Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

Frederik J Hes; Dina Ruano; Marry Nieuwenhuis; Carli M Tops; Melanie Schrumpf; Maartje Nielsen; Petra E A Huijts; Juul T Wijnen; Anja Wagner; Encarna B Gómez García; Rolf H Sijmons; Fred H Menko; Tom G W Letteboer; Nicoline Hoogerbrugge; Jan Harryvan; Ellen Kampman; Hans Morreau; Hans F A Vasen; Tom van Wezel

doi:10.1136/jmedgenet-2013-102000

Article info

Cancer genetics

Original article

Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

Authors

Frederik J Hes Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Dina Ruano Departments of Pathology, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Marry Nieuwenhuis Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, The Netherlands PubMed articles Google scholar articles
Carli M Tops Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Melanie Schrumpf Departments of Pathology, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Maartje Nielsen Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Petra E A Huijts Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Juul T Wijnen Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Anja Wagner Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands PubMed articles Google scholar articles
Encarna B Gómez García Department of Clinical Genetics, University of Maastricht, Maastricht, The Netherlands PubMed articles Google scholar articles
Rolf H Sijmons Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands PubMed articles Google scholar articles
Fred H Menko Department of Clinical Genetics, Free University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Tom G W Letteboer Department of Medical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands PubMed articles Google scholar articles
Nicoline Hoogerbrugge Department of Human Genetics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands PubMed articles Google scholar articles
Jan Harryvan Division of Human Nutrition, Wageningen University, Wageningen, The Netherlands PubMed articles Google scholar articles
Ellen Kampman Division of Human Nutrition, Wageningen University, Wageningen, The Netherlands PubMed articles Google scholar articles
Hans Morreau Departments of Pathology, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Hans F A Vasen Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, The Netherlands Department of Gastroenterology of the Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles
Tom van Wezel Departments of Pathology, Leiden University Medical Center, Leiden, The Netherlands PubMed articles Google scholar articles

Correspondence to Dr Frederik J Hes, Department of Clinical Genetics, Leiden University Medical Center (LUMC), PO Box 9600, K5-R, Leiden 2300 RC, The Netherlands; f.j.hes{at}lumc.nl

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Citation

Hes FJ, Ruano D, Nieuwenhuis M, et al

Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

Journal of Medical Genetics 2014;51:55-60.

Publication history

Received August 13, 2013
Revised October 1, 2013
Accepted October 17, 2013
First published November 19, 2013.

Online issue publication

April 27, 2016

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