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

Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.

Genes - 15 Oct 2020

Khalid Madiha, Raza Hashim, M Driessen Terri, J Lee Paul, Tejwani Leon, Sami Abdul, Nawaz Muhammad, Mehmood Baig Shahid, Lim Janghoo, Kaukab Raja Ghazala

Abstract excerpt

Autism spectrum disorder (ASD) is a group of complex multifactorial neurodevelopmental and neuropsychiatric disorders in children characterized by impairment of communication and social interaction. Several genes with associated single nucleotide polymorphisms (SNPs) have been identified for ASD in different genetic association studies, meta-analyses, and genome-wide association studies (GWAS). However,...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Biomarkers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Ethnicity

Share to Gene Frequency

Share to Pakistan

Share to Risk Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 33076578
DOI: 10.3390/genes11101206
PMCID: PMC7602870

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.PMID 33076578Read ↗

CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.Semantic proximity Read ↗

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.Semantic proximity Read ↗

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.Semantic proximity Read ↗

Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder.Semantic proximity Read ↗

Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort.Semantic proximity Read ↗

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

Biochemical and Sociodemographic Correlates of Autism Spectrum Disorder Severity in Pakistani Children: A Mixed-Methods Sibling-Matched StudySemantic proximity Read ↗

CNTNAP2 Associated Neurodevelopmental Disorders: Intellectual Disability and Epilepsy comorbidity in Pakistani population.Semantic proximity Read ↗

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.Semantic proximity Read ↗

Structural Variations Identified in Patients with Autism Spectrum Disorder (ASD) in the Chinese Population: A Systematic Review of Case-Control Studies.Semantic proximity Read ↗

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

Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder.Semantic proximity Read ↗

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