Nicoline Hoogerbrugge

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

Sharon E. Plon, Diana Eccles, Douglas F. Easton et al. · Human Mutation · 2008 · 897 citations · Full text

Genetic Testing, Cancer Pathology, Sequence Variant Classification +20

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

Marjolijn J. L. Ligtenberg, Roland P. Kuiper, Tsun Leung Chan et al. · Nature Genetics · 2008 · 803 citations

Heritable Somatic Methylation, Somatic Variant, Mendelian Disorder +9

Deficient mismatch repair system in patients with sporadic advanced colorectal cancer

Miriam Koopman, Guus A. M. Kortman, Leonie J. Mekenkamp et al. · British Journal of Cancer · 2009 · 509 citations · Full text

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

Robbert D.A. Weren, Marjolijn J. L. Ligtenberg, C. Marleen Kets et al. · Nature Genetics · 2015 · 372 citations

Genome Instability, Medicine, Genetics +7

Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

Arjen R. Mensenkamp, Ingrid P. Vogelaar, Wendy A.G. van Zelst–Stams et al. · Gastroenterology · 2013 · 320 citations

Genome Instability, Somatic Variant, Somatic Mutations +9