Tom G.W. Letteboer

5.1k total citations
27 papers, 1.2k citations indexed

About

Tom G.W. Letteboer is a scholar working on Pathology and Forensic Medicine, Genetics and Surgery. According to data from OpenAlex, Tom G.W. Letteboer has authored 27 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pathology and Forensic Medicine, 8 papers in Genetics and 7 papers in Surgery. Recurrent topics in Tom G.W. Letteboer's work include Genetic factors in colorectal cancer (11 papers), Vascular Anomalies and Treatments (8 papers) and Tracheal and airway disorders (6 papers). Tom G.W. Letteboer is often cited by papers focused on Genetic factors in colorectal cancer (11 papers), Vascular Anomalies and Treatments (8 papers) and Tracheal and airway disorders (6 papers). Tom G.W. Letteboer collaborates with scholars based in Netherlands, United States and United Kingdom. Tom G.W. Letteboer's co-authors include C. J. J. Westermann, Repke J. Snijder, Karen Duran, Victor Guryev, Ewart de Bruijn, Edwin Cuppen, Martin Poot, Ron Hochstenbach, Wigard P. Kloosterman and Diane Rushlow and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and PLoS ONE.

In The Last Decade

Tom G.W. Letteboer

25 papers receiving 1.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Tom G.W. Letteboer 410 353 347 336 283 27 1.2k
Susan Schelley 342 0.8× 385 1.1× 258 0.7× 337 1.0× 85 0.3× 17 1.0k
S. Pinson 205 0.5× 216 0.6× 123 0.4× 254 0.8× 153 0.5× 39 1.1k
Ana Novokmet 582 1.4× 153 0.4× 355 1.0× 193 0.6× 161 0.6× 15 1.3k
Reha M. Toydemir 429 1.0× 354 1.0× 223 0.6× 159 0.5× 24 0.1× 31 834
Carrie Fitzpatrick 465 1.1× 97 0.3× 439 1.3× 304 0.9× 184 0.7× 33 1.3k
Ivonne Marondel 357 0.9× 482 1.4× 72 0.2× 403 1.2× 85 0.3× 7 972
Tracey P. Leedom 148 0.4× 150 0.4× 148 0.4× 132 0.4× 50 0.2× 7 804
Glenn L. Renforth 448 1.1× 139 0.4× 355 1.0× 161 0.5× 17 0.1× 5 798
Annemarie H. van der Hout 1.2k 2.9× 131 0.4× 319 0.9× 264 0.8× 109 0.4× 36 1.8k
Manjunath Nimmakayalu 730 1.8× 491 1.4× 350 1.0× 91 0.3× 50 0.2× 24 1.6k

Countries citing papers authored by Tom G.W. Letteboer

Since Specialization
Citations

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

Fields of papers citing papers by Tom G.W. Letteboer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tom G.W. Letteboer. 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 Tom G.W. Letteboer. The network helps show where Tom G.W. Letteboer may publish in the future.

Co-authorship network of co-authors of Tom G.W. Letteboer

This figure shows the co-authorship network connecting the top 25 collaborators of Tom G.W. Letteboer. A scholar is included among the top collaborators of Tom G.W. Letteboer 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 Tom G.W. Letteboer. Tom G.W. Letteboer 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.
Lam, A., James G. Dowty, Fonnet E. Bleeker, et al.. (2025). Cancer risks for MSH6 pathogenic variant carriers. European Journal of Cancer. 231. 116098–116098.
2.
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.
3.
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
4.
Hopman, Saskia, Corianne A.J.M. de Borgie, Cora M. Aalfs, et al.. (2021). Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study. Familial Cancer. 20(4). 263–271. 6 indexed citations
5.
Mensenkamp, Arjen R., Irıs D. Nagtegaal, Wendy A.G. van Zelst–Stams, et al.. (2020). Somatic Nonepigenetic Mismatch Repair Gene Aberrations Underly Most Mismatch Repair–Deficient Lynch-Like Tumors. Gastroenterology. 160(4). 1414–1416.e3. 8 indexed citations
6.
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
7.
Hopman, Saskia, Cora M. Aalfs, Fonnet E. Bleeker, et al.. (2017). Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation. European Journal of Cancer. 80. 48–54. 18 indexed citations
8.
Nieuwenhuis, Marry H., Jeanine J. Houwing‐Duistermaat, Frederik J. Hes, et al.. (2016). Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. Familial Cancer. 15(4). 563–570. 7 indexed citations
9.
10.
Jansen, Anne M.L., Tom van Wezel, Marina Ventayol García, et al.. (2015). Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers. European Journal of Human Genetics. 24(7). 1089–1092. 96 indexed citations
11.
Kessels, Koen, Herma H. Fidder, Tom G.W. Letteboer, et al.. (2013). Adherence to Microsatellite Instability Testing in Young-Onset Colorectal Cancer Patients. Diseases of the Colon & Rectum. 56(7). 825–833. 6 indexed citations
12.
Gent, Marco W.F. van, Sebastiaan Velthuis, Martijn C. Post, et al.. (2013). Hereditary hemorrhagic telangiectasia: How accurate are the clinical criteria?. American Journal of Medical Genetics Part A. 161(3). 461–466. 39 indexed citations
13.
Boshuisen, Kim, Manon Brundel, Carolien G. F. de Kovel, et al.. (2012). Polymorphisms in ACVRL1 and Endoglin Genes are Not Associated with Sporadic and HHT-Related Brain AVMs in Dutch Patients. Translational Stroke Research. 4(3). 375–378. 14 indexed citations
14.
Kloosterman, Wigard P., Victor Guryev, Karen Duran, et al.. (2011). Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†. Human Molecular Genetics. 20(10). 1916–1924. 225 indexed citations
15.
Letteboer, Tom G.W., et al.. (2008). Genotype–phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia. American Journal of Medical Genetics Part A. 146A(21). 2733–2739. 47 indexed citations
16.
Bliek, Jet, Pauline Terhal, Saskia M. Maas, et al.. (2006). Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype. The American Journal of Human Genetics. 78(4). 604–614. 151 indexed citations
17.
Rump, Patrick, Tom G.W. Letteboer, Gilles Thomas, et al.. (2006). Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele. American Journal of Medical Genetics Part A. 140A(3). 284–290. 17 indexed citations
18.
19.
Letteboer, Tom G.W., Eveline J. Kamping, Repke J. Snijder, et al.. (2004). Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients. Human Genetics. 116(1-2). 8–16. 80 indexed citations
20.
Paul, Philip, et al.. (1993). Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposis. Human Molecular Genetics. 2(7). 925–931. 89 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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