Nicolette S. den Hollander
Leiden University Medical Center(NL)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Fetal and Pediatric Neurological Disorders, Genetics and Neurodevelopmental Disorders, Connective tissue disorders research
Most-Cited Works
- → Transcription Factor E2-2 Is an Essential and Specific Regulator of Plasmacytoid Dendritic Cell Development(2008)650 cited
- → TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands(2019)369 cited
- → Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome(2012)349 cited
- → Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients(2013)218 cited
- → The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome(2018)132 cited
- → TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations(2015)125 cited