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

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.

European journal of human genetics : EJHG - 1 May 2001

Paavola P, Heliö T, Kiuru M, Halme L, Turunen U, Terwilliger J, Karvonen A L, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K

Abstract excerpt

In inflammatory bowel diseases (IBD), certain chromosomal candidate loci have been repeatedly identified by independent studies in different populations. To investigate the contribution of the loci on chromosomes 1, 3, 7, 12, 14, and 16 to the susceptibility of IBD in Finnish population, where the predominant feature is the excess of ulcerative colitis (UC) families compared to Crohn's disease (CD) families, we...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 16
Share to Chromosomes, Human, Pair 3

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Finland

Share to Genetic Linkage

Share to Genetic Testing

Share to Inflammatory Bowel Diseases

Share to Receptors, CCR5

Share to Receptors, Interleukin-4

Source

Identifiers

PMID: 11378820
DOI: 10.1038/sj.ejhg.5200626

Genes

CCR5

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.PMID 11378820Read ↗

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.Semantic proximity Read ↗

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.Semantic proximity Read ↗

Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3).Semantic proximity Read ↗

Genome wide scan in a Flemish inflammatory bowel disease population: support for the IBD4 locus, population heterogeneity, and epistasis.Semantic proximity Read ↗

Linkage of inflammatory bowel disease to human chromosome 6p.Semantic proximity Read ↗

Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.Semantic proximity Read ↗

Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16.Semantic proximity Read ↗

Association analysis of 3p21 with Crohn's disease in a New Zealand population.Semantic proximity Read ↗

Inflammatory bowel disease is linked to 19p13 and associated with ICAM-1.Semantic proximity Read ↗

Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease.Semantic proximity Read ↗

Exclusion of linkage of Crohn's disease to previously reported regions on chromosomes 12, 7, and 3 in the Belgian population indicates genetic heterogeneity.Semantic proximity Read ↗

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease.Semantic proximity Read ↗

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