David Fasel
Impact in
- Nephrology top 10%
- Renal Diseases and Glomerulopathies
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- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genetic Associations and Epidemiology
Papers in
- Genetics 6
- Genomics and Rare Diseases 4
- BRCA gene mutations in cancer 2
- Genetic Associations and Epidemiology 1
- Genetic Mapping and Diversity in Plants and Animals 1
- Co-authors
- Ali G. Gharavi (6 shared papers)Simone Sanna‐Cherchi (4 shared papers)Miguel Verbitsky (2 shared papers)Chunhua Weng (5 shared papers)Rik Westland (2 shared papers)Wendy K. Chung (4 shared papers)Krzysztof Kiryluk (2 shared papers)Gian Marco Ghiggeri (2 shared papers)
- Journals
- The American Journal of Human Genetics (1 paper)Annals of Internal Medicine (1 paper)Kidney International Reports (1 paper)Pediatric Research (1 paper)Kidney International (1 paper)
- Partner nations
- United StatesItalyBelgium
In The Last Decade
David Fasel
8 papers receiving 226 citations
Peers
Comparison fields: 5 of 50
- Nephrology 73
- Genetics 111
- Urology 23
- Pediatrics, Perinatology and Child Health 62
- Immunology and Allergy 15
Countries citing papers authored by David Fasel
This map shows the geographic impact of David Fasel'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 Fasel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Fasel more than expected).
Fields of papers citing papers by David Fasel
This network shows the impact of papers produced by David Fasel. 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 Fasel. The network helps show where David Fasel may publish in the future.
Co-authors
The 25 scholars most cited alongside David Fasel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 54 | |
| 2 | 2015 | 51 | |
| 3 | 2018 | 46 | |
| 4 | 2020 | 26 | |
| 5 | 2020 | 19 | |
| 6 | 2020 | 17 | |
| 7 | 2023 | 9 | |
| 8 | 2021 | 6 |
About David Fasel
David Fasel is a scholar working on Genetics, Molecular Biology, Nephrology, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 8 papers that have together received 228 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Renal Diseases and Glomerulopathies (2 papers), BRCA gene mutations in cancer (2 papers), Ethics in Clinical Research (2 papers), Metabolism and Genetic Disorders (1 paper), Genetic Associations and Epidemiology (1 paper), Genetic Mapping and Diversity in Plants and Animals (1 paper) and Celiac Disease Research and Management (1 paper). The work is most often cited by research in Nephrology (73 citations), Genetics (111 citations), Urology (23 citations), Pediatrics, Perinatology and Child Health (62 citations) and Immunology and Allergy (15 citations). David Fasel has collaborated with scholars based in United States, Italy and Belgium. Frequent co-authors include Ali G. Gharavi, Simone Sanna‐Cherchi, Miguel Verbitsky, Chunhua Weng, Rik Westland, Wendy K. Chung, Krzysztof Kiryluk, Gian Marco Ghiggeri, Hila Milo Rasouly and Vivette D. D’Agati. Their work appears in journals such as The American Journal of Human Genetics, Annals of Internal Medicine, Kidney International Reports, Pediatric Research and Kidney International.
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.