Literature DB >> 35739433

Discovery of eQTL Alleles Associated with Autism Spectrum Disorder: A Case-Control Study.

Allison R Hickman1, Bradley Selee2, Rini Pauly3, Benafsh Husain3, Yuqing Hang1, Frank Alex Feltus4,5,6,7.   

Abstract

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder characterized by challenges in social communication as well as repetitive or restrictive behaviors. Many genetic associations with ASD have been identified, but most associations occur in a fraction of the ASD population. Here, we searched for eQTL-associated DNA variants with significantly different allele distributions between ASD-affected and control. Thirty significant DNA variants associated with 174 tissue-specific eQTLs from ASD individuals in the SPARK project were identified. Several significant variants fell within brain-specific regulatory regions or had been associated with a significant change in gene expression in the brain. These eQTLs are a new class of biomarkers that could control the myriad of brain and non-brain phenotypic traits seen in ASD-affected individuals.
© 2022. The Author(s).

Entities:  

Keywords:  Autism spectrum disorder; Classification; Neural network; eQTLs

Year:  2022        PMID: 35739433     DOI: 10.1007/s10803-022-05631-x

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  55 in total

1.  Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.

Authors:  Simone Berkel; Christian R Marshall; Birgit Weiss; Jennifer Howe; Ralph Roeth; Ute Moog; Volker Endris; Wendy Roberts; Peter Szatmari; Dalila Pinto; Michael Bonin; Angelika Riess; Hartmut Engels; Rolf Sprengel; Stephen W Scherer; Gudrun A Rappold
Journal:  Nat Genet       Date:  2010-05-16       Impact factor: 38.330

2.  De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth.

Authors:  Yu An; Linna Zhang; Wenwen Liu; Yunyun Jiang; Xue Chen; Xiaoping Lan; Gan Li; Qiang Hang; Jian Wang; James F Gusella; Yasong Du; Yiping Shen
Journal:  Hum Genet       Date:  2020-01-24       Impact factor: 4.132

Review 3.  The role of regulatory variation in complex traits and disease.

Authors:  Frank W Albert; Leonid Kruglyak
Journal:  Nat Rev Genet       Date:  2015-02-24       Impact factor: 53.242

Review 4.  Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.

Authors:  Catalina Betancur
Journal:  Brain Res       Date:  2010-12-01       Impact factor: 3.252

5.  A case-control family history study of autism.

Authors:  P Bolton; H Macdonald; A Pickles; P Rios; S Goode; M Crowson; A Bailey; M Rutter
Journal:  J Child Psychol Psychiatry       Date:  1994-07       Impact factor: 8.982

Review 6.  Advances in autism genetics: on the threshold of a new neurobiology.

Authors:  Brett S Abrahams; Daniel H Geschwind
Journal:  Nat Rev Genet       Date:  2008-05       Impact factor: 53.242

7.  Motor Impairment Increases in Children With Autism Spectrum Disorder as a Function of Social Communication, Cognitive and Functional Impairment, Repetitive Behavior Severity, and Comorbid Diagnoses: A SPARK Study Report.

Authors:  Anjana N Bhat
Journal:  Autism Res       Date:  2020-12-09       Impact factor: 4.633

8.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

9.  SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Authors:  Dan E Arking; Daniel B Campbell; Heather C Mefford; Eric M Morrow; Lauren A Weiss; Brett S Abrahams; Idan Menashe; Tim Wadkins; Sharmila Banerjee-Basu; Alan Packer
Journal:  Mol Autism       Date:  2013-10-03       Impact factor: 7.509

10.  The Diagnosis of Autism Spectrum Disorder Based on the Random Neural Network Cluster.

Authors:  Xia-An Bi; Yingchao Liu; Qin Jiang; Qing Shu; Qi Sun; Jianhua Dai
Journal:  Front Hum Neurosci       Date:  2018-06-26       Impact factor: 3.169

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