M Mathieu

972 total citations
24 papers, 365 citations indexed

About

M Mathieu is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, M Mathieu has authored 24 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in M Mathieu's work include Genetics and Neurodevelopmental Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Genomics and Rare Diseases (2 papers). M Mathieu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Genomics and Rare Diseases (2 papers). M Mathieu collaborates with scholars based in France, Lebanon and Germany. M Mathieu's co-authors include Martine Blayau, Anne‐Lise Delezoide, A Munnich, Véronique David, B. Le Marec, Michel Vekemans, J. Y. Le Gall, Tania Attié‐Bitach, Sylvie Odent and Gilles Mithieux and has published in prestigious journals such as Human Molecular Genetics, Vision Research and Journal of Medical Genetics.

In The Last Decade

M Mathieu

22 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M Mathieu France	8	210	156	82	43	31	24	365
Charalampos Karadimas Greece	14	473 2.3×	135 0.9×	55 0.7×	27 0.6×	32 1.0×	17	627
Linda Manwaring United States	8	136 0.6×	175 1.1×	33 0.4×	32 0.7×	33 1.1×	15	374
Gilles Morin France	9	158 0.8×	74 0.5×	156 1.9×	19 0.4×	11 0.4×	22	463
H. Goebel Germany	13	263 1.3×	29 0.2×	58 0.7×	29 0.7×	53 1.7×	37	475
Rachel Sayuri Honjo Brazil	13	205 1.0×	174 1.1×	38 0.5×	41 1.0×	12 0.4×	60	460
Catherine Bove United States	9	86 0.4×	71 0.5×	53 0.6×	18 0.4×	170 5.5×	12	441
Dustin Armstrong United States	10	365 1.7×	130 0.8×	116 1.4×	40 0.9×	46 1.5×	12	576
Marta Szybowska Canada	10	261 1.2×	141 0.9×	30 0.4×	57 1.3×	7 0.2×	17	510
Kathryn Friend Australia	12	375 1.8×	320 2.1×	20 0.2×	20 0.5×	20 0.6×	16	521
Ilse J. Anderson United States	7	164 0.8×	165 1.1×	29 0.4×	22 0.5×	28 0.9×	11	304

Countries citing papers authored by M Mathieu

Since Specialization

Citations

This map shows the geographic impact of M Mathieu'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 Mathieu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Mathieu more than expected).

Fields of papers citing papers by M Mathieu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M Mathieu. 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 Mathieu. The network helps show where M Mathieu may publish in the future.

Co-authorship network of co-authors of M Mathieu

This figure shows the co-authorship network connecting the top 25 collaborators of M Mathieu. A scholar is included among the top collaborators of M Mathieu 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 Mathieu. M Mathieu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Borck, Guntram, Clarisse Baumann, Geneviève Baujat, et al.. (2009). Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families. Journal of Medical Genetics. 47(12). 797–802. 79 indexed citations

Serfaty, D., et al.. (2003). Observance du traitement hormonal substitutif de la ménopause : résultats d’une étude prospective française de deux ans, comparant un traitement transdermique et une association fixe par voie orale. Gynécologie Obstétrique & Fertilité. 31(6). 525–533. 9 indexed citations

Gekas, Jean, et al.. (2001). Chondrodysplasie ponctuée récessive liée à l’X.Étude cytogénétique et place de la biologie moléculaire. Archives de Pédiatrie. 8(2). 176–180. 4 indexed citations

Mathieu, M, et al.. (2000). The KBG syndrome: an additional sporadic case.. PubMed. 11(1). 33–5. 6 indexed citations

Odent, Sylvie, Tania Attié‐Bitach, Martine Blayau, et al.. (1999). Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly. Human Molecular Genetics. 8(9). 1683–1689. 123 indexed citations

Bozon, Dominique, et al.. (1996). Mutation analysis in 24 French patients with glycogen storage disease type 1a.. Journal of Medical Genetics. 33(5). 358–360. 42 indexed citations

Mathieu, M, et al.. (1996). Fragile X mutation and FG syndrome-like phenotype. American Journal of Medical Genetics. 64(2). 395–398. 6 indexed citations

Hanauer, André, et al.. (1995). X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.. HAL (Le Centre pour la Communication Scientifique Directe). 20 indexed citations

Larget‐Piet, Dominique, S. Gerber, Jean‐Michel Rozet, et al.. (1995). 3234 Evidence for a fourth locus responsible for usher syndrome type I (USID). Vision Research. 35. S131–S131. 1 indexed citations

10.

Kerboull, L., et al.. (1995). [Injuries of the ligaments of the knee].. PubMed. 45(12). 1527–36. 3 indexed citations

11.

Biancalana, Valérie, Marie‐Louise Briard, A. David, et al.. (1992). Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. PubMed. 50(5). 981–7. 24 indexed citations

12.

Kaplan, Jeffrey, Anna Pelet, M Guilloud-Bataille, et al.. (1990). [An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].. PubMed. 37(1). 13–9. 2 indexed citations

13.

Mathieu, M, et al.. (1990). [Waardenburg's syndrome and severe cyanotic cardiopathy].. PubMed. 47(9). 657–9. 12 indexed citations

14.

Piussan, C, C Lenaerts, M Mathieu, & B. Boudailliez. (1983). [Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations].. PubMed. 31(2). 107–14. 4 indexed citations

15.

Maire, I, et al.. (1978). [Infantile form of Gaucher's disease. Clinical and biological studies in 1 case. Prenatal diagnosis in 2 further normal pregnancies].. PubMed. 35(9). 949–62. 1 indexed citations

16.

Mathieu, M & O Benoît. (1976). Chaine complète de traitement de l'E.E.G. Application au dépouillement automatique des tracés de sommeil. Revue d Electroencé phalographie et de Neurophysiologie Clinique. 6(2). 338–341. 1 indexed citations

17.

Cotte, J, et al.. (1968). [Our experience of 2 years oferythrocyte enzymology in pediatrics. Apropos of 250 cases].. PubMed. 25(10). 1129–54. 1 indexed citations

18.

Béthenod, M, et al.. (1967). La photothérapie dans la maladie de Crigler et Najjar. Intérêt et limites.. 14(12). 2 indexed citations

19.

Béthenod, M, et al.. (1967). [Light therapy in Crigler and Najjar's disease. Benefit and limitation].. PubMed. 14(12). 829–34. 2 indexed citations

20.

Cotte, J, et al.. (1964). [A CASE OF INTOLERANCE TO SACCHAROSE].. PubMed. 21. 240–4. 1 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.

Explore authors with similar magnitude of impact