Brigitte H. W. Faas
Radboud University Nijmegen(NL)University Medical Center(US)Radboud University Medical Center(NL)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Fetal and Pediatric Neurological Disorders, Genomic variations and chromosomal abnormalities, Parvovirus B19 Infection Studies, Congenital Anomalies and Fetal Surgery
Most-Cited Works
- → Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus(2011)475 cited
- → TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands(2019)369 cited
- → CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy(2007)298 cited
- → Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis(2015)289 cited
- → Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis(2013)215 cited
- → Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype(2008)169 cited