Hans Morreau

15.0k total citations
207 papers, 8.3k citations indexed

About

Hans Morreau is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Hans Morreau has authored 207 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 121 papers in Pathology and Forensic Medicine, 104 papers in Oncology and 76 papers in Cancer Research. Recurrent topics in Hans Morreau's work include Genetic factors in colorectal cancer (119 papers), Cancer Genomics and Diagnostics (66 papers) and Colorectal Cancer Screening and Detection (38 papers). Hans Morreau is often cited by papers focused on Genetic factors in colorectal cancer (119 papers), Cancer Genomics and Diagnostics (66 papers) and Colorectal Cancer Screening and Detection (38 papers). Hans Morreau collaborates with scholars based in Netherlands, United States and United Kingdom. Hans Morreau's co-authors include Tom van Wezel, Hans F. A. Vasen, Frederik J. Hes, Rob A.�E.�M. Tollenaar, Juul Wijnen, Marjo van Puijenbroek, Ronald van Eijk, Johannes W. A. Smit, Maartje Nielsen and Carli M.J. Tops and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Hans Morreau

201 papers receiving 8.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans Morreau Netherlands 52 4.0k 3.4k 2.5k 2.4k 1.2k 207 8.3k
Giancarlo Troncone Italy 53 3.3k 0.8× 1.4k 0.4× 4.0k 1.6× 3.0k 1.3× 1.3k 1.0× 356 9.7k
Timothy J. Yeatman United States 56 5.1k 1.3× 2.1k 0.6× 5.9k 2.3× 2.9k 1.2× 1.3k 1.1× 169 11.8k
Daniel W. Visscher United States 58 4.7k 1.2× 3.2k 0.9× 2.6k 1.0× 4.3k 1.8× 1.4k 1.2× 228 11.0k
Gyungyub Gong South Korea 51 3.1k 0.8× 1.2k 0.4× 1.7k 0.7× 1.8k 0.8× 2.0k 1.6× 297 8.1k
David J. Dabbs United States 48 3.1k 0.8× 2.0k 0.6× 1.9k 0.8× 3.2k 1.4× 1.2k 1.0× 205 7.9k
Gamze Karaca United States 28 4.6k 1.2× 1.4k 0.4× 3.4k 1.3× 4.3k 1.8× 767 0.6× 40 9.6k
Russell R. Broaddus United States 69 4.9k 1.2× 3.5k 1.0× 5.8k 2.3× 4.4k 1.8× 1.3k 1.0× 286 15.1k
Tetsunari Oyama Japan 43 2.8k 0.7× 900 0.3× 2.9k 1.1× 1.7k 0.7× 1.3k 1.0× 281 7.2k
Gabriella Fontanini Italy 56 7.2k 1.8× 1.6k 0.5× 5.3k 2.1× 2.7k 1.1× 1.3k 1.0× 320 13.4k
Andrew M. Hanby United Kingdom 49 2.6k 0.7× 1.5k 0.4× 3.3k 1.3× 2.2k 0.9× 1.2k 1.0× 128 7.5k

Countries citing papers authored by Hans Morreau

Since Specialization
Citations

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

Fields of papers citing papers by Hans Morreau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hans Morreau

