Marc Fellous
Impact in
- Reproductive Medicine top 0.2%
- Sperm and Testicular Function
- Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
- Genetics 107
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 83
- Animal Genetics and Reproduction 20
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- Sexual Differentiation and Disorders 62
- Renal and related cancers 13
- Co-authors
- Reiner A. Veitia (32 shared papers)Ken McElreavey (39 shared papers)Andrew Sinclair (3 shared papers)Philippe Berta (2 shared papers)Peter N. Goodfellow (2 shared papers)Frédéric Rosa (6 shared papers)Sandrine Barbaux (18 shared papers)B Griffiths (1 shared paper)
- Journals
- Genomics (9 papers)Human Genetics (8 papers)Nature (7 papers)Proceedings of the National Academy of Sciences (7 papers)Annals of Human Genetics (5 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Marc Fellous
175 papers receiving 9.4k citations
Marc Fellous's Hit Papers
Peers
Comparison fields: 5 of 144
- Reproductive Medicine 2.0k
- Genetics 5.7k
- Urology 534
- Molecular Biology 5.5k
- Immunology 1.3k
Countries citing papers authored by Marc Fellous
This map shows the geographic impact of Marc Fellous'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 Marc Fellous with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc Fellous more than expected).
Fields of papers citing papers by Marc Fellous
This network shows the impact of papers produced by Marc Fellous. 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 Marc Fellous. The network helps show where Marc Fellous may publish in the future.
Co-authors
The 25 scholars most cited alongside Marc Fellous, 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 179 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic evidence equating SRY and the testis-determining factor Hit paper breakdown → | 1990 | 808 |
| 2 | Donor splice-site mutations in WT1 are responsible for Frasier syndrome Hit paper breakdown → | 1997 | 563 |
| 3 | 2001 | 285 | |
| 4 | 1989 | 260 | |
| 5 | 1989 | 257 | |
| 6 | 2002 | 252 | |
| 7 | 1982 | 242 | |
| 8 | 1986 | 230 | |
| 9 | 2014 | 220 | |
| 10 | 2006 | 219 | |
| 11 | 1983 | 213 | |
| 12 | 2003 | 199 | |
| 13 | 2004 | 184 | |
| 14 | 1984 | 163 | |
| 15 | 1989 | 157 | |
| 16 | 1978 | 151 | |
| 17 | 1984 | 147 | |
| 18 | 1977 | 137 | |
| 19 | 1986 | 128 | |
| 20 | 1970 | 128 |
About Marc Fellous
Marc Fellous is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Immunology and Public Health, Environmental and Occupational Health, having authored 179 papers that have together received 10.0k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (83 papers), Sexual Differentiation and Disorders (62 papers), Sperm and Testicular Function (30 papers), Animal Genetics and Reproduction (20 papers), T-cell and B-cell Immunology (17 papers), Reproductive Biology and Fertility (15 papers), Chromosomal and Genetic Variations (14 papers) and Renal and related cancers (13 papers). The work is most often cited by research in Reproductive Medicine (2.0k citations), Genetics (5.7k citations), Urology (534 citations), Molecular Biology (5.5k citations) and Immunology (1.3k citations). Marc Fellous has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Reiner A. Veitia, Ken McElreavey, Andrew Sinclair, Philippe Berta, Peter N. Goodfellow, Frédéric Rosa, Sandrine Barbaux, B Griffiths, Francis Jaubert and Daniel Vaiman. Their work appears in journals such as Genomics, Human Genetics, Nature, Proceedings of the National Academy of Sciences and Annals of Human 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.