Stéphanie Gobin
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Neurology top 10%
- Neurological diseases and metabolism
Papers in
-
- Mitochondrial Function and Pathology 6
- Peroxisome Proliferator-Activated Receptors 2
-
- Metabolism and Genetic Disorders 11
- Co-authors
- Jean‐Paul Bonnefont (9 shared papers)Carina Prip‐Buus (5 shared papers)J. A. Phillips (4 shared papers)Laure Thuillier (4 shared papers)Nathalie Boddaert (3 shared papers)Arnold Münnich (3 shared papers)France Demaugre (3 shared papers)Alan J. Paine (4 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (5 papers)Orphanet Journal of Rare Diseases (2 papers)European Journal of Human Genetics (2 papers)European Journal of Medical Genetics (1 paper)Clinical Chemistry (1 paper)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Stéphanie Gobin
26 papers receiving 764 citations
Peers
Comparison fields: 5 of 73
- Clinical Biochemistry 309
- Neurology 114
- Biochemistry 50
- Molecular Biology 380
- Cellular and Molecular Neuroscience 83
Countries citing papers authored by Stéphanie Gobin
This map shows the geographic impact of Stéphanie Gobin'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 Stéphanie Gobin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphanie Gobin more than expected).
Fields of papers citing papers by Stéphanie Gobin
This network shows the impact of papers produced by Stéphanie Gobin. 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 Stéphanie Gobin. The network helps show where Stéphanie Gobin may publish in the future.
Co-authors
The 25 scholars most cited alongside Stéphanie Gobin, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 165 | |
| 2 | 2003 | 80 | |
| 3 | 2015 | 60 | |
| 4 | 2003 | 60 | |
| 5 | 2001 | 47 | |
| 6 | 2013 | 42 | |
| 7 | 2002 | 41 | |
| 8 | 2005 | 34 | |
| 9 | 1991 | 32 | |
| 10 | 2009 | 29 | |
| 11 | 2017 | 27 | |
| 12 | 2010 | 24 | |
| 13 | 2012 | 23 | |
| 14 | 2005 | 22 | |
| 15 | 1989 | 17 | |
| 16 | 2005 | 16 | |
| 17 | 2017 | 14 | |
| 18 | 2017 | 11 | |
| 19 | 2019 | 9 | |
| 20 | 1992 | 9 |
About Stéphanie Gobin
Stéphanie Gobin is a scholar working on Molecular Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health, Rheumatology and Cell Biology, having authored 27 papers that have together received 784 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (6 papers), Amino Acid Enzymes and Metabolism (3 papers), Folate and B Vitamins Research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Liver Disease Diagnosis and Treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Peroxisome Proliferator-Activated Receptors (2 papers). The work is most often cited by research in Clinical Biochemistry (309 citations), Neurology (114 citations), Biochemistry (50 citations), Molecular Biology (380 citations) and Cellular and Molecular Neuroscience (83 citations). Stéphanie Gobin has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Jean‐Paul Bonnefont, Carina Prip‐Buus, J. A. Phillips, Laure Thuillier, Nathalie Boddaert, Arnold Münnich, France Demaugre, Alan J. Paine, Noman Kadhom and Jean‐Marie Saudubray. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, European Journal of Human Genetics, European Journal of Medical Genetics and Clinical Chemistry.
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.