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List of works by Willy M Nillesen

Diagnostic genome profiling in mental retardation

scientific article

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

scientific article

GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila.

scientific article published on 4 May 2013

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.

scientific article published on 11 July 2016

Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome.

scientific article

Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome.

scientific article published in March 2006

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

scientific article published on 29 April 2012

Variants in CUL4B are associated with cerebral malformations

scientific article

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