Marc Fellous

12.8k citations

174 papers · 9.0k indexed · 1 hit paper · h-index 54

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

Reproductive Medicine 37
- Sperm and Testicular Function 30
Genetics 108
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 82
- Animal Genetics and Reproduction 21

Co-authors: Reiner A. Veitia Ken McElreavey Frédéric Rosa Andrew Sinclair Philippe Berta Peter N. Goodfellow B Griffiths Sandrine Barbaux
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: France United States Italy

In The Last Decade

Marc Fellous

169 papers receiving 8.7k citations

Hit Papers

align trajectories log scale

Genetic evidence equating SRY and the testis-determining factor 1990 · 734 citations

Peers

Countries citing papers authored by Marc Fellous

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

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

All Works

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20 of 20 papers shown

#	Work
1	Phase 1 Study of Rezatapopt, a p53 Reactivator, in TP53 Y220C–Mutated Tumors New England Journal of Medicine ·D. Neuschütz, Casey Thornton, Aparna R. Parikh, Melissa L. Johnson, Anthony W. Tolcher, John A. Thompson, Jule Bielfeldt, Jeanenne LaMarsh, Zengwen Yan, Dale R. Shepard, 李纪有, Ihnkee Hwang, Leila Alland, Tommi Meskanen, SK Khatik, Marc Fellous, Alison M. Schram	2026	0
2	A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing Human Reproduction ·Matthew S. Bramble, M Piskornik, Allen Lipson, Tuck C. Ngun, Ascia Eskin, Rachel Bae, Marybeth Pereira, 慶彦増渕, Hayk Barseghyan, Eric Lee, Valerie A. Arboleda, Daniel Vaiman, Zafer Yüksel, Marc Fellous, Éric Vilain	2016	63
3	Mutant Cohesin in Premature Ovarian Failure New England Journal of Medicine ·Sandrine Caburet, Valerie A. Arboleda, Elena Llano, Paul A. Overbeek, José Luís Barbero, Kazuhiro Oka, Wilbur R. Harrison, Daniel Vaiman, Ziva Ben‐Neriah, Ignacio García‐Tuñón, Marc Fellous, Alberto M. Pendás, Reiner A. Veitia, Éric Vilain	2014	196
4	North African Jewish and non-Jewish populations form distinctive, orthogonal clusters Proceedings of the National Academy of Sciences ·Christopher Campbell, Pier Francesco Palamara, Maya Dubrovsky, Laura R. Botigué, Marc Fellous, Gil Atzmon, Carole Oddoux, Alexander Pearlman, Hao Li, Brenna M. Henn, Edward R. Burns, Carlos D. Bustamante, David Comas, Eitan Friedman, Itsik Pe’er, Harry Ostrer	2012	43
5	Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) ·Sandrine Caburet, Petra Zavadáková, Ziva Ben‐Neriah, R. Ravishankar, Paul Laissue, Vered Chalifa‐Caspi, Daniel Vaiman, Giovanni Levi, Reiner A. Veitia, Marc Fellous	2012	0
6	The transcription factor FOXL2 in ovarian function and dysfunction. Folia Histochemica et Cytobiologica ·Elfride De Baere, Marc Fellous, Reiner A. Veitia	2010	13
7	Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography The International Journal of Developmental Biology ·Paul Laissue, Gaétan Burgio, David L’Hôte, Gilles Renault, Carmen Marchiol, D Fradelizi, Marc Fellous, Catherine Serres, Xavier Montagutelli, Philippe Monget, Daniel Vaiman	2009	21
8	Genetic investigation of four meiotic genes in women with premature ovarian failure European Journal of Endocrinology ·Béatrice Mandon‐Pepin, Philippe Touraine, Frédérique Kuttenn, Céline Derbois, A. Rouxel, Fumihiko Matsuda, Alain Nicolas, Corinne Cotinot, Marc Fellous	2008	91
9	Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in children Fertility and Sterility ·Nicolas Kalfa, Pascal Philibert, Catherine Patte, Joseph J. Caruso, Pierre Duvillard, Pierre Baldet, Francis Jaubert, Marc Fellous, Charles Sultan	2007	58
