Evidence map›Paper›PMID 18227837›Full record

ArticleMolecular psychiatry2009

A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.

E Z McAuley, I P Blair, Z Liu, J M Fullerton, A Scimone, M Van Herten, M R Evans, K C Kirkby, J A Donald, P B Mitchell and 1 more

Abstract read
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Article in Molecular psychiatry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

E Z McAuleyNeuroscience Research Program, Garvan Institute of Medical Research, Sydney, NSW, Australia.
I P Blair
Z Liu
J M Fullerton
A Scimone
M Van Herten
M R Evans
K C Kirkby
J A Donald
P B Mitchell
P R Schofield

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bipolar affective disorder is a heritable, relatively common, severe mood disorder with lifetime prevalence up to 4%. We report the results of a genome-wide linkage analysis conducted on a cohort of 35 Australian bipolar disorder families which identified evidence of significant linkage on chromosome 15q25-26 and suggestive evidence of linkage on chromosomes 4q, 6q and 13q. Subsequent fine-mapping of the chromosome 15q markers, using allele frequencies calculated from our cohort, gave significant results with a maximum two-point LOD score of 3.38 and multipoint LOD score of 4.58 for marker D15S130. Haplotype analysis based on pedigree-specific, identical-by-descent allele sharing, supported the location of a bipolar susceptibility gene within the Z(max-1) linkage confidence interval of 17 cM, or 6.2 Mb, between markers D15S979 and D15S816. Non-parametric and affecteds-only linkage analysis further verified the linkage signal in this region. A maximum NPL score of 3.38 (P=0.0008) obtained at 107.16 cM (near D15S130), and a maximum two-point LOD score of 2.97 obtained at marker D15S1004 (affecteds only), support the original genome-wide findings on chromosome 15q. These results are consistent with four independent positive linkage studies of mood and psychotic disorders, and raise the possibility that a common gene for susceptibility to bipolar disorder, and other psychiatric disorders may lie in this chromosome 15q25-26 region.

Indexed as

Chromosomes, Human, Pair 15Genetic Predisposition to DiseasePedigreeAdolescentAdultAustraliaBipolar DisorderChromosome MappingDNA Mutational AnalysisFemaleGenetic LinkageGenome-Wide Association StudyGenotypeHumansLod ScoreMale

Identifiers

PMID18227837

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.