Jamel Chelly

17.9k citations

128 papers · 9.7k indexed · 5 hit papers · h-index 50

Developmental Neuroscience top 0.2%
- Neurogenesis and neuroplasticity mechanisms 17
Cell Biology top 0.5%
- Microtubule and mitosis dynamics 20
- Cellular transport and secretion 11
Cellular and Molecular Neuroscience top 1%
Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 33
Molecular Biology top 1%
- Muscle Physiology and Disorders 28
- Congenital heart defects research 12
- Ubiquitin and proteasome pathways 11
- RNA modifications and cancer 10

Co-authors: Axel Kahn Fiona Francis Yoheved Berwald‐Netter A. J. Kahn Jean‐Paul Concordet Josseline Kaplan Pascal Maire Sophie Gautron
Cited by: Developmental Neuroscience Cell Biology Cellular and Molecular Neuroscience
Journals: Human Molecular Genetics (14 papers)European Journal of Human Genetics (7 papers)Human Genetics (6 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Jamel Chelly

127 papers receiving 9.6k citations

Hit Papers

5 papers align trajectories log scale

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.

1999 Neuron
1998 Cell
1993 Nature Genetics
1989 Proceedings of the National Academy of Sciences
1988 Nature

Peers

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

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.

Border = papers with Jamel Chelly Line = papers co-authored together Jamel Chelly links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development Nature Communications ·Watsatree Diteeyont,Karine Poirier,Richard Belvindrah,Imane Moutkine,Anne Houllier,Tal Ohana,Florence Petit,Anne Boland,Stephan C. Collins,Mariano Soiza‐Reilly,Binnaz Yalcin,Jamel Chelly,Jean‐François Deleuze,Nadia Bahi‐Buisson,Fiona Francis	2022	4
2	De novo and inherited private variants in MAP1B in periventricular nodular heterotopia PLoS Genetics ·Erin L. Heinzen,Adam C. O’Neill,Xiaolin Zhu,Andrew S. Allen,Melanie Bahlo,Jamel Chelly,Ming Hui Chen,William B. Dobyns,Saskia Freytag,Renzo Guerrini,Richard J. Leventer,Annapurna Poduri,Stephen P. Robertson,Christopher A. Walsh,Mengqi Zhang,(unknown)	2018	45
3	Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency Journal of Neuroscience ·Chun-Lei Zhang,Puchérie Christiane Barro-Kiki,Maria João Soares de Almeida Pereira Santos,Xander Houbaert,Hajer El Oussini,Christelle Martin,Marilyn Lepleux,Elisabeth Normand,Jamel Chelly,Étienne Herzog,Pierre Billuart,Yann Humeau	2017	7
4	New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum Brain ·Nadia Bahi‐Buisson,Isabelle Souville,Franck J. Fourniol,Aurélie Toussaint,Carolyn A. Moores,Anne Houdusse,J.A. Squier,Karine Poirier,Wendian YIN,Marie Hully,Pierre Louis Léger,Caroline Elie,Nathalie Boddaert,Chérif Beldjord,Jamel Chelly,Fiona Francis	2013	74
5	Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria European Journal of Human Genetics ·Karine Poirier,Yoann Saillour,Franck J. Fourniol,Fiona Francis,Isabelle Souville,Stéphanie Valence,Isabelle Desguerre,Saida Ayana,Nathalie Boddaert,K. Grygierek,Chérif Beldjord,Jamel Chelly,Nadia Bahi‐Buisson	2012	50
6	Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinoma Clinics and Research in Hepatology and Gastroenterology ·Philippe Couvert,Alain Carrié,Sophie Tézenas du Montcel,J Vaysse,Angéla Sutton,Nathalie Barget,Jean–Claude Trinchet,Michel Beaugrand,Nathalie Ganne‐Carrié,Philippe Giral,Jamel Chelly	2012	13
7	Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway Human Molecular Genetics ·Guoling Tian,Xavier H. Jaglin,David A. Keays,Fiona Francis,Jamel Chelly,Nicholas J. Cowan	2010	47
8	GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Brain ·Nadia Bahi‐Buisson,Karine Poirier,Nathalie Boddaert,Catherine Fallet‐Bianco,Nicola Specchio,Enrico Bertini,Ahmet Okay Çağlayan,Karine Lascelles,Caroline Elie,Jérôme Rambaud,Michel Baulac,Isabelle An,Patrícia Dias,Vincent des Portes,Marie Laure Moutard,Christine Soufflet,Dipesh Kumar Gupta,Chérif Beldjord,Laurent Villard,Jamel Chelly	2010	102
