Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder

27 Jan 2022

Abstract excerpt

Autism is a complex disease with genetic predisposition factors. Real factors for treatment and early diagnosis are yet to be defined. This study integrated transcriptome and exome genotyping for identifying functional variants associated with autism spectrum disorder and their impact on gene expression to find significant variations. More than 1800 patients were screened, and 70 (47 male/23 female) with an...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autism Spectrum Disorder Research
Share to Transgenic Plants and Applications
Share to Virology and Viral Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35215271
DOI: 10.3390/ph15020158

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum DisorderPMID 35215271Read ↗

Enrichment of genomic variation in pathways linked to autismSemantic proximity Read ↗

Potentially damaging variants’ analysis in autism subgroups uncovers early brain-expressed gene modules relevant to autism pathophysiologySemantic proximity Read ↗

Analysis of lncRNA, miRNA, mRNA-associated ceRNA networks in AutismSemantic proximity Read ↗

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autismSemantic proximity Read ↗

Whole exome sequencing in females with autism implicates novel and candidate genes.Semantic proximity Read ↗

Exome-wide analysis identify multiple variations in olfactory receptor genes (OR12D2 and OR5V1) associated with autism spectrum disorder in Saudi femalesSemantic proximity Read ↗

Genes/variants for diagnostic testing and pre-clinical research in autism spectrum disorderSemantic proximity Read ↗

Identification of Novel Gene variants for Autism Spectrum Disorder in an Indian Patient using Whole Exome SequencingSemantic proximity Read ↗

Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.Semantic proximity Read ↗

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genesSemantic proximity Read ↗

A systematic review of common genetic variation and biological pathways in autism spectrum disorder.Semantic proximity Read ↗

Autism spectrum disorders: Integration of the genome, transcriptome and the environmentSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.