It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
The core diagnostic criteria for autism comprise two symptom domains – social and communication difficulties, and unusually repetitive and restricted behaviour, interests and activities. There is some evidence to suggest that these two domains are dissociable, though this hypothesis has not yet been tested using molecular genetics. We test this using a genome-wide association study (N = 51,564) of a non-social trait related to autism, systemising, defined as the drive to analyse and build systems. We demonstrate that systemising is heritable and genetically correlated with autism. In contrast, we do not identify significant genetic correlations between social autistic traits and systemising. Supporting this, polygenic scores for systemising are significantly and positively associated with restricted and repetitive behaviour but not with social difficulties in autistic individuals. These findings strongly suggest that the two core domains of autism are genetically dissociable, and point at how to fractionate the genetics of autism.
Varun Warrier et al. report a genome-wide association study of systemising, a non-social trait associated with autism. They find 3 loci associated with systemising and show that this trait has no significant genetic correlations to social phenotypic measures, demonstrating that the social and non-social aspects of autism are genetically distinct.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Won Hyejung 3 ; Leblond, Claire S 4 ; Cliquet Freddy 4
; Delorme, Richard 5 ; De Witte Ward 6 ; Bralten Janita 7 ; Chakrabarti Bhismadev 8
; Børglum, Anders D 9
; Grove Jakob 10
; Poelmans Geert 6 ; Hinds, David A 11
; Bourgeron, Thomas 12 ; Baron-Cohen, Simon 1 1 University of Cambridge, Autism Research Centre, Department of Psychiatry, Cambridgeshire, UK (GRID:grid.5335.0) (ISNI:0000000121885934)
2 Institut Pasteur, UMR3571 CNRS, Université de Paris, Human Genetics and Cognitive Functions, Paris, France (GRID:grid.5335.0)
3 University of North Carolina, Department of Genetics and Neuroscience Center, Chapel Hill, USA (GRID:grid.410711.2) (ISNI:0000 0001 1034 1720)
4 Institut Pasteur, UMR3571 CNRS, Université de Paris, Human Genetics and Cognitive Functions, Paris, France (GRID:grid.410711.2)
5 Institut Pasteur, UMR3571 CNRS, Université de Paris, Human Genetics and Cognitive Functions, Paris, France (GRID:grid.410711.2); Robert Debré Hospital, Child and Adolescent Psychiatry Department, Paris, France (GRID:grid.413235.2) (ISNI:0000 0004 1937 0589)
6 Radboud University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands (GRID:grid.10417.33) (ISNI:0000 0004 0444 9382)
7 Radboud University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands (GRID:grid.10417.33) (ISNI:0000 0004 0444 9382); Radboud University, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands (GRID:grid.5590.9) (ISNI:0000000122931605)
8 University of Cambridge, Autism Research Centre, Department of Psychiatry, Cambridgeshire, UK (GRID:grid.5335.0) (ISNI:0000000121885934); University of Reading, Centre for Autism, School of Psychology and Clinical Language Sciences, Reading, UK (GRID:grid.9435.b) (ISNI:0000 0004 0457 9566)
9 iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark (GRID:grid.9435.b); Aarhus University, Centre for Integrative Sequencing, iSEQ, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722); Aarhus University, Department of Biomedicine - Human Genetics, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722)
10 iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark (GRID:grid.7048.b); Aarhus University, Centre for Integrative Sequencing, iSEQ, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722); Aarhus University, Department of Biomedicine - Human Genetics, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722); Aarhus University, Bioinformatics Research Centre, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722)
11 23andMe Inc., Mountain View, USA (GRID:grid.420283.f)
12 Institut Pasteur, UMR3571 CNRS, Université de Paris, Human Genetics and Cognitive Functions, Paris, France (GRID:grid.420283.f)




