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

Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes.

Human molecular genetics - 1 Jun 2013

Cortes Adrian, Field Judith, Glazov Evgeny A, Hadler Johanna, Stankovich Jim, Brown Matthew A

Abstract excerpt

Multiple sclerosis (MS) is a common chronic inflammatory disease of the central nervous system. Susceptibility to the disease is affected by both environmental and genetic factors. Genetic factors include haplotypes in the histocompatibility complex (MHC) and over 50 non-MHC loci reported by genome-wide association studies. Amongst these, we previously reported polymorphisms in chromosome 12q13-14 with a...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 12

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Loci

Share to Genome-Wide Association Study

Share to Linkage Disequilibrium

Share to Multiple Sclerosis

Share to Sequence Analysis, DNA

Share to Young Adult

Source

Identifiers

PMID: 23406874
DOI: 10.1093/hmg/ddt062

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

Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes.PMID 23406874Read ↗

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.Semantic proximity Read ↗

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.Semantic proximity Read ↗

Fine-Mapping Array Design for Multi-Ethnic Studies of Multiple Sclerosis.Semantic proximity Read ↗

Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.Semantic proximity Read ↗

A high-density screen for linkage in multiple sclerosis.Semantic proximity Read ↗

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips.Semantic proximity Read ↗

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis RiskSemantic proximity Read ↗

Genetics of multiple sclerosis: swimming in an ocean of data.Semantic proximity Read ↗

Summary-data-based mendelian randomisation reveals druggable targets for multiple sclerosisSemantic proximity Read ↗

A genome-wide association study in progressive multiple sclerosis.Semantic proximity Read ↗

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.Semantic proximity Read ↗

Utilising multi-large omics data to elucidate biological mechanisms within multiple sclerosis genetic susceptibility loci.Semantic proximity Read ↗

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