Anke Van Dijck
University of Antwerp(BE)Antwerp University Hospital(BE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Autism Spectrum Disorder Research, Genomic variations and chromosomal abnormalities, Congenital heart defects research
Most-Cited Works
- → Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling(2015)330 cited
- → Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants(2018)220 cited
- → Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders(2020)209 cited
- → Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP(2018)178 cited
- → Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes(2016)123 cited
- → Tauopathy in the young autistic brain: novel biomarker and therapeutic target(2020)105 cited
- → Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies(2018)87 cited
- → Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice(2019)84 cited
- → The transcriptional regulatorADNPlinks the BAF (SWI/SNF) complexes with autism(2014)81 cited
- → Erratum: Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children(2017)80 cited