Nicolas Lévy
Impact in
- Aging top 0.5%
- Genetics, Aging, and Longevity in Model Organisms
- Molecular Biology top 0.5%
- Nuclear Structure and Function
- Muscle Physiology and Disorders
Papers in
- Genetics 86
- Genomics and Rare Diseases 50
- Genetic and rare skin diseases. 13
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 11
-
- Muscle Physiology and Disorders 74
- Nuclear Structure and Function 65
- Co-authors
- Claire Laure Navarro (32 shared papers)Annachiara De Sandre‐Giovannoli (57 shared papers)Pierre Cau (29 shared papers)Rafaëlle Bernard (32 shared papers)Irène Boccaccio (8 shared papers)Colin L. Stewart (3 shared papers)Martin Krahn (65 shared papers)Martine F. Le Merrer (4 shared papers)
- Journals
- Neuromuscular Disorders (16 papers)Human Mutation (15 papers)European Journal of Human Genetics (11 papers)Human Molecular Genetics (11 papers)Journal of Medical Genetics (10 papers)
- Partner nations
- FranceUnited StatesSpain
In The Last Decade
Nicolas Lévy
285 papers receiving 11.7k citations
Nicolas Lévy's Hit Papers
Peers
Comparison fields: 5 of 142
- Aging 269
- Molecular Biology 6.6k
- Cellular and Molecular Neuroscience 1.2k
- Genetics 1.9k
- Genetics 353
Countries citing papers authored by Nicolas Lévy
This map shows the geographic impact of Nicolas 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 Nicolas Lévy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicolas Lévy more than expected).
Fields of papers citing papers by Nicolas Lévy
This network shows the impact of papers produced by Nicolas 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 Nicolas Lévy. The network helps show where Nicolas Lévy may publish in the future.
Co-authors
The 25 scholars most cited alongside Nicolas 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 291 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Lamin A Truncation in Hutchinson-Gilford Progeria Hit paper breakdown → | 2003 | 1192 |
| 2 | 2002 | 460 | |
| 3 | 2011 | 347 | |
| 4 | 2008 | 329 | |
| 5 | 2004 | 296 | |
| 6 | 2005 | 239 | |
| 7 | 2011 | 239 | |
| 8 | 2006 | 237 | |
| 9 | 2018 | 228 | |
| 10 | 2007 | 215 | |
| 11 | Texture Indexes and Gray Level Size Zone Matrix Application to Cell Nuclei Classification | 2009 | 206 |
| 12 | 2019 | 203 | |
| 13 | 2006 | 187 | |
| 14 | 2013 | 176 | |
| 15 | 2011 | 163 | |
| 16 | 2013 | 155 | |
| 17 | 2006 | 137 | |
| 18 | 2009 | 137 | |
| 19 | 2012 | 136 | |
| 20 | 2007 | 130 |
About Nicolas Lévy
Nicolas Lévy is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology and Genetics, having authored 291 papers that have together received 12k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (74 papers), Nuclear Structure and Function (65 papers), Genomics and Rare Diseases (50 papers), Hereditary Neurological Disorders (45 papers), Genetic and rare skin diseases. (13 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Sperm and Testicular Function (9 papers). The work is most often cited by research in Aging (269 citations), Molecular Biology (6.6k citations), Cellular and Molecular Neuroscience (1.2k citations), Genetics (1.9k citations) and Genetics (353 citations). Nicolas Lévy has collaborated with scholars based in France, United States and Spain. Frequent co-authors include Claire Laure Navarro, Annachiara De Sandre‐Giovannoli, Pierre Cau, Rafaëlle Bernard, Irène Boccaccio, Colin L. Stewart, Martin Krahn, Martine F. Le Merrer, Arnold Münnich and Stanislas Lyonnet. Their work appears in journals such as Neuromuscular Disorders, Human Mutation, European Journal of Human Genetics, Human Molecular Genetics and Journal of Medical 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.