
Jonathan G. Seidman, Ph.D.
Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
A dinucleotide repeat polymorphism in the MYBPH gene.
Authors: Authors: Watkins H, MacRae CA, Fischman DA, Seidman JG, Seidman CE.
Hum Mol Genet
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Hum Mol Genet
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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
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Nat Genet
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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
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Hum Mol Genet
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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
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Transpl Immunol
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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
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Arterioscler Thromb
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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
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Cell
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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
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Arch Ophthalmol
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T cell receptor (TCR) usage determines disease susceptibility in experimental autoimmune encephalomyelitis: studies with TCR V beta 8.2 transgenic mice.
Authors: Authors: Kuchroo VK, Collins M, al-Sabbagh A, Sobel RA, Whitters MJ, Zamvil SS, Dorf ME, Hafler DA, Seidman JG, Weiner HL, et al.
J Exp Med
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J Exp Med
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The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)
Authors: Authors: Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE.
N Engl J Med
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N Engl J Med
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A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3.
Authors: Authors: Shovlin CL, Hughes JM, Tuddenham EG, Temperley I, Perembelon YF, Scott J, Seidman CE, Seidman JG.
Nat Genet
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Nat Genet
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