Claire E. Redin
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Reproductive Medicine top 5%
- Sperm and Testicular Function
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5
- Genetic and Kidney Cyst Diseases 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
-
- Hedgehog Signaling Pathway Studies 3
- Co-authors
- Jean‐Louis Mandel (6 shared papers)Amélie Piton (4 shared papers)Gygi Steven P. (1 shared paper)Carl S. Thummel (1 shared paper)Jared P. Rutter (1 shared paper)Eric B. Taylor (1 shared paper)Audrey Boutron (1 shared paper)Sihem Boudina (1 shared paper)
- Journals
- The American Journal of Human Genetics (6 papers)European Journal of Human Genetics (5 papers)Clinical Genetics (2 papers)Journal of Medical Genetics (2 papers)JAMA Neurology (2 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Claire E. Redin
34 papers receiving 2.7k citations
Claire E. Redin's Hit Papers
Peers
Comparison fields: 5 of 113
- Genetics 1.2k
- Reproductive Medicine 190
- Molecular Biology 1.4k
- Cancer Research 244
- Clinical Biochemistry 115
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 35 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 | 704 |
| 2 | 2016 | 240 | |
| 3 | 2014 | 221 | |
| 4 | 2013 | 206 | |
| 5 | 2020 | 171 | |
| 6 | 2011 | 164 | |
| 7 | 2017 | 136 | |
| 8 | 2012 | 96 | |
| 9 | 2012 | 83 | |
| 10 | 2010 | 71 | |
| 11 | 2015 | 70 | |
| 12 | 2015 | 67 | |
| 13 | 2018 | 63 | |
| 14 | 2016 | 61 | |
| 15 | 2016 | 56 | |
| 16 | 2014 | 53 | |
| 17 | 2017 | 47 | |
| 18 | 2013 | 46 | |
| 19 | 2013 | 33 | |
| 20 | 2013 | 26 |
About Claire E. Redin
Claire E. Redin is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Reproductive Medicine and Pharmacology, having authored 35 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (5 papers), Genetic and Kidney Cyst Diseases (5 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (1.2k citations), Reproductive Medicine (190 citations), Molecular Biology (1.4k citations), Cancer Research (244 citations) and Clinical Biochemistry (115 citations). Claire E. Redin has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Jean‐Louis Mandel, Amélie Piton, Gygi Steven P., Carl S. Thummel, Jared P. Rutter, Eric B. Taylor, Audrey Boutron, Sihem Boudina, John C. Schell and M. Brivet. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Clinical Genetics, Journal of Medical Genetics and JAMA Neurology.
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.