Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.

doi:10.1186/s13229-020-00407-5

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Article

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.

Molecular autism - 10 Feb 2021

Yap Chloe X, Alvares Gail A, Henders Anjali K, Lin Tian, Wallace Leanne, Farrelly Alaina, McLaren Tiana, Berry Jolene, Vinkhuyzen Anna A E, Trzaskowski Maciej, Zeng Jian, Yang Yuanhao, Cleary Dominique, Grove Rachel, Hafekost Claire, Harun Alexis, Holdsworth Helen, Jellett Rachel, Khan Feroza, Lawson Lauren, Leslie Jodie, Levis Frenk Mira, Masi Anne, Mathew Nisha E, Muniandy Melanie, Nothard Michaela, Visscher Peter M, Dawson Paul A, Dissanayake Cheryl, Eapen Valsamma, Heussler Helen S, Whitehouse Andrew J O, Wray Naomi R, Gratten Jacob

Abstract excerpt

BACKGROUND: Autism spectrum disorder (ASD) is a complex neurodevelopmental condition whose biological basis is yet to be elucidated. The Australian Autism Biobank (AAB) is an initiative of the Cooperative Research Centre for Living with Autism (Autism CRC) to establish an Australian resource of biospecimens, phenotypes and genomic data for research on autism. METHODS: Genome-wide single-nucleotide polymorphism...

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PMID: 33568206
DOI: 10.1186/s13229-020-00407-5
PMCID: PMC7874616

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