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
Regulation of murine fetal-placental calcium metabolism by the calcium-sensing receptor.
Authors: Authors: Kovacs CS, Ho-Pao CL, Hunzelman JL, Lanske B, Fox J, Seidman JG, Seidman CE, Kronenberg HM.
J Clin Invest
View full abstract on Pubmed
Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects.
Authors: Authors: Benson DW, Sharkey A, Fatkin D, Lang P, Basson CT, McDonough B, Strauss AW, Seidman JG, Seidman CE.
Circulation
View full abstract on Pubmed
The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.
Authors: Authors: Lubianca Neto JF, Lu L, Eavey RD, Flores MA, Caldera RM, Sangwatanaroj S, Schott JJ, McDonough B, Santos JI, Seidman CE, Seidman JG.
Am J Hum Genet
View full abstract on Pubmed
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
Authors: Authors: Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE.
N Engl J Med
View full abstract on Pubmed
Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy.
Authors: Authors: Spindler M, Saupe KW, Christe ME, Sweeney HL, Seidman CE, Seidman JG, Ingwall JS.
J Clin Invest
View full abstract on Pubmed
Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalities.
Authors: Authors: Berul CI, Christe ME, Aronovitz MJ, Maguire CT, Seidman CE, Seidman JG, Mendelsohn ME.
J Interv Card Electrophysiol
View full abstract on Pubmed
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13.
Authors: Authors: Mathis BJ, Kim SH, Calabrese K, Haas M, Seidman JG, Seidman CE, Pollak MR.
Kidney Int
View full abstract on Pubmed
Molecular genetic studies of familial hypertrophic cardiomyopathy.
Authors: Authors: Seidman CE, Seidman JG.
Basic Res Cardiol
View full abstract on Pubmed
CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets.
Authors: Authors: Kelleher CL, Buckalew VM, Frederickson ED, Rhodes DJ, Conner DA, Seidman JG, Seidman CE.
Kidney Int
View full abstract on Pubmed
beta-Arrestin1 knockout mice appear normal but demonstrate altered cardiac responses to beta-adrenergic stimulation.
Authors: Authors: Conner DA, Mathier MA, Mortensen RM, Christe M, Vatner SF, Seidman CE, Seidman JG.
Circ Res
View full abstract on Pubmed