Ilse Coene

491 total citations
11 papers, 363 citations indexed

About

Ilse Coene is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Ilse Coene has authored 11 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Ilse Coene's work include BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (4 papers) and Cancer Genomics and Diagnostics (3 papers). Ilse Coene is often cited by papers focused on BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (4 papers) and Cancer Genomics and Diagnostics (3 papers). Ilse Coene collaborates with scholars based in Belgium, Czechia and South Africa. Ilse Coene's co-authors include Kathleen Claes, Bruce Poppe, Kim De Leeneer, Ludwine Messiaen, Anne De Paepe, Anne De Paepe, Eva Macháčková, Lenka Foretová, Petra Vašíčková and Marie Navrátilová and has published in prestigious journals such as Oncogene, The American Journal of Human Genetics and British Journal of Cancer.

In The Last Decade

Ilse Coene

10 papers receiving 361 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilse Coene Belgium 9 254 231 83 40 34 11 363
Jacopo Azzollini Italy 13 208 0.8× 196 0.8× 47 0.6× 31 0.8× 50 1.5× 25 324
Alison M. Hosey United Kingdom 6 279 1.1× 138 0.6× 87 1.0× 23 0.6× 117 3.4× 7 384
Magdalena Banach‐Orlowska Poland 10 254 1.0× 128 0.6× 34 0.4× 14 0.3× 26 0.8× 13 341
Eva Esteban‐Cardeñosa Spain 9 213 0.8× 216 0.9× 85 1.0× 66 1.6× 28 0.8× 13 320
Mariem Ben Rekaya Tunisia 12 195 0.8× 102 0.4× 84 1.0× 35 0.9× 20 0.6× 25 276
Hannah F. Almubarak Saudi Arabia 5 252 1.0× 94 0.4× 110 1.3× 31 0.8× 60 1.8× 7 371
Mike Stratton United Kingdom 5 136 0.5× 88 0.4× 67 0.8× 30 0.8× 26 0.8× 9 235
Jim Roberts United States 2 444 1.7× 285 1.2× 72 0.9× 49 1.2× 147 4.3× 3 535
H. Komatsubara Japan 6 320 1.3× 139 0.6× 56 0.7× 19 0.5× 16 0.5× 7 419
Maxim Pilyugin Switzerland 10 351 1.4× 67 0.3× 96 1.2× 22 0.6× 68 2.0× 16 413

Countries citing papers authored by Ilse Coene

Since Specialization
Citations

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

Fields of papers citing papers by Ilse Coene

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilse Coene

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

All Works

11 of 11 papers shown
1.
Francies, Flavia Zita, Janet L. Poole, Kim De Leeneer, et al.. (2017). Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei. DNA repair. 61. 17–24. 14 indexed citations
2.
Francies, Flavia Zita, Kim De Leeneer, Alan C. Cairns, et al.. (2015). BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer. BMC Cancer. 15(1). 912–912. 40 indexed citations
4.
Leeneer, Kim De, Ilse Coene, Bruce Poppe, Anne De Paepe, & Kathleen Claes. (2009). Genotyping of Frequent BRCA1/2 SNPs with Unlabeled Probes. Journal of Molecular Diagnostics. 11(5). 415–419. 22 indexed citations
5.
Macháčková, Eva, Lenka Foretová, Petra Vašíčková, et al.. (2008). Spectrum and characterisation of BRCA1 and BRCA2deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer. BMC Cancer. 8(1). 140–140. 63 indexed citations
6.
Leeneer, Kim De, Ilse Coene, Bruce Poppe, Anne De Paepe, & Kathleen Claes. (2008). Rapid and Sensitive Detection of BRCA1/2 Mutations in a Diagnostic Setting: Comparison of Two High-Resolution Melting Platforms. Clinical Chemistry. 54(6). 982–989. 64 indexed citations
7.
Claes, Kathleen, Bruce Poppe, Ilse Coene, Anne De Paepe, & Ludwine Messiaen. (2004). BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families. British Journal of Cancer. 90(6). 1244–1251. 38 indexed citations
8.
Claes, Kathleen, Bruce Poppe, Ilse Coene, Anne De Paepe, & Ludwine Messiaen. (2003). BRCA1/2 mutation spectrum and frequencies in Belgian breast/ovarian cancer families. The American Journal of Human Genetics. 73(5). 232–232.
9.
Claes, Kathleen, Bruce Poppe, Eva Macháčková, et al.. (2003). Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2. Genes Chromosomes and Cancer. 37(3). 314–320. 63 indexed citations
10.
Claes, Kathleen, Jo Vandesompele, Bruce Poppe, et al.. (2002). Pathological splice mutations outside the invariant AG/GT splice sites of BRCA1 exon 5 increase alternative transcript levels in the 5′ end of the BRCA1 gene. Oncogene. 21(26). 4171–4175. 32 indexed citations
11.
Claes, Kathleen, Bruce Poppe, Michel De Vos, et al.. (2000). Identification and characterisation of a founder mutation in the Belgian breast/ovarian cancer population. The American Journal of Human Genetics. 67. 80–80. 2 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026