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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Mitochondria, contractile apparatus, and ion channels in the failing myocardium: Special relationships or dangerous liaisons? von Vatta, Matteo, PhD

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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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MY APPROACH to genetic testing in cardiology practice von Vatta, Matteo, PhD, FACMG

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Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199 von Schneider, Bryan P, Li, Lang, Radovich, Milan, Shen, Fei, Miller, Kathy D, Flockhart, David A, Jiang, Guanglong, Vance, Gail, Gardner, Laura, Vatta, Matteo, Bai, Shaochun, Lai, Dongbing, Koller, Daniel, Zhao, Fengmin, O'Neill, Anne, Smith, Mary Lou, Railey, Elda, White, Carol, Partridge, Ann, Sparano, Joseph, Davidson, Nancy E, Foroud, Tatiana, Sledge, Jr, George W

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Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex von Ueda, Kazuo, Valdivia, Carmen, Medeiros-Domingo, Argelia, Tester, David J, Vatta, Matteo, Farrugia, Gianrico, Ackerman, Michael J, Makielski, Jonathan C

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Editorial commentary: Genetic testing for congenital heart disease: The future is now von Vatta, Matteo

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Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells von Turker, Isik, Makiyama, Takeru, Ueyama, Takeshi, Shimizu, Akihiko, Yamakawa, Masaru, Chen, Peng‐Sheng, Vatta, Matteo, Horie, Minoru, Ai, Tomohiko

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ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene von Moulik, Mousumi, MD, Vatta, Matteo, PhD, Witt, Stephanie H., PhD, Arola, Anita M., MD, PhD, Murphy, Ross T., MD, McKenna, William J., MD, Boriek, Aladin M., PhD, Oka, Kazuhiro, PhD, Labeit, Siegfried, MD, Bowles, Neil E., PhD, Arimura, Takuro, DVM, PhD, Kimura, Akinori, MD, PhD, Towbin, Jeffrey A., MD

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Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy von Xu, Tianhong, PhD, Yang, Zhao, MD, PhD, Vatta, Matteo, PhD, Rampazzo, Alessandra, MD, PhD, Beffagna, Giorgia, PhD, Pillichou, Kalliopi, PhD, Scherer, Steven E., PhD, Saffitz, Jeffrey, MD, PhD, Kravitz, Joshua, BS, Zareba, Wojciech, MD, Danieli, Gian Antonio, PhD, Lorenzon, Alessandra, PhD, Nava, Andrea, MD, Bauce, Barbara, MD, PhD, Thiene, Gaetano, MD, Basso, Cristina, MD, PhD, Calkins, Hugh, MD, Gear, Kathy, RN, Marcus, Frank, MD, Towbin, Jeffrey A., MD

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A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG von Turker, Isik, Makiyama, Takeru, Vatta, Matteo, Itoh, Hideki, Ueyama, Takeshi, Shimizu, Akihiko, Ai, Tomohiko, Horie, Minoru

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Moving the Boundaries of the Diagnosis of Unexplained Sudden Cardiac Arrest and Sudden Cardiac Death in the Young von Vatta, Matteo

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Use of genetic testing to identify sudden cardiac death syndromes von Vatta, Matteo, PhD, Spoonamore, Katherine G., MS

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Genetic variants and ECG pattern variability in long QT syndrome: How far are we? von Vatta, Matteo, PhD

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Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3 von Cronk, Lisa B., BA, Ye, Bin, PhD, Kaku, Toshihiko, MD, PhD, Tester, David J., BS, Vatta, Matteo, PhD, Makielski, Jonathan C., MD, Ackerman, Michael J., MD, PhD

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De novo heterozygous pathogenic FBN1 variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case report von MacGowan, Taylor, McClinchey, Taylor, Parcha, Vibhu, Vatta, Matteo, Litovsky, Silvio, Arora, Pankaj, Benson, Paul V

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Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function von Olaopa, Michael A., Ai, Tomohiko, Chao, Bo, Xiao, Xiangshu, Vatta, Matteo, Habecker, Beth A.

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Intronic variants and splicing errors in cardiovascular diseases von Vatta, Matteo, PhD

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Editorial: Current Challenges in Cardiovascular Molecular Diagnostics von Novelli, Valeria, Vatta, Matteo

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Editorial commentary: Targeting TYMP for cardiovascular disease: How far are we? von Vatta, Matteo

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