Brief Report: The Dopamine-3-Receptor Gene (DRD3) is Associated with Specific Repetitive Behavior in Autism Spectrum Disorder (ASD)

Por Staal, Wouter G., de Krom, Mariken, de Jonge, Maretha V.
Publicado em 2011

The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder

Por Stam, Arie J, Schothorst, Patricia F, Vorstman, Jacob AS, Staal, Wouter G
Publicado em 2009

Stop and Change: Inhibition and Flexibility Skills Are Related to Repetitive Behavior in Children and Young Adults with Autism Spectrum Disorders

Por Mostert-Kerckhoffs, Mandy A. L., Staal, Wouter G., Houben, Renske H., de Jonge, Maretha V.
Publicado no J Autism Dev Disord (2015)

Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism

Por Buizer-Voskamp, Jacobine E, Franke, Lude, Staal, Wouter G, van Daalen, Emma, Kemner, Chantal, Ophoff, Roel A, Vorstman, Jacob AS, van Engeland, Herman, Wijmenga, Cisca
Publicado em 2010

Paternal age and psychiatric disorders: findings from a Dutch population registry

Por Buizer-Voskamp, Jacobine E, Laan, Wijnand, Staal, Wouter G, Hennekam, Eric AM, Aukes, Maartje F, Termorshuizen, Fabian, Kahn, René S, Boks, Marco PM, Ophoff, Roel A
Publicado em 2011

Morphological Features in Children with Autism Spectrum Disorders: A Matched Case–Control Study

Por Ozgen, Heval, Hellemann, Gerhard S., Stellato, Rebecca K., Lahuis, Bertine, van Daalen, Emma, Staal, Wouter G., Rozendal, Marije, Hennekam, Raoul C., Beemer, Frits A., van Engeland, Herman
Publicado em 2010

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism

Por van Daalen, Emma, Kemner, Chantal, Verbeek, Nienke E., van der Zwaag, Bert, Dijkhuizen, Trijnie, Rump, Patrick, Houben, Renske, van ‘t Slot, Ruben, de Jonge, Maretha V., Staal, Wouter G., Beemer, Frits A., Vorstman, Jacob A. S., Burbach, J. Peter H., van Amstel, Hans Kristian Ploos, Hochstenbach, Ron, Brilstra, Eva H., Poot, Martin
Publicado em 2011

A Co-segregating Microduplication of Chromosome 15q11.2 Pinpoints Two Risk Genes for Autism Spectrum Disorder

Por van der Zwaag, Bert, Staal, Wouter G, Hochstenbach, Ron, Poot, Martin, Spierenburg, Henk A, de Jonge, Maretha V, Verbeek, Nienke E, van ’t Slot, R., van Es, Michael A, Staal, Frank J, Freitag, Christine M, Buizer-Voskamp, Jacobine E, Nelen, Marcel R, van den Berg, Leonard H, van Amstel, Hans K Ploos, van Engeland, Herman, Burbach, J Peter H
Publicado em 2010

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Por Pagnamenta, Alistair T., Bacchelli, Elena, de Jonge, Maretha V., Mirza, Ghazala, Scerri, Thomas S., Minopoli, Fiorella, Chiocchetti, Andreas, Ludwig, Kerstin U., Hoffmann, Per, Paracchini, Silvia, Lowy, Ernesto, Harold, Denise H., Chapman, Jade A., Klauck, Sabine M., Poustka, Fritz, Houben, Renske H., Staal, Wouter G., Ophoff, Roel A., O'Donovan, Michael C., Williams, Julie, Nöthen, Markus M., Schulte-Körne, Gerd, Deloukas, Panos, Ragoussis, Jiannis, Bailey, Anthony J., Maestrini, Elena, Monaco, Anthony P.
Publicado em 2010

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism

Por van der Zwaag, Bert, Franke, Lude, Poot, Martin, Hochstenbach, Ron, Spierenburg, Henk A., Vorstman, Jacob A. S., van Daalen, Emma, de Jonge, Maretha V., Verbeek, Nienke E., Brilstra, Eva H., van 't Slot, Ruben, Ophoff, Roel A., van Es, Michael A., Blauw, Hylke M., Veldink, Jan H., Buizer-Voskamp, Jacobine E., Beemer, Frits A., van den Berg, Leonard H., Wijmenga, Cisca, van Amstel, Hans Kristian Ploos, van Engeland, Herman, Burbach, J. Peter H., Staal, Wouter G.
Publicado em 2009