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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
An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy.
Authors: Authors: Fatkin D, McConnell BK, Mudd JO, Semsarian C, Moskowitz IG, Schoen FJ, Giewat M, Seidman CE, Seidman JG.
J Clin Invest
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Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy.
Authors: Authors: Ho CY, Lever HM, DeSanctis R, Farver CF, Seidman JG, Seidman CE.
Circulation
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Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease.
Authors: Authors: Kasahara H, Lee B, Schott JJ, Benson DW, Seidman JG, Seidman CE, Izumo S.
J Clin Invest
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Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.
Authors: Authors: Schönberger J, Levy H, Grünig E, Sangwatanaroj S, Fatkin D, MacRae C, Stäcker H, Halpin C, Eavey R, Philbin EF, Katus H, Seidman JG, Seidman CE.
Circulation
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Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy.
Authors: Authors: Tyska MJ, Hayes E, Giewat M, Seidman CE, Seidman JG, Warshaw DM.
Circ Res
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Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q.
Authors: Authors: Yeon HB, Lindor NM, Seidman JG, Seidman CE.
Am J Hum Genet
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Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand.
Authors: Authors: Bruneau BG, Bao ZZ, Tanaka M, Schott JJ, Izumo S, Cepko CL, Seidman JG, Seidman CE.
Dev Biol
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Clinical goals and performance measures for cholesterol management in secondary prevention of coronary heart disease.
Authors: Authors: Lee TH, Cleeman JI, Grundy SM, Gillett C, Pasternak RC, Seidman J, Sennett C.
JAMA
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Mutations in COCH (formerly Coch5b2) cause DFNA9.
Authors: Authors: Eavey RD, Manolis EN, Lubianca J, Merchant S, Seidman JG, Seidman C.
Adv Otorhinolaryngol
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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.
Authors: Authors: Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, McDonough B.
N Engl J Med
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