Michel Fardeau
- Cell Biology top 0.1%
- Skin and Cellular Biology Research 18
- Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 50
- Molecular Biology top 0.2%
- Muscle Physiology and Disorders 139
- Mitochondrial Function and Pathology 32
- Nuclear Structure and Function 21
- Genetics top 0.2%
- Neurogenetic and Muscular Disorders Research 32
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- Cardiomyopathy and Myosin Studies 48
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- Metabolism and Genetic Disorders 25
- Co-authors
- F.M.S. ToméPascale GuicheneyNorma B. RomeroB. EymardJ. BeckmannKetty SchwartzDanielle ChâteauFernando Tomé
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Michel Fardeau
265 papers receiving 14.8k citations
Hit Papers
Peers
Comparison fields: 5 of 138
- Cell Biology 3.5k
- Cellular and Molecular Neuroscience 3.7k
- Molecular Biology 12.0k
- Genetics 1.8k
- Cardiology and Cardiovascular Medicine 3.2k
Countries citing papers authored by Michel Fardeau
This map shows the geographic impact of Michel Fardeau'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 Michel Fardeau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michel Fardeau more than expected).
Fields of papers citing papers by Michel Fardeau
This network shows the impact of papers produced by Michel Fardeau. 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 Michel Fardeau. The network helps show where Michel Fardeau may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Michel Fardeau, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 35 | |
| 2 | 2018 | 16 | |
| 3 | 2014 | 1 | |
| 4 | 2010 | 75 | |
| 5 | 2004 | 20 | |
| 6 | Genetic characterisation of multi-minicore disease: identification of a first locus and evidence for genetic heterogeneity | 2001 | 1 |
| 7 | Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophybreakdown → | 1999 | 1032 |
| 8 | 1998 | 10 | |
| 9 | A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathybreakdown → | 1998 | 866 |
| 10 | 1996 | 52 | |
| 11 | 1996 | 46 | |
| 12 | 1994 | 40 | |
| 13 | 1993 | 60 | |
| 14 | 1992 | 13 | |
| 15 | [Recollections on the centenary of the death of Vulpian (5 January 1826-18 May 1887)]. | 1988 | 2 |
| 16 | 1987 | 4 | |
| 17 | Myopathie lipidique avec cardiomyopathie sévère par déficit généralisé en carnitine. Evolution favorable sous un traitement par chlorhydrate de carnitine. | 1979 | 3 |
| 18 | [Centromuclear myopathy with late clinical manifestations. Clinical, histological and ultrastructural study of a new case]. | 1976 | 10 |
| 19 | Ultrastructure des fibres musculaires squelettiques. II. | 1969 | 4 |
| 20 | 1967 | 141 |
About Michel Fardeau
Michel Fardeau is a scholar working on Clinical Biochemistry, Cell Biology and Cellular and Molecular Neuroscience, having authored 270 papers that have together received 15.2k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (139 papers), Genetic Neurodegenerative Diseases (50 papers), Cardiomyopathy and Myosin Studies (48 papers), Mitochondrial Function and Pathology (32 papers), Neurogenetic and Muscular Disorders Research (32 papers), Metabolism and Genetic Disorders (25 papers), Nuclear Structure and Function (21 papers) and Skin and Cellular Biology Research (18 papers). The work is most often cited by research in Cell Biology (3.5k citations), Cellular and Molecular Neuroscience (3.7k citations) and Molecular Biology (12.0k citations). Michel Fardeau has collaborated with scholars based in France, United States and Germany. Frequent co-authors include F.M.S. Tomé, Pascale Guicheney, Norma B. Romero, B. Eymard, J. Beckmann, Ketty Schwartz, Danielle Château, Fernando Tomé, Kevin P. Campbell and Denis Duboc. Their work appears in journals such as Nature, New England Journal of Medicine and Cell.
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.