Tom G.W. Letteboer

5.1k citations

27 papers · 1.2k indexed · h-index 16

Molecular Biology
Genetics top 2%
Genetics top 5%
Pulmonary and Respiratory Medicine top 10%
Pathology and Forensic Medicine top 5%

Co-authors: C. J. J. Westermann Repke J. Snijder Ron Hochstenbach Karen Duran Martin Poot Victor Guryev Edwin Cuppen Wigard P. Kloosterman
Topics: Genetic factors in colorectal cancer (11 papers)Vascular Anomalies and Treatments (8 papers)Tracheal and airway disorders (6 papers)
Cited by: Genetics Pathology and Forensic Medicine
Journals: Proceedings of the National Academy of Sciences Gastroenterology PLoS ONE
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Tom G.W. Letteboer

25 papers receiving 1.1k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Cancer risks for MSH6 pathogenic variant carriers 2025 ·European Journal of Cancer ·A. Lam,James G. Dowty,(unknown),(unknown),(unknown),Fonnet E. Bleeker,E. Gómez,Liselotte P. van Hest,Gilles Thomas,(unknown),Mirjam M. de Jong,Tom G.W. Letteboer,Floor A.M. Duijkers,Anja Wagner,(unknown),(unknown),Sanne W. ten Broeke,Aung Ko Win,Mark A. Jenkins,Maartje Nielsen	0
2	Delineating genotype and parent‐of‐origin effect on the phenotype in MSH6‐associated Lynch syndrome 2024 ·Genes Chromosomes and Cancer ·A. Lam,Mar Rodríguez‐Girondo,(unknown),Carli M.J. Tops,(unknown),Gilles Thomas,Floor A.M. Duijkers,Anja Wagner,(unknown),Tom G.W. Letteboer,Mirjam M. de Jong,Sanne W. ten Broeke,Fonnet E. Bleeker,E. Gómez,Mev Dominguez–Valentin,Pål Møller,Manon Suerink,Maartje Nielsen	0
3	Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers 2023 ·Modern Pathology ·A. Lam,(unknown),Carli M.J. Tops,(unknown),Liselotte P. van Hest,Gilles Thomas,Floor A.M. Duijkers,Anja Wagner,(unknown),Tom G.W. Letteboer,Mirjam M. de Jong,Sanne W. ten Broeke,Fonnet E. Bleeker,E. Gómez,Niels de Wind,Tom van Wezel,Hans Morreau,Manon Suerink,Maartje Nielsen	9
4	Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study 2021 ·Familial Cancer ·(unknown),Saskia Hopman,Corianne A.J.M. de Borgie,Cora M. Aalfs,Jakob Anninga,(unknown),Fonnet E. Bleeker,Charlotte J. Dommering,Natasha K. A. van Eijkelenburg,Peter Hammond,Marry M. van den Heuvel‐Eibrink,Janna A. Hol,Wijnanda A. Kors,Tom G.W. Letteboer,Jan Loeffen,Lisethe Meijer,Maran J.W. Olderode-Berends,Anja Wagner,Raoul C. M. Hennekam,Johannes H. M. Merks	6
5	Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation 2017 ·European Journal of Cancer ·(unknown),Saskia Hopman,Cora M. Aalfs,(unknown),Fonnet E. Bleeker,Charlotte J. Dommering,Marjolijn C.J. Jongmans,Tom G.W. Letteboer,Maran J.W. Olderode-Berends,Anja Wagner,Raoul C. M. Hennekam,Johannes H. M. Merks	18
6	Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers 2016 ·Familial Cancer ·(unknown),Marry H. Nieuwenhuis,Jeanine J. Houwing‐Duistermaat,(unknown),Frederik J. Hes,Carli M.J. Tops,Anja Wagner,Cora M. Aalfs,Senno Verhoef,E. Gómez,Rolf H. Sijmons,Fred H. Menko,Tom G.W. Letteboer,Nicoline Hoogerbrugge,Tom van Wezel,Hans F. A. Vasen,Juul Wijnen	7
7	Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14 2015 ·Frontiers in Genetics ·Tom G.W. Letteboer,Michael Benzinou,(unknown),David A. Quigley,(unknown),Il-Jin Kim,Minh D. To,David M. Jablons,Johannes Kristian Ploos van Amstel,Cornelius J.J. Westermann,Sophie Giraud,Sophie Dupuis‐Girod,Gaëtan Lesca,Jonathan Berg,Allan Balmain,Rosemary J. Akhurst	16
8	Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers 2015 ·European Journal of Human Genetics ·Anne M.L. Jansen,Tom van Wezel,(unknown),Marina Ventayol García,Dina Ruano,Carli M.J. Tops,Anja Wagner,Tom G.W. Letteboer,E. Gómez,Peter Devilee,Juul Wijnen,Frederik J. Hes,Hans Morreau	96
9	Hereditary hemorrhagic telangiectasia: How accurate are the clinical criteria? 2013 ·American Journal of Medical Genetics Part A ·Marco W.F. van Gent,Sebastiaan Velthuis,Martijn C. Post,Repke J. Snijder,Cornelis J.J. Westermann,Tom G.W. Letteboer,Johannes J. Mager	39
