F Chavin-Colin
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 3
- Congenital Ear and Nasal Anomalies 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Prenatal Screening and Diagnostics 8
- Co-authors
- C Turleau (22 shared papers)J. de Grouchy (13 shared papers)Hélène Martelli (1 shared paper)Claudine Junien (2 shared papers)de Grouchy J (7 shared papers)Claire Nihoul‐Feketé (1 shared paper)Jean‐Louis Dufier (1 shared paper)Suzette Beguı́n (1 shared paper)
- Journals
- Human Genetics (6 papers)Clinical Genetics (1 paper)European Journal of Obstetrics & Gynecology and Reproductive Biology (1 paper)Cancer Genetics and Cytogenetics (1 paper)PubMed (13 papers)
- Partner nations
- France
In The Last Decade
F Chavin-Colin
22 papers receiving 571 citations
Peers
Comparison fields: 5 of 49
- Genetics 368
- Pediatrics, Perinatology and Child Health 181
- Developmental Biology 21
- Ophthalmology 52
- Molecular Biology 332
Countries citing papers authored by F Chavin-Colin
This map shows the geographic impact of F Chavin-Colin'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 F Chavin-Colin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Chavin-Colin more than expected).
Fields of papers citing papers by F Chavin-Colin
This network shows the impact of papers produced by F Chavin-Colin. 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 F Chavin-Colin. The network helps show where F Chavin-Colin may publish in the future.
Co-authors
The 18 scholars most cited alongside F Chavin-Colin, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 135 | |
| 2 | 1985 | 57 | |
| 3 | 1984 | 49 | |
| 4 | 1979 | 46 | |
| 5 | 1984 | 39 | |
| 6 | Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin). | 1984 | 37 |
| 7 | 1977 | 36 | |
| 8 | 1982 | 35 | |
| 9 | 1980 | 32 | |
| 10 | 1980 | 23 | |
| 11 | Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertion. | 1983 | 19 |
| 12 | Chromosome Y avec satellite (Yqs) et organisateur nucléolaire survenu de novo. | 1978 | 15 |
| 13 | [Distal 14q trisomy]. | 1983 | 14 |
| 14 | [Trisomy 9p : 2 further cases]. | 1974 | 13 |
| 15 | [Distal trisomy 15q]. | 1977 | 12 |
| 16 | [Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo]. | 1978 | 12 |
| 17 | [Partial 11q monosomy and trigonocephaly. A new syndrome]. | 1975 | 9 |
| 18 | [Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case]. | 1976 | 9 |
| 19 | [Ring of the chromosome 4. II. Without facial dysmorphism]. | 1977 | 8 |
| 20 | [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child]. | 1974 | 6 |
About F Chavin-Colin
F Chavin-Colin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Oncology and Genetics, having authored 23 papers that have together received 617 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (3 papers), Cancer-related Molecular Pathways (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Genetics (368 citations), Pediatrics, Perinatology and Child Health (181 citations), Developmental Biology (21 citations), Ophthalmology (52 citations) and Molecular Biology (332 citations). F Chavin-Colin has collaborated with scholars based in France. Frequent co-authors include C Turleau, J. de Grouchy, Hélène Martelli, Claudine Junien, de Grouchy J, Claire Nihoul‐Feketé, Jean‐Louis Dufier, Suzette Beguı́n, Horacio Rivera and C Haye. Their work appears in journals such as Human Genetics, Clinical Genetics, European Journal of Obstetrics & Gynecology and Reproductive Biology, Cancer Genetics and Cytogenetics and PubMed.
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.