David Salgado
Impact in
- Genetics top 5%
- Venomous Animal Envenomation and Studies
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 5%
- Muscle Physiology and Disorders
- Biomedical Text Mining and Ontologies
- Developmental Biology and Gene Regulation
- Congenital heart defects research
Papers in
- Genetics 15
- Genomics and Rare Diseases 11
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- Biomedical Text Mining and Ontologies 7
- Muscle Physiology and Disorders 5
- Congenital heart defects research 3
- Molecular Biology Techniques and Applications 2
- Developmental Biology and Gene Regulation 2
- Co-authors
- Jean‐Pierre Desvignes (13 shared papers)Christophe Béroud (16 shared papers)Christophe Marcelle (7 shared papers)Olivier Serralbo (2 shared papers)Anne C. Rios (1 shared paper)Martin Krahn (5 shared papers)Marc Bartoli (4 shared papers)Valérie Delague (1 shared paper)
- Journals
- Human Mutation (8 papers)Database (3 papers)BMC Bioinformatics (2 papers)Bioinformatics (2 papers)Nature Communications (2 papers)
- Partner nations
- FranceSpainUnited Kingdom
In The Last Decade
David Salgado
50 papers receiving 3.6k citations
David Salgado's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 298
- Molecular Biology 1.8k
- Genetics 727
- Health Informatics 36
- Pharmacology 84
Countries citing papers authored by David Salgado
This map shows the geographic impact of David Salgado'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 David Salgado with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Salgado more than expected).
Fields of papers citing papers by David Salgado
This network shows the impact of papers produced by David Salgado. 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 David Salgado. The network helps show where David Salgado may publish in the future.
Co-authors
The 25 scholars most cited alongside David Salgado, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations Hit paper breakdown → | 2015 | 574 |
| 2 | The king cobra genome reveals dynamic gene evolution and adaptation in the snake venom system Hit paper breakdown → | 2013 | 392 |
| 3 | 2015 | 318 | |
| 4 | 2017 | 195 | |
| 5 | 2021 | 179 | |
| 6 | 2018 | 161 | |
| 7 | 2011 | 151 | |
| 8 | 2011 | 136 | |
| 9 | 2017 | 136 | |
| 10 | 2016 | 106 | |
| 11 | 2015 | 101 | |
| 12 | 2008 | 98 | |
| 13 | 2013 | 88 | |
| 14 | 2013 | 88 | |
| 15 | 2017 | 87 | |
| 16 | 2016 | 83 | |
| 17 | 2011 | 74 | |
| 18 | 2019 | 72 | |
| 19 | 2019 | 68 | |
| 20 | 2019 | 65 |
About David Salgado
David Salgado is a scholar working on Genetics, Molecular Biology, Information Systems, Information Systems and Management and Cardiology and Cardiovascular Medicine, having authored 51 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Biomedical Text Mining and Ontologies (7 papers), Research Data Management Practices (6 papers), Muscle Physiology and Disorders (5 papers), Congenital heart defects research (3 papers), Scientific Computing and Data Management (2 papers), Molecular Biology Techniques and Applications (2 papers) and Developmental Biology and Gene Regulation (2 papers). The work is most often cited by research in Genetics (298 citations), Molecular Biology (1.8k citations), Genetics (727 citations), Health Informatics (36 citations) and Pharmacology (84 citations). David Salgado has collaborated with scholars based in France, Spain and United Kingdom. Frequent co-authors include Jean‐Pierre Desvignes, Christophe Béroud, Christophe Marcelle, Olivier Serralbo, Anne C. Rios, Martin Krahn, Marc Bartoli, Valérie Delague, Gwenaëlle Collod‐Béroud and Nicolas Lévy. Their work appears in journals such as Human Mutation, Database, BMC Bioinformatics, Bioinformatics and Nature Communications.
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.