D. David
Impact in
-
- Cardiac electrophysiology and arrhythmias
- Heart Rate Variability and Autonomic Control
- Cardiac Health and Mental Health
- Hematology top 5%
- Hemophilia Treatment and Research
Papers in
-
- Cancer-related gene regulation 7
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Ilan Kutz (2 shared papers)Simcha Meisel (2 shared papers)Katia Dayan (1 shared paper)Yaron Arbel (1 shared paper)Beatrice Nolan (1 shared paper)Thomas A. Mellman (1 shared paper)Maria Guida Boavida (5 shared papers)Andreas Gal (4 shared papers)
- Journals
- Circulation (5 papers)Human Genetics (3 papers)Human Mutation (3 papers)Inflammatory Bowel Diseases (2 papers)Clinical Genetics (2 papers)
- Partner nations
- PortugalUnited StatesMozambique
In The Last Decade
D. David
51 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 103
- Cardiology and Cardiovascular Medicine 518
- Hematology 156
- Genetics 269
- Experimental and Cognitive Psychology 106
- Radiology, Nuclear Medicine and Imaging 169
Countries citing papers authored by D. David
This map shows the geographic impact of D. David'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 D. David with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. David more than expected).
Fields of papers citing papers by D. David
This network shows the impact of papers produced by D. David. 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 D. David. The network helps show where D. David may publish in the future.
Co-authors
The 25 scholars most cited alongside D. David, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 294 | |
| 2 | 2000 | 289 | |
| 3 | 1995 | 153 | |
| 4 | 1983 | 148 | |
| 5 | 1982 | 90 | |
| 6 | Post-traumatic stress disorder in myocardial infarction patients: prevalence study. | 1994 | 88 |
| 7 | 1993 | 77 | |
| 8 | 2005 | 46 | |
| 9 | 1981 | 38 | |
| 10 | 1983 | 35 | |
| 11 | 1976 | 31 | |
| 12 | 1994 | 29 | |
| 13 | 2003 | 29 | |
| 14 | The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patients. | 2006 | 25 |
| 15 | 1999 | 23 | |
| 16 | 2000 | 20 | |
| 17 | 2013 | 16 | |
| 18 | 2003 | 15 | |
| 19 | 2014 | 14 | |
| 20 | 1997 | 14 |
About D. David
D. David is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Hematology and Radiology, Nuclear Medicine and Imaging, having authored 53 papers that have together received 1.7k indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Cancer-related gene regulation (7 papers), Blood Coagulation and Thrombosis Mechanisms (6 papers), Cardiac electrophysiology and arrhythmias (5 papers), Platelet Disorders and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (518 citations), Hematology (156 citations), Genetics (269 citations), Experimental and Cognitive Psychology (106 citations) and Radiology, Nuclear Medicine and Imaging (169 citations). D. David has collaborated with scholars based in Portugal, United States and Mozambique. Frequent co-authors include Ilan Kutz, Simcha Meisel, Katia Dayan, Yaron Arbel, Beatrice Nolan, Thomas A. Mellman, Maria Guida Boavida, Andreas Gal, Eric L. Michelson and Masahito Naito. Their work appears in journals such as Circulation, Human Genetics, Human Mutation, Inflammatory Bowel Diseases and Clinical Genetics.
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.