Evidence map›Paper›PMID 22520966›Full record

ArticleBiological psychiatry2012

Estimating the genetic variance of major depressive disorder due to all single nucleotide polymorphisms.

Gitta H Lubke, Jouke Jan Hottenga, Raymond Walters, Charles Laurin, Eco J C de Geus, Gonneke Willemsen, Jan H Smit, Christel M Middeldorp, Brenda W J H Penninx, Jacqueline M Vink and 1 more

Abstract read
In one paragraph

Article in Biological psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 3 pooled it
15.1field-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

78 citing papers in PubMed, 3 syntheses or guidelines pooled it, 131 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. The Effects of Variation in the GABANeuropsychiatric disease and treatment · 2024
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  8. Pathways link environmental and genetic factors with structural brain networks and psychopathology in youth.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
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  9. Frontiers in psychiatry · 2022
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  13. Sociogenomics in the 21Sociology compass · 2018
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  15. Article
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  17. Article
  18. Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2018
    Article
  19. Article
  20. Article

18 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

11 authors at 3 institutions in 2 countries.

Gitta H LubkeDepartment of Psychology, University of Notre Dame, Notre Dame, IN 46556, USA. glubke@nd.edu
Jouke Jan Hottenga
Raymond Walters
Charles Laurin
Eco J C de Geus
Gonneke Willemsen
Jan H Smit
Christel M Middeldorp
Brenda W J H Penninx
Jacqueline M Vink
Dorret I Boomsma
Vrije Universiteit Amsterdam · NLUniversity of Notre Dame · USAmsterdam UMC Location VUmc · NL

Funding

NIMH Center Repository Supporting Stem Cell ResearchU24MH068457 · NIMH · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI BRZUSTOWICZ, LINDA M, KNOWLES, JAMES A · 2003 to 2024
$213.8M
Psychometric and Genetic Assessments of Substance UseR37DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2005 to 2014
$3.7M
Psychometric and Genetic Assessments of Substance UseR01DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2004 to 2019
$2.3M
NIDA NIH HHS DA018673NIDA NIH HHS R01 DA018673NIDA NIH HHS R37 DA018673NIMH NIH HHS U24 MH068457NIMH NIH HHS U24 MH068457-06
6 · The paper itself

Abstract

Genome-wide association studies of psychiatric disorders have been criticized for their lack of explaining a considerable proportion of the heritability established in twin and family studies. Genome-wide association studies of major depressive disorder in particular have so far been unsuccessful in detecting genome-wide significant single nucleotide polymorphisms (SNPs). Using two recently proposed methods designed to estimate the heritability of a phenotype that is attributable to genome-wide SNPs, we show that SNPs on current platforms contain substantial information concerning the additive genetic variance of major depressive disorder. To assess the consistency of these two methods, we analyzed four other complex phenotypes from different domains. The pattern of results is consistent with estimates of heritability obtained in twin studies carried out in the same population.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyFastingFemaleGenetic VariationGenotypeGlucoseHumansMajor Depressive DisorderMaleModels, StatisticalNetherlandsPolymorphism, Single NucleotideSmokingTwin Studies as TopicGlucose

Identifiers

PMID22520966
PMCPMC3404250
OpenAlexW2010083978

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.