Evidence map›Paper›PMID 20978456›Full record

ArticlePsychiatric genetics2011

Association study of polymorphisms in the autosomal mitochondrial complex I subunit gene, NADH dehydrogenase (ubiquinone) flavoprotein 2, and bipolar disorder.

Glenn A Doyle, John P Dahl, Paul J Bloch, Andrew E Weller, Falk W Lohoff, Thomas N Ferraro, Wade H Berrettini

Open access · greenAbstract readLetter
In one paragraph

Article in Psychiatric genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
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

7 authors at 2 institutions in 1 country.

Glenn A Doyle
John P Dahl
Paul J Bloch
Andrew E Weller
Falk W Lohoff
Thomas N Ferraro
Wade H Berrettini
University of Pennsylvania · USUniversity of North Carolina at Chapel Hill · US

Funding

COLLABORATIVE GENOMIC STUDY OF BIPOLAR DISORDERR01MH059553 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BERRETTINI, WADE H · 1998 to 2007
$2.1M
VMAT1 in bipolar disorder and schizophreniaK08MH080372 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI LOHOFF, FALK W · 2008 to 2012
$949k
NIMH NIH HHS K08 MH080372NIMH NIH HHS R01 MH059553NIMH NIH HHS R01 MH59553
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseBipolar DisorderElectron Transport Complex IHaplotypesHumansLinkage DisequilibriumNADH DehydrogenasePolymorphism, Single NucleotideProtein SubunitsElectron Transport Complex INADH DehydrogenaseNDUFV2 protein, humanProtein Subunits

Identifiers

PMID20978456
PMCPMC3073549
OpenAlexW2332429154

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.