Contemporary Cardiac Issues in Duchenne Muscular Dystrophy von McNally, Elizabeth M, Kaltman, Jonathan R, Benson, D Woodrow, Canter, Charles E, Cripe, Linda H, Duan, Dongsheng, Finder, Jonathan D, Hoffman, Eric P, Judge, Daniel P, Kertesz, Naomi, Kinnett, Kathi, Kirsch, Roxanne, Metzger, Joseph M, Pearson, Gail D, Rafael-Fortney, Jill A, Raman, Subha V, Spurney, Christopher F, Targum, Shari L, Wagner, Kathryn R, Markham, Larry W

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Extracellular Matrix Remodeling and Organization in Developing and Diseased Aortic Valves von Hinton, Robert B, Lincoln, Joy, Deutsch, Gail H, Osinska, Hanna, Manning, Peter B, Benson, D Woodrow, Yutzey, Katherine E

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Fetal Heart Rate Predictors of Long QT Syndrome von MITCHELL, Jason L, CUNEO, Bettina F, ETHERIDGE, Susan P, HORIGOME, Hitoshi, WENG, Hsin-Yi, WOODROW BENSON, D

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Spectrum of heart disease associated with murine and human GATA4 mutation von Rajagopal, Satish K, Ma, Qing, Obler, Dita, Shen, Jie, Manichaikul, Ani, Tomita-Mitchell, Aoy, Boardman, Kari, Briggs, Christine, Garg, Vidu, Srivastava, Deepak, Goldmuntz, Elizabeth, Broman, Karl W, Woodrow Benson, D, Smoot, Leslie B, Pu, William T

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Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice von Ye, Maoqing, Coldren, Chris, Liang, Xingqun, Mattina, Teresa, Goldmuntz, Elizabeth, Benson, D. Woodrow, Ivy, Dunbar, Perryman, M.B., Garrett-Sinha, Lee Ann, Grossfeld, Paul

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Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy von Markham, Larry W, Kinnett, Kathi, Wong, Brenda L, Woodrow Benson, D, Cripe, Linda H

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Comparison of Magnetic Resonance Feature Tracking for Strain Calculation With Harmonic Phase Imaging Analysis von Hor, Kan N., MD, Gottliebson, William M., MD, Carson, Christopher, MD, Wash, Erin, BS, Cnota, James, MD, Fleck, Robert, MD, Wansapura, Janaka, PhD, Klimeczek, Piotr, MD, Al-Khalidi, Hussein R., PhD, Chung, Eugene S., MD, Benson, D. Woodrow, MD, PhD, Mazur, Wojciech, MD

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Inherited Arrhythmias : A national heart, lung, and blood institute and office of rare diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, an... von LEHNART, Stephan E, ACKERMAN, Michael J, LATHROP, David A, LEDERER, W. Jonathan, MAKIELSKI, Jonathan C, MOHLER, Peter J, MOSS, Arthur, NERBONNE, Jeanne M, OLSON, Timothy M, PRZYWARA, Dennis A, TOWBIN, Jeffrey A, WANG, Lan-Hsiang, BENSON, D. Woodrow, MARKS, Andrew R, BRUGADA, Ramon, CLANCY, Colleen E, DONAHUE, J. Kevin, GEORGE, Alfred L, GRANT, Augustus O, GROFT, Stephen C, JANUARY, Craig T

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Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm von Chetaille, Philippe, Preuss, Christoph, Burkhard, Silja, Côté, Jean-Marc, Houde, Christine, Castilloux, Julie, Piché, Jessica, Gosset, Natacha, Leclerc, Séverine, Wünnemann, Florian, Thibeault, Maryse, Gagnon, Carmen, Galli, Antonella, Tuck, Elizabeth, Hickson, Gilles R, Amine, Nour El, Boufaied, Ines, Lemyre, Emmanuelle, de Santa Barbara, Pascal, Faure, Sandrine, Jonzon, Anders, Cameron, Michel, Dietz, Harry C, Gallo-McFarlane, Elena, Benson, D Woodrow, Moreau, Claudia, Labuda, Damian, Zhan, Shing H, Shen, Yaoqing, Jomphe, Michèle, Jones, Steven J M, Bakkers, Jeroen, Andelfinger, Gregor

