Evidence map›Paper›PMID 42625058›Full record

ArticleNature genetics2026

Distinguishing different psychiatric disorders using DDx-PRS.

Wouter J Peyrot, Georgia Panagiotaropoulou, Loes M Olde Loohuis, Mark J Adams, Ole A Andreassen, Swapnil Awasthi, Andreas J Forstner, Tian Ge, Andrew M McIntosh, Brittany L Mitchell and 14 more

Abstract read
In one paragraph

Article in Nature genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Wouter J PeyrotDepartment of Psychiatry, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands. w.peyrot@amsterdamumc.nl.ORCID http://orcid.org/0000-0001-7954-8383
Georgia PanagiotaropoulouDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin, Berlin, Germany.ORCID http://orcid.org/0000-0001-9516-6158
Loes M Olde LoohuisCenter for Neurobehavioral Genetics, University of California Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-3327-7837
Mark J AdamsInstitute of Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-3599-6018
Ole A AndreassenDivision of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-4461-3568
Swapnil AwasthiDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin, Berlin, Germany.ORCID http://orcid.org/0000-0002-9692-8123
Andreas J ForstnerInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.
Tian GePsychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4785-4444
Andrew M McIntoshInstitute of Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-0198-4588
Brittany L MitchellMental Health and Neuroscience, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.ORCID http://orcid.org/0000-0002-9050-1516
Niamh MullinsDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-8021-839X
Kevin S O'ConnellDivision of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.
Brenda W J H PenninxDepartment of Psychiatry, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-7779-9672
Danielle PosthumaDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin, Berlin, Germany.ORCID http://orcid.org/0000-0003-3622-835X
Douglas M RuderferCenter for Digital Genomic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-2365-386X
Emil UffelmannDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Bjarni J VilhjalmssonNational Centre for Register-based Research, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0003-2277-9249
Zhihong ZhuNational Centre for Register-based Research, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-6783-3037
Schizophrenia Working Group of the Psychiatric Genomics Consortium
Bipolar Disorder Working Group of the Psychiatric Genomics Consortium
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Jordan W SmollerPsychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0381-6334
Alkes L PriceDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA. aprice@hsph.harvard.edu.ORCID http://orcid.org/0000-0002-2971-7975

Funding

Statistical methods to localize disease heritability and identify biological mechanismsR37MH107649 · NIMH · BROAD INSTITUTE, INC. · PI Benjamin Michael Neale · 2019 to 2026
$7.0M
Methods for Genome-wide Association Studies in Admixed PopulationsR01HG006399 · NHGRI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI PRICE, ALKES L · 2011 to 2024
$6.3M
1/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109528 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2016 to 2020
$2.5M
3/7 Psychiatric Genomics Consortium: Advancing Discovery and ImpactR01MH124839 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ANDREASSEN, OLE A, HUCKINS, LAURA MARIANNE · 2021 to 2025
$2.0M
1/4 Psychiatric GWAS Consortium: Genomic Follow-up Next-Gen Sequencing & GenotypiU01MH094421 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2012 to 2015
$1.9M
1/5-The Psychiatric GWAS Consortium: Integrated & Coordinated GWAS Meta-AnalysesU01MH085520 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2008 to 2008
$642k
NHGRI NIH HHS R01 HG006399NIMH NIH HHS R01 MH124839NIMH NIH HHS R37 MH107649NIMH NIH HHS U01 MH085520NIMH NIH HHS U01 MH094421NIMH NIH HHS U01 MH109528U.S. Department of Health & Human Services | National Institutes of Health (NIH) HG006399U.S. Department of Health & Human Services | National Institutes of Health (NIH) MH107649U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH085520U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH094421U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH109528U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01MH124839
6 · The paper itself

Abstract

Despite great progress on case-control polygenic prediction, an unmet need remains for a method that genetically distinguishes clinically related disorders (e.g., schizophrenia (SCZ) versus bipolar disorder (BIP) versus major depressive disorder (MDD) versus controls). We introduce differential diagnosis-polygenic risk score (DDx-PRS), which jointly estimates the posterior probabilities of each diagnostic category (e.g., SCZ = 50%, BIP = 25%, MDD = 15%, control = 10%) by modeling variance-covariance structure across disorders, leveraging case-control polygenic risk scores and prior clinical probabilities for each diagnostic category. We applied DDx-PRS to Psychiatric Genomics Consortium SCZ, BIP, MDD and control data, including summary-level training data from three case-control genome-wide association studies (n = 41,917-173,140 cases; total n = 1,048,683) and held-out test data from different cohorts with equal numbers for each diagnostic category (total n = 11,460). DDx-PRS was well calibrated and well powered (consistent with simulations) and produced comparable results to methods that require tuning data. True diagnosis probabilities in the top deciles of predicted diagnosis probabilities were considerably larger than prior baseline probabilities, implying appreciable potential for clinical utility in certain settings.

Indexed as

Bipolar DisorderDEAD-box RNA HelicasesMajor Depressive DisorderMental DisordersCase-Control StudiesDiagnosis, DifferentialGenetic Predisposition to DiseaseGenetic Risk ScoreGenome-Wide Association StudyHumansMultifactorial InheritancePolymorphism, Single NucleotideSchizophreniaDEAD-box RNA Helicases

Identifiers

PMID42625058
PMCPMC13559851

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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.