Jamel Chelly
Impact in
- Developmental Neuroscience top 0.05%
- Neurogenesis and neuroplasticity mechanisms
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 202
- Genetics and Neurodevelopmental Disorders 164
- Genomic variations and chromosomal abnormalities 24
- Genomics and Rare Diseases 21
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- Fetal and Pediatric Neurological Disorders 55
- Co-authors
- Axel Kahn (31 shared papers)Thierry Bienvenu (58 shared papers)Cherif Beldjord (45 shared papers)Fiona Francis (28 shared papers)Jean‐Claude Kaplan (17 shared papers)Pierre Billuart (31 shared papers)Claude Moraine (31 shared papers)Anthony P. Monaco (23 shared papers)
- Journals
- European Journal of Human Genetics (26 papers)Human Molecular Genetics (25 papers)The American Journal of Human Genetics (16 papers)Journal of Medical Genetics (13 papers)Nature Genetics (13 papers)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Jamel Chelly
360 papers receiving 25.5k citations
Jamel Chelly's Hit Papers
Peers
Comparison fields: 5 of 153
- Developmental Neuroscience 2.6k
- Genetics 8.6k
- Pediatrics, Perinatology and Child Health 2.4k
- Cellular and Molecular Neuroscience 2.1k
- Cell Biology 1.7k
Countries citing papers authored by Jamel Chelly
This map shows the geographic impact of Jamel Chelly'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 Jamel Chelly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamel Chelly more than expected).
Fields of papers citing papers by Jamel Chelly
This network shows the impact of papers produced by Jamel Chelly. 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 Jamel Chelly. The network helps show where Jamel Chelly may publish in the future.
Co-authors
The 25 scholars most cited alongside Jamel Chelly, 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 361 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas Hit paper breakdown → | 1998 | 970 |
| 2 | 1999 | 876 | |
| 3 | The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Hit paper breakdown → | 1989 | 832 |
| 4 | Transcription of the dystrophin gene in human muscle and non-muscle tissues Hit paper breakdown → | 1988 | 652 |
| 5 | 1998 | 639 | |
| 6 | X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family Hit paper breakdown → | 2004 | 636 |
| 7 | Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein Hit paper breakdown → | 1993 | 619 |
| 8 | 1989 | 555 | |
| 9 | A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation Hit paper breakdown → | 2009 | 505 |
| 10 | 1998 | 425 | |
| 11 | 2007 | 384 | |
| 12 | 2013 | 380 | |
| 13 | 2012 | 343 | |
| 14 | 2005 | 325 | |
| 15 | 2000 | 314 | |
| 16 | 2009 | 306 | |
| 17 | 2009 | 299 | |
| 18 | 1998 | 288 | |
| 19 | 1999 | 265 | |
| 20 | 2002 | 253 |
About Jamel Chelly
Jamel Chelly is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Neuroscience, Molecular Biology and Psychiatry and Mental health, having authored 361 papers that have together received 26.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (164 papers), Fetal and Pediatric Neurological Disorders (55 papers), Muscle Physiology and Disorders (38 papers), Neurogenesis and neuroplasticity mechanisms (26 papers), Genomic variations and chromosomal abnormalities (24 papers), Genomics and Rare Diseases (21 papers), Epilepsy research and treatment (18 papers) and Microtubule and mitosis dynamics (11 papers). The work is most often cited by research in Developmental Neuroscience (2.6k citations), Genetics (8.6k citations), Pediatrics, Perinatology and Child Health (2.4k citations), Cellular and Molecular Neuroscience (2.1k citations) and Cell Biology (1.7k citations). Jamel Chelly has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Axel Kahn, Thierry Bienvenu, Cherif Beldjord, Fiona Francis, Jean‐Claude Kaplan, Pierre Billuart, Claude Moraine, Anthony P. Monaco, Karine Poirier and Jean‐Pierre Fryns. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Journal of Medical Genetics 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.