Manon Suerink

1.1k total citations
21 papers, 212 citations indexed

About

Manon Suerink is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Manon Suerink has authored 21 papers receiving a total of 212 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pathology and Forensic Medicine, 11 papers in Oncology and 8 papers in Cancer Research. Recurrent topics in Manon Suerink's work include Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (8 papers) and Colorectal Cancer Screening and Detection (5 papers). Manon Suerink is often cited by papers focused on Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (8 papers) and Colorectal Cancer Screening and Detection (5 papers). Manon Suerink collaborates with scholars based in Netherlands, Germany and Austria. Manon Suerink's co-authors include Maartje Nielsen, Hans Morreau, Tom van Wezel, Sanne W. ten Broeke, Katharina Wimmer, Carli M.J. Tops, Hans F. A. Vasen, Alexandra M. J. Langers, Yael Goldberg and Thomas P. Potjer and has published in prestigious journals such as Gastroenterology, Frontiers in Immunology and Journal of Clinical Pathology.

In The Last Decade

Manon Suerink

18 papers receiving 211 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Manon Suerink Netherlands	9	145	94	88	46	42	21	212
Eric Ruano France	5	179 1.2×	104 1.1×	63 0.7×	95 2.1×	37 0.9×	9	243
Chelsea Mullins United States	7	98 0.7×	105 1.1×	114 1.3×	99 2.2×	24 0.6×	17	265
Richard Gallon United Kingdom	8	237 1.6×	197 2.1×	132 1.5×	81 1.8×	47 1.1×	20	299
Theofanis Zagoras Sweden	8	173 1.2×	100 1.1×	87 1.0×	72 1.6×	48 1.1×	10	269
Emmanouil Volikos United Kingdom	6	126 0.9×	36 0.4×	91 1.0×	44 1.0×	30 0.7×	7	187
Raffaella Liccardo Italy	11	227 1.6×	161 1.7×	144 1.6×	118 2.6×	38 0.9×	23	330
Alicia Latham United States	7	112 0.8×	84 0.9×	75 0.9×	31 0.7×	41 1.0×	26	209
Rebecca P. M. Brosens Netherlands	8	131 0.9×	98 1.0×	176 2.0×	88 1.9×	77 1.8×	10	324
P. Yussanne United Kingdom	6	158 1.1×	90 1.0×	101 1.1×	119 2.6×	14 0.3×	7	307
Khazi M. Nayeemuddin United States	6	202 1.4×	166 1.8×	144 1.6×	11 0.2×	32 0.8×	6	303

Countries citing papers authored by Manon Suerink

Since Specialization

Citations

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

Fields of papers citing papers by Manon Suerink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manon Suerink

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

All Works

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20 of 20 papers shown

Srebniak, Malgorzata I., Donald R. Hahn, Karin E. M. Diderich, et al.. (2025). Prenatal Variants of Uncertain Significance (VUS): to report or not to report?. European Journal of Human Genetics. 33(10). 1300–1308.

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

Colas, Chrystelle, et al.. (2024). ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management. European Journal of Human Genetics. 32(12). 1526–1541. 5 indexed citations

Haak, Monique C., Xiao Han, Martina Ruiterkamp‐Versteeg, et al.. (2024). De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of Medical Genetics. 61(6). 549–552. 1 indexed citations

Lam, A., Mar Rodríguez‐Girondo, Carli M.J. Tops, et al.. (2024). Delineating genotype and parent‐of‐origin effect on the phenotype in MSH6‐associated Lynch syndrome. Genes Chromosomes and Cancer. 63(5). e23237–e23237.

Giordano, Jessica L., et al.. (2024). Prenatal Ultrasonographic Features Associated With ARSL and X‐Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series. Prenatal Diagnosis. 44(13). 1663–1670.

Haeringen, Arie van, Lisenka E.L.M. Vissers, Emilia K. Bijlsma, et al.. (2023). Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context. European Journal of Pediatrics. 183(1). 345–355. 8 indexed citations

Lam, A., Carli M.J. Tops, Liselotte P. van Hest, et al.. (2023). Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers. Modern Pathology. 36(9). 100240–100240. 9 indexed citations

Nielsen, Maartje, Manon Suerink, Jan J. Koornstra, et al.. (2023). PMS2-associated Lynch syndrome: Past, present and future. Frontiers in Oncology. 13. 1127329–1127329. 7 indexed citations

10.

Suerink, Manon, et al.. (2023). Relation between WHO Classification and Location- and Functionality-Based Classifications of Neuroendocrine Neoplasms of the Digestive Tract. Neuroendocrinology. 114(2). 120–133. 5 indexed citations

11.

Elsayed, Fadwa A., Tom van Wezel, Alexandra M. J. Langers, et al.. (2022). Mismatch repair deficiency and MUTYH variants in small intestine-neuroendocrine tumors. Human Pathology. 125. 11–17. 5 indexed citations

12.

Broeke, Sanne W. ten, Hans Morreau, Manon Suerink, et al.. (2021). The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations. Critical Reviews in Oncology/Hematology. 163. 103338–103338. 20 indexed citations

13.

Suerink, Manon, et al.. (2020). Recurrent APC Splice Variant c.835-8A>G in Patients With Unexplained Colorectal Polyposis Fulfilling the Colibactin Mutational Signature. Gastroenterology. 159(4). 1612–1614.e5. 14 indexed citations

14.

Suerink, Manon, Katharina Wimmer, Laurence Brugières, et al.. (2020). Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019. Familial Cancer. 20(1). 67–73. 12 indexed citations

15.

Suerink, Manon, Arantza Fariña Sarasqueta, Alexandra M. J. Langers, et al.. (2020). Prevalence of mismatch repair deficiency and Lynch syndrome in a cohort of unselected small bowel adenocarcinomas. Journal of Clinical Pathology. 74(11). 724–729. 11 indexed citations

16.

Suerink, Manon, Frederik J. Hes, Alexandra M. J. Langers, et al.. (2019). Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy. European Journal of Human Genetics. 28(2). 222–230. 12 indexed citations

17.

IJspeert, Hanna, Pauline A. van Schouwenburg, Ingrid Pico‐Knijnenburg, et al.. (2019). Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans. Frontiers in Immunology. 10. 1913–1913. 7 indexed citations

18.

Broeke, Sanne W. ten, E. Gómez, Frederik J. Hes, et al.. (2018). Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2. Gastroenterology. 155(3). 844–851. 29 indexed citations

19.

Suerink, Manon, Tim Ripperger, Ludwine Messiaen, et al.. (2018). Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy. Journal of Medical Genetics. 56(2). 53–62. 34 indexed citations

20.

Suerink, Manon, Thomas P. Potjer, A. Birgitta Versluijs, et al.. (2017). Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?. Clinical Genetics. 93(1). 134–137. 20 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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