Annick Vogels

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

Femke Hannes, Andrew J. Sharp, Heather C. Mefford et al. · Journal of Medical Genetics · 2008 · 346 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

Jacob Vorstman, Elemi Breetvelt, Sasja N. Duijff et al. · JAMA Psychiatry · 2015 · 297 citations · Full text

Medicine, Psychiatry, Psychology +16

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

J. K. J. VAN HOUDT, Beata Nowakowska, Sérgio B. Sousa et al. · Nature Genetics · 2012 · 244 citations

Life Sciences, Genetics, Molecular Genetics +10

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Ann Swillen, Koenraad Devriendt, Eric Legius et al. · PubMed · 1999 · 209 citations

Education, Behavioral Sciences, Human Development +17

Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders

Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen et al. · European Journal of Human Genetics · 2003 · 185 citations

Public Health, Obstetrics, Pediatrics +11