M Fellous

1.1k citations
16 papers · 924 · h-index 12

Impact in

    • Sperm and Testicular Function
  • Genetics top 5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Animal Genetics and Reproduction

Papers in

    • Sperm and Testicular Function 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
    • Animal Genetics and Reproduction 1
    • Genetic diversity and population structure 1

M Fellous

16 papers receiving 840 citations

Peers

M Fellous
Comparison fields: 5 of 49
  • Reproductive Medicine 289
  • Genetics 750
  • Urology 99
  • Molecular Biology 687
  • Nephrology 31
Replace Joëlle Bignon‐Topalovic with:
Joëlle Bignon‐Topalovic France
Lucile Gouédard France
Jocelyn A. van den Bergen Australia
Christopher Tilmann United States
Fernando Pierucci‐Alves United States
Radu Harbuz France
Miriam Post Netherlands
Saunders T. Ching United States
Wen-Hui Shen China
Jocelyn van den Bergen Australia
M Fellous relative to Joëlle Bignon‐Topalovic France Joëlle Bignon‐Topalovic's profile →
Citations per field
00.5×5×10×15.5×
Joëlle Bignon‐Topalovic · 1×
Citations per year

Countries citing papers authored by M Fellous

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

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

All Works

16 of 16 papers shown
#Work
1 1993312
2 199298
3 200080
4 200080
5
Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.
199274
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.
199657
7
Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.
199346
8 199344
9 200838
10 199328
11 199025
12 200219
13
Gonad development in Drash and Frasier syndromes depends on WT1 mutations.
20049
14 20129
15 20054
16 19861

About M Fellous

M Fellous is a scholar working on Reproductive Medicine, Genetics, Molecular Biology, Urology and Archeology, having authored 16 papers that have together received 924 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 (6 papers), Renal and related cancers (3 papers), Animal Genetics and Reproduction (1 paper), CRISPR and Genetic Engineering (1 paper), Genetic diversity and population structure (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Reproductive Medicine (289 citations), Genetics (750 citations), Urology (99 citations), Molecular Biology (687 citations) and Nephrology (31 citations). M Fellous has collaborated with scholars based in France, Italy and Cuba. Frequent co-authors include Ken McElreavey, Eric J. N. Vilain, N. Abbas, Ira Herskowitz, Francis Jaubert, Fran�ois Richaud, Reiner A. Veitia, Francis Jaubert, Claire Nihoul‐Feketé and Roland Berger. Their work appears in journals such as Human Genetics, Bulletins et Mémoires de la Société d anthropologie de Paris, Differentiation, Kidney International 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.

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