M Mathieu
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Cleft Lip and Palate Research
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- Glycogen Storage Diseases and Myoclonus
- Moyamoya disease diagnosis and treatment
Papers in
- Genetics 8
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
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- Protein Tyrosine Phosphatases 1
- Co-authors
- Michel Vekemans (1 shared paper)Martine Blayau (1 shared paper)Véronique David (1 shared paper)A Munnich (1 shared paper)Anne‐Lise Delezoide (1 shared paper)J. Y. Le Gall (1 shared paper)Tania Attié‐Bitach (1 shared paper)Sylvie Odent (1 shared paper)
In The Last Decade
M Mathieu
22 papers receiving 352 citations
Peers
Comparison fields: 5 of 67
- Genetics 156
- Rheumatology 82
- Developmental Biology 11
- Sensory Systems 22
- Molecular Biology 210
Countries citing papers authored by M Mathieu
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
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-authors
The 25 scholars most cited alongside M Mathieu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 123 | |
| 2 | 2009 | 79 | |
| 3 | 1996 | 42 | |
| 4 | 1992 | 24 | |
| 5 | X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21. | 1995 | 20 |
| 6 | [Waardenburg's syndrome and severe cyanotic cardiopathy]. | 1990 | 12 |
| 7 | 2003 | 9 | |
| 8 | [Syndrome of compression of the external saphenous nerve (or the sural nerve)]. | 1989 | 8 |
| 9 | [Still's disease in adults and Wissler-Fanconi syndrome]. | 1973 | 7 |
| 10 | 1996 | 6 | |
| 11 | The KBG syndrome: an additional sporadic case. | 2000 | 6 |
| 12 | 1996 | 5 | |
| 13 | 2001 | 4 | |
| 14 | [Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations]. | 1983 | 4 |
| 15 | [Injuries of the ligaments of the knee]. | 1995 | 3 |
| 16 | [An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]. | 1990 | 2 |
| 17 | La photothérapie dans la maladie de Crigler et Najjar. Intérêt et limites. | 1967 | 2 |
| 18 | 2024 | 2 | |
| 19 | [Light therapy in Crigler and Najjar's disease. Benefit and limitation]. | 1967 | 2 |
| 20 | 1995 | 1 |
About M Mathieu
M Mathieu is a scholar working on Genetics, Molecular Biology, Surgery, Rheumatology and Pathology and Forensic Medicine, having authored 24 papers that have together received 365 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Neonatal Health and Biochemistry (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Hydrogen's biological and therapeutic effects (1 paper), Moyamoya disease diagnosis and treatment (1 paper) and Protein Tyrosine Phosphatases (1 paper). The work is most often cited by research in Genetics (156 citations), Rheumatology (82 citations), Developmental Biology (11 citations), Sensory Systems (22 citations) and Molecular Biology (210 citations). M Mathieu has collaborated with scholars based in France, Lebanon and Germany. Frequent co-authors include Michel Vekemans, Martine Blayau, Véronique David, A Munnich, Anne‐Lise Delezoide, J. Y. Le Gall, Tania Attié‐Bitach, Sylvie Odent, B. Le Marec and Dominique Bozon. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Vision Research, CIRP journal of manufacturing science and technology and American Journal of Medical 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.