Josette Lucas
- Molecular Biology
- Epidemiology top 5%
- Hepatology top 2%
- Genetics top 10%
- Surgery
- Co-authors
- Christiane Guguen‐GuillouzoSylvie RuminStephan UrbanClaire GuyomardIsabelle CannieJacques Le SeyecDenise GlaiseChristian Trépo
- Topics
- Genomic variations and chromosomal abnormalities (13 papers)Prenatal Screening and Diagnostics (7 papers)Chromosomal and Genetic Variations (5 papers)
- Cited by
- HepatologyPharmacologyEpidemiology
- Partner nations
- FranceUnited StatesAustralia
In The Last Decade
Josette Lucas
27 papers receiving 1.5k citations
Hit Papers
Peers
Comparison fields: 5 of 103
- Molecular Biology 561
- Epidemiology 491
- Hepatology 461
- Genetics 305
- Surgery 176
Countries citing papers authored by Josette Lucas
This map shows the geographic impact of Josette Lucas'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 Josette Lucas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Josette Lucas more than expected).
Fields of papers citing papers by Josette Lucas
This network shows the impact of papers produced by Josette Lucas. 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 Josette Lucas. The network helps show where Josette Lucas may publish in the future.
Co-authorship network of co-authors of Josette Lucas
This figure shows the co-authorship network connecting the top 25 collaborators of Josette Lucas. A scholar is included among the top collaborators of Josette Lucas 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 Josette Lucas. Josette Lucas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 12 | |
| 2 | 31 | |
| 3 | 1 | |
| 4 | 6 | |
| 5 | 19 | |
| 6 | 45 | |
| 7 | 31 | |
| 8 | 2 | |
| 9 | 69 | |
| 10 | 27 | |
| 11 | 3 | |
| 12 | 18 | |
| 13 | 18 | |
| 14 | 15 | |
| 15 | 43 | |
| 16 | 6 | |
| 17 | 43 | |
| 18 | 49 | |
| 19 | 2 | |
| 20 | [Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion]. | 5 |
About Josette Lucas
Josette Lucas is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 27 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Hepatology (461 citations), Pharmacology (155 citations) and Epidemiology (491 citations). Josette Lucas has collaborated with scholars based in France, United States and Australia. Frequent co-authors include Christiane Guguen‐Guillouzo, Sylvie Rumin, Stephan Urban, Claire Guyomard, Isabelle Cannie, Jacques Le Seyec, Denise Glaise, Christian Trépo, Philippe Gripon and Sylvie Odent. Their work appears in journals such as Proceedings of the National Academy of Sciences, Clinical Endocrinology 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.