
Jonathan G. Seidman, Ph.D.
Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
AMP-activated protein kinase in the heart: role during health and disease.
Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome.
Authors: Authors: Hinson JT, Fantin VR, Schönberger J, Breivik N, Siem G, McDonough B, Sharma P, Keogh I, Godinho R, Santos F, Esparza A, Nicolau Y, Selvaag E, Cohen BH, Hoppel CL, Tranebjaerg L, Eavey RD, Seidman JG, Seidman CE.
N Engl J Med
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N Engl J Med
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Complex genomic rearrangement in CCS-LacZ transgenic mice.
Authors: Authors: Stroud DM, Darrow BJ, Kim SD, Zhang J, Jongbloed MR, Rentschler S, Moskowitz IP, Seidman J, Fishman GI.
Genesis
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Genesis
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Cardiac myosin binding protein C phosphorylation is cardioprotective.
Authors: Authors: Sadayappan S, Osinska H, Klevitsky R, Lorenz JN, Sargent M, Molkentin JD, Seidman CE, Seidman JG, Robbins J.
Proc Natl Acad Sci U S A
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Proc Natl Acad Sci U S A
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Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
Authors: Authors: Schmitt JP, Debold EP, Ahmad F, Armstrong A, Frederico A, Conner DA, Mende U, Lohse MJ, Warshaw D, Seidman CE, Seidman JG.
Proc Natl Acad Sci U S A
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Proc Natl Acad Sci U S A
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Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis.
Authors: Authors: Mori AD, Zhu Y, Vahora I, Nieman B, Koshiba-Takeuchi K, Davidson L, Pizard A, Seidman JG, Seidman CE, Chen XJ, Henkelman RM, Bruneau BG.
Dev Biol
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Dev Biol
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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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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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Circulation
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Cardiovascular genomics.
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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Novartis Found Symp
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