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Author
Christine E. Seidman
also known as C E Seidman, C SEIDMAN, C Seidman
Harvard University · University of Utah · Roosevelt University · Kagoshima University
About this author
Works
707
Cited by
91,364
h-index
151
i10
467
ORCID ↗
Top papers
Contemporary Definitions and Classification of the Cardiomyopathies
Barry J. Maron, Jeffrey A. Towbin, Gaetano Thiene, et al.
·
2006
·
Circulation
↗ 3,395
Fulminant Myocarditis with Combination Immune Checkpoint Blockade
Douglas B. Johnson, Justin M. Balko, Margaret Compton, et al.
·
2016
·
New England Journal of Medicine
↗ 2,236
OA
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
Bernard J. Gersh, Barry J. Maron, Robert O. Bonow, et al.
·
2011
·
Circulation
↗ 2,113
OA
Cells of the adult human heart
Monika Litviňuková, Carlos Talavera‐López, Henrike Maatz, et al.
·
2020
·
Nature
↗ 1,726
OA
American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy
Barry J. Maron, William J. McKenna, Gordon K. Danielson, et al.
·
2003
·
Journal of the American College of Cardiology
↗ 1,576
OA
Truncations of Titin Causing Dilated Cardiomyopathy
Daniel S. Herman, Lien Lam, Matthew R.G. Taylor, et al.
·
2012
·
New England Journal of Medicine
↗ 1,456
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
Anja A. T. Geisterfer-Lowrance, Susan Kass, G Tanigawa, et al.
·
1990
·
Cell
↗ 1,385
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
Diane Fatkin, Calum A. MacRae, Takeshi Sasaki, et al.
·
1999
·
New England Journal of Medicine
↗ 1,345
OA
Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i>
Jean‐Jacques Schott, D. Woodrow Benson, Craig T. Basson, et al.
·
1998
·
Science
↗ 1,303
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
Bernard J. Gersh, Barry J. Maron, Robert O. Bonow, et al.
·
2011
·
Journal of the American College of Cardiology
↗ 1,273
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
Craig T. Basson, David R. Bachinsky, Robert C. Lin, et al.
·
1997
·
Nature Genetics
↗ 1,105
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
Martin R. Pollak, Edward M. Brown, Yah‐Huei Wu Chou, et al.
·
1993
·
Cell
↗ 1,051