Tom Letteboer

Assistant Professor - medical

Recent publications

Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome Anne Sophie van der Werf-'t Lam, Mar Rodriguez-Girondo, Mandy Villasmil, Carli M. Tops, Liselotte van Hest, Hans J.P. Gille, Floor A.M. Duijkers, Anja Wagner, Ellis Eikenboom, Tom G.W. Letteboer, Mirjam M. de Jong, Sanne W. Bajwa-ten Broeke, Fonnet Bleeker, Encarna B. Gomez Garcia, Mev Dominguez-Valentin, Pal Møller, Manon Suerink, Maartje Nielsen
Genes Chromosomes and Cancer, 2024, vol. 63
Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS) Floor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, Cora M Aalfs, Jakob K Anninga, Lieke P V Berger, 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 L C M Loeffen, Lisethe Meijer, Maran J W Olderode-Berends, Anja Wagner, Raoul C Hennekam, Johannes H M Merks
Familial Cancer, 2021, vol. 20, p.263-271
Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2 Sanne W. ten Broeke, Tom C. van Bavel, Anne M.L. Jansen, Encarnca Gómez-García, Frederik J. Hes, Liselot P. van Hest, Tom G.W. Letteboer, Maran J.W. Olderode-Berends, Dina Ruano, Liesbeth Spruijt, Manon Suerink, Carli M. Tops, Ronald van Eijk, Hans Morreau, Tom van Wezel, Maartje Nielsen
Gastroenterology, 2018, vol. 155, p.844-851
SNP association study in PMS2-associated Lynch syndrome Sanne W. Ten Broeke, Fadwa A. Elsayed, Lisa Pagan, Maran J W Olderode-Berends, Encarna Gomez Garcia, Hans J J P Gille, Liselot P. van Hest, Tom G.W. Letteboer, Lizet E. Van Der Kolk, Arjen R. Mensenkamp, Theo A. Van Os, Liesbeth Spruijt, Bert J W Redeker, Manon Suerink, Yvonne J. Vos, Anja Wagner, Juul T. Wijnen, Ewout W. Steyerberg, Carli M J Tops, Tom van Wezel, Maartje Nielsen
Familial Cancer, 2018, vol. 17, p.507-515
Cancer Risks for PMS2-associated lynch syndrom Sanne W.Ten Broeke, Heleen M.Vander Klift, Carli M.J. Tops, Stefan Aretz, Inge Bernstein, Daniel D. Buchanan, Albert Dela Chapelle, Gabriel Capella, Mark Clendenning, Christoph Engel, Steven Gallinger, Encarna Gomez Garcia, Jane C. Figueiredo, Robert Haile, Heather L. Hampel, John L. Hopper, Nicoline Hoogerbrugge, Magnus Von Knebel Doeberitz, Loic Le Marchand, Tom G.W. Letteboer, Mark A. Jenkins, Annika Lindblom, Noralane M. Lindor, Arjen R. Mensenkamp, Pal Møller, Polly A. Newcomb, Theo A.M. Van Os, Rachel Pearlman, Marta Pineda, Nils Rahner, Egbert J.W. Redeker, Maran J.W. Olderode-Berends, Christophe Rosty, Hans K. Schackert, Rodney Scott, Leigha Senter, Liesbeth Spruijt, Verena Steinke-Lange, Manon Suerink, Stephen Thibodeau, Yvonne J. Vos, Anja Wagner, Ingrid Winship, J. Frederik Hes, Hans F.A. Vasen, Juul T. Wijnen, Maartje Nielsen, Aung Ko Win
Journal of Clinical Oncology, 2018, vol. 36, p.2961-2968
Sending family history questionnaires to patients before a colonoscopy improves genetic counseling for hereditary colorectal cancer Koen Kessels, Joey D Eisinger, Tom G Letteboer, G Johan A Offerhaus, Peter D Siersema, Leon M G Moons
Rare diseases (Austin, Tex.), 2017, vol. 18, p.343-348

Fellowships & Awards

2005: To a promising doctor for research into Hereditary Hemorrhagic Telangiectasia

2004: The Robert I. White Jr., M.D. Young HHT Clinician of the Year Award for his work on Osler-Weber-Rendu syndrome