Evidence map›Paper›PMID 20368705›Full record

ArticleMolecular psychiatry2011

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.

A Erhardt, L Czibere, D Roeske, S Lucae, P G Unschuld, S Ripke, M Specht, M A Kohli, S Kloiber, M Ising and 30 more

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In one paragraph

Article in Molecular psychiatry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 12 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 12 pooled it
7.9field-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

82 citing papers in PubMed, 12 syntheses or guidelines pooled it, 183 citations in OpenAlex.

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  6. Genome-wide association study of shared liability to anxiety disorders in Army STARRS.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2020
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  17. Cortex-SpecificThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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22 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

40 authors at 7 institutions in 1 country.

A ErhardtMax Planck Institute of Psychiatry, München, Germany. erhardt@mpipsykl.mpg.de
L Czibere
D Roeske
S Lucae
P G Unschuld
S Ripke
M Specht
M A Kohli
S Kloiber
M Ising
A Heck
H Pfister
P Zimmermann
R Lieb
B Pütz
M Uhr
P Weber
J M Deussing
M Gonik
M Bunck
M S Kebler
E Frank
C Hohoff
K Domschke
P Krakowitzky
W Maier
B Bandelow
C Jacob
J Deckert
S Schreiber
J Strohmaier
M Nöthen
S Cichon
M Rietschel
T Bettecken
M E Keck
R Landgraf
B Müller-Myhsok
F Holsboer
E B Binder
Max Planck Institute of Psychiatry · DEUniversity of Bonn · DEUniversity of Münster · DEHeidelberg University · DEUniversity of Würzburg · DEKiel University · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lifetime prevalence of panic disorder (PD) is up to 4% worldwide and there is substantial evidence that genetic factors contribute to the development of PD. Single-nucleotide polymorphisms (SNPs) in TMEM132D, identified in a whole-genome association study (GWAS), were found to be associated with PD in three independent samples, with a two-SNP haplotype associated in each of three samples in the same direction, and with a P-value of 1.2e-7 in the combined sample (909 cases and 915 controls). Independent SNPs in this gene were also associated with the severity of anxiety symptoms in patients affected by PD or panic attacks as well as in patients suffering from unipolar depression. Risk genotypes for PD were associated with higher TMEM132D mRNA expression levels in the frontal cortex. In parallel, using a mouse model of extremes in trait anxiety, we could further show that anxiety-related behavior was positively correlated with Tmem132d mRNA expression in the anterior cingulate cortex, central to the processing of anxiety/fear-related stimuli, and that in this animal model a Tmem132d SNP is associated with anxiety-related behavior in an F2 panel. TMEM132D may thus be an important new candidate gene for PD as well as more generally for anxiety-related behavior.

Indexed as

AdultAnimalsAnxietyDisease Models, AnimalFemaleFrontal LobeGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMembrane ProteinsMiceMiddle AgedPhenotypePolymorphism, Single NucleotidePsychiatric Status Rating ScalesMembrane ProteinsRNA, Messenger

Identifiers

PMID20368705
OpenAlexW2029776070

What OpenQuestion holds

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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.