F. Hes

发表

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)

E. Kuipers, J. Houwing-Duistermaat, T. Reinards, 2005, Journal of Medical Genetics.

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

J. Houwing-Duistermaat, S. Verhoef, A. Wagner, 2016, Familial Cancer.

Evidence for accelerated colorectal adenoma–carcinoma progression in MUTYH-associated polyposis?

J. Sampson, H. Vasen, S. Aretz, 2011, Gut.

Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review

E. Kampman, R. Sijmons, C. Tops, 2013, Familial Cancer.

Duodenal adenomas and cancer in MUTYH-associated polyposis: an international cohort study.

M. Mort, G. Capellá, E. Dekker, 2020, Gastroenterology.

Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps

E. Kampman, R. Sijmons, C. Tops, 2013 .

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis

H. Morreau, M. Weiss, M. Breuning, 2007, Clinical genetics.

High frequency of copy‐neutral LOH in MUTYH‐associated polyposis carcinomas

H. Morreau, T. van Wezel, N. T. Ter Haar, 2008, The Journal of pathology.

Guidelines for the clinical management of familial adenomatous polyposis (FAP)

P. Møller, G. Capellá, S. Tejpar, 2008, Gut.

Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3

V. Moskvina, R. Houlston, D. Evans, 2008, Gut.

A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature

A. V. D. van den Ouweland, H. Morreau, T. van Wezel, 2019, Familial Cancer.

Frequency of Von Hippel‐Lindau germline mutations in classic and non‐classic Von Hippel‐Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation‐dependent probe amplification

P. Pearson, D. Halley, R. Sijmons, 2007, Clinical genetics.

Psychosocial impact of Von Hippel–Lindau disease: levels and sources of distress

S. Verhoef, N. Hoogerbrugge, D. Majoor-Krakauer, 2010, Clinical genetics.

Is colorectal surveillance indicated in patients with PTEN mutations?

A. Spigelman, N. Lindor, P. Möller, 2012, Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland.

Duodenal carcinoma in MUTYH-associated polyposis

E. Kuipers, S. Verhoef, A. Wagner, 2006, Journal of Clinical Pathology.

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded tissue

H. Morreau, D. Ruano, R. Eijk, 2018 .

Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome

P. Møller, D. Evans, A. Spigelman, 2014, Familial Cancer.

Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review

Y. Vos, F. Hes, A. Knopperts, 2012, Familial Cancer.