Cees J. Cornelisse

23.3k total citations · 3 hit papers
201 papers, 12.4k citations indexed

About

Cees J. Cornelisse is a scholar working on Cancer Research, Molecular Biology and Genetics. According to data from OpenAlex, Cees J. Cornelisse has authored 201 papers receiving a total of 12.4k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Cancer Research, 70 papers in Molecular Biology and 65 papers in Genetics. Recurrent topics in Cees J. Cornelisse's work include Cancer Genomics and Diagnostics (49 papers), Genetic factors in colorectal cancer (37 papers) and BRCA gene mutations in cancer (33 papers). Cees J. Cornelisse is often cited by papers focused on Cancer Genomics and Diagnostics (49 papers), Genetic factors in colorectal cancer (37 papers) and BRCA gene mutations in cancer (33 papers). Cees J. Cornelisse collaborates with scholars based in Netherlands, United States and Russia. Cees J. Cornelisse's co-authors include Peter Devilee, Gert Jan Fleuren, Vincent T.H.B.M. Smit, Marc J. van de Vijver, Anne‐Marie Cleton-Jansen, Peter E.M. Taschner, Geert Berx, Frans van Roy, Anne‐Marie Cleton‐Jansen and Bora E. Baysal and has published in prestigious journals such as Science, New England Journal of Medicine and Nucleic Acids Research.

In The Last Decade

Cees J. Cornelisse

200 papers receiving 12.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

2000 1.3k citations Bora E. Baysal, David Myssiorek et al. profile →
E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers.

1995 628 citations Cees J. Cornelisse et al. profile →
KRAS codon 12 mutations occur very frequently in pancreatic adenocarcinomas

1988 531 citations Cees J. Cornelisse et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cees J. Cornelisse Netherlands	55	5.1k	4.4k	3.5k	2.7k	2.6k	201	12.4k
Catharina Larsson Sweden	62	6.1k 1.2×	2.9k 0.7×	4.2k 1.2×	2.1k 0.8×	2.8k 1.1×	358	14.4k
Peter Devilee Netherlands	63	8.1k 1.6×	6.6k 1.5×	5.2k 1.5×	3.0k 1.1×	6.5k 2.5×	220	18.6k
Allen M. Gown United States	68	5.0k 1.0×	3.7k 0.8×	6.4k 1.8×	2.2k 0.8×	2.1k 0.8×	191	16.1k
Paul J. Goodfellow United States	51	5.1k 1.0×	3.0k 0.7×	2.8k 0.8×	1.3k 0.5×	2.2k 0.8×	222	11.1k
Giovanni Tallini Italy	65	4.5k 0.9×	2.4k 0.5×	3.7k 1.1×	2.2k 0.8×	1.7k 0.6×	288	14.6k
Gilbert Lenoir France	64	6.3k 1.2×	1.9k 0.4×	5.2k 1.5×	852 0.3×	3.4k 1.3×	254	15.5k
Silvana Pilotti Italy	68	5.1k 1.0×	2.7k 0.6×	6.6k 1.9×	2.7k 1.0×	1.2k 0.5×	294	16.2k
S. Pilotti Italy	54	3.1k 0.6×	1.5k 0.3×	4.0k 1.1×	1.6k 0.6×	1.0k 0.4×	175	9.2k
Manuel Sobrinho‐Simões Portugal	65	5.0k 1.0×	1.5k 0.3×	3.6k 1.0×	4.4k 1.7×	1.9k 0.7×	357	14.9k
Ronald A. DeLellis United States	51	2.6k 0.5×	1.3k 0.3×	2.6k 0.7×	2.3k 0.9×	1.4k 0.5×	204	9.8k

Countries citing papers authored by Cees J. Cornelisse

Since Specialization

Citations

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

Fields of papers citing papers by Cees J. Cornelisse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cees J. Cornelisse. 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 Cees J. Cornelisse. The network helps show where Cees J. Cornelisse may publish in the future.

