Sandra Mercier
Impact in
- Developmental Biology top 10%
- Genetics top 10%
- Neurogenetic and Muscular Disorders Research
- Virus-based gene therapy research
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
Papers in
-
- Hedgehog Signaling Pathway Studies 9
- Muscle Physiology and Disorders 5
- RNA regulation and disease 4
- Genetics 12
- Neurogenetic and Muscular Disorders Research 4
- Genomics and Rare Diseases 4
- Co-authors
- Sylvie Odent (11 shared papers)Christèle Dubourg (7 shared papers)Véronique David (6 shared papers)Yann Péréon (13 shared papers)Maximilian Muenke (3 shared papers)Daniel Pineda‐Alvarez (3 shared papers)Benjamin D. Solomon (2 shared papers)Claude Bendavid (4 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)Journal of Medical Genetics (3 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)Neuromuscular Disorders (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Sandra Mercier
35 papers receiving 670 citations
Peers
Comparison fields: 5 of 57
- Developmental Biology 24
- Genetics 289
- Genetics 92
- Molecular Biology 456
- Pediatrics, Perinatology and Child Health 77
Countries citing papers authored by Sandra Mercier
This map shows the geographic impact of Sandra Mercier'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 Sandra Mercier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Mercier more than expected).
Fields of papers citing papers by Sandra Mercier
This network shows the impact of papers produced by Sandra Mercier. 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 Sandra Mercier. The network helps show where Sandra Mercier may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Mercier, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 109 | |
| 2 | 2022 | 109 | |
| 3 | 2011 | 74 | |
| 4 | 1999 | 54 | |
| 5 | 2012 | 52 | |
| 6 | 2010 | 38 | |
| 7 | 2021 | 31 | |
| 8 | 2010 | 31 | |
| 9 | 2011 | 23 | |
| 10 | 2016 | 17 | |
| 11 | 2012 | 16 | |
| 12 | 2016 | 15 | |
| 13 | 2010 | 14 | |
| 14 | 2013 | 11 | |
| 15 | 2010 | 11 | |
| 16 | 2015 | 8 | |
| 17 | 2020 | 7 | |
| 18 | 2018 | 6 | |
| 19 | 2018 | 6 | |
| 20 | 2018 | 5 |
About Sandra Mercier
Sandra Mercier is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Genetics and Pediatrics, Perinatology and Child Health, having authored 41 papers that have together received 680 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (9 papers), Muscle Physiology and Disorders (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), RNA regulation and disease (4 papers), Hereditary Neurological Disorders (4 papers), Genomics and Rare Diseases (4 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Developmental Biology (24 citations), Genetics (289 citations), Genetics (92 citations), Molecular Biology (456 citations) and Pediatrics, Perinatology and Child Health (77 citations). Sandra Mercier has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Sylvie Odent, Christèle Dubourg, Véronique David, Yann Péréon, Maximilian Muenke, Daniel Pineda‐Alvarez, Benjamin D. Solomon, Claude Bendavid, Isabelle Gicquel and Erich Roessler. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Neuromuscular Disorders and Human Molecular 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.