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

[Characterization of copy number variations in concomitant exotropia using single nucleotide polymorphism microarray].

[Zhonghua yan ke za zhi] Chinese journal of ophthalmology - 11 May 2026

Zhou W T, Zhao Y Z, Li J, Shi X F

Abstract excerpt

Objective: To investigate the genetic characteristics of copy number variations (CNVs) in families with concomitant exotropia. Methods: A family-based molecular genetic study. The study included 25 unrelated concomitant exotropia families who visited Tianjin Eye Hospital between August 2019 and August 2021. Patients and healthy individuals from these families were included as subjects. Clinical data were...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to RB1 gene

Share to Genotype

Share to Oligonucleotide Array Sequence Analysis

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 42103667
DOI: 10.3760/cma.j.cn112142-20250815-00350

Genes

BRAF
ESCO2
RB1
IFT80
ROCK2
CCDC25
PBK
SYCP2
VPS13C

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Characterization of copy number variations in concomitant exotropia using single nucleotide polymorphism microarray].PMID 42103667Read ↗

Presence of Copy Number Variants Associated With Esotropia in Patients With Exotropia.Semantic proximity Read ↗

Recurrent Rare Copy Number Variants Increase Risk for Esotropia.Semantic proximity Read ↗

Whole-exome sequencing uncovers the genetic basis of hereditary concomitant exotropia in ten Chinese pedigrees.Semantic proximity Read ↗

Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.Semantic proximity Read ↗

Genome-Wide Association Study with Three Control Cohorts of Japanese Patients with Esotropia and Exotropia of Comitant Strabismus and Idiopathic Superior Oblique Muscle Palsy.Semantic proximity Read ↗

Integrative Transcriptomic Profiling and WGCNA Reveals Key Genetic Determinants of StrabismusSemantic proximity Read ↗

A Shared Genetic Basis Underlying Myopia-Exotropia Comorbidity.Semantic proximity Read ↗

[Genome-wide association study on complex diseases: study design and genetic markers].Semantic proximity Read ↗

[Schizophrenia and ocular misalignment: phenotypic and genetic association analysis].Semantic proximity Read ↗

Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus.Semantic proximity Read ↗

Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.Semantic proximity Read ↗

Genome-wide search for strabismus susceptibility loci.Semantic proximity Read ↗

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