Bénédicte Gérard
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Nephrology top 2%
- Parathyroid Disorders and Treatments
Papers in
- Genetics 21
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- Dominique Chrétien (2 shared papers)Jean‐Marie Saudubray (2 shared papers)Agnès Rötig (2 shared papers)Arnold Münnich (2 shared papers)Pierre Rustin (2 shared papers)Thomas Bourgeron (1 shared paper)Bernard Grandchamp (20 shared papers)Érick Denamur (3 shared papers)
- Journals
- Human Mutation (4 papers)European Journal of Pediatrics (3 papers)Blood (2 papers)Clinical Genetics (2 papers)British Journal of Cancer (2 papers)
- Partner nations
- FranceUnited KingdomGermany
In The Last Decade
Bénédicte Gérard
58 papers receiving 3.2k citations
Bénédicte Gérard's Hit Papers
Peers
Comparison fields: 5 of 135
- Clinical Biochemistry 349
- Nephrology 289
- Genetics 692
- Molecular Biology 1.6k
- Biological Psychiatry 33
Countries citing papers authored by Bénédicte Gérard
This map shows the geographic impact of Bénédicte Gérard'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 Bénédicte Gérard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bénédicte Gérard more than expected).
Fields of papers citing papers by Bénédicte Gérard
This network shows the impact of papers produced by Bénédicte Gérard. 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 Bénédicte Gérard. The network helps show where Bénédicte Gérard may publish in the future.
Co-authors
The 25 scholars most cited alongside Bénédicte Gérard, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Biochemical and molecular investigations in respiratory chain deficiencies Hit paper breakdown → | 1994 | 1059 |
| 2 | 2003 | 443 | |
| 3 | 2002 | 245 | |
| 4 | 2008 | 140 | |
| 5 | 2009 | 140 | |
| 6 | 2004 | 112 | |
| 7 | 2009 | 66 | |
| 8 | 2005 | 66 | |
| 9 | 2003 | 64 | |
| 10 | 2008 | 61 | |
| 11 | 2007 | 59 | |
| 12 | 2009 | 54 | |
| 13 | 1995 | 54 | |
| 14 | 2017 | 50 | |
| 15 | 2006 | 45 | |
| 16 | 1998 | 41 | |
| 17 | 1997 | 39 | |
| 18 | 2008 | 37 | |
| 19 | 2018 | 37 | |
| 20 | 2015 | 28 |
About Bénédicte Gérard
Bénédicte Gérard is a scholar working on Molecular Biology, Genetics, Surgery, Immunology and Cell Biology, having authored 59 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), melanin and skin pigmentation (3 papers), Immune cells in cancer (3 papers), Acute Lymphoblastic Leukemia research (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). The work is most often cited by research in Clinical Biochemistry (349 citations), Nephrology (289 citations), Genetics (692 citations), Molecular Biology (1.6k citations) and Biological Psychiatry (33 citations). Bénédicte Gérard has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Dominique Chrétien, Jean‐Marie Saudubray, Agnès Rötig, Arnold Münnich, Pierre Rustin, Thomas Bourgeron, Bernard Grandchamp, Érick Denamur, François Taddéi and Ivan Matić. Their work appears in journals such as Human Mutation, European Journal of Pediatrics, Blood, Clinical Genetics and British Journal of Cancer.
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.