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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 human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
Authors: Authors: Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.
Nat Genet
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Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency.
Authors: Authors: Georgopoulos NA, Pralong FP, Seidman CE, Seidman JG, Crowley WF, Vallejo M.
J Clin Endocrinol Metab
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Deficient cation channel regulation in neurons from mice with targeted disruption of the extracellular Ca2+-sensing receptor gene.
Authors: Authors: Ye C, Ho-Pao CL, Kanazirska M, Quinn S, Seidman CE, Seidman JG, Brown EM, Vassilev PM.
Brain Res Bull
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Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action.
Authors: Authors: Watkins H, Seidman CE, Seidman JG, Feng HS, Sweeney HL.
J Clin Invest
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Genetic analysis of susceptibility to experimental autoimmune encephalomyelitis in a cross between SJL/J and B10.S mice.
Authors: Authors: Encinas JA, Lees MB, Sobel RA, Symonowicz C, Greer JM, Shovlin CL, Weiner HL, Seidman CE, Seidman JG, Kuchroo VK.
J Immunol
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Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130.
Authors: Authors: Basson CT, MacRae CA, Schoenberg-Fejzo M, Morton CC, Spinner NB, Genin A, Krug E, Seidman JG, Seidman CE.
Genomics
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A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
Authors: Authors: Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
Nat Genet
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Lack of association of secretory component with IgA in J chain-deficient mice.
Authors: Authors: Hendrickson BA, Rindisbacher L, Corthesy B, Kendall D, Waltz DA, Neutra MR, Seidman JG.
J Immunol
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A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.
Authors: Authors: Manolis EN, Yandavi N, Nadol JB, Eavey RD, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant SN, Duyk GM, MacRae C, Seidman CE, Seidman JG.
Hum Mol Genet
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Missense mutation in the pore region of HERG causes familial long QT syndrome.
Authors: Authors: Benson DW, MacRae CA, Vesely MR, Walsh EP, Seidman JG, Seidman CE, Satler CA.
Circulation
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