Kaplan Jc

6.5k citations

153 papers · 5.3k · 2 hit papers · h-index 32

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Molecular Biology top 2%
- Muscle Physiology and Disorders

Papers in

Genetics 40
- Genomic variations and chromosomal abnormalities 22
- Genomics and Rare Diseases 13
- Genetic Associations and Epidemiology 8
- Hemoglobinopathies and Related Disorders 7
Pulmonary and Respiratory Medicine 36
- Cystic Fibrosis Research Advances 21
- Methemoglobinemia and Tumor Lysis Syndrome 14

Co-authors: Axel Kahn (13 shared papers)Jamel Chelly (9 shared papers)Jean‐Paul Concordet (1 shared paper)Ernest Beutler (3 shared papers)Bracha Ramot (2 shared papers)G. W. Löhr (2 shared papers)Karl G. Blume (2 shared papers)William N. Valentine (2 shared papers)
Journals: Human Genetics (17 papers)Neuromuscular Disorders (16 papers)Journal of Medical Genetics (6 papers)Journal of Clinical Investigation (5 papers)Nucleic Acids Research (5 papers)
Partner nations: France United States Algeria

In The Last Decade

Kaplan Jc

142 papers receiving 5k citations

Kaplan Jc's Hit Papers

align trajectories log scale

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. 1989 · 832 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

1989 PubMed
1977 British Journal of Haematology

Peers

Countries citing papers authored by Kaplan Jc

Since Specialization

Citations

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

Fields of papers citing papers by Kaplan Jc

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Kaplan Jc, 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 Kaplan Jc Line = papers co-authored together Kaplan Jc links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 153 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. PubMed ·Michel Koenig, Alan H. Beggs, S. Scherpf, K. Heindrich, Thomas Bettecken, Gerhard Meng, C. R. Müller, Mikael Lindlöf Hit paper breakdown →	1989	832
2	Illegitimate transcription: transcription of any gene in any cell type. Proceedings of the National Academy of Sciences ·Jamel Chelly, Jean‐Paul Concordet, Kaplan Jc, Axel Kahn	1989	555
3	International Committee for Standardization in Haematology: Recommended Methods for Red‐Cell Enzyme Analysis* British Journal of Haematology ·Ernest Beutler, Karl G. Blume, Kaplan Jc, G. W. Löhr, Bracha Ramot, William N. Valentine Hit paper breakdown →	1977	483
4	Modification of enzymatic-ally amplified DNA for the detection of point mutations Nucleic Acids Research ·Alexandre Haliassos, Jean‐Claude Chomel, Laurent Tesson, M. Baudis, J Kruh, Kaplan Jc, Alain Kitzis	1989	284
5	Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity Nature Genetics ·Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre, France Leturcq, Kemal Azibi, Cherif Beldjord, Alain Carrié, Dominique Récan	1995	169
6	Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers Nucleic Acids Research ·Alexandre Haliassos, Jean‐Claude Chomel, Sophie Grandjouan, J Kruh, Kaplan Jc, Alain Kitzis	1989	158
7	International Committee for Standardization in Haematology: Recommended Screening Test for Glucose‐6‐Phosphate Dehydrogenase (G‐6‐PD) Deficiency British Journal of Haematology ·Ernest Beutler, Karl G. Blume, Kaplan Jc, G. W. Löhr, Bracha Ramot, William N. Valentine	1979	148
8	Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues. Proceedings of the National Academy of Sciences ·Jean‐Philippe Hugnot, Hélène Gilgenkrantz, Nathalie Vincent, Philippe Chafey, Glenn E. Morris, Anthony P. Monaco, Yoheved Berwald‐Netter, Annette Koulakoff	1992	138
9	Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression Human Molecular Genetics ·Fatma Daoud, Nathalie Angeard, B. Demerre, I. Martie, Rabah Ben Yaou, France Leturcq, Mireille Cossée, Nathalie Deburgrave	2009	137
10	LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene Brain ·Amets Sáenz, France Leturcq, Anna Maria Cobo, Juan José Poza, Xavier Ferrer, David Otaegui, Pilar Camaño, Miguel Urtasun	2005	129
11	Human type I procollagen genes are located on different chromosomes. Proceedings of the National Academy of Sciences ·C Huerre, Claudine Junien, Dominique Weil, Mon‐Li Chu, Maria A. Morabito, N. Van Cong, Jeanne C. Myers, Chantal Foubert	1982	112
12	Primary adhalinopathy (α‐sarcoglycanopathy) Neurology ·B. Eymard, Norma Beatriz Romero, France Leturcq, Fédérica Piccolo, Alain Carrié, Marc Jeanpierre, Nathalie Deburgrave, Kemal Azibi	1997	108
13	Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Journal of Medical Genetics ·Alain Carrié, Fédérica Piccolo, France Leturcq, Claudia de Toma, Kemal Azibi, Cherif Beldjord, Jean‐Michel Vallat, Luciano Merlini	1997	102
14	The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number Nucleic Acids Research ·Melanie Anderson, Marie‐France Szajnert, Kaplan Jc, L A McColl, Bryan D. Young	1984	84
15	Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization. PubMed ·Claudine Junien, Dominique Weil, Jeanne C. Myers, N. Van Cong, Mon‐Li Chu, Chantal Foubert, Marie‐Sylvie Gross, Darwin J. Prockop	1982	69
16	Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. Journal of Clinical Investigation ·Kiichiro Matsumura, Fernando M. S. Tomé, Victor V. Ionasescu, James M. Ervasti, Norma Beatriz Romero, Dominique Simon, Dominique Récan, Kaplan Jc	1993	66
17	Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects. Journal of Clinical Investigation ·D. Choury, A Leroux, Kaplan Jc	1981	53
18	The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2. PubMed ·Isabelle Marie Henry, Georges Uzan, Dominique Weil, Kaplan Jc, Christopher Marguerie, Axel Kahn, Claudine Junien +1 other	1984	53
19	Homogeneous phenotype of the gypsy limb-girdle MD with the γ-sarcoglycan C283Y mutation Neurology ·Luciano Merlini, Kaplan Jc, Annie Barois, Dominique Bonneau, J. Brasa, Bernard Échenne, P. Gallano, Laura Jarre	2000	51
20	Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II Blood ·LM Vieira, Kaplan Jc, Axel Kahn, A Leroux	1995	48

About Kaplan Jc

Kaplan Jc is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Molecular Biology, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 153 papers that have together received 5.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (45 papers), Genomic variations and chromosomal abnormalities (22 papers), Cystic Fibrosis Research Advances (21 papers), Neonatal Health and Biochemistry (14 papers), Methemoglobinemia and Tumor Lysis Syndrome (14 papers), Genomics and Rare Diseases (13 papers), Genetic Associations and Epidemiology (8 papers) and Hemoglobinopathies and Related Disorders (7 papers). The work is most often cited by research in Genetics (382 citations), Molecular Biology (2.7k citations), Genetics (885 citations), Pediatrics, Perinatology and Child Health (386 citations) and Clinical Biochemistry (99 citations). Kaplan Jc has collaborated with scholars based in France, United States and Algeria. Frequent co-authors include Axel Kahn, Jamel Chelly, Jean‐Paul Concordet, Ernest Beutler, Bracha Ramot, G. W. Löhr, Karl G. Blume, William N. Valentine, Alain Kitzis and Jean‐Claude Chomel. Their work appears in journals such as Human Genetics, Neuromuscular Disorders, Journal of Medical Genetics, Journal of Clinical Investigation and Nucleic Acids Research.

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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Kaplan Jc's Hit Papers

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