Ilse M. van der Werf

Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP

Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns et al. · Biological Psychiatry · 2018 · 177 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Mendelian Disorder +13

Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndrome

Ilse M. van der Werf, Karin Buiting, Johanna Christina Czeschik et al. · European Journal of Human Genetics · 2016 · 62 citations · Full text

Chromatin, Gene Deletion Data, Developmental Biology +11

Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities

Anke Van Dijck, Ilse M. van der Werf, Edwin Reyniers et al. · European Journal of Medical Genetics · 2015 · 48 citations

Triplication Show Macrocephaly, Chromatin, Chromosome 1Q21.1 +10

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Jasmin Beygo, Alma Küchler, Gabriele Gillessen‐Kaesbach et al. · European Journal of Human Genetics · 2017 · 43 citations · Full text

Imprinted Meg8-dmr, Mendelian Disorder, Genetic Disorder +9

Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability

Ilse M. van der Werf, Anke Van Dijck, Edwin Reyniers et al. · Gene · 2016 · 37 citations · Full text

Mendelian Disorder, Genetic Disorder, Large Pedigrees +8