Michèle Mathieu

2.2k total citations
18 papers, 622 citations indexed

About

Michèle Mathieu is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Michèle Mathieu has authored 18 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Michèle Mathieu's work include Genetic factors in colorectal cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (2 papers). Michèle Mathieu is often cited by papers focused on Genetic factors in colorectal cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (2 papers). Michèle Mathieu collaborates with scholars based in France, Switzerland and Belgium. Michèle Mathieu's co-authors include Christine Petit, Marc Delpech, Jacques Young, Anne Lienhardt-Roussie, Catherine Dodé, Graeme Morgan, Arnaud Murat, Jean-Pierre Hardelin, Jacqueline Levilliers and Sławomir Wołczyński and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Michèle Mathieu

16 papers receiving 601 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michèle Mathieu France 9 341 310 247 64 60 18 622
P A de Zoysa United Kingdom 6 291 0.9× 221 0.7× 237 1.0× 20 0.3× 66 1.1× 7 676
Naoyuki Takuma Japan 12 330 1.0× 169 0.5× 157 0.6× 63 1.0× 137 2.3× 15 635
Corinne Fouveaut France 8 332 1.0× 297 1.0× 428 1.7× 19 0.3× 99 1.6× 12 722
Marie-Laure Kottler France 15 456 1.3× 406 1.3× 361 1.5× 56 0.9× 253 4.2× 23 981
Maria Tereza Matias Baptista Brazil 16 413 1.2× 366 1.2× 267 1.1× 34 0.5× 187 3.1× 46 687
Susan J. Allen United States 15 439 1.3× 367 1.2× 71 0.3× 128 2.0× 28 0.5× 25 752
Rachel Larder United Kingdom 14 480 1.4× 288 0.9× 108 0.4× 31 0.5× 58 1.0× 19 997
Kirsi Vaaralahti Finland 16 332 1.0× 283 0.9× 438 1.8× 17 0.3× 198 3.3× 35 719
Hélène Buteau France 9 384 1.1× 246 0.8× 137 0.6× 42 0.7× 370 6.2× 9 914
Bruno Francou France 15 498 1.5× 459 1.5× 711 2.9× 35 0.5× 155 2.6× 37 1.1k

Countries citing papers authored by Michèle Mathieu

Since Specialization
Citations

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

Fields of papers citing papers by Michèle Mathieu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michèle Mathieu

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

All Works

18 of 18 papers shown
1.
Jedraszak, Guillaume, Aline Receveur, Matthieu Décamp, et al.. (2015). Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: A family report. Annales d Endocrinologie. 76(5). 629–634. 17 indexed citations
2.
Madariaga, Leire, Vincent Morinière, Marc Jeanpierre, et al.. (2013). Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes. Clinical Journal of the American Society of Nephrology. 8(7). 1179–1187. 73 indexed citations
3.
4.
Crépin, Michel, Sophie Lejeune, Fabienne Escande, et al.. (2011). Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility. Human Mutation. 33(1). 180–188. 47 indexed citations
5.
Andrieux, Joris, Christèle Dubourg, Marlène Rio, et al.. (2009). Genotype–phenotype correlation in four 15q24 deleted patients identified by array‐CGH. American Journal of Medical Genetics Part A. 149A(12). 2813–2819. 27 indexed citations
6.
Piussan, C, et al.. (2009). Acquisitions des performances dans un cas d’ectrodactylie. Bulletin de l Académie Nationale de Médecine. 193(3). 709–712.
7.
Morin, Gilles, et al.. (2008). Additional familial case of subtotal leukonychia and sebaceous cysts (Bauer syndrome): Belong the nervous tumours to the phenotype?. European Journal of Medical Genetics. 51(5). 436–443. 4 indexed citations
8.
Dodé, Catherine, Luís Teixeira, Jacqueline Levilliers, et al.. (2006). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. 2(10). e175–e175. 315 indexed citations
9.
Yılmaz, Saliha, Thierry Bienvenu, Anne Moncla, et al.. (2005). Deleterious mutations in exon 1 of MECP2 in Rett syndrome. European Journal of Medical Genetics. 49(4). 313–322. 24 indexed citations
10.
Dodé, Catherine, Luís Augusto Teixeira, Jacqueline Levilliers, et al.. (2005). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. preprint(2006). e175–e175. 5 indexed citations
11.
Viot, Géraldine, Didier Lacombe, Albert David, et al.. (2002). Osteopathia striata cranial sclerosis: Non‐random X‐inactivation suggestive of X‐linked dominant inheritance. American Journal of Medical Genetics. 107(1). 1–4. 28 indexed citations
12.
Morin, Gilles, Jean Gekas, Jean Gondry, et al.. (2001). Cerebro‐costo‐mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission. Prenatal Diagnosis. 21(10). 890–893. 8 indexed citations
13.
Mathieu, Michèle. (2000). Changing Managed-care Model Offers Opportunities for Nutrition Coverage. Journal of the American Dietetic Association. 100(4). 415–415. 1 indexed citations
14.
Bonnet, Damien, Anna Pelet, Laurence Legeai‐Mallet, et al.. (1994). A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12. Nature Genetics. 6(4). 405–408. 33 indexed citations
15.
Mornet, Étienne, Brigitte Simon‐Bouy, Michèle Mathieu, et al.. (1993). Molecular analysis of a ring chromosome X in a family with fragile X syndrome. Human Genetics. 92(4). 373–378. 4 indexed citations
16.
17.
Mathieu, Michèle. (1981). LEGISLATIVE HIGHLIGHTS. Journal of the American Dietetic Association. 79(2). 175–175.
18.
Mathieu, Michèle. (1981). LEGISLATIVE HIGHLIGHTS. Journal of the American Dietetic Association. 79(6). 718–718. 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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