee, Nakorn, Vitayakritsirikul, Vorapot, Ratanarapee, Samrerng, Sharma, Sanjay, van der Wal, Allard C., Christiansen, Michael, Tan, Hanno L., Wilde, Arthur A., Nogami, Akihiko, Sheppard, Mary N., Veerakul, Gumpanart, Behr, Elijah R.
Publicado no J Am Coll Cardiol (2015)

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice

Por Muggenthaler, Martina M. A., Chowdhury, Biswajit, Hasan, S. Naimul, Cross, Harold E., Mark, Brian, Harlalka, Gaurav V., Patton, Michael A., Ishida, Miho, Behr, Elijah R., Sharma, Sanjay, Zahka, Kenneth, Faqeih, Eissa, Blakley, Brian, Jackson, Mike, Lees, Melissa, Dolinsky, Vernon, Cross, Leroy, Stanier, Philip, Salter, Claire, Baple, Emma L., Alkuraya, Fowzan S., Crosby, Andrew H., Triggs-Raine, Barbara, Chioza, Barry A.
Publicado no PLoS Genet (2017)

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

Por Behr, Elijah R., Savio-Galimberti, Eleonora, Barc, Julien, Holst, Anders G., Petropoulou, Evmorfia, Prins, Bram P., Jabbari, Javad, Torchio, Margherita, Berthet, Myriam, Mizusawa, Yuka, Yang, Tao, Nannenberg, Eline A., Dagradi, Federica, Weeke, Peter, Bastiaenan, Rachel, Ackerman, Michael J., Haunso, Stig, Leenhardt, Antoine, Kääb, Stefan, Probst, Vincent, Redon, Richard, Sharma, Sanjay, Wilde, Arthur, Tfelt-Hansen, Jacob, Schwartz, Peter, Roden, Dan M., Bezzina, Connie R., Olesen, Morten, Darbar, Dawood, Guicheney, Pascale, Crotti, Lia, Jamshidi, Yalda
Publicado no Cardiovasc Res (2015)

Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes

Por Behr, Elijah R., Ritchie, Marylyn D., Tanaka, Toshihiro, Kääb, Stefan, Crawford, Dana C., Nicoletti, Paola, Floratos, Aris, Sinner, Moritz F., Kannankeril, Prince J., Wilde, Arthur A. M., Bezzina, Connie R., Schulze-Bahr, Eric, Zumhagen, Sven, Guicheney, Pascale, Bishopric, Nanette H., Marshall, Vanessa, Shakir, Saad, Dalageorgou, Chrysoula, Bevan, Steve, Jamshidi, Yalda, Bastiaenen, Rachel, Myerburg, Robert J., Schott, Jean-Jacques, Camm, A. John, Steinbeck, Gerhard, Norris, Kris, Altman, Russ B., Tatonetti, Nicholas P., Jeffery, Steve, Kubo, Michiaki, Nakamura, Yusuke, Shen, Yufeng, George, Alfred L., Roden, Dan M.
Publicado em 2013