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Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
Cold compressive dressing after total knee arthroplasty.
Authors: Authors: Healy WL, Seidman J, Pfeifer BA, Brown DG.
Clin Orthop Relat Res
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Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.
Authors: Authors: Straceski AJ, Geisterfer-Lowrance A, Seidman CE, Seidman JG, Leinwand LA.
Proc Natl Acad Sci U S A
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Inactivation of G-protein genes: double knockout in cell lines.
Authors: Authors: Mortensen RM, Seidman JG.
Methods Enzymol
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An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.
Authors: Authors: MacRae CA, Watkins HC, Jarcho JA, Thierfelder L, McKenna WJ, Seidman JG, Seidman CE.
Circulation
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Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
Authors: Authors: Pollak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, Levi T, Seidman CE, Seidman JG.
Cell
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Response.
Authors: Authors: Lipes MA, Rosenzweig A, Tan KN, Tanigawa G, Seidman JG, Eisenbarth GS.
Science
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Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, Thierfelder L, Anan R, Jarcho J, Matsumori A, McKenna W, Seidman JG, Seidman CE.
Am J Hum Genet
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Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
Authors: Authors: Pollak MR, Chou YH, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE.
Nat Genet
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Flagellar and acrosomal abnormalities associated with testicular HSV-tk expression in the mouse.
Authors: Authors: Huttner KM, Pudney J, Milstone DS, Ladd D, Seidman JG.
Biol Reprod
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A dinucleotide repeat polymorphism in the human LAMB2 gene on chromosome 1q.
Authors: Authors: Watkins HC, MacRae CA, Thierfelder L, McKenna WJ, Seidman CE, Seidman JG.
Hum Mol Genet
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