Myocardial Fibrosis as an Early Manifestation of Hypertrophic Cardiomyopathy von Ho, Carolyn Y, López, Begoña, Coelho-Filho, Otavio R, Lakdawala, Neal K, Cirino, Allison L, Jarolim, Petr, Kwong, Raymond, González, Arantxa, Colan, Steven D, Seidman, J.G, Seidman, Christine E, Díez, Javier

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Identifying Sarcomere Gene Mutations in Hypertrophic Cardiomyopathy: A Personal History von Seidman, Christine E, Seidman, J.G

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A common genetic variant within SCN10A modulates cardiac SCN5A expression von van den Boogaard, Malou, Smemo, Scott, Burnicka-Turek, Ozanna, Arnolds, David E, van de Werken, Harmen J G, Klous, Petra, McKean, David, Muehlschlegel, Jochen D, Moosmann, Julia, Toka, Okan, Yang, Xinan H, Koopmann, Tamara T, Adriaens, Michiel E, Bezzina, Connie R, de Laat, Wouter, Seidman, Christine, Seidman, J G, Christoffels, Vincent M, Nobrega, Marcelo A, Barnett, Phil, Moskowitz, Ivan P

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults von Morita, Hiroyuki, Rehm, Heidi L, Menesses, Andres, McDonough, Barbara, Roberts, Amy E, Kucherlapati, Raju, Towbin, Jeffrey A, Seidman, J.G, Seidman, Christine E

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poly(UG)-tailed RNAs in genome protection and epigenetic inheritance von Shukla, Aditi, Yan, Jenny, Pagano, Daniel J., Dodson, Anne E., Fei, Yuhan, Gorham, Josh, Seidman, J. G., Wickens, Marvin, Kennedy, Scott

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Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis von Delgado-Olguín, Paul, Huang, Yu, Li, Xue, Christodoulou, Danos, Seidman, Christine E, Seidman, J G, Tarakhovsky, Alexander, Bruneau, Benoit G

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AMP-Activated Protein Kinase in the Heart: Role During Health and Disease von Arad, Michael, Seidman, Christine E, Seidman, J G

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Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy von Arad, Michael, Maron, Barry J, Gorham, Joshua M, Johnson, Walter H, Saul, J. Philip, Perez-Atayde, Antonio R, Spirito, Paolo, Wright, Gregory B, Kanter, Ronald J, Seidman, J.G, Seidman, Christine E

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Transcription factor protein interactomes reveal genetic determinants in heart disease von Gonzalez-Teran, Barbara, Pittman, Maureen, Felix, Franco, Thomas, Reuben, Richmond-Buccola, Desmond, Hüttenhain, Ruth, Choudhary, Krishna, Moroni, Elisabetta, Costa, Mauro W., Huang, Yu, Padmanabhan, Arun, Alexanian, Michael, Lee, Clara Youngna, Maven, Bonnie E.J., Samse-Knapp, Kaitlen, Morton, Sarah U., McGregor, Michael, Gifford, Casey A., Seidman, J.G., Seidman, Christine E., Gelb, Bruce D., Colombo, Giorgio, Conklin, Bruce R., Black, Brian L., Bruneau, Benoit G., Krogan, Nevan J., Pollard, Katherine S., Srivastava, Deepak

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The genetic basis for cardiac remodeling von Ahmad, Ferhaan, Seidman, J G, Seidman, Christine E

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy von Minoche, Andre E., Horvat, Claire, Johnson, Renee, Gayevskiy, Velimir, Morton, Sarah U., Drew, Alexander P., Woo, Kerhan, Statham, Aaron L., Lundie, Ben, Bagnall, Richard D., Ingles, Jodie, Semsarian, Christopher, Seidman, J. G., Seidman, Christine E., Dinger, Marcel E., Cowley, Mark J., Fatkin, Diane

