Arie P.T. Smits
Radboud University Nijmegen(NL)Radboud University Medical Center(NL)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Autism Spectrum Disorder Research, Congenital heart defects research
Most-Cited Works
- → Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15(1992)192 cited
- → Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?(1999)163 cited
- → Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis(2010)144 cited
- → Imprinting Effect in Premature Ovarian Failure Confined to Paternally Inherited Fragile X Premutations(2000)130 cited
- → CGG-Repeat Expansion in the DIP2B Gene Is Associated with the Fragile Site FRA12A on Chromosome 12q13.1(2007)129 cited
- → Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice(2011)109 cited