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Hypoplastic Left Heart Syndrome Links to Chromosomes 10q and 6q and Is Genetically Related to Bicuspid Aortic Valve von Hinton, Robert B., MD, Martin, Lisa J., PhD, Rame-Gowda, Smitha, PhD, Tabangin, Meredith E., MPH, Cripe, Linda H., MD, Benson, D. Woodrow, MD, PhD

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Genetics of Hypoplastic Left Heart Syndrome von Benson, D. Woodrow, MD, PhD, Martin, Lisa J., PhD, Lo, Cecilia W., PhD

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Autonomic Dysfunction: A Driving Force for Myocardial Fibrosis in Young Duchenne Muscular Dystrophy Patients? von Thomas, Tamara O., Jefferies, John L., Lorts, Angela, Anderson, Jeffrey B., Gao, Zhiqian, Woodrow Benson, D., Hor, Kan N., Cripe, Linda H., Urbina, Elaine M.

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Impact of MYH6 variants in hypoplastic left heart syndrome von Tomita-Mitchell, Aoy, Stamm, Karl D, Mahnke, Donna K, Kim, Min-Su, Hidestrand, Pip M, Liang, Huan Ling, Goetsch, Mary A, Hidestrand, Mats, Simpson, Pippa, Pelech, Andrew N, Tweddell, James S, Benson, D Woodrow, Lough, John W, Mitchell, Michael E

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NKX2.5 mutations in patients with congenital heart disease von MCELHINNEY, Doff B, GEIGER, Elizabeth, BLINDER, Joshua, BENSON, D. Woodrow, GOLDMUNTZ, Elizabeth

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Hypoplastic Left Heart Syndrome Is Heritable von Hinton, Robert B., MD, Martin, Lisa J., PhD, Tabangin, Meredith E., MPH, Mazwi, Mjaye L., MD, Cripe, Linda H., MD, Benson, D. Woodrow, MD, PhD

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Highly Sensitive Noninvasive Cardiac Transplant Rejection Monitoring Using Targeted Quantification of Donor-Specific Cell-Free Deoxyribonucleic Acid von Hidestrand, Mats, PhD, Tomita-Mitchell, Aoy, PhD, Hidestrand, Pip M., MD, Oliphant, Arnold, PhD, Goetsch, Mary, MS, Stamm, Karl, MS, Liang, Huan-Ling, MD, Castleberry, Chesney, MD, Benson, D. Woodrow, MD, PhD, Stendahl, Gail, DNP, Simpson, Pippa M., PhD, Berger, Stuart, MD, Tweddell, James S., MD, Zangwill, Steven, MD, Mitchell, Michael E., MD

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Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy von Arad, Michael, Benson, D Woodrow, Perez-Atayde, Antonio R, McKenna, William J, Sparks, Elizabeth A, Kanter, Ronald J, McGarry, Kate, Seidman, J G, Seidman, Christine E

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Detection of Progressive Cardiac Dysfunction by Serial Evaluation of Circumferential Strain in Patients With Duchenne Muscular Dystrophy von Hagenbuch, Sean C., MD, Gottliebson, William M., MD, MS, Wansapura, Janaka, PhD, Mazur, Wojciech, MD, Fleck, Robert, MD, Benson, D. Woodrow, MD, PhD, Hor, Kan N., MD

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Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging von Tandon, Animesh, MD, MS, Jefferies, John L., MD, MPH, Villa, Chet R., MD, Hor, Kan N., MD, Wong, Brenda L., MD, Ware, Stephanie M., MD, PhD, Gao, Zhiqian, PhD, Towbin, Jeffrey A., MD, MS, Mazur, Wojciech, MD, Fleck, Robert J., MD, Sticka, Joshua J., MD, Benson, D. Woodrow, MD, PhD, Taylor, Michael D., MD, PhD

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Arrhythmia Phenotype During Fetal Life Suggests Long-QT Syndrome Genotype: Risk Stratification of Perinatal Long-QT Syndrome von Cuneo, Bettina F, Etheridge, Susan P, Horigome, Hitoshi, Sallee, Denver, Moon-Grady, Anita, Weng, Hsin-Yi, Ackerman, Michael J, Benson, D Woodrow

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