Christine E. Seidman
Impact in
- Cardiology and Cardiovascular Medicine top 0.01%
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Viral Infections and Immunology Research
- Cardiovascular Function and Risk Factors
- Cardiac electrophysiology and arrhythmias
- Molecular Biology top 0.05%
- Congenital heart defects research
- Muscle Physiology and Disorders
Papers in
-
- Congenital heart defects research 93
- Muscle Physiology and Disorders 38
- Ion channel regulation and function 25
-
- Cardiomyopathy and Myosin Studies 212
- Cardiovascular Effects of Exercise 78
- Viral Infections and Immunology Research 61
- Cardiovascular Function and Risk Factors 34
- Cardiac electrophysiology and arrhythmias 34
- Co-authors
- Jonathan G. Seidman (222 shared papers)Barry J. Maron (26 shared papers)J G Seidman (46 shared papers)William J. McKenna (22 shared papers)J.G. Seidman (47 shared papers)Jeffrey A. Towbin (12 shared papers)Hugh Watkins (24 shared papers)David A. Conner (23 shared papers)
- Journals
- Circulation (44 papers)Journal of Clinical Investigation (34 papers)Circulation Research (30 papers)Proceedings of the National Academy of Sciences (18 papers)New England Journal of Medicine (14 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Christine E. Seidman
409 papers receiving 44.4k citations
Christine E. Seidman's Hit Papers
Peers
Comparison fields: 5 of 180
- Cardiology and Cardiovascular Medicine 28.1k
- Molecular Biology 24.1k
- Nephrology 1.6k
- Developmental Neuroscience 940
- Epidemiology 5.2k
Countries citing papers authored by Christine E. Seidman
This map shows the geographic impact of Christine E. Seidman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christine E. Seidman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christine E. Seidman more than expected).
Fields of papers citing papers by Christine E. Seidman
This network shows the impact of papers produced by Christine E. Seidman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christine E. Seidman. The network helps show where Christine E. Seidman may publish in the future.
Co-authors
The 25 scholars most cited alongside Christine E. Seidman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 416 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Contemporary Definitions and Classification of the Cardiomyopathies Hit paper breakdown → | 2006 | 2222 |
| 2 | 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy Hit paper breakdown → | 2011 | 1597 |
| 3 | Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease Hit paper breakdown → | 1999 | 984 |
| 4 | A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation Hit paper breakdown → | 1990 | 975 |
| 5 | Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5 Hit paper breakdown → | 1998 | 944 |
| 6 | 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy Hit paper breakdown → | 2011 | 869 |
| 7 | Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome Hit paper breakdown → | 1997 | 787 |
| 8 | α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere Hit paper breakdown → | 1994 | 779 |
| 9 | The Genetic Basis for Cardiomyopathy Hit paper breakdown → | 2001 | 767 |
| 10 | Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Hit paper breakdown → | 1993 | 739 |
| 11 | The Management of Hypertrophic Cardiomyopathy Hit paper breakdown → | 1997 | 688 |
| 12 | Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy Hit paper breakdown → | 1995 | 673 |
| 13 | 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: Executive Summary Hit paper breakdown → | 2011 | 585 |
| 14 | A human MSX1 homeodomain missense mutation causes selective tooth agenesis Hit paper breakdown → | 1996 | 565 |
| 15 | Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy Hit paper breakdown → | 2000 | 527 |
| 16 | Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy Hit paper breakdown → | 1992 | 526 |
| 17 | Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline Hit paper breakdown → | 2009 | 493 |
| 18 | Myocardial Fibrosis as an Early Manifestation of Hypertrophic Cardiomyopathy Hit paper breakdown → | 2010 | 484 |
| 19 | A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice Hit paper breakdown → | 2016 | 467 |
| 20 | 2003 | 460 |
About Christine E. Seidman
Christine E. Seidman is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Genetics, Epidemiology and Surgery, having authored 416 papers that have together received 45.6k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (212 papers), Congenital heart defects research (93 papers), Cardiovascular Effects of Exercise (78 papers), Viral Infections and Immunology Research (61 papers), Muscle Physiology and Disorders (38 papers), Cardiovascular Function and Risk Factors (34 papers), Cardiac electrophysiology and arrhythmias (34 papers) and Ion channel regulation and function (25 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (28.1k citations), Molecular Biology (24.1k citations), Nephrology (1.6k citations), Developmental Neuroscience (940 citations) and Epidemiology (5.2k citations). Christine E. Seidman has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Jonathan G. Seidman, Barry J. Maron, J G Seidman, William J. McKenna, J.G. Seidman, Jeffrey A. Towbin, Hugh Watkins, David A. Conner, Michael Arad and Ludwig Thierfelder. Their work appears in journals such as Circulation, Journal of Clinical Investigation, Circulation Research, Proceedings of the National Academy of Sciences and New England Journal of Medicine.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.