M Fellous
Impact in
- Reproductive Medicine top 2%
- Sperm and Testicular Function
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
-
- Sexual Differentiation and Disorders 9
- Renal and related cancers 3
- Genomics and Chromatin Dynamics 1
- Genetics 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
- Genetics and Neurodevelopmental Disorders 1
- Animal Genetics and Reproduction 1
- Co-authors
- Ken McElreavey (7 shared papers)Éric Vilain (5 shared papers)N. Abbas (2 shared papers)Ira Herskowitz (1 shared paper)F Jaubert (2 shared papers)F Richaud (2 shared papers)Reiner A. Veitia (2 shared papers)Claire Nihoul‐Feketé (3 shared papers)
In The Last Decade
M Fellous
15 papers receiving 806 citations
Peers
Comparison fields: 5 of 46
- Reproductive Medicine 290
- Genetics 726
- Urology 93
- Molecular Biology 656
- Nephrology 30
Countries citing papers authored by M Fellous
This map shows the geographic impact of M 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 M Fellous with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Fellous more than expected).
Fields of papers citing papers by M Fellous
This network shows the impact of papers produced by M 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 M Fellous. The network helps show where M Fellous may publish in the future.
Co-authors
The 25 scholars most cited alongside M 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
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 308 | |
| 2 | 1992 | 95 | |
| 3 | 2000 | 78 | |
| 4 | 2000 | 78 | |
| 5 | Familial case with sequence variant in the testis-determining region associated with two sex phenotypes. | 1992 | 71 |
| 6 | A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome. | 1996 | 57 |
| 7 | 1993 | 43 | |
| 8 | Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. | 1993 | 43 |
| 9 | 2008 | 38 | |
| 10 | 1993 | 27 | |
| 11 | 1990 | 25 | |
| 12 | Gonad development in Drash and Frasier syndromes depends on WT1 mutations. | 2004 | 10 |
| 13 | 2012 | 9 | |
| 14 | [beta2-Microglobulin in human seminal fluid (author's transl)]. | 1978 | 3 |
| 15 | 1986 | 1 | |
| 16 | [Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)]. | 1980 | 1 |
About M Fellous
M Fellous is a scholar working on Molecular Biology, Genetics, Reproductive Medicine, Pediatrics, Perinatology and Child Health and Urology, having authored 16 papers that have together received 887 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Sexual Differentiation and Disorders (9 papers), Sperm and Testicular Function (7 papers), Renal and related cancers (3 papers), Genomics and Chromatin Dynamics (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Animal Genetics and Reproduction (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Reproductive Medicine (290 citations), Genetics (726 citations), Urology (93 citations), Molecular Biology (656 citations) and Nephrology (30 citations). M Fellous has collaborated with scholars based in France, Italy and Egypt. Frequent co-authors include Ken McElreavey, Éric Vilain, N. Abbas, Ira Herskowitz, F Jaubert, F Richaud, Reiner A. Veitia, Claire Nihoul‐Feketé, Roland Berger and Francis Jaubert. Their work appears in journals such as Human Genetics, European Journal of Biochemistry, Pediatric Research, The Journal of Urology and Genomics.
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.