Jamel Chelly - Concepedia

Author

Jamel Chelly

Also Known As

Chelly, J, Chelly, J., Chelly, Jamel, Chérif Beldjord, J Chelly, J. Chelly, Jamel CHELLY, Jamel Chelly, Jamel Chelly (93238), Maria-Victoria Hinckelmann

234

Publications

17.8K

Citations

H-Index

170

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique Institut Cochin Université Paris Cité Assistance Publique – Hôpitaux de Paris

About

Jamel Chelly is an author at Inserm specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	90	11.3K
2	Natural Sciences	10	10	2.1K
3	Health Sciences	7	7	688
4	Public Health	5	5	525
5	Engineering	2	2	183

Jamel Chelly

147

Publications

16.1K

Citations

H-Index

Page 1

	Year	Citations
Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons Fiona Francis, Annette Koulakoff, Dominique Boucher, Neuron Microtubule-associated ProteinNeuroregenerationDevelopmental BiologyMolecular NeuroscienceNeural Stem Cell	1999	997
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome Vincent des Portes, Jean Marc Pinard, Pierre Billuart, Cell Neurobiology Of DiseaseDevelopmental BiologyNeurogenomicsNeurological DisorderNeuroanatomy	1998	736
Transcription of the dystrophin gene in human muscle and non-muscle tissues Jamel Chelly, Jean-Claude Kaplan, Pascal Maire, Nature Human MuscleMuscle FunctionMolecular PhysiologyDystrophin GeneMuscle Injury	1988	727
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein Jamel Chelly, Zeynep Tümer, T. Tønnesen, Nature Genetics Mendelian DisorderDisease MechanismMenkes DiseaseMedicineGenetics	1993	726
Illegitimate transcription: transcription of any gene in any cell type. Jamel Chelly, Jean‐Paul Concordet, Josseline Kaplan, Proceedings of the National Academy of Sciences Vitro AmplificationTranscriptional RegulationSystems BiologyMolecular PhysiologyFactor Viiic	1989	638
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly Karine Poirier, Nicolas Lebrun, Loïc Broix, Nature Genetics Developmental AnomalyDevelopmental BiologyBrain DevelopmentDevelopmental GeneticsGenetics	2013	488
Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans David A. Keays, Guoling Tian, Karine Poirier, Cell	2007	435
Differentially Activated Macrophages Orchestrate Myogenic Precursor Cell Fate During Human Skeletal Muscle Regeneration Marielle Saclier, Houda Yacoub‐Youssef, Abigail L. Mackey, Stem Cells Regenerative MedicineRegenerationMechanobiologyInflammationDevelopmental Biology	2012	396
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation Lars Riff Jensen, M Amende, Ulf Gurok, The American Journal of Human Genetics ChromatinTranscriptional RegulationGenome InstabilityJarid1c GeneChromatin Remodeling	2005	374
Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria Xavier H. Jaglin, Karine Poirier, Yoann Saillour, Nature Genetics BiologyNatural SciencesGeneticsMolecular BiologyAsymmetrical Polymicrogyria	2009	365

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