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Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE.
Nat Genet
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A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
Authors: Authors: Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE.
Nat Genet
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Altered hepatic transport of immunoglobulin A in mice lacking the J chain.
Authors: Authors: Hendrickson BA, Conner DA, Ladd DJ, Kendall D, Casanova JE, Corthesy B, Max EE, Neutra MR, Seidman CE, Seidman JG.
J Exp Med
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Cloning and functional characterization of extracellular Ca(2+)-sensing receptors from parathyroid and kidney.
Authors: Authors: Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC.
Bone
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Calcium-ion-sensing cell-surface receptors.
Authors: Authors: Brown EM, Pollak M, Seidman CE, Seidman JG, Chou YH, Riccardi D, Hebert SC.
N Engl J Med
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The cloning of extracellular Ca(2+)-sensing receptors from parathyroid and kidney: molecular mechanisms of extracellular Ca(2+)-sensing.
Authors: Authors: Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC.
J Nutr
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A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, Anan R, Coviello DA, Spirito P, Seidman JG, Seidman CE.
Circulation
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Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemia.
Authors: Authors: Chou YH, Pollak MR, Brandi ML, Toss G, Arnqvist H, Atkinson AB, Papapoulos SE, Marx S, Brown EM, Seidman JG, et al.
Am J Hum Genet
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Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG, et al.
N Engl J Med
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Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.
Authors: Authors: Watkins H, Seidman JG, Seidman CE.
Hum Mol Genet
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