B. Mousson
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
-
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- Biochemical and Molecular Research
- RNA modifications and cancer
Papers in
-
- Mitochondrial Function and Pathology 23
- ATP Synthase and ATPases Research 7
- Biochemical and Molecular Research 3
-
- Metabolism and Genetic Disorders 28
- Co-authors
- G. Stepien (4 shared papers)Georges Stepien (5 shared papers)Dominique Bozon (1 shared paper)H Carrier (8 shared papers)P. Divry (5 shared papers)Christine Vianey‐Saban (4 shared papers)Catherine Godinot (5 shared papers)Alain Lachaux (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (4 papers)Molecular and Cellular Biochemistry (2 papers)European Journal of Pediatrics (2 papers)Neuromuscular Disorders (2 papers)Mammalian Genome (1 paper)
- Partner nations
- FranceSwitzerlandNetherlands
In The Last Decade
B. Mousson
35 papers receiving 591 citations
Peers
Comparison fields: 5 of 58
- Clinical Biochemistry 406
- Molecular Biology 499
- Biochemistry 26
- Pediatrics, Perinatology and Child Health 52
- Cellular and Molecular Neuroscience 48
Countries citing papers authored by B. Mousson
This map shows the geographic impact of B. Mousson'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 B. Mousson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. Mousson more than expected).
Fields of papers citing papers by B. Mousson
This network shows the impact of papers produced by B. Mousson. 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 B. Mousson. The network helps show where B. Mousson may publish in the future.
Co-authors
The 25 scholars most cited alongside B. Mousson, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 84 | |
| 2 | 1999 | 63 | |
| 3 | 1993 | 41 | |
| 4 | 1993 | 37 | |
| 5 | 1993 | 34 | |
| 6 | 1999 | 34 | |
| 7 | 1997 | 34 | |
| 8 | 1997 | 33 | |
| 9 | 1994 | 33 | |
| 10 | 1993 | 26 | |
| 11 | 1998 | 20 | |
| 12 | [MNGIE syndrome in 2 siblings]. | 1997 | 20 |
| 13 | 1988 | 16 | |
| 14 | 1997 | 14 | |
| 15 | 1985 | 13 | |
| 16 | 2000 | 12 | |
| 17 | 1995 | 12 | |
| 18 | 1997 | 11 | |
| 19 | 1999 | 11 | |
| 20 | 1996 | 11 |
About B. Mousson
B. Mousson is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Nephrology, having authored 37 papers that have together received 624 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (28 papers), Mitochondrial Function and Pathology (23 papers), ATP Synthase and ATPases Research (7 papers), Genetic Neurodegenerative Diseases (6 papers), Neonatal Health and Biochemistry (4 papers), Gout, Hyperuricemia, Uric Acid (3 papers), Biochemical and Molecular Research (3 papers) and Diet and metabolism studies (3 papers). The work is most often cited by research in Clinical Biochemistry (406 citations), Molecular Biology (499 citations), Biochemistry (26 citations), Pediatrics, Perinatology and Child Health (52 citations) and Cellular and Molecular Neuroscience (48 citations). B. Mousson has collaborated with scholars based in France, Switzerland and Netherlands. Frequent co-authors include G. Stepien, Georges Stepien, Dominique Bozon, H Carrier, P. Divry, Christine Vianey‐Saban, Catherine Godinot, Alain Lachaux, Nathalie Streichenberger and Pierre‐Henri Ducluzeau. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular and Cellular Biochemistry, European Journal of Pediatrics, Neuromuscular Disorders and Mammalian Genome.
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.