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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
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
Authors: Authors: Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE.
N Engl J Med
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Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy.
Authors: Authors: Spindler M, Saupe KW, Christe ME, Sweeney HL, Seidman CE, Seidman JG, Ingwall JS.
J Clin Invest
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Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalities.
Authors: Authors: Berul CI, Christe ME, Aronovitz MJ, Maguire CT, Seidman CE, Seidman JG, Mendelsohn ME.
J Interv Card Electrophysiol
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A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13.
Authors: Authors: Mathis BJ, Kim SH, Calabrese K, Haas M, Seidman JG, Seidman CE, Pollak MR.
Kidney Int
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Molecular genetic studies of familial hypertrophic cardiomyopathy.
Authors: Authors: Seidman CE, Seidman JG.
Basic Res Cardiol
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CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets.
Authors: Authors: Kelleher CL, Buckalew VM, Frederickson ED, Rhodes DJ, Conner DA, Seidman JG, Seidman CE.
Kidney Int
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beta-Arrestin1 knockout mice appear normal but demonstrate altered cardiac responses to beta-adrenergic stimulation.
Authors: Authors: Conner DA, Mathier MA, Mortensen RM, Christe M, Vatner SF, Seidman CE, Seidman JG.
Circ Res
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Targeted ablation of the murine alpha-tropomyosin gene.
Authors: Authors: Blanchard EM, Iizuka K, Christe M, Conner DA, Geisterfer-Lowrance A, Schoen FJ, Maughan DW, Seidman CE, Seidman JG.
Circ Res
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Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.
Authors: Authors: Shovlin CL, Hughes JM, Scott J, Seidman CE, Seidman JG.
Am J Hum Genet
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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome.
Authors: Authors: Bamshad M, Lin RC, Law DJ, Watkins WC, Krakowiak PA, Moore ME, Franceschini P, Lala R, Holmes LB, Gebuhr TC, Bruneau BG, Schinzel A, Seidman JG, Seidman CE, Jorde LB.
Nat Genet
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