Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy von Hershberger, Ray E., MD, Siegfried, Jill D., MS

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Considering complexity in the genetic evaluation of dilated cardiomyopathy von Jordan, Elizabeth, Hershberger, Ray E

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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) von Miller, David T., Lee, Kristy, Chung, Wendy K., Gordon, Adam S., Herman, Gail E., Klein, Teri E., Stewart, Douglas R., Amendola, Laura M., Adelman, Kathy, Bale, Sherri J., Gollob, Michael H., Harrison, Steven M., Hershberger, Ray E., McKelvey, Kent, Richards, C. Sue, Vlangos, Christopher N., Watson, Michael S., Martin, Christa Lese

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Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline von Hershberger, Ray E., Givertz, Michael M., Ho, Carolyn Y., Judge, Daniel P., Kantor, Paul F., McBride, Kim L., Morales, Ana, Taylor, Matthew R.G., Vatta, Matteo, Ware, Stephanie M.

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Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association von Musunuru, Kiran, Hershberger, Ray E., Day, Sharlene M., Klinedinst, N. Jennifer, Landstrom, Andrew P., Parikh, Victoria N., Prakash, Siddharth, Semsarian, Christopher, Sturm, Amy C.

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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) von Hershberger, Ray E., Givertz, Michael M., Ho, Carolyn Y, Judge, Daniel P., Kantor, Paul F., McBride, Kim L., Morales, Ana, Taylor, Matthew R. G., Vatta, Matteo, Ware, Stephanie M.

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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) von Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, C. Sue, Stewart, Douglas R., Martin, Christa Lese

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Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rieder, Mark J., Siegfried, Jill D., Rampersaud, Evadnie, Züchner, Stephan, Mangos, Steve, Gonzalez-Quintana, Jorge, Wang, Libin, McGee, Sean, Reiser, Jochen, Martin, Eden, Nickerson, Deborah A., Hershberger, Ray E.

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2021 ACC/AHA Key Data Elements and Definitions for Heart Failure: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Data Standards (W... von Bozkurt, Biykem, Hershberger, Ray E., Butler, Javed, Grady, Kathleen L., Heidenreich, Paul A., Isler, Maria Lizza, Kirklin, James K., Weintraub, William S.

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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death von Walsh, Roddy, Adler, Arnon, Amin, Ahmad S, Abiusi, Emanuela, Care, Melanie, Bikker, Hennie, Amenta, Simona, Feilotter, Harriet, Nannenberg, Eline A, Mazzarotto, Francesco, Trevisan, Valentina, Garcia, John, Hershberger, Ray E, Perez, Marco V, Sturm, Amy C, Ware, James S, Zareba, Wojciech, Novelli, Valeria, Wilde, Arthur A M, Gollob, Michael H

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ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene‐level specification of the ACMG/AMP guidelines for sequence variant interpretation... von Rivera‐Muñoz, Edgar A., Milko, Laura V., Harrison, Steven M., Azzariti, Danielle R., Kurtz, C. Lisa, Lee, Kristy, Mester, Jessica L., Weaver, Meredith A., Currey, Erin, Craigen, William, Eng, Charis, Funke, Birgit, Hegde, Madhuri, Hershberger, Ray E., Mao, Rong, Steiner, Robert D., Vincent, Lisa M., Martin, Christa L., Plon, Sharon E., Ramos, Erin, Rehm, Heidi L., Watson, Michael, Berg, Jonathan S.

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Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy von MORALES, Ana, PAINTER, Thomas, RAN LI, SIEGFRIED, Jill D, DUANXIANG LI, NORTON, Nadine, HERSHBERGER, Ray E

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Clinical and genetic issues in familial dilated cardiomyopathy von Burkett, Emily L., Hershberger, Ray E.

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Advanced (Stage D) Heart Failure: A Statement From the Heart Failure Society of America Guidelines Committee von Fang, James C., MD, Ewald, Gregory A., MD, Allen, Larry A., MD, MHS, Butler, Javed, MD, Westlake Canary, Cheryl A., RN, PhD, Colvin-Adams, Monica, MD, Dickinson, Michael G., MD, Levy, Phillip, MD, MPH, Stough, Wendy Gattis, PharmD, Sweitzer, Nancy K., MD, PhD, Teerlink, John R., MD, Whellan, David J., MD, MHS, Albert, Nancy M., RN, PhD, Krishnamani, Rajan, MD, Rich, Michael W., MD, Walsh, Mary N., MD, Bonnell, Mark R., MD, Carson, Peter E., MD, Chan, Michael C., MBBS, Dries, Daniel L., MD, Hernandez, Adrian F., MD, Hershberger, Ray E., MD, Katz, Stuart D., MD, Moore, Stephanie, MD, Rodgers, Jo E., PharmD, Rogers, Joseph G., MD, Vest, Amanda R., MBBS, Givertz, Michael M., MD

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HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies von Ackerman, Michael J., MD, PhD, Priori, Silvia G., MD, PhD, Willems, Stephan, MD, PhD, Berul, Charles, MD, FHRS, CCDS, Brugada, Ramon, MD, PhD, Calkins, Hugh, MD, FHRS, CCDS, Camm, A. John, MD, FHRS, Ellinor, Patrick T., MD, PhD, Gollob, Michael, MD, Hamilton, Robert, MD, CCDS, Hershberger, Ray E., MD, Judge, Daniel P., MD, Le Marec, Hervè, MD, McKenna, William J., MD, Schulze-Bahr, Eric, MD, PhD, Semsarian, Chris, MBBS, PhD, Towbin, Jeffrey A., MD, Watkins, Hugh, MD, PhD, Wilde, Arthur, MD, PhD, Wolpert, Christian, MD, Zipes, Douglas P., MD, FHRS

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Where Genome Meets Phenome: Rationale for Integrating Genetic and Protein Biomarkers in the Diagnosis and Management of Dilated Cardiomyopathy and Heart Failure von Piran, Sanaz, MD, Liu, Peter, MD, Morales, Ana, MS, Hershberger, Ray E., MD

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The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy von Hershberger, Ray E., Cowan, Jason, Jordan, Elizabeth, Kinnamon, Daniel D.

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A human mitofusin 2 mutation can cause mitophagic cardiomyopathy von Franco, Antonietta, Li, Jiajia, Kelly, Daniel P, Hershberger, Ray E, Marian, Ali J, Lewis, Renate M, Song, Moshi, Dang, Xiawei, Schmidt, Alina D, Mathyer, Mary E, Edwards, John R, Strong, Cristina de Guzman, Dorn, Gerald W

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Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy von Parks, Sharie B., PhD, Kushner, Jessica D., MS, CGC, Nauman, Deirdre, BSN, Burgess, Donna, BSN, Ludwigsen, Susan, MA, Peterson, Amanda, BS, Li, Duanxiang, MD, Jakobs, Petra, PhD, Litt, Michael, PhD, Porter, Charles B., MD, FACC, Rahko, Peter S., MD, FACC, Hershberger, Ray E., MD, FACC

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Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era von Norton, Nadine, Robertson, Peggy D, Rieder, Mark J, Züchner, Stephan, Rampersaud, Evadnie, Martin, Eden, Li, Duanxiang, Nickerson, Deborah A, Hershberger, Ray E

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