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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
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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Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
Authors: Authors: Benson DW, Silberbach GM, Kavanaugh-McHugh A, Cottrill C, Zhang Y, Riggs S, Smalls O, Johnson MC, Watson MS, Seidman JG, Seidman CE, Plowden J, Kugler JD.
J Clin Invest
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Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.
Authors: Authors: McConnell BK, Jones KA, Fatkin D, Arroyo LH, Lee RT, Aristizabal O, Turnbull DH, Georgakopoulos D, Kass D, Bond M, Niimura H, Schoen FJ, Conner D, Fischman DA, Seidman CE, Seidman JG, Fischman DH.
J Clin Invest
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Altered regulatory function of two familial hypertrophic cardiomyopathy troponin T mutants.
Authors: Authors: Mukherjea P, Tong L, Seidman JG, Seidman CE, Hitchcock-DeGregori SE.
Biochemistry
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Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
Authors: Authors: Manolis EN, Eavey RD, Sangwatanaroj S, Halpin C, Rosenbaum S, Watkins H, Jarcho J, Seidman CE, Seidman JG.
Am J Otol
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Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.
Authors: Authors: Bruneau BG, Logan M, Davis N, Levi T, Tabin CJ, Seidman JG, Seidman CE.
Dev Biol
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