Jonathan Seidman headshot

Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
617-432-7830
Seidman Lab Website
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
View full abstract on Pubmed
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
View full abstract on Pubmed
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
View full abstract on Pubmed
A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
Authors: Authors: Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
Nat Genet
View full abstract on Pubmed
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
View full abstract on Pubmed
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
View full abstract on Pubmed
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
View full abstract on Pubmed
A mouse model of familial hypertrophic cardiomyopathy.
Authors: Authors: Geisterfer-Lowrance AA, Christe M, Conner DA, Ingwall JS, Schoen FJ, Seidman CE, Seidman JG.
Science
View full abstract on Pubmed
T cell responses in calcineurin A alpha-deficient mice.
Authors: Authors: Zhang BW, Zimmer G, Chen J, Ladd D, Li E, Alt FW, Wiederrecht G, Cryan J, O'Neill EA, Seidman CE, Abbas AK, Seidman JG.
J Exp Med
View full abstract on Pubmed
Hereditary inclusion body myopathy maps to chromosome 9p1-q1.
Authors: Authors: Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, Seidman CE, Seidman JG.
Hum Mol Genet
View full abstract on Pubmed