Florence Petit
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Congenital heart defects research 9
- Developmental Biology and Gene Regulation 6
- RNA Research and Splicing 6
- RNA modifications and cancer 6
- Genetics 27
- Genomic variations and chromosomal abnormalities 9
- Genetic Syndromes and Imprinting 5
- Co-authors
- Nadav Ahituv (2 shared papers)Karen E. Sears (1 shared paper)Sylvie Manouvrier‐Hanu (23 shared papers)Muriel Holder‐Espinasse (11 shared papers)Fabienne Escande (14 shared papers)Joris Andrieux (13 shared papers)Nicole Porchet (5 shared papers)Anne‐Sophie Jourdain (7 shared papers)
- Journals
- European Journal of Medical Genetics (10 papers)Clinical Genetics (9 papers)European Journal of Human Genetics (4 papers)Genetics in Medicine (4 papers)Human Mutation (3 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Florence Petit
56 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 82
- Developmental Biology 87
- Genetics 434
- Genetics 90
- Molecular Biology 578
- Developmental Neuroscience 20
Countries citing papers authored by Florence Petit
This map shows the geographic impact of Florence Petit'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 Florence Petit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florence Petit more than expected).
Fields of papers citing papers by Florence Petit
This network shows the impact of papers produced by Florence Petit. 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 Florence Petit. The network helps show where Florence Petit may publish in the future.
Co-authors
The 25 scholars most cited alongside Florence Petit, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 120 | |
| 2 | 2019 | 86 | |
| 3 | 2012 | 84 | |
| 4 | 2013 | 60 | |
| 5 | 2012 | 42 | |
| 6 | 2019 | 42 | |
| 7 | 2016 | 39 | |
| 8 | 2017 | 39 | |
| 9 | 2021 | 38 | |
| 10 | 2014 | 38 | |
| 11 | 2015 | 37 | |
| 12 | 2020 | 33 | |
| 13 | 2018 | 31 | |
| 14 | 2017 | 30 | |
| 15 | 2010 | 29 | |
| 16 | 2016 | 29 | |
| 17 | 2014 | 28 | |
| 18 | 2013 | 27 | |
| 19 | 2010 | 23 | |
| 20 | 2015 | 21 |
About Florence Petit
Florence Petit is a scholar working on Molecular Biology, Genetics, Developmental Biology, Surgery and Pediatrics, Perinatology and Child Health, having authored 62 papers that have together received 1.1k indexed citations. Recurring topics across this work include Congenital heart defects research (9 papers), Congenital limb and hand anomalies (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Developmental Biology and Gene Regulation (6 papers), RNA Research and Splicing (6 papers), Prenatal Screening and Diagnostics (6 papers), RNA modifications and cancer (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Developmental Biology (87 citations), Genetics (434 citations), Genetics (90 citations), Molecular Biology (578 citations) and Developmental Neuroscience (20 citations). Florence Petit has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Nadav Ahituv, Karen E. Sears, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse, Fabienne Escande, Joris Andrieux, Nicole Porchet, Anne‐Sophie Jourdain, Didier Lacombe and Jamal Ghoumid. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, European Journal of Human Genetics, Genetics in Medicine and Human Mutation.
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.