J.‐C. Kaplan - Concepedia

Author

J.‐C. Kaplan

Also Known As

J C Kaplan, J Kaplan, J-C. Kaplan, J. -C. Kaplan, J. C. KAPLAN, J. C. Kaplan, J. Cl. Kaplan, J. Kaplan, J.-C Kaplan, J.-C. Kaplan

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Inserm Institut Cochin Centre National de la Recherche Scientifique Hôpital Cochin Château de Longchamp

About

J.‐C. Kaplan is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	21	1.2K
2	Natural Sciences	5	5	151
3	Health Sciences	3	3	251
4	Engineering	2	2	353
5	Public Health	1	1	12

J.‐C. Kaplan

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Alan H. Beggs, Mary B. Moyer, S. Scherpf, PubMed	1989	961
Modification of enzymatic-ally amplified DNA for the detection of point mutations A. Haliassos, Jean‐Claude Chomel, Laurent Tesson, Nucleic Acids Research EngineeringGeneticsDna AnalysisMolecular BiologyNucleic Acid Amplification Test	1989	322
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers A. Haliassos, Jean‐Claude Chomel, S Grandjouan, Nucleic Acids Research GeneticsDna AnalysisPathologyRestriction SiteArtificial Restriction Site	1989	178
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Alain Carrié, Fédérica Piccolo, France Leturcq, Journal of Medical Genetics Rare DiseasesMendelian DisorderGenetic DisorderMutational DiversityGenetics	1997	115
The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number Melanie Anderson, Marie‐France Szajnert, J.‐C. Kaplan, Nucleic Acids Research	1984	93
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. Kiichiro Matsumura, F.M.S. Tomé, Victor Ionâşescu, Journal of Clinical Investigation Molecular BiologyPathologyCytoskeletonCellular PhysiologyDmd Patients	1993	77
Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects. D. Choury, A Leroux, J.‐C. Kaplan Journal of Clinical Investigation Aldo-keto ReductaseIron MetabolismMethemoglobin ReductaseRedox BiologyOxidative Stress	1981	56
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy Jamel Chelly, F. Marlhens, B. Le Marec, Human Genetics Mendelian DisorderGenetic DisorderDuchenne Muscular DystrophyGeneticsDna Microdeletion	1986	55
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients. Jamel Chelly, Hélène Gilgenkrantz, Jean‐Philippe Hugnot, Journal of Clinical Investigation Muscle TissueTranscriptional RegulationCell LineageGene Deletion DataBecker Patients	1991	54
β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate Franck Duclos, Odile Broux, Nathalie Bourg, Neuromuscular Disorders Somatic VariantMedicineGeneticsGenomic AnalysisPathology	1998	54

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