Co-authorship network of co-authors of Cees J. Cornelisse

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Hoekstra, Attje S., Erik F. Hensen, Ekaterina S. Jordanova, et al.. (2017). Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas. Oncotarget. 8(9). 14525–14536. 17 indexed citations

Russnes, Hege G., Ekatherina Sh. Kuligina, Evgeny N. Suspitsin, et al.. (2011). Paired distribution of molecular subtypes in bilateral breast carcinomas. Cancer Genetics. 204(2). 96–102. 9 indexed citations

Corver, Willem E., Anneke Middeldorp, Natalja T. ter Haar, et al.. (2008). Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations. Cancer Research. 68(24). 10333–10340. 30 indexed citations

Oldenburg, Reinhard, Hanne Meijers‐Heijboer, Cees J. Cornelisse, & Peter Devilee. (2007). Genetic susceptibility for breast cancer: How many more genes to be found?. Critical Reviews in Oncology/Hematology. 63(2). 125–149. 91 indexed citations

Lombaerts, Marcel, Tom van Wezel, Katja Philippo, et al.. (2006). E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines. British Journal of Cancer. 94(5). 661–671. 279 indexed citations

Suspitsin, Evgeny N., Anna P. Sokolenko, Alexandr V. Togo, et al.. (2006). Nonrandom distribution of oncogene amplifications in bilateral breast carcinomas: Possible role of host factors and survival bias. International Journal of Cancer. 120(2). 297–302. 7 indexed citations

Hoya, Miguel de la, Hanne Meijers‐Heijboer, Juan Manuel Fernández, et al.. (2004). Mutant BRCA1 alleles transmission: Different approaches and different biases. International Journal of Cancer. 113(1). 166–167.

Hensen, Erik F., Ekaterina S. Jordanova, Pancras C.W. Hogendoorn, et al.. (2004). Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families. Oncogene. 23(23). 4076–4083. 110 indexed citations

Bovée, Judith V.M.G., Raf Sciot, Paola Dal Cin, et al.. (2001). Chromosome 9 Alterations and Trisomy 22 in Central Chondrosarcoma: A Cytogenetic and DNA Flow Cytometric Analysis of Chondrosarcoma Subtypes. Diagnostic Molecular Pathology. 10(4). 228–235. 33 indexed citations

10.

Baysal, Bora E., Evert M. van Schothorst, David Myssiorek, et al.. (1999). Repositioning the hereditary paraganglioma critical region on chromosome band 11q23. Human Genetics. 104(3). 219–225. 46 indexed citations

11.

Rosenberg, Carla, R.P.M. van Gijlswijk, J. Wiegant, et al.. (1998). Comparative genomic hybridization with lissamine- and fluorescein-labeled nucleotides. Cytometry. 32(4). 337–341. 9 indexed citations

12.

Sugihara, Hiroyuki, et al.. (1997). Identification of host and donor cells in porcine homograft heart valve explants by fluorescence in situ hybridization. Pure Amsterdam UMC. 2 indexed citations

13.

Tollenaar, Rob A.�E.�M., Bert A. Bonsing, Nel J. Kuipers‐Dijkshoorn, et al.. (1997). Evidence of clonal divergence in colorectal carcinoma. Cancer. 79(7). 1304–1314. 2 indexed citations

14.

Tollenaar, Rob A.�E.�M., Bert A. Bonsing, Nel J. Kuipers‐Dijkshoorn, et al.. (1997). Evidence of clonal divergence in colorectal carcinoma. Cancer. 79(7). 1304–1314. 22 indexed citations

15.

Hellmén, Eva, et al.. (1997). P53 mutations in mammary tumor cell lines and corresponding tumor tissues in the dog.. PubMed. 16(6B). 3737–44. 50 indexed citations

16.

Kibbelaar, Robby E., et al.. (1993). Statistical methods in interphase cytogenetics: An experimental approach. Cytometry. 14(7). 716–724. 43 indexed citations

17.

Dierendonck, Jan Hein van, et al.. (1991). Cell-cycle-related staining patterns of anti-proliferating cell nuclear antigen monoclonal antibodies. Comparison with BrdUrd labeling and Ki-67 staining.. PubMed. 138(5). 1165–72. 183 indexed citations

18.

Rosekrans, P C, C. J. L. M. Meijer, A M van der Wal, Cees J. Cornelisse, & J. Lindeman. (1980). Immunoglobulin containing cells in inflammatory bowel disease of the colon: a morphometric and immunohistochemical study.. Gut. 21(11). 941–947. 78 indexed citations

19.

Smeulders, A.W.M., Cees J. Cornelisse, A.M. Vossepoel, & J. S. Ploem. (1979). An image segmentation approach to the analysis of nuclear texture of cervical cells.. PubMed. 20. 217–22. 3 indexed citations

20.

Velde, Cornelis J.�H. van de, Chris Meyer, Cees J. Cornelisse, et al.. (1978). A morphometrical analysis of lymph node responses to tumors of different immunogenicity.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 38(3). 661–7. 18 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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