Evidence map›Paper›PMID 18762858›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2009

Association analysis of Rgs7 variants with panic disorder.

Christa Hohoff, Anna Neumann, Katharina Domschke, Christian Jacob, Wolfgang Maier, Jürgen Fritze, Borwin Bandelow, Petra Krakowitzky, Matthias Rothermundt, Volker Arolt and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2017
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Anxiety in mice and men: a comparison.Journal of neural transmission (Vienna, Austria : 1996) · 2009
    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

11 authors at 5 institutions in 1 country.

Christa HohoffDepartment of Psychiatry, University of Muenster, Muenster, Germany. hohoffch@uni-muenster.de
Anna Neumann
Katharina Domschke
Christian Jacob
Wolfgang Maier
Jürgen Fritze
Borwin Bandelow
Petra Krakowitzky
Matthias Rothermundt
Volker Arolt
Jürgen Deckert
University of Münster · DEUniversity of Würzburg · DEGoethe University Frankfurt · DEUniversity of Bonn · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following our recent finding of Rgs2 playing a role in the development of human panic disorder (PD), we examine another positional and functional candidate from the functionally interwoven Rgs (regulator of G-protein signaling) family, Rgs7, in the pathogenesis of PD. A German PD sample (N = 224) was compared with matched controls (N = 224) for seven SNPs within and flanking the gene. The intronic SNP3 (rs11805657) and its corresponding haplotypes were found to be associated with PD, particularly PD with comorbid agoraphobia (PDAgP), with the effect originating from the female subgroup (P values 0.008-0.047). The rare A-allele was underrepresented in patients, suggesting a protective effect with carriers possessing an about 2-fold lower risk for developing the disorder compared to G/G homozygotes. Our results argue against a major role of Rgs7 gene variants in the pathogenesis of PD, but are consistent with a minor gender-specific effect on PD, particularly PDAgP.

Indexed as

AdultAgoraphobiaBrain ChemistryCohort StudiesDNA Mutational AnalysisFemaleGene FrequencyGenetic MarkersGenetic Predisposition to DiseaseGenetic TestingGenotypeHaplotypesHeterozygoteHomozygoteHumansIntronsGenetic MarkersRGS7 protein, humanRGS Proteins

Identifiers

PMID18762858
OpenAlexW1986487393

What OpenQuestion holds

Textmetadata
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.