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

Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32.

American journal of medical genetics - 8 May 2001

Liu C, Badner J A, Christian S L, Guroff J J, Detera-Wadleigh S D, Gershon E S

Abstract excerpt

A region between D13S71 and D13S274 on 13q32 showed linkage to bipolar disorder (BP) based on a genome scan using markers with an average spacing of approximately 6 cM and an average heterozygosity of approximately 60% [Detera-Wadleigh et al., 1999: Proc Natl Acad Sci USA 96:5604-5609]. In an attempt to confirm this finding and achieve fine mapping of the susceptibility region, nine additional microsatellite...

Read the complete abstract on PubMed

Topics

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

Share to Bipolar Disorder
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 13

Share to Family Health

Share to Genetic Linkage

Share to Genetic Predisposition to Disease

Share to Lod Score

Share to Microsatellite Repeats

Source

Identifiers

PMID: 11378853
DOI: 10.1002/ajmg.1358

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

Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32.PMID 11378853Read ↗

Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series.Semantic proximity Read ↗

A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q.Semantic proximity Read ↗

SNP fine mapping of chromosome 8q24 in bipolar disorder.Semantic proximity Read ↗

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.Semantic proximity Read ↗

Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.Semantic proximity Read ↗

Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q.Semantic proximity Read ↗

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.Semantic proximity Read ↗

Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.Semantic proximity Read ↗

A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.Semantic proximity Read ↗

A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.Semantic proximity Read ↗

Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3.Semantic proximity Read ↗

Family-based SNP association study on 8q24 in bipolar disorder.Semantic proximity Read ↗

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