Ivonne J.H.M. van Minderhout

Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients

Gijs W.E. Santen, Emmelien Aten, Anneke T. Vulto‐van Silfhout et al. · Human Mutation · 2013 · 214 citations

Genetics, Genetic Epidemiology, Pathology +20

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families

Erik F. Hensen, Ekaterina S. Jordanova, Ivonne J.H.M. van Minderhout et al. · Oncogene · 2004 · 152 citations

Somatic Variant, Cytogenetics, Somatic Loss +10

Leiden open variation database of the MUTYH gene

Astrid A. Out, Carli M.J. Tops, Maartje Nielsen et al. · Human Mutation · 2010 · 79 citations · Full text

Deep sequencing to reveal new variants in pooled DNA samples

Astrid A. Out, Ivonne J.H.M. van Minderhout, Jelle J. Goeman et al. · Human Mutation · 2009 · 76 citations

Genetics, Pathology, Allele Frequency Estimation +19

MUTYH gene variants and breast cancer in a Dutch case–control study

Astrid A. Out, Marijke Wasielewski, Petra E.A. Huijts et al. · Breast Cancer Research and Treatment · 2012 · 50 citations · Full text