Audrey Putoux
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Fetal and Pediatric Neurological Disorders
Papers in
-
- RNA modifications and cancer 8
- Hedgehog Signaling Pathway Studies 5
- RNA Research and Splicing 5
- Genetics 20
- Genetic and Kidney Cyst Diseases 6
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Tania Attié‐Bitach (5 shared papers)Marie-Claire Gübler (2 shared papers)Damien Sanlaville (12 shared papers)Jelena Martinović (1 shared paper)Patrick Edery (15 shared papers)Audrey Labalme (8 shared papers)Gaëtan Lesca (14 shared papers)Laurent Guibaud (7 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Ultrasound in Obstetrics and Gynecology (2 papers)Clinical Genetics (2 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Audrey Putoux
26 papers receiving 354 citations
Peers
Comparison fields: 5 of 55
- Genetics 215
- Pediatrics, Perinatology and Child Health 72
- Molecular Biology 236
- Cellular and Molecular Neuroscience 36
- Genetics 21
Countries citing papers authored by Audrey Putoux
This map shows the geographic impact of Audrey Putoux'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 Audrey Putoux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Audrey Putoux more than expected).
Fields of papers citing papers by Audrey Putoux
This network shows the impact of papers produced by Audrey Putoux. 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 Audrey Putoux. The network helps show where Audrey Putoux may publish in the future.
Co-authors
The 25 scholars most cited alongside Audrey Putoux, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 65 | |
| 2 | 2014 | 49 | |
| 3 | 2019 | 26 | |
| 4 | 2012 | 26 | |
| 5 | 2015 | 24 | |
| 6 | 2010 | 20 | |
| 7 | 2015 | 19 | |
| 8 | 2019 | 18 | |
| 9 | 2018 | 16 | |
| 10 | 2013 | 13 | |
| 11 | 2014 | 11 | |
| 12 | 2020 | 10 | |
| 13 | 2021 | 9 | |
| 14 | 2019 | 8 | |
| 15 | 2020 | 8 | |
| 16 | 2019 | 6 | |
| 17 | 2022 | 6 | |
| 18 | 2021 | 5 | |
| 19 | 2020 | 5 | |
| 20 | 2019 | 5 |
About Audrey Putoux
Audrey Putoux is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Clinical Biochemistry, having authored 32 papers that have together received 369 indexed citations. Recurring topics across this work include RNA modifications and cancer (8 papers), Genetic and Kidney Cyst Diseases (6 papers), Fetal and Pediatric Neurological Disorders (6 papers), Hedgehog Signaling Pathway Studies (5 papers), RNA Research and Splicing (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (215 citations), Pediatrics, Perinatology and Child Health (72 citations), Molecular Biology (236 citations), Cellular and Molecular Neuroscience (36 citations) and Genetics (21 citations). Audrey Putoux has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Tania Attié‐Bitach, Marie-Claire Gübler, Damien Sanlaville, Jelena Martinović, Patrick Edery, Audrey Labalme, Gaëtan Lesca, Laurent Guibaud, Estelle Dubruc and Christelle Rougeot. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, Prenatal Diagnosis, Ultrasound in Obstetrics and Gynecology and Clinical 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.