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

All Works

20 of 20 papers shown
1.
Boot, Arnoud, Quinten R. Ducarmon, Sam Nooij, et al.. (2024). Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients. BMC Cancer. 24(1). 104–104. 5 indexed citations
2.
Ruano, Dina, Sebastien M. Joruiz, Mar Rodríguez‐Girondo, et al.. (2024). Germline variant affecting p53β isoforms predisposes to familial cancer. Nature Communications. 15(1). 8208–8208. 1 indexed citations
3.
Terradas, Mariona, Dina Ruano, Gemma Aiza, et al.. (2024). Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European Journal of Human Genetics. 32(7). 871–875. 2 indexed citations
4.
Bakker, Leontine E. H., Marco J. T. Verstegen, Iris C. M. Pelsma, et al.. (2024). Chromosomal alteration patterns in PitNETs: massive losses in aggressive tumors. Endocrine Related Cancer. 32(1). 2 indexed citations
5.
Morreau, Hans, Adriana C. H. van Engen–van Grunsven, Lioe‐Fee de Geus‐Oei, et al.. (2023). Molecular Diagnostics and [ 18 F]FDG-PET/CT in Indeterminate Thyroid Nodules: Complementing Techniques or Waste of Valuable Resources?. Thyroid. 34(1). 41–53. 10 indexed citations
6.
Roelands, Jessica, Manon van der Ploeg, Marieke E. Ijsselsteijn, et al.. (2022). Transcriptomic and immunophenotypic profiling reveals molecular and immunological hallmarks of colorectal cancer tumourigenesis. Gut. 72(7). 1326–1339. 47 indexed citations
7.
Lam, Suk Wai, Marie Kostine, Noel F.C.C. de Miranda, et al.. (2021). Mismatch repair deficiency is rare in bone and soft tissue tumors. Histopathology. 79(4). 509–520. 29 indexed citations
8.
Soer, Eline C., Lodewijk A.A. Brosens, Marc J. van de Vijver, et al.. (2018). Dilemmas for the pathologist in the oncologic assessment of pancreatoduodenectomy specimens. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 472(4). 533–543. 27 indexed citations
9.
Mulder, Babs G. Sibinga, J. Sven D. Mieog, Arantza Fariña Sarasqueta, et al.. (2017). Diagnostic value of targeted next-generation sequencing in patients with suspected pancreatic or periampullary cancer. Journal of Clinical Pathology. 71(3). 246–252. 9 indexed citations
10.
Geus, Susanna W.L. de, J. Sven D. Mieog, Rutger‐Jan Swijnenburg, et al.. (2016). Predictive Biomarkers for Short-Term Survival After Curative Intent Pancreatic Cancer Surgery : Identifying the Biologically Ill-Fated. Pancreas. 45(10). 1502–1502. 3 indexed citations
11.
Miranda, Noel F.C.C. de, Maarten van Dinther, Brendy E.W.M. van den Akker, et al.. (2015). Transforming Growth Factor beta Signaling in Colorectal Cancer Cells With Microsatellite Instability Despite Biallelic Mutations in TGFBR2. PLoS ONE. 148(7). 1 indexed citations
12.
Miranda, Noel F.C.C. de, Ekaterina S. Jordanova, Carli M.J. Tops, et al.. (2012). Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases. Clinical Cancer Research. 18(5). 1237–1245. 28 indexed citations
13.
Fransen, Marieke F., Marjolein Sluijter, Hans Morreau, Ramon Arens, & Cornelis J.M. Melief. (2011). Local Activation of CD8 T Cells and Systemic Tumor Eradication without Toxicity via Slow Release and Local Delivery of Agonistic CD40 Antibody. Clinical Cancer Research. 17(8). 2270–2280. 128 indexed citations
14.
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
15.
Lips, Esther H., Ronald van Eijk, Eelco J. R. de Graaf, et al.. (2008). Progression and Tumor Heterogeneity Analysis in Early Rectal Cancer. Clinical Cancer Research. 14(3). 772–781. 35 indexed citations
16.
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
17.
Kodach, Liudmila L., Eliza Wiercinska, Noel F.C.C. de Miranda, et al.. (2008). The Bone Morphogenetic Protein Pathway Is Inactivated in the Majority of Sporadic Colorectal Cancers. EUR Research Repository (Erasmus University Rotterdam). 1 indexed citations
18.
Capella, Matías, Ryan K. van Laar, Corrie A.M. Marijnen, et al.. (2007). Prognosis prediction of stage II colon cancer by gene expression profiling. Annals of Oncology. 18. 2 indexed citations
19.
Cardoso, Joana, Renée X. de Menezes, Monique E. van Leerdam, et al.. (2006). Chromosomal Instability in MYH - and APC -Mutant Adenomatous Polyps. Cancer Research. 66(5). 2514–2519. 45 indexed citations
20.
Jong, Andrea E. van der Meulen‐de, Hans Morreau, Fokko M. Nagengast, et al.. (2005). Prevalence of Adenomas among Young Individuals at Average Risk for Colorectal Cancer. The American Journal of Gastroenterology. 100(1). 139–143. 51 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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