TY  -  
T1  - Identification of common genetic risk variants for autism spectrum disorder 
SN  -  /  
UR  - http://hdl.handle.net/10138/313330 
T3  -  
A1  - Psychiat Genomics Consortium; BUPGEN; 23andMe Res Team; Grove, Jakob; Ripke, Stephan; Als, Thomas D.; Palotie, Aarno; Daly, Mark J. 
A2  -  
PB  -  
Y1  - 2019 
LA  - eng 
AB  - Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual variants have been robustly associated with ASD. With a marked sample-size increase from a unique Danish population resource, we report a genome-wide association meta-analysis of 18,381 individuals with ASD and 27,969 controls that identified five genom... 
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KW  - GENOME-WIDE ASSOCIATION; SIMONS SIMPLEX COLLECTION; LD SCORE REGRESSION; DE-NOVO; SYNAPTIC PLASTICITY; NEURITE OUTGROWTH; CELL-SURFACE; LOCI; HERITABILITY; METAANALYSIS; 3111 Biomedicine; 1184 Genetics, developmental biology, physiology 
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PP  -  
ER  -