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Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants von Ito, Kaoru, Bick, Alexander G, Flannick, Jason, Friedman, David J, Genovese, Giulio, Parfenov, Michael G, DePalma, Steven R, Gupta, Namrata, Gabriel, Stacey B, Taylor, Herman A, Fox, Ervin R, Newton-Cheh, Christopher, Kathiresan, Sekar, Hirschhorn, Joel N, Altshuler, David M, Pollak, Martin R, Wilson, James G, Seidman, J.G, Seidman, Christine

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Genetic Testing for Dilated Cardiomyopathy in Clinical Practice von Lakdawala, Neal K., MD, Funke, Birgit H., PhD, Baxter, Samantha, MS, CGC, Cirino, Allison L., MS, CGC, Roberts, Amy E., MD, Judge, Daniel P., MD, Johnson, Nicole, MS, CGC, Mendelsohn, Nancy J., MD, Morel, Chantal, MD, Care, Melanie, MS, CGC, Chung, Wendy K., MD, Jones, Carolyn, MD, PhD, Psychogios, Apostolos, MD, Duffy, Elizabeth, Rehm, Heidi L., PhD, White, Emily, MS, Seidman, J.G., PhD, Seidman, Christine E., MD, Ho, Carolyn Y., MD

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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes von Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noël P, Florez, Jose C, Meigs, James B, Taylor, Herman, Lyssenko, Valeriya, Irgens, Henrik, Fox, Ervin, Burslem, Frank, Johansson, Stefan, Brosnan, M Julia, Trimmer, Jeff K, Newton-Cheh, Christopher, Tuomi, Tiinamaija, Molven, Anders, Wilson, James G, O'Donnell, Christopher J, Kathiresan, Sekar, Hirschhorn, Joel N, Njølstad, Pål R, Rolph, Tim, Seidman, J G, Gabriel, Stacey, Cox, David R, Seidman, Christine E, Groop, Leif, Altshuler, David

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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia von Song, Lei, Alcalai, Ronny, Arad, Michael, Wolf, Cordula M, Toka, Okan, Conner, David A, Berul, Charles I, Eldar, Michael, Seidman, Christine E, Seidman, J G

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Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease von Fatkin, Diane, MacRae, Calum, Sasaki, Takeshi, Wolff, Matthew R, Porcu, Maurizio, Frenneaux, Michael, Atherton, John, Vidaillet, Humberto J, Spudich, Serena, De Girolami, Umberto, Seidman, Christine E, Seidman, J.G, Muntoni, Francesco, Müehle, Gerry, Johnson, Wendy, McDonough, Barbara

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Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy von Gerull, Brenda, Gramlich, Michael, Atherton, John, McNabb, Mark, Trombitás, Karoly, Sasse-Klaassen, Sabine, Seidman, J.G., Seidman, Christine, Granzier, Henk, Labeit, Siegfried, Frenneaux, Michael, Thierfelder, Ludwig

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Gene mutations in apical hypertrophic cardiomyopathy von ARAD, Michael, PENAS-LADO, Manual, SEIDMAN, J. G, SEIDMAN, Christine E, MONSERRAT, Lorenzo, MARON, Barry J, SHERRID, Mark, HO, Carolyn Y, BARR, Scott, KARIM, Ahmad, OLSON, Timothy M, KAMISAGO, Mitsohiro

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Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease von Wolf, Cordula M, Wang, Libin, Alcalai, Ronny, Pizard, Anne, Burgon, Patrick G, Ahmad, Ferhaan, Sherwood, Megan, Branco, Dorothy M, Wakimoto, Hiroko, Fishman, Glenn I, See, Vincent, Stewart, Colin L, Conner, David A, Berul, Charles I, Seidman, Christine E, Seidman, J.G

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Precision Medicine in the Management of Dilated Cardiomyopathy von Fatkin, Diane, Huttner, Inken G., Kovacic, Jason C., Seidman, J.G., Seidman, Christine E.

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