Robert Dumas
Impact in
- Nephrology top 10%
- Renal Diseases and Glomerulopathies
- Urology top 10%
- Urological Disorders and Treatments
Papers in
-
- Sexual Differentiation and Disorders 4
- Renal and related cancers 4
- Genetics 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Co-authors
- Philippe Berta (5 shared papers)Charles Sultan (4 shared papers)Charles Belon (6 shared papers)Chantal Loirat (2 shared papers)Michel Fischbach (2 shared papers)Maud Dehennault (2 shared papers)E. Bérard (2 shared papers)Philippe Eckart (2 shared papers)
- Journals
- Archives of Disease in Childhood (3 papers)Human Genetics (2 papers)Pediatric Nephrology (2 papers)Human Mutation (2 papers)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- FranceUnited StatesHungary
In The Last Decade
Robert Dumas
49 papers receiving 347 citations
Peers
Comparison fields: 5 of 79
- Nephrology 63
- Urology 49
- Genetics 116
- Pediatrics, Perinatology and Child Health 62
- Molecular Biology 185
Countries citing papers authored by Robert Dumas
This map shows the geographic impact of Robert Dumas'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 Robert Dumas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Dumas more than expected).
Fields of papers citing papers by Robert Dumas
This network shows the impact of papers produced by Robert Dumas. 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 Robert Dumas. The network helps show where Robert Dumas may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Dumas, 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 | 1999 | 51 | |
| 2 | 1992 | 42 | |
| 3 | 2005 | 27 | |
| 4 | 1980 | 23 | |
| 5 | 1993 | 22 | |
| 6 | 1999 | 22 | |
| 7 | 1971 | 22 | |
| 8 | Syndrome néphrotique pur (ou néphrose) corticosensible de l'enfant: Protocole de traitement proposé par la Société de Néphrologie Pédiatrique☆ | 2005 | 19 |
| 9 | 1993 | 13 | |
| 10 | 1992 | 13 | |
| 11 | 1997 | 11 | |
| 12 | 1996 | 9 | |
| 13 | 1993 | 8 | |
| 14 | 1986 | 8 | |
| 15 | 1999 | 8 | |
| 16 | 1985 | 7 | |
| 17 | 1996 | 6 | |
| 18 | 1981 | 6 | |
| 19 | 1999 | 5 | |
| 20 | [Hereditary deficiency of the 4th component of complement (C4) associated with a lupic syndrome]. | 1986 | 4 |
About Robert Dumas
Robert Dumas is a scholar working on Molecular Biology, Genetics, Nephrology, Pulmonary and Respiratory Medicine and Surgery, having authored 51 papers that have together received 376 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Renal Diseases and Glomerulopathies (4 papers), Sexual Differentiation and Disorders (4 papers), Renal and related cancers (4 papers), Parathyroid Disorders and Treatments (4 papers), Neonatal Health and Biochemistry (3 papers), Agriculture and Rural Development Research (3 papers) and Electrolyte and hormonal disorders (3 papers). The work is most often cited by research in Nephrology (63 citations), Urology (49 citations), Genetics (116 citations), Pediatrics, Perinatology and Child Health (62 citations) and Molecular Biology (185 citations). Robert Dumas has collaborated with scholars based in France, United States and Hungary. Frequent co-authors include Philippe Berta, Charles Sultan, Charles Belon, Chantal Loirat, Michel Fischbach, Maud Dehennault, E. Bérard, Philippe Eckart, R. Medlej and M. Broyer. Their work appears in journals such as Archives of Disease in Childhood, Human Genetics, Pediatric Nephrology, Human Mutation and Journal of Inherited Metabolic Disease.
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.