Andrea K. Vaags

Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder

Andrea K. Vaags, Anath C. Lionel, Daisuke Sato et al. · The American Journal of Human Genetics · 2011 · 215 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 175 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

Anath C. Lionel, Andrea K. Vaags, Daisuke Sato et al. · Human Molecular Genetics · 2013 · 159 citations · Full text

Life Sciences, Genetics, Neuroscience +17

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

Sébastien Chénier, Grace Yoon, Bob Argiropoulos et al. · Journal of Neurodevelopmental Disorders · 2014 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Derivation and Characterization of Canine Embryonic Stem Cell Lines with In Vitro and In Vivo Differentiation Potential

Andrea K. Vaags, Suzana Rosic-Kablar, Cathy Gartley et al. · Stem Cells · 2008 · 81 citations · Full text

Life Sciences, Cell Biology, Developmental Biology +17