J.‐C. Kaplan

2.9k total citations
54 papers, 1.5k citations indexed

About

J.‐C. Kaplan is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, J.‐C. Kaplan has authored 54 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 13 papers in Pediatrics, Perinatology and Child Health and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in J.‐C. Kaplan's work include Muscle Physiology and Disorders (16 papers), Neonatal Health and Biochemistry (12 papers) and Methemoglobinemia and Tumor Lysis Syndrome (8 papers). J.‐C. Kaplan is often cited by papers focused on Muscle Physiology and Disorders (16 papers), Neonatal Health and Biochemistry (12 papers) and Methemoglobinemia and Tumor Lysis Syndrome (8 papers). J.‐C. Kaplan collaborates with scholars based in France, United States and Algeria. J.‐C. Kaplan's co-authors include Alain Kitzis, A. Haliassos, J Kruh, Jean‐Claude Chomel, Laurent Tesson, Marie‐France Szajnert, S Grandjouan, Dominique Récan, Michel Fardeau and Marc Jeanpierre and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Blood.

In The Last Decade

J.‐C. Kaplan

54 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.‐C. Kaplan France 22 988 279 217 175 168 54 1.5k
Anthony N. Corps United Kingdom 29 902 0.9× 236 0.8× 119 0.5× 200 1.1× 195 1.2× 47 2.3k
Irene E. Zohn United States 22 1.3k 1.3× 171 0.6× 117 0.5× 110 0.6× 257 1.5× 42 2.0k
Mitsunobu Shimadzu Japan 22 812 0.8× 195 0.7× 176 0.8× 452 2.6× 87 0.5× 43 1.7k
Yoko Hamazaki Japan 25 752 0.8× 171 0.6× 244 1.1× 86 0.5× 281 1.7× 49 2.2k
J N Wilcox United States 13 1.0k 1.0× 173 0.6× 150 0.7× 297 1.7× 122 0.7× 17 2.4k
James G. Simmons United States 23 906 0.9× 491 1.8× 163 0.8× 159 0.9× 75 0.4× 36 2.3k
Céline Schaeffer Italy 20 1.3k 1.3× 544 1.9× 68 0.3× 78 0.4× 131 0.8× 32 2.0k
W. Putt United Kingdom 20 756 0.8× 375 1.3× 84 0.4× 88 0.5× 133 0.8× 44 1.3k
Patrick Spielmann Switzerland 21 935 0.9× 241 0.9× 249 1.1× 97 0.6× 109 0.6× 35 1.7k
Paul T. Massa United States 27 824 0.8× 188 0.7× 157 0.7× 197 1.1× 64 0.4× 63 2.4k

Countries citing papers authored by J.‐C. Kaplan

Since Specialization
Citations

This map shows the geographic impact of J.‐C. Kaplan'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 J.‐C. Kaplan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.‐C. Kaplan more than expected).

Fields of papers citing papers by J.‐C. Kaplan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.‐C. Kaplan. 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 J.‐C. Kaplan. The network helps show where J.‐C. Kaplan may publish in the future.

Co-authorship network of co-authors of J.‐C. Kaplan

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

All Works

20 of 20 papers shown
1.
Plaisancié, Julie, Patrícia Locosque Ramos, Véronique Gaston, et al.. (2018). Implication of non-coding PAX6 mutations in aniridia. Human Genetics. 137(10). 831–846. 34 indexed citations
2.
Plaisancié, Julie, Nicola Ragge, Hélène Dollfus, et al.. (2017). FOXE3 mutations: genotype‐phenotype correlations. Clinical Genetics. 93(4). 837–845. 26 indexed citations
3.
Kaplan, J.‐C.. (2000). Génomique et médecine: réflexions prospectives. De la génétique booléeene des lois de Mendel à une médecine moléculaire multifactorielle.. Comptes Rendus Biologies. 323(12). 1167–1174. 12 indexed citations
4.
Duclos, Franck, Odile Broux, Nathalie Bourg, et al.. (1998). β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders. 8(1). 30–38. 43 indexed citations
5.
Jeanpierre, Marc, Alain Carrié, Fédérica Piccolo, et al.. (1996). From adhalinopathies to alpha-sarcoglycanopathies: An overview. Neuromuscular Disorders. 6(6). 463–465. 13 indexed citations
6.
Dürr, Alexandra, Catherine Dodé, Christophe Pécheux, et al.. (1995). Diagnosis of “sporadic” Huntington's disease. Journal of the Neurological Sciences. 129(1). 51–55. 23 indexed citations
7.
Matsumura, Kiichiro, Arthur H.M. Burghes, Marina Mora, et al.. (1994). Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.. Journal of Clinical Investigation. 93(1). 99–105. 45 indexed citations
8.
Philippe, Christophe, M. Chery, Hélène Gilgenkrantz, et al.. (1994). Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X‐chromosome inactivation. American Journal of Medical Genetics. 52(2). 198–206. 32 indexed citations
9.
Matsumura, Kiichiro, F.M.S. Tomé, Victor Ionâşescu, et al.. (1993). Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.. Journal of Clinical Investigation. 92(2). 866–871. 60 indexed citations
10.
Hugnot, Jean‐Philippe, Dominique Récan, Marc Jeanpierre, J.‐C. Kaplan, & Aslıhan Tolun. (1991). A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD). Nucleic Acids Research. 19(11). 3159–3159. 16 indexed citations
11.
Chelly, Jamel, Hélène Gilgenkrantz, Jean‐Philippe Hugnot, et al.. (1991). 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. 88(4). 1161–1166. 46 indexed citations
12.
Nafa, Khédoudja, Abderrezak Reghis, M. Benabadji, et al.. (1990). Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria. Human Genetics. 84(5). 401–5. 8 indexed citations
13.
Haliassos, A., Jean‐Claude Chomel, Laurent Tesson, et al.. (1989). Modification of enzymatic-ally amplified DNA for the detection of point mutations. Nucleic Acids Research. 17(9). 3606–3606. 265 indexed citations
14.
Haliassos, A., Jean‐Claude Chomel, S Grandjouan, et al.. (1989). Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers. Nucleic Acids Research. 17(20). 8093–8099. 156 indexed citations
15.
Gilgenkrantz, Hélène, et al.. (1989). Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies. Genomics. 5(3). 574–580. 26 indexed citations
16.
Chelly, Jamel, F. Marlhens, Bernard Dutrillaux, et al.. (1988). Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia. Human Genetics. 78(3). 222–227. 15 indexed citations
17.
Marlhens, F., Jamel Chelly, J.‐C. Kaplan, et al.. (1987). Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia. Human Genetics. 77(4). 379–383. 12 indexed citations
18.
19.
Wajcman, Henri, et al.. (1981). Evidence for endogenous proteolytic solubilization of human red‐cell membrane NADH‐cytochrome b5 reductase. FEBS Letters. 126(2). 172–174. 11 indexed citations
20.
Kaplan, J.‐C., et al.. (1968). Electrophoretic abnormality in triosephosphate isomerase deficiency. Biochemical and Biophysical Research Communications. 31(5). 768–773. 45 indexed citations

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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