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Kaplan Jc

Observed names: J C KAPLAN, J C Kaplan, J Kaplan, J-C. Kaplan, J-c. Kaplan, J. -C. Kaplan, J. -c. Kaplan, J. C. KAPLAN, J. C. Kaplan, J. Cl. Kaplan, J. KAPLAN, J. Kaplan, J.-C Kaplan, J.-C. Kaplan, J.C. Kaplan, J.‐C. Kaplan, JC Kaplan, KAPLAN JC, Kaplan, J. C., Kaplan, J-C, Kaplan, JC
Observed institutions: University of Iowa, Centre National de la Recherche Scientifique, City Of Hope National Medical Center, Harvard University, Inserm, Université Paris Cité, Hospital de Sant Pau, Ghent University, Hôpital Cochin, Assistance Publique – Hôpitaux de Paris, City of Hope, Centre Hospitalier Universitaire de Poitiers, Laboratoire de Biochimie, Institut de Myologie, Istituto Ortopedico Rizzoli, Groupe Hospitalier Cochin - Port-Royal, Hôtel-Dieu, Broca - La Collégiale, Hôpital Raymond-Poincaré, Institut Cochin, Hôpital Saint Eloi, Hôpital Mustapha Pacha, Centre international de recherche sur le cancer, Université Laval, Université Paris Descartes, Faculté de médecine de Tunis, The Ohio State University, Universitat de Barcelona
OpenAlex ID: A5113735558
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
1989 · M Koenig, A H Beggs, et al. · Europe PMC (PubMed Central) · 958
Illegitimate transcription: transcription of any gene in any cell type.
1989 · J Chelly, J P Concordet, et al. · Proceedings of the National Academy of Sciences · 629
International Committee for Standardization in Haematology: Recommended Methods for Red‐Cell Enzyme Analysis*
1977 · E. Beutler, K. G. Blume, et al. · British Journal of Haematology · 532
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Modification of enzymatic-ally amplified DNA for the detection of point mutations
1989 · A. Haliassos, J.C. Chomel, et al. · Nucleic Acids Research · 316
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
1995 · F. Piccolo, S.L. Roberds, et al. · Nature Genetics · 188
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers
1989 · A. Haliassos, J.C. Chomel, et al. · Nucleic Acids Research · 178
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LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene
2005 · A. Sáenz, F. Leturcq, et al. · Brain · 176
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression
2009 · F. Daoud, N. Angeard, et al. · Human Molecular Genetics · 167
International Committee for Standardization in Haematology: Recommended Screening Test for Glucose‐6‐Phosphate Dehydrogenase (G‐6‐PD) Deficiency
1979 · E. Beutler, K. G. Blume, et al. · British Journal of Haematology · 167
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Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.
1992 · J P Hugnot, H Gilgenkrantz, et al. · Proceedings of the National Academy of Sciences · 155
Guidelines for Human Gene Nomenclature
2008 · Jean Frézal, P.J. McAlpine, et al. · Cytogenetics and Cell Genetics · 135
Primary adhalinopathy (α‐sarcoglycanopathy)
1997 · B. Eymard, N. B. Romero, et al. · Neurology · 129
Human type I procollagen genes are located on different chromosomes.
1982 · C Huerre, C Junien, et al. · Proceedings of the National Academy of Sciences · 116
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
1997 · A Carrié, F Piccolo, et al. · Journal of Medical Genetics · 112
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The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number
1984 · M.L.M. Anderson, M.F. Szajnert, et al. · Nucleic Acids Research · 92
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.
1993 · K Matsumura, F M Tomé, et al. · Journal of Clinical Investigation · 78
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Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization.
1982 · C Junien, D Weil, et al. · PubMed · 76
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2.
1984 · I Henry, G Uzan, et al. · Europe PMC (PubMed Central) · 64
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy
1986 · J. Chelly, F. Marlhens, et al. · Human Genetics · 61
Homogeneous phenotype of the gypsy limb-girdle MD with the γ-sarcoglycan C283Y mutation
2000 · L. Merlini, J-C. Kaplan, et al. · Neurology · 60
Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II
1995 · LM Vieira, JC Kaplan, et al. · Blood · 57
Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.
1981 · D Choury, A Leroux, et al. · Journal of Clinical Investigation · 55
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β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate
1998 · F Duclos, O Broux, et al. · Neuromuscular Disorders · 54
Human chromosome 22.
1987 · J C Kaplan, A Aurias, et al. · Journal of Medical Genetics · 54
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Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.
1991 · J Chelly, H Gilgenkrantz, et al. · Journal of Clinical Investigation · 52
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Works count: 254
Citation count: 6,519
H-index: 35
I10-index: 95
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