Jamel Chelly

17.9k total citations · 5 hit papers
128 papers, 9.7k citations indexed

About

Jamel Chelly is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Jamel Chelly has authored 128 papers receiving a total of 9.7k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 55 papers in Genetics and 32 papers in Cell Biology. Recurrent topics in Jamel Chelly's work include Genetics and Neurodevelopmental Disorders (33 papers), Muscle Physiology and Disorders (28 papers) and Microtubule and mitosis dynamics (20 papers). Jamel Chelly is often cited by papers focused on Genetics and Neurodevelopmental Disorders (33 papers), Muscle Physiology and Disorders (28 papers) and Microtubule and mitosis dynamics (20 papers). Jamel Chelly collaborates with scholars based in France, United Kingdom and United States. Jamel Chelly's co-authors include Axel Kahn, Fiona Francis, Yoheved Berwald‐Netter, A. J. Kahn, Jean‐Paul Concordet, Josseline Kaplan, Pascal Maire, Sophie Gautron, Anthony P. Monaco and Annette Koulakoff and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jamel Chelly

127 papers receiving 9.6k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons

1999 837 citations Fiona Francis, Annette Koulakoff et al. profile →
Transcription of the dystrophin gene in human muscle and non-muscle tissues

1988 640 citations Jamel Chelly, Pascal Maire et al. Nature profile →
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

1998 589 citations Vincent des Portes, Pierre Billuart et al. Cell profile →
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

1993 557 citations Jamel Chelly et al. profile →
Illegitimate transcription: transcription of any gene in any cell type.

1989 539 citations Jamel Chelly et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Jamel Chelly France	50	5.8k	2.4k	1.9k	1.8k	1.4k	128	9.7k
Katsuhiko Mikoshiba Japan	65	9.0k 1.5×	1.6k 0.6×	2.0k 1.0×	2.5k 1.4×	1.2k 0.8×	205	12.6k
Alexander Grinberg United States	46	6.3k 1.1×	1.9k 0.8×	1.1k 0.6×	1.5k 0.8×	637 0.4×	61	11.0k
Noriko Osumi Japan	53	6.2k 1.1×	1.7k 0.7×	774 0.4×	1.8k 1.0×	2.0k 1.4×	223	9.0k
Muriel T. Davisson United States	56	7.2k 1.2×	3.4k 1.4×	1.4k 0.8×	1.9k 1.0×	472 0.3×	183	12.0k
Vassilis Pachnis United Kingdom	65	7.4k 1.3×	2.5k 1.0×	620 0.3×	3.4k 1.9×	2.5k 1.7×	120	14.9k
Kazuki Nakao Japan	58	9.6k 1.6×	1.7k 0.7×	2.0k 1.0×	2.3k 1.3×	590 0.4×	221	15.7k
Albee Messing United States	65	8.8k 1.5×	1.7k 0.7×	1.3k 0.7×	4.8k 2.7×	2.2k 1.5×	174	14.5k
Kazuhiro Ikenaka Japan	55	5.3k 0.9×	1.2k 0.5×	946 0.5×	3.2k 1.8×	3.2k 2.2×	251	10.4k
Fiona Francis France	39	2.9k 0.5×	1.8k 0.7×	1.3k 0.7×	1.2k 0.7×	1.6k 1.1×	103	6.5k
Simon W. M. John United States	64	7.6k 1.3×	1.0k 0.4×	1.3k 0.7×	1.9k 1.1×	542 0.4×	155	15.3k

Countries citing papers authored by Jamel Chelly

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Jamel Chelly

This figure shows the co-authorship network connecting the top 25 collaborators of Jamel Chelly. A scholar is included among the top collaborators of Jamel Chelly 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 Jamel Chelly. Jamel Chelly is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Poirier, Karine, Richard Belvindrah, Imane Moutkine, et al.. (2022). Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13(1). 2746–2746. 4 indexed citations

Heinzen, Erin L., Adam C. O’Neill, Xiaolin Zhu, et al.. (2018). De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. PLoS Genetics. 14(5). e1007281–e1007281. 45 indexed citations

