Jamel Chelly
Impact in
- Genetics top 0.2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Developmental Neuroscience top 1%
Papers in
- Genetics 95
- Genetics and Neurodevelopmental Disorders 90
- Genomic variations and chromosomal abnormalities 23
-
- Ubiquitin and proteasome pathways 18
- RNA modifications and cancer 17
- Congenital heart defects research 10
- Epigenetics and DNA Methylation 9
- Co-authors
- Thierry Bienvenu (34 shared papers)Claude Moraine (20 shared papers)Ben C.J. Hamel (10 shared papers)Hans‐Hilger Ropers (14 shared papers)Martine Raynaud (14 shared papers)Chérif Beldjord (11 shared papers)Jean‐Pierre Fryns (9 shared papers)Juliette Nectoux (15 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)Neurogenetics (6 papers)European Journal of Medical Genetics (5 papers)Human Molecular Genetics (5 papers)The American Journal of Human Genetics (4 papers)
- Partner nations
- FranceGermanyNetherlands
In The Last Decade
Jamel Chelly
111 papers receiving 5.4k citations
Jamel Chelly's Hit Papers
Peers
Comparison fields: 5 of 106
- Genetics 3.2k
- Developmental Neuroscience 301
- Cellular and Molecular Neuroscience 938
- Cognitive Neuroscience 948
- Molecular Biology 3.2k
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 111 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 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 | 552 |
| 2 | 2000 | 289 | |
| 3 | 1998 | 265 | |
| 4 | 2002 | 231 | |
| 5 | 1999 | 226 | |
| 6 | 2008 | 209 | |
| 7 | 2006 | 206 | |
| 8 | 2006 | 179 | |
| 9 | 1994 | 156 | |
| 10 | 2000 | 154 | |
| 11 | 2002 | 113 | |
| 12 | 2006 | 105 | |
| 13 | 1999 | 93 | |
| 14 | 2008 | 90 | |
| 15 | 2009 | 89 | |
| 16 | 2006 | 87 | |
| 17 | 2008 | 85 | |
| 18 | 2008 | 83 | |
| 19 | 2004 | 82 | |
| 20 | 2012 | 80 |
About Jamel Chelly
Jamel Chelly is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Cellular and Molecular Neuroscience, having authored 111 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (90 papers), Genomic variations and chromosomal abnormalities (23 papers), Ubiquitin and proteasome pathways (18 papers), RNA modifications and cancer (17 papers), Autism Spectrum Disorder Research (16 papers), Chromosomal and Genetic Variations (12 papers), Congenital heart defects research (10 papers) and Epigenetics and DNA Methylation (9 papers). The work is most often cited by research in Genetics (3.2k citations), Developmental Neuroscience (301 citations), Cellular and Molecular Neuroscience (938 citations), Cognitive Neuroscience (948 citations) and Molecular Biology (3.2k citations). Jamel Chelly has collaborated with scholars based in France, Germany and Netherlands. Frequent co-authors include Thierry Bienvenu, Claude Moraine, Ben C.J. Hamel, Hans‐Hilger Ropers, Martine Raynaud, Chérif Beldjord, Jean‐Pierre Fryns, Juliette Nectoux, Fiona Francis and Nathalie Ronce. Their work appears in journals such as European Journal of Human Genetics, Neurogenetics, European Journal of Medical Genetics, Human Molecular Genetics and The American Journal of Human 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.