Ray E. Hershberger
Active 1988–2025
- Also published as
- Ray E Hershberger
- 93
- Papers
- 22,396
- Citations
- 72
- h-index
- 90
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1%
- Brigham and Women's Hospital0.9%
- Massachusetts General Hospital0.6%
- University College London0.6%
- Stanford University0.6%
- Inserm0.6%
- Other95.7%
Fields
- Medicine69.1%
- Biochemistry, Genetics and Molecular Biology26.3%
- Engineering1.4%
- Neuroscience0.8%
- Immunology and Microbiology0.4%
- Computer Science0.3%
- Other1.7%
Topics
- Cardiomyopathy and Myosin Studies8.8%
- Cardiac electrophysiology and arrhythmias6.3%
- Cardiovascular Effects of Exercise4.7%
- Heart Failure Treatment and Management4.7%
- Cardiovascular Function and Risk Factors3.9%
- Genomics and Rare Diseases3.7%
- Other67.9%
Coauthors
- Ana Morales18
- Daniel P. Judge14
- Elizabeth Jordan13
- Duanxiang Li12
- Michael H. Gollob12
- Steven M. Harrison10
- Daniel D. Kinnamon9
- Michael R. Bristow9
- Christa Lese Martin8
- Deirdre Nauman8
- Jill D. Siegfried8
- Kristy Lee8
- Matthew T. Wheeler8
- Stuart D. Katz8
- Allan Gordon7
- Christopher Semsarian7
- David T. Miller7
- Donna R. Burgess7
- Douglas R. Stewart7
- Hanyu Ni7
- Laura M. Amendola7
- Nadine Norton7
- Nancy K. Sweitzer7
- Palak Shah7
All papers
- 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis
Authors: M. Kittleson, Frederick L. Ruberg, Amrut V. Ambardekar, Thomas H. Brannagan, Richard K. Cheng, John O. Clarke, Laura M. Dember, Janell Grazzini Frantz, Ray E. Hershberger, Matthew J. Maurer, José Nativi-Nicolau, Vaishali Sanchorawala, Farooq H. Sheikh - Journal of the American College of Cardiology 2023 cited by 569
- Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Authors: Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, Babken Asatryan, Lucas Bronicki, Emily Brown, Rudy Celeghin, Matthew Edwards, Judy Fan, Jodie Ingles, Cynthia A. James, Olga Jarinova, Renée Johnson, Daniel P. Judge, Najim Lahrouchi, Ronald H. Lekanne Deprez, R Thomas Lumbers, Francesco Mazzarotto, Argelia Medeiros‐Domingo, Rebecca L. Miller, Ana Morales, Brittney Murray, Stacey Peters, Kalliopi Pilichou, Alexandros Protonotarios, Christopher Semsarian, Palak Shah, Petros Syrris, Courtney Thaxton, J. Peter van Tintelen, Roddy Walsh, Jessica Wang, James S. Ware, Ray E. Hershberger - Circulation 2021 cited by 512
- ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Authors: David T. Miller, Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob, Allan Gordon, Steven M. Harrison, Ray E. Hershberger, Teri E. Klein, C. Sue Richards, Douglas R. Stewart, Christa Lese Martin - Genetics in Medicine 2023 cited by 417
- Dilated cardiomyopathy
Authors: Heinz‐Peter Schultheiß, DeLisa Fairweather, Alida L.P. Caforio, Felicitas Escher, Ray E. Hershberger, Steven E. Lipshultz, Peter P. Liu, Akira Matsumori, Andrea Mazzanti, John J.V. McMurray, Silvia G. Priori - Nature Reviews Disease Primers 2019 cited by 674
- Dilated cardiomyopathy: the complexity of a diverse genetic architecture
Authors: Ray E. Hershberger, Dale J. Hedges, Ana Morales - Nature Reviews Cardiology 2013 cited by 1,013
- Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes
Authors: Jodie Ingles, Jennifer Goldstein, Courtney Thaxton, Colleen Caleshu, Edward W. Corty, Stephanie B. Crowley, Kristen Dougherty, Steven M. Harrison, Jennifer McGlaughon, Laura V. Milko, Ana Morales, Bryce A. Seifert, Natasha T. Strande, Kate Thomson, J. Peter van Tintelen, Kathleen Wallace, Roddy Walsh, Quinn S. Wells, Nicola Whiffin, Leora Witkowski, Christopher Semsarian, James S. Ware, Ray E. Hershberger, Birgit Funke - Circulation Genomic and Precision Medicine 2019 cited by 450
- Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association
Authors: Kiran Musunuru, Ray E. Hershberger, Sharlene M. Day, N. Jennifer Klinedinst, Andrew P. Landstrom, Victoria N. Parikh, Siddharth K. Prakash, Christopher Semsarian, Amy C. Sturm - Circulation Genomic and Precision Medicine 2020 cited by 372
- ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Authors: David T. Miller, Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob, Allan Gordon, Steven M. Harrison, Ray E. Hershberger, Teri E. Klein, Carolyn Sue Richards, Douglas R. Stewart, Christa Lese Martin - Genetics in Medicine 2022 cited by 288
- Clinical Genetic Testing for Familial Hypercholesterolemia
Authors: Amy C. Sturm, Joshua W. Knowles, Samuel S. Gidding, Zahid Ahmad, Catherine D. Ahmed, Christie M. Ballantyne, Seth J. Baum, Mafalda Bourbon, Alain Carrié, Marina Cuchel, Sarah D. de Ferranti, Joep C. Defesche, Tomáš Freiberger, Ray E. Hershberger, G. Kees Hovingh, Lala Karayan, Johannes J.P. Kastelein, Iris Kindt, Stacey R. Lane, S. E. A. Leigh, MacRae F. Linton, Pedro Mata, William A. Neal, Børge G. Nordestgaard, Raúl D. Santos, Mariko Harada‐Shiba, Eric J.G. Sijbrands, Nathan O. Stitziel, Shizuya Yamashita, Katherine Wilemon, David H. Ledbetter, Daniel J. Rader - Journal of the American College of Cardiology 2018 cited by 597
- ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Authors: David T. Miller, Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein, Douglas R. Stewart, Laura M. Amendola, Kathy Adelman, Sherri J. Bale, Michael H. Gollob, Steven M. Harrison, Ray E. Hershberger, Kent D. McKelvey, C. Sue Richards, Christopher N. Vlangos, Michael S. Watson, Christa Lese Martin - Genetics in Medicine 2021 cited by 562
- An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome
Authors: Arnon Adler, Valeria Novelli, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Eline A. Nannenberg, Harriet Feilotter, Simona Amenta, Daniela Mazzà, Hennie Bikker, Amy C. Sturm, John Garcia, Michael J. Ackerman, Ray E. Hershberger, Marco Pérez, Wojciech Zaręba, James S. Ware, Arthur A.M. Wilde, Michael H. Gollob - Circulation 2020 cited by 399
- International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework
Authors: Cynthia A. James, Jan D.H. Jongbloed, Ray E. Hershberger, Ana Morales, Daniel P. Judge, Petros Syrris, Kalliopi Pilichou, Argelia Medeiros‐Domingo, Brittney Murray, Julia Cadrin‐Tourigny, Ronald H. Lekanne Deprez, Rudy Celeghin, Alexandros Protonotarios, Babken Asatryan, Emily Brown, Elizabeth Jordan, Jennifer McGlaughon, Courtney Thaxton, C. Lisa Kurtz, J. Peter van Tintelen - Circulation Genomic and Precision Medicine 2021 cited by 234
- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
Authors: Michael J. Ackerman, Silvia G. Priori, Stephan Willems, Charles I. Berul, Ramón Brugada, Hugh Calkins, A. John Camm, Patrick T. Ellinor, Michael H. Gollob, Robert M. Hamilton, Ray E. Hershberger, Daniel P. Judge, Hervé Le Marec, William J. McKenna, Eric Schulze‐Bahr, Chris Semsarian, Jeffrey A. Towbin, Hugh Watkins, Arthur A.M. Wilde, Christian Wolpert, Douglas P. Zipes - Heart Rhythm 2011 cited by 1,468
- Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Authors: David T. Miller, Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale, Wendy K. Chung, Michael H. Gollob, Steven M. Harrison, Gail E. Herman, Ray E. Hershberger, Teri E. Klein, Kent D. McKelvey, C. Sue Richards, Christopher N. Vlangos, Douglas R. Stewart, Michael S. Watson, Christa Lese Martin - Genetics in Medicine 2021 cited by 263
- Reappraisal of Reported Genes for Sudden Arrhythmic Death
Authors: S. Mohsen Hosseini, Raymond H. Kim, Sharmila Udupa, Gregory Costain, Rebekah Jobling, Eriskay Liston, Seema M. Jamal, Marta Szybowska, Chantal F. Morel, Sarah Bowdin, John Garcia, Melanie Care, Amy C. Sturm, Valeria Novelli, Michael Ackerman, James S. Ware, Ray E. Hershberger, Arthur A.M. Wilde, Michael H. Gollob - Circulation 2018 cited by 370
- Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Authors: Roddy Walsh, Arnon Adler, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Hennie Bikker, Simona Amenta, Harriet Feilotter, Eline A. Nannenberg, Francesco Mazzarotto, Valentina Trevisan, John Garcia, Ray E. Hershberger, Marco Pérez, Amy C. Sturm, James S. Ware, Wojciech Zaręba, Valeria Novelli, Arthur A.M. Wilde, Michael H. Gollob - European Heart Journal 2021 cited by 143
- Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel
Authors: Melissa Kelly, Colleen Caleshu, Ana Morales, Jillian G. Buchan, Zena Wolf, Steven M. Harrison, Stuart A. Cook, Mitchell W. Dillon, John Garcia, Eden Haverfield, Jan D.H. Jongbloed, Daniela Macaya, Arjun K. Manrai, Kate M. Orland, Gabriele Richard, Katherine G. Spoonamore, Matthew Thomas, Kate Thomson, Lisa M. Vincent, Roddy Walsh, Hugh Watkins, Nicola Whiffin, Jodie Ingles, J. Peter van Tintelen, Christopher Semsarian, James S. Ware, Ray E. Hershberger, Birgit Funke - Genetics in Medicine 2018 cited by 371
- ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene‐level specification of the ACMG/AMP guidelines for sequence variant interpretation
Authors: E. Andres Rivera-Munoz, Laura V. Milko, Steven M. Harrison, Danielle R. Azzariti, C. Lisa Kurtz, Kristy Lee, Jessica L. Mester, Meredith Weaver, Erin Currey, William Craigen, Charis Eng, Birgit Funke, Madhuri Hegde, Ray E. Hershberger, Rong Mao, Robert D. Steiner, Lisa M. Vincent, Christa Lese Martin, Sharon E. Plon, Erin M. Ramos, Heidi L. Rehm, Michael S. Watson, Jonathan S. Berg - Human Mutation 2018 cited by 219
- Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Authors: Ray E. Hershberger, Michael M. Givertz, Carolyn Y. Ho, Daniel P. Judge, Paul F. Kantor, Kim L. McBride, Ana Morales, Matthew R.G. Taylor, Matteo Vatta, Stephanie M. Ware - Genetics in Medicine 2018 cited by 283
- Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline
Authors: Ray E. Hershberger, JoAnn Lindenfeld, Luisa Mestroni, Christine E. Seidman, Matthew R.G. Taylor, Jeffrey A. Towbin - Journal of Cardiac Failure 2009 cited by 705
- Carvedilol Produces Dose-Related Improvements in Left Ventricular Function and Survival in Subjects With Chronic Heart Failure
Authors: Michael R. Bristow, Edward M. Gilbert, William T. Abraham, Kirkwood F. Adams, Michael B. Fowler, Ray E. Hershberger, Spencer H. Kubo, Kenneth A. Narahara, Henry Ingersoll, Steven K. Krueger, Sarah Young, Neil H. Shusterman - Circulation 1996 cited by 1,306
- Effects of Danicamtiv, a Novel Cardiac Myosin Activator, in Heart Failure with Reduced Ejection Fraction: Experimental Data and Clinical Results from a Phase 2a Trial
Authors: Adriaan A. Voors, Jean‐François Tamby, John G.F. Cleland, Michael J. Koren, Leslie B. Forgosh, Dinesh Gupta, Lars H. Lund, Albert Camacho, Ravi Karra, Henk P. Swart, Pierpaolo Pellicori, Frank Wagner, Ray E. Hershberger, Narayana Prasad, Robert L. Anderson, Anu Anto, Kaylyn M. Bell, Jay M. Edelberg, Liang Fang, Marcus Henze, Cynthia M. Kelly, Gregory Kurio, Wanying Li, Kate Wells, Chun Yang, Sam L. Teichman, Carlos del Río, Scott D. Solomon - European Journal of Heart Failure 2020 cited by 106
- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
Authors: Michael J. Ackerman, Silvia G. Priori, Stephan Willems, Charles I. Berul, Ramón Brugada, Hugh Calkins, A. John Camm, Patrick T. Ellinor, Michael H. Gollob, Robert M. Hamilton, Ray E. Hershberger, Daniel P. Judge, Hervé Le Marec, William J. McKenna, Eric Schulze‐Bahr, Christopher Semsarian, Jeffrey A. Towbin, Hugh Watkins, Arthur A.M. Wilde, Christian Wolpert, Douglas P. Zipes - EP Europace 2011 cited by 901
- Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy
Authors: Victoria N. Parikh, Colleen Caleshu, Chloe M. Reuter, Laura C. Lazzeroni, Jodie Ingles, John Garcia, Kristen McCaleb, Tolulope Adesiyun, Farbod Sedaghat‐Hamedani, Saurabh Kumar, Sharon Graw, Marta Gigli, Davide Stolfo, Matteo Dal Ferro, Alexander Ing, Robert L. Nussbaum, Birgit H. Funke, Matthew T. Wheeler, Ray E. Hershberger, Stuart A. Cook, Lars M. Steinmetz, Neal K. Lakdawala, Matthew R.G. Taylor, Luisa Mestroni, Marco Merlo, Gianfranco Sinagra, Christopher Semsarian, Benjamin Meder, Daniel P. Judge, Euan A. Ashley - Circulation Heart Failure 2019 cited by 147
