Carli Tops

1.5k total citations
11 papers, 508 citations indexed

About

Carli Tops is a scholar working on Pathology and Forensic Medicine, Oncology and Molecular Biology. According to data from OpenAlex, Carli Tops has authored 11 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pathology and Forensic Medicine, 8 papers in Oncology and 3 papers in Molecular Biology. Recurrent topics in Carli Tops's work include Genetic factors in colorectal cancer (10 papers), Colorectal Cancer Screening and Detection (7 papers) and Cancer Genomics and Diagnostics (3 papers). Carli Tops is often cited by papers focused on Genetic factors in colorectal cancer (10 papers), Colorectal Cancer Screening and Detection (7 papers) and Cancer Genomics and Diagnostics (3 papers). Carli Tops collaborates with scholars based in Netherlands, United Kingdom and Germany. Carli Tops's co-authors include Hans F. A. Vasen, Juul Wijnen, Hans Morreau, Yvonne Hendriks, Annette Bröcker‐Vriends, Marjo van Puijenbroek, Andrea E. van der Meulen‐de Jong, Hanne Meijers‐Heijboer, Margreet G.E.M. Ausems and Anja Wagner and has published in prestigious journals such as Clinical Cancer Research, American Journal Of Pathology and Cancer Epidemiology Biomarkers & Prevention.

In The Last Decade

Carli Tops

10 papers receiving 489 citations

Peers

Carli Tops

PFM

ONCOL

GENET

Shannon A. Kuismanen United States

H Sato Japan

Ester Borràs United States

Fernando Bellido Spain

Hicham Ouchene Netherlands

Rohan Gnanaolivu United States

Kun Y. Lee United States

Steven A. Narod Canada

Maggie Gorman United Kingdom

Julian Alexander United States

Shannon A. Kuismanen United States

Carli Tops

563 ×1.3

PFM

390 ×1.3

ONCOL

282 ×1.4

189 ×1.4

82 ×0.9

GENET

Citations per year, relative to Carli Tops Carli Tops (= 1×) peers Shannon A. Kuismanen

Countries citing papers authored by Carli Tops

Since Specialization

Citations

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

Fields of papers citing papers by Carli Tops

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carli Tops

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

All Works

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11 of 11 papers shown

Krijger, Ronald R. de, Lennart Kester, Saskia Hopman, et al.. (2025). Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant. Pediatric Blood & Cancer. 72(9). e31872–e31872.

Rahner, Nils, Felix F. Brockschmidt, Verena Steinke, et al.. (2011). Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors. Familial Cancer. 11(1). 19–26. 1 indexed citations

Middeldorp, Anneke, Shantie Jagmohan–Changur, Heleen M. van der Klift, et al.. (2010). Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer. Genes Chromosomes and Cancer. 49(6). 539–548. 14 indexed citations

Middeldorp, Anneke, Shantie Jagmohan–Changur, Ronald van Eijk, et al.. (2009). Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort. Cancer Epidemiology Biomarkers & Prevention. 18(11). 3062–3067. 53 indexed citations

Wasielewski, Marijke, Hans F. A. Vasen, Juul Wijnen, et al.. (2008). CHEK2 1100delC Is a Susceptibility Allele for HNPCC-Related Colorectal Cancer. Clinical Cancer Research. 14(15). 4989–4994. 28 indexed citations

Vasen, Hans F. A., Yvonne Hendriks, Andrea E. van der Meulen‐de Jong, et al.. (2004). Identification of HNPCC by Molecular Analysis of Colorectal and Endometrial Tumors. Disease Markers. 20(4-5). 207–213. 33 indexed citations

Jong, Andrea E. van der Meulen‐de, Marjo van Puijenbroek, Yvonne Hendriks, et al.. (2004). Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer. Clinical Cancer Research. 10(3). 972–980. 173 indexed citations

Hendriks, Yvonne, Patrick Franken, Jan Willem F Dierssen, et al.. (2003). Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors. American Journal Of Pathology. 162(2). 469–477. 137 indexed citations

Jagmohan–Changur, Shantie, Virpi Launonen, Friedrik P. Wikman, et al.. (2003). EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.. PubMed. 63(1). 154–8. 50 indexed citations

10.

Marcelis, Carlo, H.W.H.M. van der Putten, Carli Tops, Ludy Lutgens, & Ute Moog. (2001). Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?. Familial Cancer. 1(2). 109–111. 18 indexed citations

11.

Gerdes, Hans, et al.. (1989). Genetics of colon cancer: Abnormalities of chromosomes 5 and 17 correlate with the loss of alleles on these chromosomes in colorectal cancer cell lines. Cancer Genetics and Cytogenetics. 41(2). 221–221. 1 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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