F Kerangueven

736 total citations
15 papers, 609 citations indexed

About

F Kerangueven is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, F Kerangueven has authored 15 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in F Kerangueven's work include RNA modifications and cancer (5 papers), BRCA gene mutations in cancer (5 papers) and RNA Research and Splicing (4 papers). F Kerangueven is often cited by papers focused on RNA modifications and cancer (5 papers), BRCA gene mutations in cancer (5 papers) and RNA Research and Splicing (4 papers). F Kerangueven collaborates with scholars based in France, Netherlands and United States. F Kerangueven's co-authors include Daniel Birnbaum, François Eisinger, Michel Longy, Hagay Sobol, Florence Allione, T Noguchi, Clément Bailly, Laurent Essioux, Anne Vincent‐Salomon and D Stoppa-Lyonnet and has published in prestigious journals such as Oncogene, European Journal of Cancer and Genomics.

In The Last Decade

F Kerangueven

15 papers receiving 576 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F Kerangueven France 10 326 325 214 212 164 15 609
Keri Fair United States 7 323 1.0× 111 0.3× 179 0.8× 151 0.7× 144 0.9× 7 501
Kenneth Offit United States 12 445 1.4× 488 1.5× 223 1.0× 187 0.9× 274 1.7× 14 843
Florence Allione France 6 271 0.8× 176 0.5× 156 0.7× 150 0.7× 123 0.8× 8 429
Markéta Janatová Czechia 12 268 0.8× 259 0.8× 133 0.6× 100 0.5× 127 0.8× 35 483
Anitta Tamminen Finland 12 648 2.0× 633 1.9× 314 1.5× 267 1.3× 406 2.5× 13 1.1k
Fitsum Hagos United States 9 457 1.4× 225 0.7× 167 0.8× 45 0.2× 215 1.3× 10 657
Agnès Chompret France 5 252 0.8× 171 0.5× 120 0.6× 68 0.3× 219 1.3× 5 441
Elizabeth L. Schubert United States 8 241 0.7× 251 0.8× 171 0.8× 85 0.4× 125 0.8× 9 466
Munaza Ahmed United Kingdom 5 636 2.0× 734 2.3× 344 1.6× 252 1.2× 245 1.5× 8 1.1k
Åke Borg Sweden 7 234 0.7× 163 0.5× 153 0.7× 66 0.3× 226 1.4× 7 461

Countries citing papers authored by F Kerangueven

Since Specialization
Citations

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

Fields of papers citing papers by F Kerangueven

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Kerangueven

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

All Works

15 of 15 papers shown
1.
Sobol, Hagay, F Kerangueven, Yin Luo, et al.. (2001). Genome‐wide search for loss of heterozygosity in Burkitt lymphoma cell lines. Genes Chromosomes and Cancer. 33(2). 217–224. 12 indexed citations
2.
Kerangueven, F, François Eisinger, Tetsuro Noguchi, et al.. (1997). Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions. Oncogene. 14(3). 339–347. 54 indexed citations
3.
Kerangueven, F, T Noguchi, François Coulier, et al.. (1997). Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas.. PubMed. 57(24). 5469–74. 137 indexed citations
4.
Chaffanet, Max, Laurent Essioux, Tetsuro Noguchi, et al.. (1996). Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome. Genomics. 32(1). 29–38. 31 indexed citations
5.
Eisinger, François, D Stoppa-Lyonnet, Michel Longy, et al.. (1996). Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer.. PubMed. 56(3). 471–4. 129 indexed citations
6.
Sobol, H., Dominique Stoppa‐Lyonnet, J Jacquemier, et al.. (1996). PP-4-6 Germline mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer. European Journal of Cancer. 32. 28–28. 1 indexed citations
7.
Kerangueven, F, T Noguchi, Florence Allione, et al.. (1996). Multiple sites of loss of heterozygosity on chromosome arms 3p and 3q in human breast carcinomas. Oncology Reports. 3(2). 313–6. 4 indexed citations
8.
Kerangueven, F, François Eisinger, Florence Allione, et al.. (1996). Cumulative regional allelotyping of human breast carcinomas. International Journal of Oncology. 8(6). 1155–63. 2 indexed citations
9.
Sobol, H., Brigitte Bressac–de Paillerets, J.P. Peyrat, et al.. (1996). Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers.. PubMed. 56(14). 3216–9. 49 indexed citations
10.
Kerangueven, F, Florence Allione, José Adélaı̈de, et al.. (1995). Patterns of loss of heterozygosity at loci from chromosome arm 13q suggest a possible involvement of BRCA2 in sporadic breast tumors. Genes Chromosomes and Cancer. 13(4). 291–294. 38 indexed citations
11.
Kerangueven, F, Laurent Essioux, T Noguchi, et al.. (1995). Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8.. PubMed. 10(5). 1023–6. 105 indexed citations
12.
Kerangueven, F, T Noguchi, José Adélaı̈de, et al.. (1995). ALLELIC LOSS AT MARKERS OF CHROMOSOMAL BAND 7Q31 IS NOT A FREQUENT EVENT IN HUMAN BREAST-CANCER. Oncology Reports. 2(1). 89–90. 4 indexed citations
13.
Kerangueven, F, José Adélaı̈de, Michel Longy, et al.. (1994). ALLELIC LOSS AT CHROMOSOME 8P IN HUMAN BREAST-CANCER. Oncology Reports. 1(2). 393–5. 8 indexed citations
14.
Kerangueven, F, et al.. (1991). Effects of transforming growth factor beta, tumor necrosis factor alpha, interferon gamma and LIF-HILDA on the proliferation of acute myeloid leukemia cells.. PubMed. 1(2). 99–107. 9 indexed citations
15.
Lopez, Marc, N Maroc, F Kerangueven, et al.. (1991). Coexpression of the genes for interleukin 6 and its receptor without apparent involvement in the proliferation of acute myeloid leukemia cells.. PubMed. 19(8). 797–803. 26 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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