Evidence map›Paper›PMID 42431851›Full record

ArticleTranslational psychiatry2026

Investigation of polygenic risk scores and subphenotypes in social anxiety disorder.

Lisa Sindermann, Angelina Röhrig, Friederike S David, Börge Schmidt, Katharina Domschke, Verena Nieratschker, Udo Dannlowski, Elisabeth J Leehr, Eric Leibing, Markus M Nöthen and 5 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lisa Sindermann *Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany. sinderma@uni-bonn.de.
Angelina Röhrig *Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.
Friederike S DavidInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0001-9521-5669
Börge SchmidtInstitute for Medical Informatics, University Hospital of Essen, Essen, Germany.
Katharina DomschkeDepartment of Psychiatry and Psychotherapy, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-2550-9132
Verena NieratschkerDepartment of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7884-4500
Udo DannlowskiUniversity of Münster, Institute for Translational Psychiatry, Münster, Germany.ORCID http://orcid.org/0000-0002-0623-3759
Elisabeth J LeehrUniversity of Münster, Institute for Translational Psychiatry, Münster, Germany.ORCID http://orcid.org/0000-0002-9264-5003
Eric LeibingClinic of Psychosomatic Medicine and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany.
Markus M NöthenInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-8770-2464
Franziska GeiserDepartment of Psychosomatic Medicine and Psychotherapy, University Hospital Bonn, University of Bonn, Bonn, Germany.
Johannes SchumacherInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0001-9217-6457
Carlo MajCentre for Human Genetics, University of Marburg, Marburg, Germany.
Rupert ConradDepartment of Psychosomatic Medicine and Psychotherapy, University of Münster, Münster, Germany.
Andreas J ForstnerInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany. forstner@uni-bonn.de.ORCID http://orcid.org/0000-0002-1876-6368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Social anxiety disorder (SAD) is a common anxiety disorder (ANX) with moderate heritability that often co-occurs with other mental disorders. Until now, sample sizes in genetic analyses of SAD have been limited, so that the genetic basis of SAD and its subphenotypes is still largely unknown. In a large cohort comprising n = 1,194 SAD patients derived from five German cohorts and n = 3,409 controls from the Heinz Nixdorf Recall Study, we computed polygenic risk scores (PRS) at six p-thresholds using PRSice-2 based on large-scale genome-wide association studies for depression, major depressive disorder (MDD), ANX, schizophrenia (SCZ), bipolar disorder (BD), attention-deficit/hyperactivity disorder (ADHD), anorexia nervosa (AN), autism spectrum disorder (ASD), and alcohol dependence (AD). We used general linear models to examine the association between the PRS and SAD status. In SAD subsamples, we investigated whether the PRS are associated with SAD subphenotypes (i.e., SAD severity, current depressive symptoms, comorbid MDD) using correlation analyses and a general linear model. Results were corrected for multiple testing. The SAD status was significantly associated with PRS for depression, MDD, ANX, SCZ, BD, AN, and ASD (p

Indexed as

Multifactorial InheritancePhobia, SocialAdultAttention Deficit Disorder with HyperactivityBipolar DisorderComorbidityFemaleGenetic Predisposition to DiseaseGenetic Risk ScoreGenome-Wide Association StudyGermanyHumansMajor Depressive DisorderMaleMiddle AgedPhenotype

Identifiers

PMID42431851
PMCPMC13354785

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.