Sandra J. B. Hendriks-Cornelissen

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 · 819 citations

Life Sciences, Genetics, Molecular Genetics +11

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 · 324 citations

Life Sciences, Genetics, Molecular Genetics +14

Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags

Astrid Eijkelenboom, Eveline J. Kamping, Annemiek W. Kastner-van Raaij et al. · Journal of Molecular Diagnostics · 2016 · 143 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Phenotypic and Genotypic Characterization of Orthotopic Human Glioma Models and Its Relevance for the Study of Anti‐glioma Therapy

An Claes, Janneke Schuuring, Sandra Boots‐Sprenger et al. · Brain Pathology · 2008 · 73 citations · Full text

Medicine, Neuroscience, Oncology +17

Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material

Elisabeth M. P. Steeghs, Leonie I. Kroeze, Bastiaan B.J. Tops et al. · BMC Cancer · 2020 · 37 citations · Full text

Medicine, Genetics, Oncology +17