Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy von Marian, Ali J, Braunwald, Eugene

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Current state of vaccine development and targeted therapies for COVID-19: impact of basic science discoveries von Marian, Ali J.

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Sporadic dilated cardiomyopathy is often familial von Marian, Ali J

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COVID-19 and the cardiovascular system: implications for risk assessment, diagnosis, and treatment options von Guzik, Tomasz J, Mohiddin, Saidi A, Dimarco, Anthony, Patel, Vimal, Savvatis, Kostas, Marelli-Berg, Federica M, Madhur, Meena S, Tomaszewski, Maciej, Maffia, Pasquale, D’Acquisto, Fulvio, Nicklin, Stuart A, Marian, Ali J, Nosalski, Ryszard, Murray, Eleanor C, Guzik, Bartlomiej, Berry, Colin, Touyz, Rhian M, Kreutz, Reinhold, Wang, Dao Wen, Bhella, David, Sagliocco, Orlando, Crea, Filippo, Thomson, Emma C, McInnes, Iain B

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A tribute to James Thornton Willerson, M.D. November 16, 1939–September 16, 2020 von Marian, Ali J

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Clinical Interpretation and Management of Genetic Variants von Marian, Ali J.

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Challenges in the Diagnosis of Anderson-Fabry Disease: A Deceptively Simple and Yet Complicated Genetic Disease von Marian, Ali J.

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Hypertrophic cardiomyopathy: from genetics to treatment von Marian, Ali J.

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BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific lamin A/C-deficient mice von Auguste, Gaelle, Rouhi, Leila, Matkovich, Scot J, Coarfa, Cristian, Robertson, Matthew J, Czernuszewicz, Grazyna, Gurha, Priyatansh, Marian, Ali J

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DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations von Chen, Suet Nee, Lombardi, Raffaella, Karmouch, Jennifer, Tsai, Ju-Yun, Czernuszewicz, Grace, Taylor, Matthew R.G, Mestroni, Luisa, Coarfa, Cristian, Gurha, Priyatansh, Marian, Ali J

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Genetic basis and molecular biology of cardiac arrhythmias in cardiomyopathies von Marian, Ali J, Asatryan, Babken, Wehrens, Xander H T

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Highlights of American Heart Association Scientific Sessions 2020: a virtual experience von Adão, Rui, Marian, Ali J

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Evaluation of Mavacamten in Symptomatic Patients With Nonobstructive Hypertrophic Cardiomyopathy von Ho, Carolyn Y, Mealiffe, Matthew E, Bach, Richard G, Bhattacharya, Mondira, Choudhury, Lubna, Edelberg, Jay M, Hegde, Sheila M, Jacoby, Daniel, Lakdawala, Neal K, Lester, Steven J, Ma, Yanfei, Marian, Ali J, Nagueh, Sherif F, Owens, Anjali, Rader, Florian, Saberi, Sara, Sehnert, Amy J, Sherrid, Mark V, Solomon, Scott D, Wang, Andrew, Wever-Pinzon, Omar, Wong, Timothy C, Heitner, Stephen B

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DNA double-stranded breaks, a hallmark of aging, defined at the nucleotide resolution, are increased and associated with transcription in the cardiac myocytes in LMNA-cardiomyopath... von Cathcart, Benjamin, Cheedipudi, Sirisha M, Rouhi, Leila, Zhao, Zhongming, Gurha, Priyatansh, Marian, Ali J

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Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders von Marian, Ali J, van Rooij, Eva, Roberts, Robert

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Single-Cell RNA Sequencing Uncovers Paracrine Functions of the Epicardial-Derived Cells in Arrhythmogenic Cardiomyopathy von Yuan, Ping, Cheedipudi, Sirisha M., Rouhi, Leila, Fan, Siyang, Simon, Lukas, Zhao, Zhongming, Hong, Kui, Gurha, Priyatansh, Marian, Ali J.

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Cardiac Fibro-Adipocyte Progenitors Express Desmosome Proteins and Preferentially Differentiate to Adipocytes Upon Deletion of the Desmoplakin Gene von Lombardi, Raffaella, Chen, Suet Nee, Ruggiero, Alessandra, Gurha, Priyatansh, Czernuszewicz, Grazyna Z, Willerson, James T, Marian, Ali J

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Suppression of Activated FOXO Transcription Factors in the Heart Prolongs Survival in a Mouse Model of Laminopathies von Auguste, Gaelle, Gurha, Priyatansh, Lombardi, Raffaella, Coarfa, Cristian, Willerson, James T, Marian, Ali J

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Domain-specific association of single-nucleotide variants in the LMNA gene with the phenotypic expression of dilated cardiomyopathy von Zhuo, Wen, Jiang, Zhenhong, Xun, Mengwei, Lin, Mouwen, Zhou, Qiongqiong, Marian, Ali J, Hong, Kui

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Molecular genetic studies of complex phenotypes von Marian, Ali J

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