Roos van der Donk

De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism

Illja J. Diets, Roos van der Donk, Kristina Baltrunaite et al. · The American Journal of Human Genetics · 2019 · 50 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders

Roos van der Donk, Sandra Jansen, Janneke Schuurs-Hoeijmakers et al. · Genetics in Medicine · 2018 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome

Alexander J.M. Dingemans, Diante E. Stremmelaar, Roos van der Donk et al. · European Journal of Human Genetics · 2021 · 14 citations · Full text

Life Sciences, Genetics, Craniofacial Genetics +7