Françoise Devillard
Impact in
- Reproductive Medicine top 5%
- Sperm and Testicular Function
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genomics and Rare Diseases 2
- Genetic Syndromes and Imprinting 2
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- Epigenetics and DNA Methylation 2
- Co-authors
- Florence Amblard (14 shared papers)Véronique Satre (13 shared papers)Charles Coutton (12 shared papers)Pierre‐Simon Jouk (10 shared papers)Gaëlle Vieville (7 shared papers)Guillaume Martinez (4 shared papers)Sophie Brouillet (5 shared papers)Sylviane Hennebicq (4 shared papers)
- Journals
- Human Reproduction (3 papers)Prenatal Diagnosis (3 papers)Clinical Genetics (3 papers)Neurogenetics (1 paper)International Journal of Molecular Sciences (1 paper)
- Partner nations
- FranceItalyNew Zealand
In The Last Decade
Françoise Devillard
26 papers receiving 389 citations
Peers
Comparison fields: 5 of 50
- Reproductive Medicine 133
- Genetics 196
- Pediatrics, Perinatology and Child Health 99
- Developmental Neuroscience 14
- Public Health, Environmental and Occupational Health 75
Countries citing papers authored by Françoise Devillard
This map shows the geographic impact of Françoise Devillard'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 Françoise Devillard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Françoise Devillard more than expected).
Fields of papers citing papers by Françoise Devillard
This network shows the impact of papers produced by Françoise Devillard. 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 Françoise Devillard. The network helps show where Françoise Devillard may publish in the future.
Co-authors
The 25 scholars most cited alongside Françoise Devillard, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 107 | |
| 2 | 2016 | 78 | |
| 3 | 2020 | 43 | |
| 4 | 2012 | 28 | |
| 5 | 2008 | 20 | |
| 6 | 2010 | 16 | |
| 7 | 2004 | 15 | |
| 8 | 2014 | 15 | |
| 9 | 2014 | 14 | |
| 10 | 1998 | 13 | |
| 11 | 2019 | 11 | |
| 12 | 1991 | 10 | |
| 13 | 2007 | 10 | |
| 14 | 2018 | 10 | |
| 15 | 2013 | 9 | |
| 16 | 2014 | 7 | |
| 17 | 2024 | 6 | |
| 18 | 2015 | 5 | |
| 19 | 2018 | 5 | |
| 20 | 2015 | 4 |
About Françoise Devillard
Françoise Devillard is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Public Health, Environmental and Occupational Health, having authored 27 papers that have together received 436 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (5 papers), Chromosomal and Genetic Variations (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Rare Diseases (2 papers), Epigenetics and DNA Methylation (2 papers), Genetic Syndromes and Imprinting (2 papers) and Down syndrome and intellectual disability research (2 papers). The work is most often cited by research in Reproductive Medicine (133 citations), Genetics (196 citations), Pediatrics, Perinatology and Child Health (99 citations), Developmental Neuroscience (14 citations) and Public Health, Environmental and Occupational Health (75 citations). Françoise Devillard has collaborated with scholars based in France, Italy and New Zealand. Frequent co-authors include Florence Amblard, Véronique Satre, Charles Coutton, Pierre‐Simon Jouk, Gaëlle Vieville, Guillaume Martinez, Sophie Brouillet, Sylviane Hennebicq, Christophe Arnoult and Habib Latrous. Their work appears in journals such as Human Reproduction, Prenatal Diagnosis, Clinical Genetics, Neurogenetics and International Journal of Molecular Sciences.
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.