Evidence map›Paper›PMID 18228528›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2008

Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm.

Jiajun Shi, Jacqueline K Wittke-Thompson, Judith A Badner, Eiji Hattori, James B Potash, Virginia L Willour, Francis J McMahon, Elliot S Gershon, Chunyu Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 1 pooled it
6.4field-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

86 citing papers in PubMed, 1 synthesis or guideline pooled it, 206 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The genetics of bipolar disorder.Molecular psychiatry · 2020
    Review
  19. Article
  20. Review

26 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

Jiajun ShiDepartment of Psychiatry, University of Chicago, Chicago, Illinois 60637, USA.
Jacqueline K Wittke-Thompson
Judith A Badner
Eiji Hattori
James B Potash
Virginia L Willour
Francis J McMahon
Elliot S Gershon
Chunyu Liu
University of Chicago · USJohns Hopkins Medicine · USRIKEN Center for Brain Science · JPUnited States Department of Health and Human Services · US

Funding

Identification of Genes Involved in Major Mood DisordersZIAMH002843 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2025
$24.5M
Fine Genomic Mapping of 13q32 in Bipolar DisorderR01MH065560 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S · 2002 to 2006
$3.0M
GENETIC LINKAGE STUDIES IN BIPOLAR DISORDERSR01MH061613 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S · 2000 to 2009
$2.8M
Training in Emerging Multidisciplinary Approaches to Mental Health and DiseaseT32MH020065 · NIMH · UNIVERSITY OF CHICAGO · PI NICOLAE, DAN LIVIU, RZHETSKY, ANDREY · 2002 to 2017
$2.3M
COLLABORATIVE STUDY OF BIPOLAR DISORDERR01MH059535 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S · 1998 to 2007
$1.9M
A Collaborative Genomic Study of Bipolar DisorderZIAMH002842 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2010
$1.0M
Intramural NIH HHSNIMH NIH HHS MH065560-02NIMH NIH HHS MH61613-05A1NIMH NIH HHS R01 MH059535NIMH NIH HHS R01 MH061613NIMH NIH HHS R01 MH065560NIMH NIH HHS T32 MH020065NIMH NIH HHS T32 MH200065Wellcome TrustWellcome Trust 076113
6 · The paper itself

Abstract

Several previous studies suggest that dysfunction of circadian rhythms may increase susceptibility to bipolar disorder (BP). We conducted an association study of five circadian genes (CRY2, PER1-3, and TIMELESS) in a family collection of 36 trios and 79 quads (Sample I), and 10 circadian genes (ARNTL, ARNTL2, BHLHB2, BHLHB3, CLOCK, CRY1, CSNK1D, CSNK1E, DBP, and NR1D1) in an extended family collection of 70 trios and 237 quads (Sample II), which includes the same 114 families but not necessarily the same individuals as Sample I. In Sample II, the Sibling-Transmission Disequilibrium Test (sib-tdt) analysis showed nominally significant association of BP with three SNPs within or near the CLOCK gene (rs534654, P = 0.0097; rs6850524, P = 0.012; rs4340844, P = 0.015). In addition, SNPs in the ARNTL2, CLOCK, DBP, and TIMELESS genes and haplotypes in the ARNTL, CLOCK, CSNK1E, and TIMELESS genes showed suggestive evidence of association with several circadian phenotypes identified in BP patients. However, none of these associations reached gene-wide or experiment-wide significance after correction for multiple-testing. A multi-locus interaction between rs6442925 in the 5' upstream of BHLHB2, rs1534891 in CSNK1E, and rs534654 near the 3' end of the CLOCK gene, however, is significantly associated with BP (P = 0.00000172). It remains significant after correcting for multiple testing using the False Discovery Rate method. Our results indicate an interaction between three circadian genes in susceptibility to bipolar disorder.

Indexed as

Genetic Predisposition to DiseaseBasic Helix-Loop-Helix ProteinsBipolar DisorderCasein Kinase 1 epsilonCircadian RhythmCLOCK ProteinsEpistasis, GeneticFamily HealthFemaleGene Regulatory NetworksHaplotypesHomeodomain ProteinsHumansLinkage DisequilibriumMalePolymorphism, Single NucleotideBasic Helix-Loop-Helix ProteinsBHLHE40 protein, humanCasein Kinase 1 epsilonCLOCK protein, humanCLOCK ProteinsHomeodomain ProteinsTrans-Activators

Identifiers

PMID18228528
PMCPMC2574897
OpenAlexW2126862274

What OpenQuestion holds

Textmetadata
LicenceTDM
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.