Annick Vogels
KU Leuven(BE)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Congenital heart defects research, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Congenital Heart Disease Studies
Most-Cited Works
- → Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant(2008)346 cited
- → Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome(2015)295 cited
- → Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome(2012)243 cited
- The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.(1999)
- → Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications(2000)189 cited
- → Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders(2003)185 cited
- → Intellectual abilities in a large sample of children with Velo–Cardio–Facial Syndrome: an update