Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
Abstract Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a strong genetic component in which rare variants contribute significantly to risk. We performed whole genome and/or exome sequencing (WGS and WES) and SNP-array analysis to identify both rare sequence and copy nu...
Main Authors: | , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2024-03-01
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Series: | npj Genomic Medicine |
Online Access: | https://doi.org/10.1038/s41525-024-00411-1 |