James S. Ware
Impact in
-
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Cardiac electrophysiology and arrhythmias
- Genetics top 0.1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Papers in
-
- Cardiomyopathy and Myosin Studies 91
- Cardiac electrophysiology and arrhythmias 24
- Cardiovascular Effects of Exercise 23
- Genetics 67
- Genomics and Rare Diseases 47
- Genetic Associations and Epidemiology 16
- Co-authors
- Michael Simons (9 shared papers)Robert E. Tarone (2 shared papers)Marie Tarrant (6 shared papers)Stuart A. Cook (36 shared papers)Kenneth Craig Kent (10 shared papers)Shaoqing Tang (7 shared papers)Roddy Walsh (25 shared papers)Anthony W. Ashton (8 shared papers)
- Journals
- Circulation (28 papers)European Heart Journal (21 papers)Journal of the American College of Cardiology (18 papers)Genetics in Medicine (16 papers)Journal of Biological Chemistry (15 papers)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
James S. Ware
388 papers receiving 38.9k citations
James S. Ware's Hit Papers
Peers
Comparison fields: 5 of 207
- Cardiology and Cardiovascular Medicine 11.4k
- Genetics 8.8k
- Molecular Biology 14.0k
- Cancer Research 2.3k
- Genetics 1.3k
Countries citing papers authored by James S. Ware
This map shows the geographic impact of James S. Ware'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 James S. Ware with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James S. Ware more than expected).
Fields of papers citing papers by James S. Ware
This network shows the impact of papers produced by James S. Ware. 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 James S. Ware. The network helps show where James S. Ware may publish in the future.
Co-authors
The 25 scholars most cited alongside James S. Ware, 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 410 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Analysis of protein-coding genetic variation in 60,706 humans Hit paper breakdown → | 2016 | 7751 |
| 2 | The mutational constraint spectrum quantified from variation in 141,456 humans Hit paper breakdown → | 2020 | 6616 |
| 3 | 2023 ESC Guidelines for the management of cardiomyopathies Hit paper breakdown → | 2023 | 1451 |
| 4 | A genomic mutational constraint map using variation in 76,156 human genomes Hit paper breakdown → | 2023 | 736 |
| 5 | A structural variation reference for medical and population genetics Hit paper breakdown → | 2020 | 636 |
| 6 | De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies Hit paper breakdown → | 2015 | 622 |
| 7 | Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy Hit paper breakdown → | 2018 | 621 |
| 8 | Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples Hit paper breakdown → | 2016 | 594 |
| 9 | 1977 | 581 | |
| 10 | Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies Hit paper breakdown → | 2016 | 472 |
| 11 | Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial Hit paper breakdown → | 2018 | 453 |
| 12 | 1986 | 406 | |
| 13 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 395 |
| 14 | 2015 | 382 | |
| 15 | Evidence-Based Assessment of Genes in Dilated Cardiomyopathy Hit paper breakdown → | 2021 | 353 |
| 16 | 1999 | 342 | |
| 17 | 2017 | 333 | |
| 18 | Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes Hit paper breakdown → | 2019 | 330 |
| 19 | 1994 | 317 | |
| 20 | 2018 | 283 |
About James S. Ware
James S. Ware is a scholar working on Cardiology and Cardiovascular Medicine, Genetics, Molecular Biology, Physiology and Immunology and Allergy, having authored 410 papers that have together received 40.3k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (91 papers), Genomics and Rare Diseases (47 papers), Cardiac electrophysiology and arrhythmias (24 papers), Cardiovascular Effects of Exercise (23 papers), Protein Kinase Regulation and GTPase Signaling (21 papers), Congenital heart defects research (21 papers), Angiogenesis and VEGF in Cancer (17 papers) and Genetic Associations and Epidemiology (16 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (11.4k citations), Genetics (8.8k citations), Molecular Biology (14.0k citations), Cancer Research (2.3k citations) and Genetics (1.3k citations). James S. Ware has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Michael Simons, Robert E. Tarone, Marie Tarrant, Stuart A. Cook, Kenneth Craig Kent, Shaoqing Tang, Roddy Walsh, Anthony W. Ashton, E W Salzman and Malay K. Raychowdhury. Their work appears in journals such as Circulation, European Heart Journal, Journal of the American College of Cardiology, Genetics in Medicine and Journal of Biological Chemistry.
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.