Reza Asadollahi (Zurich, Switzerland): "The use of small CNVs to identify novel disease genes in neurodevelopmental disorders"
Evan Eichler (Seattle, USA): "Advances in Understanding the Genetic Basis of Autism and Intellectual Disability"
Jozef Gecz (Adelaide, Australia): "Defining the role of mRNA export and mRNA decay in neurodevelopmental disorders, intellectual disability and autism"
Yann Herault (Strasbourg, France): "Modelling 16p11 and 17q21.31 copy number variants affecting intellectual disabilities in the mouse"
Vera Kalscheuer (Berlin, Germany): "XLID genes and networks"
Frank Kooy (Antwerpen, Belgium): "FRA2A is a CGG repeat expansion associated with silencing of AFF3"
Sebastien Jacquemont (Lausanne, Switzerland): "Neuroimaging and cognitive correlates in 16p patients"
Björn Menten (Ghent, Belgium): “Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations”
Alexandre Reymond (Lausanne, Switzerland): "Chromatin loops and CNVs: the complex spatial organization of the 16p11.2 locus"
Lisenka Vissers (Nijmegen, The Netherlands): “Genome sequencing identifies major causes of severe intellectual disability”