Jonathan G. Seidman

Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School

617-432-7830

Publications

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 1995-05-01
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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 1995-04-20
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Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.

Authors: Authors: Watkins H, Seidman JG, Seidman CE.
Hum Mol Genet 1995-01-01
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A dinucleotide repeat polymorphism in the MYBPH gene.

Authors: Authors: Watkins H, MacRae CA, Fischman DA, Seidman JG, Seidman CE.
Hum Mol Genet 1994-12-01
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Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Authors: Authors: Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG.
Nat Genet 1994-11-01
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Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Authors: Authors: Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML.
Hum Mol Genet 1994-09-01
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T cell receptor (beta chain) transgenic mice have selective deficits in gamma delta T cell subpopulations.

Authors: Authors: Rimm IJ, Fruman DA, Abhyankar S, Sakamoto H, Orme IM, Milstone D, Seidman JG, Ferrara JL.
Transpl Immunol 1994-09-01
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Diversity of T-cell antigen receptor V beta gene utilization in advanced human atheroma.

Authors: Authors: Swanson SJ, Rosenzweig A, Seidman JG, Libby P.
Arterioscler Thromb 1994-07-01
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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Authors: Authors: Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE.
Cell 1994-06-03
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A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34.

Authors: Authors: Zhang K, Bither PP, Park R, Donoso LA, Seidman JG, Seidman CE.
Arch Ophthalmol 1994-06-01
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