Craig T. Basson - Concepedia

Author

Craig T. Basson

Also Known As

Basson, Craig, C Basson, C T Basson, C. BASSON, C. Basson, CRAIG T. BASSON, Craig Basson, Craig T Basson, Craig T. Basson, Craig Todd Basson

137

Publications

11.9K

Citations

H-Index

132

Concepts

All Affiliations

Cornell University Harvard University Brigham and Women's Hospital Howard Hughes Medical Institute Johns Hopkins University

About

Craig T. Basson is an author at Cornell University specializing in medicine, cardiology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	32	4.6K
2	Public Health	7	7	569
3	Natural Sciences	3	3	145
4	Engineering	2	2	174
5	Health Sciences	2	2	251

Craig T. Basson

Publications

9.5K

Citations

H-Index

Page 1

	Year	Citations
Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i> Jean‐Jacques Schott, D. Woodrow Benson, Craig T. Basson, Science	1998	1.3K
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome Craig T. Basson, David R. Bachinsky, Robert C. Lin, Nature Genetics Developmental AnomalyCardiac MalformationDevelopmental BiologyHuman Cause LimbGenetic Disorder	1997	1.1K
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy Brenda Gerull, Arnd Heuser, Thomas Wichter, Nature Genetics Cardiac MuscleCardiomyopathyHeart FailureStructural Heart DiseaseGenetics	2004	822
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome) Craig T. Basson, Glenn S. Cowley, Scott D. Solomon, New England Journal of Medicine	1994	392
Different <i>TBX5</i> interactions in heart and limb defined by Holt–Oram syndrome mutations Craig T. Basson, Taosheng Huang, Robert C. Lin, Proceedings of the National Academy of Sciences	1999	365
<i>TET2</i>-Driven Clonal Hematopoiesis and Response to Canakinumab E. C. Svensson, Aviv Madar, Catarina D. Campbell, JAMA Cardiology	2022	333
Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex Mairead Casey, Carl J. Vaughan, Jie He, Journal of Clinical Investigation	2000	276
Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy Arnd Heuser, Eva Plovie, Patrick T. Ellinor, The American Journal of Human Genetics Cardiac MuscleCardiomyopathyHeart FailureMolecular PhysiologyCardiovascular Disease	2006	258
Secreted Frizzled-related protein 2 is a procollagen C proteinase enhancer with a role in fibrosis associated with myocardial infarction Koichi S. Kobayashi, Min Luo, Yue Zhang, Nature Cell Biology InflammationFibrosisCardiovascular DiseasePathologyFrizzled-related Protein 2	2008	220
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. Calum A. MacRae, Nitin Ghaisas, Susan Kass, Journal of Clinical Investigation Wolff-parkinson-white Syndrome MapsCardiomyopathyDisease LocusMendelian DisorderFamilial Hypertrophic Cardiomyopathy	1995	219

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