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Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
617-432-7830
Seidman Lab Website
Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study.
Authors: Authors: Morita H, Larson MG, Barr SC, Vasan RS, O'Donnell CJ, Hirschhorn JN, Levy D, Corey D, Seidman CE, Seidman JG, Benjamin EJ.
Circulation
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Novel locus for an inherited cardiomyopathy maps to chromosome 7.
Authors: Authors: Song L, DePalma SR, Kharlap M, Zenovich AG, Cirino A, Mitchell R, McDonough B, Maron BJ, Seidman CE, Seidman JG, Ho CY.
Circulation
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Cardiovascular genomics.
Authors: Authors: Sabatine MS, Seidman JG, Seidman CE.
Circulation
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Sarcomere protein gene mutations and inherited heart disease: a beta-cardiac myosin heavy chain mutation causing endocardial fibroelastosis and heart failure.
Authors: Authors: Kamisago M, Schmitt JP, McNamara D, Seidman C, Seidman JG.
Novartis Found Symp
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Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.
Authors: Authors: Wolf CM, Moskowitz IP, Arno S, Branco DM, Semsarian C, Bernstein SA, Peterson M, Maida M, Morley GE, Fishman G, Berul CI, Seidman CE, Seidman JG.
Proc Natl Acad Sci U S A
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Cardiac myosin-binding protein-C phosphorylation and cardiac function.
Authors: Authors: Sadayappan S, Gulick J, Osinska H, Martin LA, Hahn HS, Dorn GW, Klevitsky R, Seidman CE, Seidman JG, Robbins J.
Circ Res
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Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy.
Authors: Authors: Ahmad F, Arad M, Musi N, He H, Wolf C, Branco D, Perez-Atayde AR, Stapleton D, Bali D, Xing Y, Tian R, Goodyear LJ, Berul CI, Ingwall JS, Seidman CE, Seidman JG.
Circulation
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Gene mutations in apical hypertrophic cardiomyopathy.
Authors: Authors: Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE.
Circulation
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Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.
Authors: Authors: Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C.
J Med Genet
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N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activity.
Authors: Authors: Zou L, Shen M, Arad M, He H, Løfgren B, Ingwall JS, Seidman CE, Seidman JG, Tian R.
Circ Res
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