Monique Goossens

1.8k total citations · 1 hit paper
7 papers, 873 citations indexed

About

Monique Goossens is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology. According to data from OpenAlex, Monique Goossens has authored 7 papers receiving a total of 873 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 6 papers in Cancer Research and 4 papers in Oncology. Recurrent topics in Monique Goossens's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Screening and Detection (3 papers). Monique Goossens is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Screening and Detection (3 papers). Monique Goossens collaborates with scholars based in Netherlands, Germany and United Kingdom. Monique Goossens's co-authors include Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, Han G. Brunner, Konnie M. Hebeda, J. Han van Krieken, Daniëlle Bodmer, Suet Yi Leung, Tsun Leung Chan, Siu Tsan Yuen and Ad Geurts van Kessel and has published in prestigious journals such as Nature Genetics, Gastroenterology and PLoS ONE.

In The Last Decade

Monique Goossens

7 papers receiving 862 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.

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

2008 546 citations Marjolijn J. L. Ligtenberg, Roland P. Kuiper et al. Nature Genetics profile →

Peers

Monique Goossens

PFM

ONCOL

CR

MB

GENET

Renée C. Niessen Netherlands

Verena Steinke Germany

Maran J.W. Berends Netherlands

Prathap Bandipalliam United States

Margot G F van Lier Netherlands

N E Beck United Kingdom

Dietlinde Stienen Germany

T I Andersen Norway

Ingrid P. Vogelaar Netherlands

I. Tomlinson United Kingdom

Renée C. Niessen Netherlands

Monique Goossens

594 ×0.8

PFM

385 ×0.8

ONCOL

327 ×0.7

CR

163 ×0.8

MB

123 ×0.9

GENET

Citations per year, relative to Monique Goossens Monique Goossens (= 1×) peers Renée C. Niessen

Countries citing papers authored by Monique Goossens

Since Specialization

Citations

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

Fields of papers citing papers by Monique Goossens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monique Goossens

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

All Works

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7 of 7 papers shown

1.

Venderbosch, Sabine, Shannon van Vliet, Anton F. J. de Haan, et al.. (2015). EMAST Is Associated with a Poor Prognosis in Microsatellite Instable Metastatic Colorectal Cancer. PLoS ONE. 10(4). e0124538–e0124538. 27 indexed citations

2.

Mensenkamp, Arjen R., Ingrid P. Vogelaar, Wendy A.G. van Zelst–Stams, et al.. (2013). Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors. Gastroenterology. 146(3). 643–646.e8. 230 indexed citations

3.

Venkatachalam, Ramprasath, Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, et al.. (2010). Germline epimutation of the tumor suppressor gene PTPRJ in early onset familial colorectal cancer. Cancer Genetics and Cytogenetics. 203(1). 59–59. 1 indexed citations

4.

Ligtenberg, Marjolijn J. L., Roland P. Kuiper, Tsun Leung Chan, et al.. (2008). Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1. Nature Genetics. 41(1). 112–117. 546 indexed citations breakdown →

5.

Kets, Carolien M., et al.. (2008). Compound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2. European Journal of Human Genetics. 17(2). 159–164. 16 indexed citations

6.

Overbeek, Lucy, C. Marleen Kets, Konnie M. Hebeda, et al.. (2007). Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer. British Journal of Cancer. 96(10). 1605–1612. 40 indexed citations

7.

Kets, C. Marleen, J. Han van Krieken, Konnie M. Hebeda, et al.. (2006). Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability. British Journal of Cancer. 95(12). 1678–1682. 13 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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