Evidence map›Paper›PMID 12660806›Full record

ArticleMolecular psychiatry2003

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.

J Liu, S H Juo, A Dewan, A Grunn, X Tong, M Brito, N Park, J E Loth, K Kanyas, B Lerer and 6 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 123 citations in OpenAlex.

  1. Pooled it
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  14. The phenotype of recurrent 10q22q23 deletions and duplications.European journal of human genetics : EJHG · 2011
    Article
  15. Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2011
    Article
  16. An investigation of candidate regions for association with bipolar disorder.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2010
    Article
  17. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

J LiuColumbia Genome Center and Department o fPsychiatry, Columbia University , New York, NY 10032, USA.
S H Juo
A Dewan
A Grunn
X Tong
M Brito
N Park
J E Loth
K Kanyas
B Lerer
J Endicott
G Penchaszadeh
J A Knowles
J Ott
T C Gilliam
M Baron
Columbia University · USNew York Genome Center · USHadassah Medical Center · ILRockefeller University · US

Funding

LINKAGE ANALYSIS METHODS IN SCHIZOPHRENIAR01MH044292 · NIMH · ROCKEFELLER UNIVERSITY · PI OTT, JURG · 1989 to 2008
$1.3M
LINKAGE ANALYSIS METHODS IN SCHIZOPHRENIAR37MH044292 · NIMH · ROCKEFELLER UNIVERSITY · PI OTT, JURG · 1993 to 2002
$788k
GENETIC LINKAGE STUDIES IN AFFECTIVE DISORDERSR01MH043979 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE · PI BARON, MIRON · 1989 to 1997
–
IMMUNITY IN PREPUBESCENT MAJOR DEPRESSIVE DISORDERR03MH045235 · NIMH · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BARTLETT, JACQUELINE · 1989 to 1989
–
NIMH NIH HHS MH00176NIMH NIH HHS MH43979NIMH NIH HHS MH44292NIMH NIH HHS MH45235
6 · The paper itself

Abstract

Bipolar disorder (BP) is a severe and common psychiatric disorder characterized by extreme mood swings. Family, twin and adoption studies strongly support a genetic component. The mode of inheritance is complex and likely involves multiple, as yet unidentified genes. To identify susceptibility loci, we conducted a genome-wide scan with 343 microsatellite markers in one of the largest, well-characterized pedigree samples assembled to date (373 individuals in 40 pedigrees). To increase power to detect linkage, scan statistics were used to examine the logarithm of odds (lod) scores based on evidence at adjacent chromosomal loci. This analysis yielded significant evidence of linkage (genome-wide P&<0.05) for markers on 2p13-16. Standard linkage analysis was also supportive of linkage to 2p13-16 (lod=3.20), and identified several other interesting regions: 4q31 (lod=3.16), 7q34 (lod=2.78), 8q13 (lod=2.06), 9q31 (lod=2.07), 10q24 (lod=2.79), 13q32 (lod=2.2), 14q21 (lod=2.36) and 17q11-12 (lod=2.75). In this systematic, large-scale study, we identified novel putative loci for BP (on 2p13-16, 8q13 and 14q21) and found support for previously proposed loci (on 4q31, 7q34, 9q31, 10q21-24, 13q32 and 17q11-12). Two of the regions implicated in our study, 2p13-14 and 13q32, have also been linked to schizophrenia, suggesting that the two disorders may have susceptibility genes in common.

Indexed as

Chromosomes, Human, Pair 2Lod ScoreAdolescentAdultBipolar DisorderChromosomes, Human, Pair 10Chromosomes, Human, Pair 13Chromosomes, Human, Pair 14Chromosomes, Human, Pair 17Chromosomes, Human, Pair 4Chromosomes, Human, Pair 7Chromosomes, Human, Pair 8Chromosomes, Human, Pair 9Genetic Predisposition to DiseaseHumans

Identifiers

PMID12660806
OpenAlexW1977247394

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.