9	A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization Human Mutation ·Tangui Le Guen,Yann Fichou,Juliette Nectoux,Nadia Bahi‐Buisson,François Rivier,Nathalie Boddaert,Karen Elaine Smith,Delphine Héron,Jamel Chelly,Thierry Bienvenu	2010	15
10	Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects Trends in Genetics ·Xavier H. Jaglin,Jamel Chelly	2009	126
11	A Pachygyria-causing α-Tubulin Mutation Results in Inefficient Cycling with CCT and a Deficient Interaction with TBCB Molecular Biology of the Cell ·Guoling Tian,Xiang‐Peng Kong,Xavier H. Jaglin,Jamel Chelly,David A. Keays,Nicholas J. Cowan	2008	37
12	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 ·Malik Khelfaoui,Cécile V. Denis,张文质,Frédéric de Bock,Alain Schmitt,Christophe Houbron,Élise Morice,Bruno Giros,G.J.A. Ramakers,Sharmila Mudgal,Jamel Chelly,Marika Nosten‐Bertrand,Pierre Billuart	2007	112
13	Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans Cell ·David A. Keays,Guoling Tian,Karine Poirier,Guo‐Jen Huang,Christian Siebold,James Cleak,Peter L. Oliver,Martin Fray,Victoria L. Harvey,Zoltán Molnár,Maria Carmen Piñon,Neil Dear,William Valdar,Steve D. M. Brown,Kay E. Davies,J. N. P. Rawlins,Nicholas J. Cowan,Patrick M. Nolan,Jamel Chelly,Jonathan Flint	2007	322
14	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 ·Purushothaman Pichandi,S. V. Neklyudov,S. Llense,M. Akhtar,Dominique Récan,Cécile Peccate,Arthur H.M. Burghes,Christophe Béroud,Luis Garcı́a,Jean‐Claude Kaplan,Jamel Chelly,France Leturcq	2006	95
15	Calpain 10 and development of diabetes mellitus in cystic fibrosis Journal of Cystic Fibrosis ·蒋晓冬,Sheikh Hategekimana Assan,D. Hubert,Chaitanya Kini S,Sophie Grabar,Jamel Chelly,Thierry Bienvenu	2005	27
16	Mechanism of Microtubule Stabilization by Doublecortin Molecular Cell ·Carolyn A. Moores,Mylène Perderiset,Fiona Francis,Jamel Chelly,Anne Houdusse,Ronald A. Milligan	2004	183
17	Active Caspase-8 Translocates into the Nucleus of Apoptotic Cells to Inactivate Poly(ADP-ribose) Polymerase-2 Journal of Biological Chemistry ·Alexandra Benchoua,F. Ertl,Ruthleia Leoncio de Almeida,Laurence Tartier,Philippe Couvert,Gaëlle Friocourt,Jamel Chelly,Abdelmoumen Saci,J. WANG	2002	69
18	Breakthroughs in molecular andcellular mechanisms underlying X-linked mental retardation Human Molecular Genetics ·Jamel Chelly	1999	55
19	Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients. Journal of Clinical Investigation ·Jamel Chelly,Hélène Gilgenkrantz,Jean‐Philippe Hugnot,G. Hamard,J Misković,Dominique Récan,Saïd Akli,Haardik Gupta,A Kahn,J.‐C. Kaplan	1991	46
20	Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia Human Genetics ·F. Marlhens,Jamel Chelly,J.‐C. Kaplan,D. Lefrançois,J P Harpey,Bernard Dutrillaux	1987	12

About Jamel Chelly

Jamel Chelly is a scholar working on Developmental Neuroscience, Genetics and Cell Biology, having authored 128 papers that have together received 9.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (33 papers), Muscle Physiology and Disorders (28 papers), Microtubule and mitosis dynamics (20 papers), Neurogenesis and neuroplasticity mechanisms (17 papers), Congenital heart defects research (12 papers), Ubiquitin and proteasome pathways (11 papers), Cellular transport and secretion (11 papers) and RNA modifications and cancer (10 papers). The work is most often cited by research in Developmental Neuroscience (1.4k citations), Cell Biology (1.9k citations) and Cellular and Molecular Neuroscience (1.8k citations). Jamel Chelly has collaborated with scholars based in France, United Kingdom and United States. Frequent 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. Their work appears in journals such as Human Molecular Genetics, European Journal of Human Genetics, Human Genetics, Genomics and European 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.

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