Liselotte P. Hest

Compliance with periodic surveillance for Von-Hippel-Lindau disease

N. Aaronson, S. Verhoef, E. Bleiker, 2011, Genetics in Medicine.

Germ-line and somatic DICER1 mutations in pineoblastoma

J. Lupski, S. Jhangiani, W. Foulkes, 2014, Acta Neuropathologica.

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

Aung Ko Win, M. Kloor, B. Bonanni, 2022, Hereditary Cancer in Clinical Practice.

Two TP53 germline mutations in a classical Li-Fraumeni syndrome family

H. Meijers-Heijboer, S. Verhoef, A. Wagner, 2007, Familial Cancer.

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

P. Devilee, C. Asperen, S. Verhoef, 2016, Human mutation.

Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

L. Vissers, A. Hoischen, J. Lupski, 2017, European Journal of Human Genetics.