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

Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populations.

Lupus science & medicine - 8 Mar 2024

Tangtanatakul Pattarin, Lei Yao, Jaiwan Krisana, Yang Wanling, Boonbangyang Manon, Kunhapan Punna, Sodsai Pimpayao, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Yang Yi, Eu-Ahsunthornwattana Jakris, Aekplakorn Wichai, Jinawath Natini, Neelapaichit Nareemarn, Hirankarn Nattiya, Wang Yong-Fei

Abstract excerpt

OBJECTIVES: X chromosome has been considered as a risk factor for SLE, which is a prototype of autoimmune diseases with a significant sex difference (female:male ratio is around 9:1). Our study aimed at exploring the association of genetic variants in X chromosome and investigating the influence of trisomy X in the development of SLE. METHODS: X chromosome-wide association studies were conducted using data from...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Lupus Erythematosus, Systemic

Share to Membrane Proteins

Share to Sex Chromosome Aberrations

Share to Thailand

Share to Trisomy

Source

Open in PubMed Open full text

Identifiers

PMID: 38458775
DOI: 10.1136/lupus-2023-001061
PMCID: PMC10928741

Genes

TMEM187
GPR173
IRAK1
MECP2
PRPS2
TLR7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populations.PMID 38458775Read ↗

Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE.Semantic proximity Read ↗

Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus.Semantic proximity Read ↗

Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.Semantic proximity Read ↗

Associated genetic polymorphisms and clinical manifestations in systemic lupus erythematosus in Asian populations - A systematic literature review.Semantic proximity Read ↗

Association study between X-linked susceptibility genes and clinical features in Chinese female patients with systemic lupus erythematosus.Semantic proximity Read ↗

Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus.Semantic proximity Read ↗

Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.Semantic proximity Read ↗

Exome-wide association study identifies four novel loci for systemic lupus erythematosus in Han Chinese population.Semantic proximity Read ↗

Evaluation of 10 SLE susceptibility loci in Asian populations, which were initially identified in European populations.Semantic proximity Read ↗

Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population.Semantic proximity Read ↗

A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene.Semantic proximity Read ↗

Genetics, Epigenetics, and Gender Impact in Axial-Spondyloarthritis Susceptibility: An Update on Genetic Polymorphisms and Their Sex Related AssociationsSemantic proximity Read ↗

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