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

Rare MED12L Variants Are Associated with Susceptibility to Guttate Psoriasis in the Han Chinese Population.

Dermatology (Basel, Switzerland) - 1 Jan 2024

Wu Kejia, Wang Wanrong, Cheng Qianhui, Xiao Duncheng, Li Yunxiao, Chen Mengyun, Zheng Xiaodong

Abstract excerpt

INTRODUCTION: According to the common disease/rare variant hypothesis, it is important to study the role of rare variants in complex diseases. The association of rare variants with psoriasis has been demonstrated, but the association between rare variants and specific clinical subtypes of psoriasis has not been investigated. METHODS: Gene-based and gene-level meta-analyses were performed on data extracted 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 East Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Haplotypes

Share to Mediator Complex

Share to Polymorphism, Single Nucleotide

Share to Psoriasis

Source

Identifiers

PMID: 38735287
DOI: 10.1159/000538805

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

Rare MED12L Variants Are Associated with Susceptibility to Guttate Psoriasis in the Han Chinese Population.PMID 38735287Read ↗

Genome-wide meta-analysis identifies ten new psoriasis susceptibility loci in the Chinese population.Semantic proximity Read ↗

Association of IL-12B gene rs6887695 polymorphism with hereditary susceptibility and clinical characterization of psoriasis vulgaris in the Chinese Han population.Semantic proximity Read ↗

Association of the novel susceptible locus rs9266150 with clinical features of psoriasis vulgaris in the Chinese Han population.Semantic proximity Read ↗

Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.Semantic proximity Read ↗

Sequencing-based approach identified three new susceptibility loci for psoriasis.Semantic proximity Read ↗

Multi-ancestry genome-wide meta-analysis with 472,819 individuals identifies 32 novel risk loci for psoriasisSemantic proximity Read ↗

A new perspective on population genetics: Deciphering the relationship between genetic variants and disease prevalence in Psoriasis.Semantic proximity Read ↗

Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21.Semantic proximity Read ↗

Polygenicity and prevalence contribute to investigating the genetic signature of common diseasesSemantic proximity Read ↗

A large-scale screen for coding variants predisposing to psoriasis.Semantic proximity Read ↗

Common variants explain a large fraction of the variability in the liability to psoriasis in a Han Chinese population.Semantic proximity Read ↗

Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.Semantic proximity Read ↗

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