Claire E. Redin
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
- Reproductive Medicine top 2%
- Sperm and Testicular Function
Papers in
- Genetics 17
- Genetic and Kidney Cyst Diseases 6
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
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- Pharmacogenetics and Drug Metabolism 3
- Co-authors
- Jean‐Louis Mandel (6 shared papers)Amélie Piton (4 shared papers)John C. Schell (1 shared paper)M. Brivet (1 shared paper)Jared P. Rutter (1 shared paper)Jonathan G. Van Vranken (1 shared paper)Carl S. Thummel (1 shared paper)Eric B. Taylor (1 shared paper)
- Journals
- The American Journal of Human Genetics (6 papers)European Journal of Human Genetics (6 papers)JAMA Neurology (2 papers)Clinical Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Claire E. Redin
40 papers receiving 2.9k citations
Claire E. Redin's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 888
- Reproductive Medicine 218
- Cancer Research 84
- Molecular Biology 403
- Immunology 120
Countries citing papers authored by Claire E. Redin
This map shows the geographic impact of Claire E. Redin'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 Claire E. Redin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claire E. Redin more than expected).
Fields of papers citing papers by Claire E. Redin
This network shows the impact of papers produced by Claire E. Redin. 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 Claire E. Redin. The network helps show where Claire E. Redin may publish in the future.
Co-authors
The 25 scholars most cited alongside Claire E. Redin, 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 | A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans Hit paper breakdown → | 2012 | 710 |
| 2 | 2016 | 241 | |
| 3 | 2014 | 223 | |
| 4 | 2013 | 208 | |
| 5 | 2020 | 174 | |
| 6 | 2011 | 165 | |
| 7 | 2022 | 145 | |
| 8 | 2017 | 144 | |
| 9 | 2012 | 96 | |
| 10 | 2012 | 82 | |
| 11 | 2010 | 71 | |
| 12 | 2015 | 70 | |
| 13 | 2015 | 68 | |
| 14 | 2018 | 65 | |
| 15 | 2023 | 63 | |
| 16 | 2016 | 61 | |
| 17 | 2016 | 58 | |
| 18 | 2014 | 53 | |
| 19 | 2017 | 47 | |
| 20 | 2013 | 46 |
About Claire E. Redin
Claire E. Redin is a scholar working on Genetics, Pharmacology, Infectious Diseases, Reproductive Medicine and Cellular and Molecular Neuroscience, having authored 41 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Pharmacogenetics and Drug Metabolism (3 papers), SARS-CoV-2 and COVID-19 Research (3 papers), Sperm and Testicular Function (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (888 citations), Reproductive Medicine (218 citations), Cancer Research (84 citations), Molecular Biology (403 citations) and Immunology (120 citations). Claire E. Redin has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Jean‐Louis Mandel, Amélie Piton, John C. Schell, M. Brivet, Jared P. Rutter, Jonathan G. Van Vranken, Carl S. Thummel, Eric B. Taylor, James Eric Cox and Sihem Boudina. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, JAMA Neurology, Clinical Genetics and Journal of Medical 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.