Broix, Loïc, Carla G. Silva, Peggy Tilly, et al.. (2017). Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development. Human Molecular Genetics. 27(2). 224–238. 27 indexed citations

Zhang, Chun-Lei, Xander Houbaert, Hajer El Oussini, et al.. (2017). Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency. Journal of Neuroscience. 37(46). 11114–11126. 7 indexed citations

Tian, Guoling, Xavier H. Jaglin, David A. Keays, et al.. (2010). Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway. Human Molecular Genetics. 19(18). 3599–3613. 47 indexed citations

Bahi‐Buisson, Nadia, Karine Poirier, Nathalie Boddaert, et al.. (2010). GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Brain. 133(11). 3194–3209. 102 indexed citations

Pavlowsky, Alice, Antonella Gianfelice, Marta Pallotto, et al.. (2010). A Postsynaptic Signaling Pathway that May Account for the Cognitive Defect Due to IL1RAPL1 Mutation. Current Biology. 20(2). 103–115. 94 indexed citations

Lecourtois, Magalie, Karine Poirier, Gaëlle Friocourt, et al.. (2010). Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype. Acta Neuropathologica. 119(6). 779–789. 39 indexed citations

Bashiardes, Stavros, Hans van Bokhoven, Hans‐Hilger Ropers, et al.. (2009). A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients with X-Linked Disorders. Journal of Molecular Diagnostics. 11(6). 562–568. 4 indexed citations

10.

Gambino, Frédéric, Alice Pavlowsky, Henriette Skala, et al.. (2009). IL1RAPL1 controls inhibitory networks during cerebellar development in mice. European Journal of Neuroscience. 30(8). 1476–1486. 30 indexed citations

11.

Nosten‐Bertrand, Marika, Caroline Kappeler, Céline Dinocourt, et al.. (2008). Epilepsy in Dcx Knockout Mice Associated with Discrete Lamination Defects and Enhanced Excitability in the Hippocampus. PLoS ONE. 3(6). e2473–e2473. 54 indexed citations

12.

Khelfaoui, Malik, Cécile V. Denis, Frédéric de Bock, et al.. (2007). Loss of X-Linked Mental Retardation Gene Oligophrenin1 in Mice Impairs Spatial Memory and Leads to Ventricular Enlargement and Dendritic Spine Immaturity. Journal of Neuroscience. 27(35). 9439–9450. 112 indexed citations

13.

Llense, S., Dominique Récan, Cécile Peccate, et al.. (2006). Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. Human Mutation. 28(2). 183–195. 95 indexed citations

14.

Poirier, Karine, Isabelle Souville, Cécile Laroche-Raynaud, et al.. (2005). Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation. Human Genetics. 118(1). 45–48. 19 indexed citations

15.

Moores, Carolyn A., Mylène Perderiset, Fiona Francis, et al.. (2004). Mechanism of Microtubule Stabilization by Doublecortin. Molecular Cell. 14(6). 833–839. 183 indexed citations

16.

Friocourt, Gaëlle, Caroline Kappeler, Yoann Saillour, et al.. (2004). Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes. Molecular and Cellular Neuroscience. 28(1). 153–164. 33 indexed citations

17.

Poirier, Karine, Céline Chalas, Frédérique Tissier, et al.. (2003). Loss of parental‐specific methylation at the IGF2 locus in human hepatocellular carcinoma. The Journal of Pathology. 201(3). 473–479. 27 indexed citations

18.

Portes, Vincent des, Pierre Billuart, Marie Claude Vinet, et al.. (1998). A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome. Cell. 92(1). 51–61. 589 indexed citations breakdown →

19.

Hugnot, Jean‐Philippe, et al.. (1993). Striking conservation of the brain-specific region of the dystrophin gene. Mammalian Genome. 4(7). 393–396. 4 indexed citations

20.

Chelly, Jamel, et al.. (1988). Transcription of the dystrophin gene in human muscle and non-muscle tissues. Nature. 333(6176). 858–860. 640 indexed citations breakdown →

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.

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