Véronique Geoffroy
- Genetics top 5%
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
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- Hedgehog Signaling Pathway Studies 5
- Genomics and Phylogenetic Studies 4
- dental development and anomalies 4
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- Bone and Dental Protein Studies 3
- Co-authors
- Corinne StoetzelHélène DollfusJean MullerAmélie PitonArnaud KressYvan HerengerSophie ScheideckerChristelle Etard
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Véronique Geoffroy
17 papers receiving 769 citations
Peers
Comparison fields: 5 of 72
- Genetics 510
- Molecular Biology 559
- Cancer Research 70
- Developmental Biology 9
- Cell Biology 64
Countries citing papers authored by Véronique Geoffroy
This map shows the geographic impact of Véronique Geoffroy'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 Véronique Geoffroy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Véronique Geoffroy more than expected).
Fields of papers citing papers by Véronique Geoffroy
This network shows the impact of papers produced by Véronique Geoffroy. 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 Véronique Geoffroy. The network helps show where Véronique Geoffroy may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Véronique Geoffroy, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 6 | |
| 2 | 2023 | 5 | |
| 3 | 2021 | 34 | |
| 4 | 2019 | 15 | |
| 5 | 2019 | 5 | |
| 6 | 2019 | 10 | |
| 7 | 2019 | 29 | |
| 8 | 2018 | 207 | |
| 9 | 2018 | 9 | |
| 10 | 2016 | 11 | |
| 11 | 2016 | 40 | |
| 12 | 2016 | 57 | |
| 13 | 2015 | 50 | |
| 14 | 2015 | 47 | |
| 15 | 2013 | 104 | |
| 16 | 2012 | 81 | |
| 17 | 2011 | 65 |
About Véronique Geoffroy
Véronique Geoffroy is a scholar working on Genetics, Developmental Biology and Oral Surgery, having authored 17 papers that have together received 775 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (5 papers), Hedgehog Signaling Pathway Studies (5 papers), Genomics and Rare Diseases (4 papers), Genomics and Phylogenetic Studies (4 papers), dental development and anomalies (4 papers), Bone and Dental Protein Studies (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (510 citations), Molecular Biology (559 citations) and Cancer Research (70 citations). Véronique Geoffroy has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Corinne Stoetzel, Hélène Dollfus, Jean Muller, Amélie Piton, Arnaud Kress, Yvan Herenger, Sophie Scheidecker, Christelle Etard, Uwe Strähle and Élise Schaefer. Their work appears in journals such as Nucleic Acids Research, Nature Communications and Bioinformatics.
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.