Kaplan Jc
Impact in
-
- Cystic Fibrosis Research Advances
- Methemoglobinemia and Tumor Lysis Syndrome
- Neonatal Respiratory Health Research
-
- Neonatal Health and Biochemistry
Papers in
-
- Muscle Physiology and Disorders 7
-
- Methemoglobinemia and Tumor Lysis Syndrome 7
- Cystic Fibrosis Research Advances 7
- Neonatal Respiratory Health Research 4
- Co-authors
- A Leroux (5 shared papers)Claudine Junien (7 shared papers)Thierry Bienvenu (5 shared papers)A Kahn (2 shared papers)D. Hubert (5 shared papers)Isabelle Fajac (3 shared papers)Kevin P. Campbell (4 shared papers)N. Desmazes-Dufeu (2 shared papers)
- Journals
- European Respiratory Journal (3 papers)Human Molecular Genetics (1 paper)Blood (1 paper)Prenatal Diagnosis (1 paper)Neuropediatrics (1 paper)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Kaplan Jc
47 papers receiving 383 citations
Peers
Comparison fields: 5 of 65
- Pulmonary and Respiratory Medicine 171
- Pediatrics, Perinatology and Child Health 88
- Physiology 76
- Genetics 29
- Molecular Biology 179
Countries citing papers authored by Kaplan Jc
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
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.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 50 | |
| 2 | 1996 | 40 | |
| 3 | 1999 | 31 | |
| 4 | Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin. | 1993 | 31 |
| 5 | Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries. | 1993 | 28 |
| 6 | 1998 | 23 | |
| 7 | Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients. | 1997 | 18 |
| 8 | 2000 | 16 | |
| 9 | Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case. | 1975 | 14 |
| 10 | 1996 | 12 | |
| 11 | Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy. | 2000 | 12 |
| 12 | [Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]. | 1976 | 12 |
| 13 | [Clinical and biological forms of cytochrome b5 reductase deficiency]. | 1979 | 10 |
| 14 | [The enzyme defect in recessive congenital methemoglobinemia with encephalopathy. A new defective variant of NADH-diaphorase (Beni-Messous variant)]. | 1975 | 9 |
| 15 | [Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) (author's transl)]. | 1981 | 9 |
| 16 | Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis. | 1993 | 9 |
| 17 | 1997 | 8 | |
| 18 | 1994 | 7 | |
| 19 | Adenovirus-mediated transfer of a human dystrophin gene to skeletal muscle of mdx mouse. | 1994 | 6 |
| 20 | Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification. | 1992 | 5 |
About Kaplan Jc
Kaplan Jc is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health, Genetics and Physiology, having authored 50 papers that have together received 406 indexed citations. Recurring topics across this work include Neonatal Health and Biochemistry (10 papers), Methemoglobinemia and Tumor Lysis Syndrome (7 papers), Muscle Physiology and Disorders (7 papers), Cystic Fibrosis Research Advances (7 papers), Erythrocyte Function and Pathophysiology (6 papers), Genetic Neurodegenerative Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Neonatal Respiratory Health Research (4 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (171 citations), Pediatrics, Perinatology and Child Health (88 citations), Physiology (76 citations), Genetics (29 citations) and Molecular Biology (179 citations). Kaplan Jc has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include A Leroux, Claudine Junien, Thierry Bienvenu, A Kahn, D. Hubert, Isabelle Fajac, Kevin P. Campbell, N. Desmazes-Dufeu, Régis Matran and F.M.S. Tomé. Their work appears in journals such as European Respiratory Journal, Human Molecular Genetics, Blood, Prenatal Diagnosis and Neuropediatrics.
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.