10	Infertilité humaine : des gènes de méiose comme candidats potentiels Gynécologie Obstétrique & Fertilité ·Béatrice Mandon‐Pepin, Céline Derbois, Fumihiko Matsuda, Corinne Cotinot, Debra J. Wolgemuth, Kathleen N. Smith, Ken McElreavey, Alain Nicolas, Marc Fellous	2002	14
11	Novel Paralogy Relations Among Human Chromosomes Support a Link between the Phylogeny of doublesex -Related Genes and the Evolution of Sex Determination Genomics ·Chris Ottolenghi, Marc Fellous, Marcello Barbieri, Ken McElreavey	2002	88
12	Uncoordinated HLA-D Gene Expression in a RFXANK -Defective Patient with MHC Class II Deficiency The Journal of Immunology ·Ana‐Maria Lennon‐Duménil, Mohamed‐Ridha Barbouche, Gregg F. Martin, Thomas Prod’homme, Mohamed Béjaoui, Z Detko, Dominique Charron, Marc Fellous, Koussay Dellagi, Catherine Alcaïde‐Loridan	2001	13
13	A 11.7-kb deletion triggers intersexuality and polledness in goats Nature Genetics ·Éric Pailhoux, B. Vigier, Stéphane Chaffaux, Nathalie Servel, Séad Taourit, Jean‐Pierre Furet, Marc Fellous, François Grosclaude, Edmond Cribiu, Corinne Cotinot, Daniel Vaiman	2001	262
14	The Human Doublesex-Related Gene, DMRT2, Is Homologous to a Gene Involved in Somitogenesis and Encodes a Potential Bicistronic Transcript Genomics ·Chris Ottolenghi, Reiner A. Veitia, Marcello Barbieri, Marc Fellous, Ken McElreavey	2000	51
15	The human SRY protein is present in fetal and adult Sertoli cells and germ cells The International Journal of Developmental Biology ·Laura Salas‐Cortés, Francis Jaubert, Sandrine Barbaux, C Nessmann, BS Cheon, Marc Fellous, Ken McElreavey, Mario Rosemblatt	1999	50
16	The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome Cytogenetic and Genome Research ·Reiner A. Veitia, Anne Laurent, Lluís Quintana‐Murci, Chris Ottolenghi, Marc Fellous, Michel Vidaud, Ken McElreavey	1998	5
17	Déterminisme et différenciation sexuels chez l'homme: de la pathologie aux gènes Archives de Pédiatrie ·Reiner A. Veitia, Marta C. Nunes, Ken McElreavey, Marc Fellous	1997	1
18	Dysgerminoma in a Pure 45,X Turner Syndrome: Report of a Case and Review of the Literature Gynecologic Oncology ·J-Y Pierga, Sylvie Giacchetti, Éric Vilain, J.M. Extra, Yves Houde, Theobald Nemetschek, K. B. Luk, Marc Fellous, 차문성	1994	10
19	XY Sex reversal associated with a nonsense mutation in SRY Genomics ·Mariana Rossi Corregliano, Éric Vilain, C. Boucekkine, Michel Vidaud, Yen-Yi Chan, François Richaud, Marc Fellous	1992	49
20	Genetic mapping of a male germ cell-expressed gene Tpx-2 to mouse chromosome 17 Immunogenetics ·Masanori Kasahara, Eric Seboun, Marc Fellous, Sung Yoon Kim	1991	2

About Marc Fellous

Marc Fellous is a scholar working on Reproductive Medicine, Genetics, Molecular Biology, Urology and Immunology, having authored 174 papers that have together received 9.0k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (82 papers), Sexual Differentiation and Disorders (63 papers), Sperm and Testicular Function (30 papers), Animal Genetics and Reproduction (21 papers), Reproductive Biology and Fertility (18 papers), T-cell and B-cell Immunology (17 papers), Renal and related cancers (13 papers) and Chromosomal and Genetic Variations (13 papers). The work is most often cited by research in Reproductive Medicine (2.0k citations), Genetics (5.3k citations), Molecular Biology (5.3k citations), Urology (455 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, Frédéric Rosa, Andrew Sinclair, Philippe Berta, Peter N. Goodfellow, B Griffiths, Sandrine Barbaux, J Hawkins 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.

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