10	Adherence to Microsatellite Instability Testing in Young-Onset Colorectal Cancer Patients 2013 ·Diseases of the Colon & Rectum ·Koen Kessels,Herma H. Fidder,(unknown),Tom G.W. Letteboer,Robin Timmer,Thijs van Dalen,Esther C. J. Consten,G. Johan A. Offerhaus,Peter D. Siersema	6
11	Polymorphisms in ACVRL1 and Endoglin Genes are Not Associated with Sporadic and HHT-Related Brain AVMs in Dutch Patients 2012 ·Translational Stroke Research ·Kim Boshuisen,Manon Brundel,Carolien G. F. de Kovel,Tom G.W. Letteboer,Gabriël J.E. Rinkel,Cornelis J.J. Westermann,Helen Kim,Ludmila Pawlikowska,Bobby P. C. Koeleman,Catharina J.M. Klijn	14
12	Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline† 2011 ·Human Molecular Genetics ·Wigard P. Kloosterman,Victor Guryev,(unknown),Karen Duran,Ewart de Bruijn,(unknown),Tom G.W. Letteboer,(unknown),Ron Hochstenbach,Martin Poot,Edwin Cuppen	225
13	Genotype–phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia 2008 ·American Journal of Medical Genetics Part A ·Tom G.W. Letteboer,(unknown),Repke J. Snijder,Dick Lindhout,(unknown),Pieter Zanen,(unknown)	47
14	Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia 2007 ·European Journal of Gastroenterology & Hepatology ·Sebastiaan A.C. van Tuyl,Tom G.W. Letteboer,(unknown),Ernst J. Kuipers,Repke J. Snijder,C. J. J. Westermann,Mark F.J. Stolk	15
15	Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype 2006 ·The American Journal of Human Genetics ·Jet Bliek,Pauline Terhal,(unknown),Saskia M. Maas,Ben C.J. Hamel,Georgette B. Salieb–Beugelaar,Marleen Simon,Tom G.W. Letteboer,Jasper van der Smagt,(unknown),Marcel M. A. M. Mannens	151
16	SMAD4 mutations found in unselected HHT patients 2006 ·Journal of Medical Genetics ·Carol J. Gallione,(unknown),Tom G.W. Letteboer,Diane Rushlow,(unknown),Tracey P. Leedom,Arupa Ganguly,Antoni Castells,Hans Kristian Ploos van Amstel,C. J. J. Westermann,Reed E. Pyeritz,Douglas A. Marchuk	174
17	Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele 2006 ·American Journal of Medical Genetics Part A ·Patrick Rump,Tom G.W. Letteboer,Gilles Thomas,(unknown),W. Baerts,Josephus P. J. van Gestel,Joanne Verheij,Anthonie J. van Essen	17
18	A Pulmonary Right-to-Left Shunt in Patients With Hereditary Hemorrhagic Telangiectasia Is Associated With an Increased Prevalence of Migraine 2005 ·CHEST Journal ·Martijn C. Post,Tom G.W. Letteboer,Johannes J. Mager,(unknown),Johannes C. Kelder,Cornelius J.J. Westermann	51
19	Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients 2004 ·Human Genetics ·Tom G.W. Letteboer,(unknown),Eveline J. Kamping,(unknown),(unknown),Repke J. Snijder,Dick Lindhout,Frederic A. M. Hennekam,C. J. J. Westermann,Johannes Kristian Ploos van Amstel	80
20	Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposis 1993 ·Human Molecular Genetics ·Philip Paul,Tom G.W. Letteboer,(unknown),Joanna Groden,R. White,Max J. Coppes	89

About Tom G.W. Letteboer

Tom G.W. Letteboer is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research, having authored 27 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (11 papers), Vascular Anomalies and Treatments (8 papers) and Tracheal and airway disorders (6 papers). The work is most often cited by research in Genetics (353 citations), Pathology and Forensic Medicine (283 citations) and Genetics (347 citations). Tom G.W. Letteboer has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include C. J. J. Westermann, Repke J. Snijder, Ron Hochstenbach, Karen Duran, Martin Poot, Victor Guryev, Edwin Cuppen, Wigard P. Kloosterman, Ewart de Bruijn and R. White. Their work appears in journals such as Proceedings of the National Academy of Sciences, Gastroenterology and PLoS ONE.

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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