F Chavin-Colin

759 total citations
24 papers, 640 citations indexed

About

F Chavin-Colin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, F Chavin-Colin has authored 24 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in F Chavin-Colin's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (3 papers). F Chavin-Colin is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (3 papers). F Chavin-Colin collaborates with scholars based in France. F Chavin-Colin's co-authors include C Turleau, J. de Grouchy, Hélène Martelli, Claudine Junien, de Grouchy J, Suzette Beguı́n, Claire Nihoul‐Feketé, Jean‐Louis Dufier, C Haye and P Schlienger and has published in prestigious journals such as Human Genetics, European Journal of Obstetrics & Gynecology and Reproductive Biology and Clinical Genetics.

In The Last Decade

F Chavin-Colin

23 papers receiving 605 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F Chavin-Colin France	14	413	352	202	133	57	24	640
E. Orye Belgium	14	311 0.8×	233 0.7×	137 0.7×	122 0.9×	65 1.1×	35	590
K. L. Ying United States	12	252 0.6×	267 0.8×	75 0.4×	81 0.6×	54 0.9×	18	497
J W Towner United States	9	232 0.6×	136 0.4×	102 0.5×	85 0.6×	55 1.0×	13	352
Nataline B. Kardon United States	13	329 0.8×	232 0.7×	281 1.4×	108 0.8×	35 0.6×	26	640
Lydia E. McMorrow United States	11	320 0.8×	505 1.4×	137 0.7×	110 0.8×	43 0.8×	22	699
Sparkes Rs United States	11	132 0.3×	143 0.4×	72 0.4×	42 0.3×	30 0.5×	30	382
M. L. Kwee Netherlands	13	320 0.8×	426 1.2×	91 0.5×	57 0.4×	59 1.0×	24	640
Salah Ebrahim United States	14	165 0.4×	127 0.4×	93 0.5×	51 0.4×	89 1.6×	33	447
Ulrike Gamerdinger Germany	11	105 0.3×	190 0.5×	44 0.2×	60 0.5×	94 1.6×	20	398
P. Mollevanger Netherlands	13	189 0.5×	196 0.6×	59 0.3×	95 0.7×	52 0.9×	19	428

Countries citing papers authored by F Chavin-Colin

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of F Chavin-Colin

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

All Works

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20 of 20 papers shown

Turleau, C, J. de Grouchy, F Chavin-Colin, et al.. (1985). Cytogenetic forms of retinoblastoma: Their incidence in a survey of 66 patients. Cancer Genetics and Cytogenetics. 16(4). 321–334. 54 indexed citations

Turleau, C, et al.. (1984). Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin).. PubMed. 27(4). 237–40. 34 indexed citations

Grouchy, J. de, et al.. (1984). Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8. Human Genetics. 66(2-3). 230–233. 39 indexed citations

Turleau, C, J. de Grouchy, Claire Nihoul‐Feketé, et al.. (1984). Del11p13/nephroblastoma without aniridia. Human Genetics. 67(4). 455–456. 45 indexed citations

Turleau, C, et al.. (1983). [Distal 14q trisomy].. PubMed. 26(3). 165–70. 14 indexed citations

Turleau, C, et al.. (1983). Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertion.. PubMed. 26(3). 158–60. 18 indexed citations

Turleau, C, F Chavin-Colin, J. de Grouchy, P Maroteaux, & Horacio Rivera. (1982). Langer-Giedion syndrome with and without del 8q. Assignment of critical segment to 8q23. Human Genetics. 62(3). 183–187. 34 indexed citations

Turleau, C, F Chavin-Colin, & J. de Grouchy. (1980). A 45,X male with translocation of euchromatic Y chromosome material. Human Genetics. 53(3). 299–302. 22 indexed citations

Turleau, C, et al.. (1980). [Trisomy 21 by mirror duplication 46,XX,psu dic(21)ter rea (21q21q) (author's transl)].. PubMed. 23(3). 187–9. 4 indexed citations

10.

Turleau, C, et al.. (1980). Trisomy 18q‐. Trisomy mapping of chromosome 18 revisited. Clinical Genetics. 18(1). 20–26. 32 indexed citations

11.

Turleau, C, F Chavin-Colin, & J. de Grouchy. (1979). Cytogenetic investigation in 413 couples with spontaneous abortions. European Journal of Obstetrics & Gynecology and Reproductive Biology. 9(2). 65–74. 36 indexed citations

12.

Turleau, C, et al.. (1978). Chromosome Y avec satellite (Yqs) et organisateur nucléolaire survenu de novo.. Annales de Génétique. 21(4). 15 indexed citations

13.

Turleau, C, et al.. (1978). [Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo].. PubMed. 21(4). 239–42. 12 indexed citations

14.

Turleau, C, et al.. (1977). [Distal trisomy 15q].. PubMed. 20(3). 214–6. 12 indexed citations

15.

Chavin-Colin, F, et al.. (1977). [Ring of the chromosome 4. II. Without facial dysmorphism].. PubMed. 20(2). 105–9. 8 indexed citations

16.

Turleau, C, et al.. (1977). Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers. Human Genetics. 37(1). 97–104. 36 indexed citations

17.

Turleau, C, et al.. (1975). [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].. PubMed. 18(2). 125–9. 5 indexed citations

18.

Turleau, C, et al.. (1975). [Partial 11q monosomy and trigonocephaly. A new syndrome].. PubMed. 18(4). 257–60. 9 indexed citations

19.

Turleau, C, et al.. (1974). [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child].. PubMed. 17(4). 291–4. 6 indexed citations

20.

Turleau, C, et al.. (1974). [Trisomy 9p : 2 further cases].. PubMed. 17(3). 167–74. 13 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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