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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
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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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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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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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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Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function.
Authors: Authors: Golitsina N, An Y, Greenfield NJ, Thierfelder L, Iizuka K, Seidman JG, Seidman CE, Lehrer SS, Hitchcock-DeGregori SE.
Biochemistry
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Cao-sensing receptor (CaR)-mediated activation of K+ channels is blunted in CaR gene-deficient mouse neurons.
Authors: Authors: Vassilev PM, Ho-Pao CL, Kanazirska MP, Ye C, Hong K, Seidman CE, Seidman JG, Brown EM.
Neuroreport
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Cytoskeletal changes in the brains of mice lacking calcineurin A alpha.
Authors: Authors: Kayyali US, Zhang W, Yee AG, Seidman JG, Potter H.
J Neurochem
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Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Authors: Authors: Argov Z, Tiram E, Eisenberg I, Sadeh M, Seidman CE, Seidman JG, Karpati G, Mitrani-Rosenbaum S.
Ann Neurol
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