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

Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patients

18 Aug 2022

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Autoimmune and Inflammatory Disorders Research
Share to Ocular Diseases and Behçet’s Syndrome
Share to Otitis Media and Relapsing Polychondritis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 35987173
DOI: 10.1016/j.jaut.2022.102882

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

Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patientsPMID 35987173Read ↗

Different phenotypes identified for Behçet syndrome.Semantic proximity Read ↗

Phenotypes in Behçet’s syndromeSemantic proximity Read ↗

PW03-013 - Behçet's disease: genotype-phenotype correlationsSemantic proximity Read ↗

Epigenetic alterations in chronic disease focusing on Behçet’s disease: ReviewSemantic proximity Read ↗

Genetics of Behçet's Disease: Functional Genetic Analysis and Estimating Disease HeritabilitySemantic proximity Read ↗

Genetics of Behçet's DiseaseSemantic proximity Read ↗

HLA and non-HLA genes in Behçet’s disease: a multicentric study in the Spanish populationSemantic proximity Read ↗

The potential of genetically guided treatment in Behçet's disease.Semantic proximity Read ↗

Genetics of Behçet's disease.Semantic proximity Read ↗

OR9-001 - Exome sequencing in monogenic Behçet-like diseaseSemantic proximity Read ↗

Approaches based on miRNAs in Behçet's Disease: Unveiling pathogenic mechanisms, diagnostic strategies, and therapeutic applicationsSemantic proximity Read ↗

Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement.Semantic proximity Read ↗

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