Alain Verloès
- Molecular Biology top 1%
- Genetics top 0.2%
- Surgery top 5%
- Genetics top 0.5%
- Pulmonary and Respiratory Medicine top 2%
- Co-authors
- Damien SanlavilleL KoulischerClarisse BaumannSandrine PassemardNatzi SakalihasanIsabelle Bailleul‐ForestierRaymond LimetAriane Berdal
- Topics
- Genomic variations and chromosomal abnormalities (55 papers)Genetics and Neurodevelopmental Disorders (39 papers)Hedgehog Signaling Pathway Studies (30 papers)
- Cited by
- GeneticsMolecular Biology
- Partner nations
- FranceBelgiumUnited States
In The Last Decade
Alain Verloès
307 papers receiving 8.4k citations
Peers
Comparison fields: 5 of 143
- Molecular Biology 4.4k
- Genetics 3.8k
- Surgery 1.1k
- Genetics 1.1k
- Pulmonary and Respiratory Medicine 1.0k
Countries citing papers authored by Alain Verloès
This map shows the geographic impact of Alain Verloès'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 Alain Verloès with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alain Verloès more than expected).
Fields of papers citing papers by Alain Verloès
This network shows the impact of papers produced by Alain Verloès. 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 Alain Verloès. The network helps show where Alain Verloès may publish in the future.
Co-authorship network of co-authors of Alain Verloès
This figure shows the co-authorship network connecting the top 25 collaborators of Alain Verloès. A scholar is included among the top collaborators of Alain Verloès based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alain Verloès. Alain Verloès is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 8 | |
| 3 | 18 | |
| 4 | 12 | |
| 5 | 10 | |
| 6 | Gonadal Function of Female Patients with Noonan Syndrome | 1 |
| 7 | 6 | |
| 8 | 19 | |
| 9 | 25 | |
| 10 | 15 | |
| 11 | 47 | |
| 12 | 24 | |
| 13 | 33 | |
| 14 | 2 | |
| 15 | 90 | |
| 16 | 9 | |
| 17 | 51 | |
| 18 | 3 | |
| 19 | 48 | |
| 20 | 10 |
About Alain Verloès
Alain Verloès is a scholar working on Developmental Biology, Genetics and Genetics, having authored 314 papers that have together received 8.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (55 papers), Genetics and Neurodevelopmental Disorders (39 papers) and Hedgehog Signaling Pathway Studies (30 papers). The work is most often cited by research in Genetics (3.8k citations), Genetics (1.1k citations) and Molecular Biology (4.4k citations). Alain Verloès has collaborated with scholars based in France, Belgium and United States. Frequent co-authors include Damien Sanlaville, L Koulischer, Clarisse Baumann, Sandrine Passemard, Natzi Sakalihasan, Isabelle Bailleul‐Forestier, Raymond Limet, Ariane Berdal, Didier Lacombe and Pierre Gressèns. Their work appears in journals such as Circulation, Journal of Clinical Investigation and Nature 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.