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

WDR13: A Novel Gene Implicated in Non-Syndromic Intellectual Disability.

Genes - 28 Nov 2021

Rzońca-Niewczas Sylwia, Wierzba Jolanta, Kaczorowska Ewa, Poryszewska Milena, Kosińska Joanna, Stawiński Piotr, Płoski Rafał, Bal Jerzy

Abstract excerpt

Investigating novel genetic variants involved in intellectual disability (ID) development is essential. X-linked intellectual disability (XLID) accounts for over 10% of all cases of ID in males. XLID genes are involved in many cellular pathways and processes. Some of them are not specific to the development and functioning of the neural system. The implementation of exome sequencing simplifies the search for...

Read the complete abstract on PubMed

Topics

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

Share to Cell Cycle Proteins
Share to Exome Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation

Share to Genes, X-Linked

Share to Intellectual Disability

Share to Pedigree

Share to X-Linked Intellectual Disability

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 34946860
DOI: 10.3390/genes12121911
PMCID: PMC8701106

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

WDR13: A Novel Gene Implicated in Non-Syndromic Intellectual Disability.PMID 34946860Read ↗

Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.Semantic proximity Read ↗

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.Semantic proximity Read ↗

Four families with X-linked intellectual disability affected males: Novel deleterious variants and clinical features with the review of literatureSemantic proximity Read ↗

FBXO11 variants are associated with intellectual disability and variable clinical manifestation in Chinese affected individuals.Semantic proximity Read ↗

FBXO11 Variants are Associated with Intellectual Disability and Variable Clinical Manifestation in Chinese PatientsSemantic proximity Read ↗

De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.Semantic proximity Read ↗

X-Linked intellectual disability update 2022.Semantic proximity Read ↗

Two novel pathogenic variants in MED13L: one familial and one isolated case.Semantic proximity Read ↗

KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.Semantic proximity Read ↗

Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with Ataxia.Semantic proximity Read ↗

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.Semantic proximity Read ↗

High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing.Semantic proximity Read ↗

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