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

[Molecular diagnosis of genetic polymorphisms related to autism spectrum disorder in children based on multi-PCR targeted sequencing technology].

Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] - 6 Feb 2026

Xie F, Li S, Mao W H, Sun Y, Wang J, Li Y F, Deng Y X, Chen J

Abstract excerpt

Establish a multiplex PCR targeted sequencing technology to detect the single nucleotide polymorphism (SNP) sites of disease-related genes in children with autism spectrum disorder, and explore its application value as a diagnostic biomarker for autism spectrum disorder. Through a literature review, 357 candidate risk genes and their 603 mutation sites highly associated with the occurrence of autism spectrum...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cell Adhesion Molecules, Neuronal

Share to Child, Preschool

Share to Multiplex Polymerase Chain Reaction

Share to Nerve Tissue Proteins

Share to Reelin Protein

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 41606982
DOI: 10.3760/cma.j.cn112150-20250528-00492

Genes

AUTS2
RELN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular diagnosis of genetic polymorphisms related to autism spectrum disorder in children based on multi-PCR targeted sequencing technology].PMID 41606982Read ↗

Clinical Targeted Panel Sequencing Analysis in Clinical Evaluation of Children with Autism Spectrum Disorder in China.Semantic proximity Read ↗

Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.Semantic proximity Read ↗

Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses.Semantic proximity Read ↗

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

Pathogenic/likely pathogenic mutations identified in Vietnamese children diagnosed with autism spectrum disorder using high-resolution SNP genotyping platform.Semantic proximity Read ↗

Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum DisorderSemantic proximity Read ↗

Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.Semantic proximity Read ↗

Molecular diagnosis of 405 individuals with autism spectrum disorder.Semantic proximity Read ↗

High-throughput sequencing of autism spectrum disorders comes of age.Semantic proximity Read ↗

Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.Semantic proximity Read ↗

A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder.Semantic proximity Read ↗

Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.Semantic proximity Read ↗

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