V. Cacheux

594 total citations
10 papers, 453 citations indexed

About

V. Cacheux is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, V. Cacheux has authored 10 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in V. Cacheux's work include Chromosomal and Genetic Variations (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). V. Cacheux is often cited by papers focused on Chromosomal and Genetic Variations (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). V. Cacheux collaborates with scholars based in France and Belgium. V. Cacheux's co-authors include Gérard Tachdjian, Bernard Grandchamp, C Nessmann, Hélène Cavé, Claude Preudhomme, J.-F. Oury, JL Laï, E Vilmer, Pascale Cochaux and Marleen Bâkkus and has published in prestigious journals such as Biochemical Journal, Human Molecular Genetics and Leukemia.

In The Last Decade

V. Cacheux

10 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Cacheux France 8 165 156 135 129 71 10 453
D E Rooney United Kingdom 10 245 1.5× 243 1.6× 84 0.6× 291 2.3× 68 1.0× 14 631
P. Wieacker Germany 12 198 1.2× 109 0.7× 43 0.3× 177 1.4× 51 0.7× 43 455
Zhanhe Wu Australia 11 102 0.6× 135 0.9× 27 0.2× 179 1.4× 39 0.5× 23 340
Nataline B. Kardon United States 13 232 1.4× 281 1.8× 66 0.5× 329 2.6× 85 1.2× 26 640
Paolo Guanciali‐Franchi Italy 10 222 1.3× 154 1.0× 21 0.2× 144 1.1× 67 0.9× 24 443
Martha Weinstein United States 7 90 0.5× 177 1.1× 50 0.4× 211 1.6× 91 1.3× 8 390
Brian Thiel United States 10 186 1.1× 201 1.3× 89 0.7× 348 2.7× 11 0.2× 11 598
Paolo Guanciali Franchi Italy 14 220 1.3× 80 0.5× 25 0.2× 298 2.3× 80 1.1× 31 484
Catarina Lundin Sweden 11 85 0.5× 106 0.7× 24 0.2× 98 0.8× 63 0.9× 17 287
Brigitte Pabst Germany 12 137 0.8× 65 0.4× 38 0.3× 109 0.8× 32 0.5× 29 374

Countries citing papers authored by V. Cacheux

Since Specialization
Citations

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

Fields of papers citing papers by V. Cacheux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Cacheux

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

All Works

10 of 10 papers shown
1.
Cacheux, V.. (2001). Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease. Human Molecular Genetics. 10(14). 1503–1510. 171 indexed citations
2.
Callebaut, Isabelle, et al.. (2000). Polydom: a secreted protein with pentraxin, complement control protein, epidermal growth factor and von Willebrand factor A domains. Biochemical Journal. 352(1). 49–49. 3 indexed citations
3.
Cacheux, V., et al.. (2000). Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study. Prenatal Diagnosis. 20(2). 123–131. 22 indexed citations
4.
Callebaut, Isabelle, et al.. (2000). Polydom: a secreted protein with pentraxin, complement control protein, epidermal growth factor and von Willebrand factor A domains. Biochemical Journal. 352(1). 49–59. 46 indexed citations
5.
Sanlaville, Damien, Clarisse Baumann, Serge Romana, et al.. (1999). De novo inverted duplication 9p21pter involving telomeric repeated sequences. American Journal of Medical Genetics. 83(2). 125–131. 16 indexed citations
6.
Cavé, Hélène, V. Cacheux, Sophie Raynaud, et al.. (1997). ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia. Leukemia. 11(9). 1459–1464. 84 indexed citations
7.
8.
Cacheux, V., et al.. (1994). Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12. Human Genetics. 94(5). 557–9. 24 indexed citations
9.
Cacheux, V., Gérard Tachdjian, J.-F. Oury, et al.. (1994). Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescencein situhybridization. Prenatal Diagnosis. 14(2). 79–86. 37 indexed citations
10.

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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