Jonathan Lévy
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 52
- Genetics and Neurodevelopmental Disorders 33
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 15
- Genetic and Kidney Cyst Diseases 2
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- RNA Research and Splicing 4
- Co-authors
- David M. Winder (1 shared paper)Jane Carolyn Sterling (1 shared paper)Peter K. C. Goon (1 shared paper)Alain Verloès (8 shared papers)Siolian L.R. Ball (1 shared paper)Margaret Stanley (1 shared paper)Céline Dupont (5 shared papers)Anne‐Claude Tabet (8 shared papers)
- Journals
- Clinical Genetics (10 papers)The American Journal of Human Genetics (7 papers)Genetics in Medicine (7 papers)European Journal of Human Genetics (7 papers)Human Mutation (3 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Jonathan Lévy
55 papers receiving 696 citations
Jonathan Lévy's Hit Papers
Peers
Comparison fields: 5 of 72
- Genetics 320
- Developmental Neuroscience 12
- Molecular Biology 160
- Epidemiology 76
- Developmental Biology 5
Countries citing papers authored by Jonathan Lévy
This map shows the geographic impact of Jonathan Lévy'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 Jonathan Lévy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Lévy more than expected).
Fields of papers citing papers by Jonathan Lévy
This network shows the impact of papers produced by Jonathan Lévy. 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 Jonathan Lévy. The network helps show where Jonathan Lévy may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan Lévy, 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 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 70 | |
| 2 | 2017 | 64 | |
| 3 | 2019 | 51 | |
| 4 | 2012 | 40 | |
| 5 | 2021 | 30 | |
| 6 | 2018 | 29 | |
| 7 | 2019 | 27 | |
| 8 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 9 | 2020 | 24 | |
| 10 | 2019 | 23 | |
| 11 | 2017 | 20 | |
| 12 | 2018 | 20 | |
| 13 | 2025 | 20 | |
| 14 | 2021 | 19 | |
| 15 | 2021 | 18 | |
| 16 | 2020 | 16 | |
| 17 | 2022 | 16 | |
| 18 | 2022 | 16 | |
| 19 | 2022 | 12 | |
| 20 | 2023 | 12 |
About Jonathan Lévy
Jonathan Lévy is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Developmental Biology and Immunology, having authored 64 papers that have together received 719 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (33 papers), Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (15 papers), RNA Research and Splicing (4 papers), Hereditary Neurological Disorders (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Cervical Cancer and HPV Research (1 paper). The work is most often cited by research in Genetics (320 citations), Developmental Neuroscience (12 citations), Molecular Biology (160 citations), Epidemiology (76 citations) and Developmental Biology (5 citations). Jonathan Lévy has collaborated with scholars based in France, United States and Germany. Frequent co-authors include David M. Winder, Jane Carolyn Sterling, Peter K. C. Goon, Alain Verloès, Siolian L.R. Ball, Margaret Stanley, Céline Dupont, Anne‐Claude Tabet, Boris Keren and Marie‐France Portnoï. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, Genetics in Medicine, European Journal of Human Genetics 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.