David Fasel

3.0k citations
8 papers · 233 · h-index 7

Impact in

  • Nephrology top 10%
    • Renal Diseases and Glomerulopathies
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Genetic Associations and Epidemiology
    • Genetic and Kidney Cyst Diseases

Papers in

    • Genomics and Rare Diseases 3
    • BRCA gene mutations in cancer 2
    • Genetic Mapping and Diversity in Plants and Animals 1
    • Genetic Associations and Epidemiology 1
    • Epigenetics and DNA Methylation 1

David Fasel

8 papers receiving 231 citations

Peers

David Fasel
Comparison fields: 5 of 44
  • Nephrology 57
  • Genetics 92
  • Urology 16
  • Pediatrics, Perinatology and Child Health 48
  • Immunology and Allergy 15
Replace Brigitte Leroy with:
Brigitte Leroy France
Yasufumi Ohtsuka Japan
V. Steinbicker Germany
C. Steinkamm Germany
Camille Humbert France
Fabian Küpper Germany
Charles D. Madsen United States
Leah Contrino United States
Guilherme De Sena Brandine United States
Zeineb Bakey Germany
David Fasel relative to Brigitte Leroy France Brigitte Leroy's profile →
Citations per field
00.5×7.1×
Brigitte Leroy · 1×
Citations per year

Countries citing papers authored by David Fasel

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with David Fasel Line = papers co-authored together David Fasel links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1 201555
2 201551
3 201846
4 202026
5 202021
6 202018
7 202310
8 20216

About David Fasel

David Fasel is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Nephrology and Pathology and Forensic Medicine, having authored 8 papers that have together received 233 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Ethics in Clinical Research (2 papers), BRCA gene mutations in cancer (2 papers), Celiac Disease Research and Management (1 paper), Epigenetics and DNA Methylation (1 paper), Genetic Mapping and Diversity in Plants and Animals (1 paper), Renal Diseases and Glomerulopathies (1 paper) and Genetic Associations and Epidemiology (1 paper). The work is most often cited by research in Nephrology (57 citations), Genetics (92 citations), Urology (16 citations), Pediatrics, Perinatology and Child Health (48 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, Hila Milo Rasouly, Vivette D. D’Agati, Emily Groopman and Gian Marco Ghiggeri. Their work appears in journals such as Pediatric Research, Kidney International Reports, Annals of Internal Medicine, Journal of Clinical Investigation 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.

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