Interactions of genetic risks for autism and the broad autism phenotypes

Bibliographic Data

ID15525630
AuthorsLijie Dong (0000-0001-9720-8227, Central South University), Yijing Wang (0000-0002-7886-8366, Central South University), Xiaomeng Wang (0000-0002-2409-2419, Central South University), Tengfei Luo (Central South University), Qiao Zhou (0000-0001-6568-0260, Central South University), Guihu Zhao (0000-0003-4033-1843, Central South University), Bin Li (0000-0002-9633-0033, Central South University), Lu Xia (0000-0003-1859-9755, Central South University, corresponding author), Kun Xia (0000-0001-8090-6002, Central South University, corresponding author), Jinchen Li (0000-0003-3335-9303, Central South University, corresponding author)
Year2023
Volume14
Pages1110080-1110080
Publication date2023-03-21
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2023.1110080
PMID37102084
OpenAlexW4328119016
LanguageEN
References cited48

Our study revealed that the risk for ASD and the autism broad phenotypes likely arises from a combination of common polygenic risk, damaging DNVs (including those in ASD risk genes), and sex

Autism · Autism spectrum disorder · Biology · Gene · Genotype · Mutation · Phenotype · Polygenic risk score · Proband · Psychiatry · Single-nucleotide polymorphism · Autism Spectrum Disorder Research · Clinical Psychology · Genomic variations and chromosomal abnormalities · Genomics and Rare Diseases · Medicine · Psychology · Genetics

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