Barbara McDonough - Concepedia

Author

Barbara McDonough

Also Known As

B McDonough, B. MCDONOUGH, B. McDonough, BARBARA MCDONOUGH, Barbara A. McDonough, Barbara McDonough, Calum MacRae, Mark McCarthy, McDonough, Barbara

Publications

8.3K

Citations

H-Index

Concepts

All Affiliations

Harvard University Howard Hughes Medical Institute Brigham and Women's Hospital Boston Children's Hospital German Centre for Cardiovascular Research

About

Barbara McDonough is an author at Harvard University specializing in medicine, genetics, and cardiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	601
2	Health Sciences	2	2	63
3	Cell Biology	2	2	242
4	Cellular Physiology	1	1	20
5	Hearing Sciences	1	1	51

Barbara McDonough

Publications

7.9K

Citations

H-Index

Page 1

	Year	Citations
Cells of the adult human heart Monika Litviňuková, Carlos Talavera‐López, Henrike Maatz, Nature	2020	1.7K
Truncations of Titin Causing Dilated Cardiomyopathy Daniel S. Herman, Lien Lam, Matthew R.G. Taylor, New England Journal of Medicine	2012	1.4K
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, New England Journal of Medicine	1999	1.3K
Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy Mitsuhiro Kamisago, Sapna Sharma, Steven R. DePalma, New England Journal of Medicine	2000	724
Assessment of Diastolic Function With Doppler Tissue Imaging to Predict Genotype in Preclinical Hypertrophic Cardiomyopathy Carolyn Y. Ho, Nancy K. Sweitzer, Barbara McDonough, Circulation	2002	421
Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults Hiroyuki Morita, Heidi L. Rehm, Andres Menesses, New England Journal of Medicine	2008	407
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies Daniel Reichart, Eric L. Lindberg, Henrike Maatz, Science Cardiac MuscleHeart FailureGeneticsCardiac Progenitor CellsCongenital Heart Anomaly	2022	222
Missense Mutations in the<i>BCS1L</i>Gene as a Cause of the Björnstad Syndrome J. Travis Hinson, Valeria R. Fantin, Jost Schönberger, New England Journal of Medicine	2007	210
Hypertrophic cardiomyopathy mutations in <i>MYBPC3</i> dysregulate myosin Christopher N. Toepfer, Hiroko Wakimoto, Amanda C. Garfinkel, Science Translational Medicine	2019	207
The Congenital Heart Disease Genetic Network Study Bruce D. Gelb, Martina Brueckner, Wendy Chung, Circulation Research Heart FailureCongenital Heart DefectsPediatric Heart DiseaseGeneticsGenetic Epidemiology	2013	166

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