W.M. Wissink-Lindhout
Radboud University Nijmegen(NL)Radboud University Medical Center(NL)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Chromatin Remodeling and Cancer, Diverse Scientific and Economic Studies
Most-Cited Works
- → Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling(2015)330 cited
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability(2012)267 cited
- → Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability(2011)202 cited
- → Update on Kleefstra Syndrome(2011)178 cited
- → Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability(2016)154 cited
- → Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function(2014)102 cited
- → Homozygous SLC6A17 Mutations Cause Autosomal-Recessive Intellectual Disability with Progressive Tremor, Speech Impairment, and Behavioral Problems(2015)42 cited
- → B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies(2017)14 cited
- → Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability(2018)1 cited