M Fellous

1.1k total citations
16 papers, 779 citations indexed

About

M Fellous is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, M Fellous has authored 16 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Reproductive Medicine. Recurrent topics in M Fellous's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Sexual Differentiation and Disorders (10 papers) and Sperm and Testicular Function (8 papers). M Fellous is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Sexual Differentiation and Disorders (10 papers) and Sperm and Testicular Function (8 papers). M Fellous collaborates with scholars based in France, Italy and India. M Fellous's co-authors include Ken McElreavey, Éric Vilain, N. Abbas, Ira Herskowitz, F Jaubert, F Richaud, Reiner A. Veitia, Claire Nihoul‐Feketé, Roland Berger and Nacer Abbas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Kidney International and The Journal of Urology.

In The Last Decade

M Fellous

15 papers receiving 749 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M Fellous France	11	663	617	294	72	57	16	779
M Post Netherlands	8	380 0.6×	496 0.8×	483 1.6×	40 0.6×	8 0.1×	8	891
François Cuzin France	7	142 0.2×	576 0.9×	57 0.2×	28 0.4×	28 0.5×	8	677
Katrien Stouffs Belgium	21	649 1.0×	618 1.0×	534 1.8×	7 0.1×	78 1.4×	47	1.0k
Jocelyn A. van den Bergen Australia	14	341 0.5×	545 0.9×	203 0.7×	35 0.5×	17 0.3×	18	665
Anne M. Wikström Finland	11	616 0.9×	573 0.9×	577 2.0×	20 0.3×	16 0.3×	14	895
J Teter Poland	13	265 0.4×	301 0.5×	150 0.5×	42 0.6×	27 0.5×	42	480
G. Bourrouillou France	14	398 0.6×	279 0.5×	147 0.5×	4 0.1×	95 1.7×	40	587
Jean Pierre Siffroi France	16	483 0.7×	387 0.6×	376 1.3×	16 0.2×	93 1.6×	35	792
K Boczkowski Poland	10	272 0.4×	266 0.4×	100 0.3×	31 0.4×	56 1.0×	44	389
Lucile Gouédard France	7	267 0.4×	344 0.6×	328 1.1×	41 0.6×	6 0.1×	7	673

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-authorship network of co-authors of M Fellous

This figure shows the co-authorship network connecting the top 25 collaborators of M Fellous. A scholar is included among the top collaborators of M Fellous based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M Fellous. M Fellous is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Fellous, M, et al.. (2012). Genetic Counseling for the Orthodox Jewish Couple Undergoing Preimplantation Genetic Diagnosis. Journal of Genetic Counseling. 21(5). 625–630. 7 indexed citations

Kalfa, Nicolas, M Fellous, Catherine Patte, et al.. (2008). Aberrant Expression of Ovary Determining Gene FOXL2 in the Testis and Juvenile Granulosa Cell Tumor in Children. The Journal of Urology. 180(4S). 1810–1813. 33 indexed citations

Jaubert, Francis, et al.. (2004). Gonad development in Drash and Frasier syndromes depends on WT1 mutations.. PubMed. 65(2). 40–4. 9 indexed citations

Denamur, Erick, N. Bocquet, Véronique Baudouin, et al.. (2000). WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis. Kidney International. 57(5). 1868–1872. 66 indexed citations

Ottolenghi, Chris, Reiner A. Veitia, Lluís Quintana‐Murci, et al.. (2000). The Region on 9p Associated with 46,XY Sex Reversal Contains Several Transcripts Expressed in the Urogenital System and a Novel Doublesex-Related Domain. Genomics. 64(2). 170–178. 72 indexed citations

Ion, Alexandra, Louise Telvi, Jean‐Louis Chaussain, et al.. (1996). 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.. PubMed. 58(6). 1185–91. 47 indexed citations

Vilain, Éric, F Jaubert, M Fellous, & Ken McElreavey. (1993). Pathology of 46, XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor. Differentiation. 52(2). 151–159. 35 indexed citations

McElreavey, Ken, Éric Vilain, Corinne Cotinot, Emmanuel Payen, & M Fellous. (1993). Control of sex determination in animals. European Journal of Biochemistry. 218(3). 769–783. 25 indexed citations

Abbas, N., Éric Vilain, Francis Jaubert, et al.. (1993). Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.. PubMed. 316(4). 375–83. 33 indexed citations

10.

McElreavey, Ken, Éric Vilain, N. Abbas, Ira Herskowitz, & M Fellous. (1993). A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.. Proceedings of the National Academy of Sciences. 90(8). 3368–3372. 280 indexed citations

11.

McElreavey, Ken, R Rappaport, Éric Vilain, et al.. (1992). A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY. Human Genetics. 90(1-2). 121–5. 82 indexed citations

12.

Vilain, Éric, et al.. (1992). Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.. PubMed. 50(5). 1008–11. 62 indexed citations

13.

Abbas, Nacer, Giuseppe Novelli, Francesco Corrado, et al.. (1990). A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1. Human Genetics. 86(1). 94–8. 24 indexed citations

14.

Seboun, Eric, J E Toublanc, Pascale Leroy, et al.. (1986). DNA ANALYSIS OF XX MALES WITH GENITAL ABNORMALITIES COMPARED TO "CLASSICAL" XX MALES. Pediatric Research. 20(11). 1183–1183. 1 indexed citations

15.

Roger, M, Christopher D. Roy, M Fellous, et al.. (1980). [Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)].. PubMed. 41(1). 73–5. 1 indexed citations

16.

Sire, Jean-Marie, et al.. (1978). [beta2-Microglobulin in human seminal fluid (author's transl)].. PubMed. 26(6). 392–4. 2 indexed citations

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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