Evidence map›Paper›PMID 16402137›Full record

ArticleMolecular psychiatry2006

Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder.

R Cheng, S H Juo, J E Loth, J Nee, I Iossifov, R Blumenthal, L Sharpe, K Kanyas, B Lerer, B Lilliston and 5 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 5 pooled it
13.8field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 5 syntheses or guidelines pooled it, 155 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Genetics of suicide: a systematic review of twin studies.Wiener klinische Wochenschrift · 2007
    Pooled it
  6. Review
  7. Article
  8. Article
  9. Article
  10. Inflammation as a Mechanism of Bipolar Disorder Neuroprogression.Current topics in behavioral neurosciences · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Do we need pharmacogenetics to personalize antidepressant therapy?Cellular and molecular life sciences : CMLS · 2013
    Review
  20. Endophenotypes as a measure of suicidality.Journal of applied genetics · 2012
    Review
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

15 authors at 5 institutions in 3 countries.

R ChengColumbia Genome Center, Columbia University, New York, NY 10032, USA.
S H Juo
J E Loth
J Nee
I Iossifov
R Blumenthal
L Sharpe
K Kanyas
B Lerer
B Lilliston
M Smith
K Trautman
T C Gilliam
J Endicott
M Baron
Columbia University · USHebrew University of Jerusalem · ILKaohsiung Medical University · TWNew York Genome Center · USUniversity of Chicago · US

Funding

MOLECULAR GENETICS OF BIPOLAR DISORDERR01MH059602 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BARON, MIRON · 1998 to 2001
$1.8M
GENOTYPING FOR LOCATING HUMAN DISEASE GENESN01HG065403 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID L · 1996 to 2000
$1.7M
NHGRI NIH HHS N01-HG-65403NIMH NIH HHS MH59602
6 · The paper itself

Abstract

We conducted a 9-cM genome scan in a large bipolar pedigree sample from the National Institute of Mental Health genetics initiative (1060 individuals from 154 multiplex families). We performed parametric and nonparametric analyses using both standard diagnostic models and comorbid conditions thought to identify phenotypic subtypes: psychosis, suicidal behavior, and panic disorder. Our strongest linkage signals (genome-wide significance) were observed on chromosomes 10q25, 10p12, 16q24, 16p13, and 16p12 using standard diagnostic models, and on 6q25 (suicidal behavior), 7q21 (panic disorder) and 16p12 (psychosis) using phenotypic subtypes. Several other regions were suggestive of linkage, including 1p13 (psychosis), 1p21 (psychosis), 1q44, 2q24 (suicidal behavior), 2p25 (psychosis), 4p16 (psychosis, suicidal behavior), 5p15, 6p25 (psychosis), 8p22 (psychosis), 8q24, 10q21, 10q25 (suicidal behavior), 10p11 (psychosis), 13q32 and 19p13 (psychosis). Over half the implicated regions were identified using phenotypic subtypes. Several regions - 1p, 1q, 6q, 8p, 13q and 16p - have been previously reported to be linked to bipolar disorder. Our results suggest that dissection of the disease phenotype can enrich the harvest of linkage signals and expedite the search for susceptibility genes. This is the first large-scale linkage scan of bipolar disorder to analyze simultaneously bipolar disorder, psychosis, suicidal behavior, and panic disorder.

Indexed as

Chromosome MappingGenetic LinkageGenome, HumanSuicideBipolar DisorderGenetic MarkersHumansNational Institutes of Health (U.S.)Panic DisorderPsychotic DisordersUnited StatesGenetic Markers

Identifiers

PMID16402137
OpenAlexW1991109311

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Registered trials

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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.