Evidence map›Paper›PMID 40240380›Full record

ArticleNPJ Parkinson's disease2025

Prioritizing Parkinson's disease risk genes in genome-wide association loci.

Lara M Lange, Catalina Cerquera-Cleves, Marijn Schipper, Georgia Panagiotaropoulou, Alice Braun, Julia Kraft, Swapnil Awasthi, Nathaniel Bell, Danielle Posthuma, Stephan Ripke and 2 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Genetic and Proteomic Investigation of the Smoking-Parkinson's Disease Association.medRxiv : the preprint server for health sciences · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Lara M Lange *Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
Catalina Cerquera-Cleves *Neurology Unit, Department of Neurosciences, Hospital Universitario San Ignacio, Bogotá, Colombia.
Marijn SchipperVrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Georgia PanagiotaropoulouDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Alice BraunDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Julia KraftDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Swapnil AwasthiDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Nathaniel BellVrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Danielle PosthumaVrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Cornelis BlauwendraatLaboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
Karl HeilbronDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Berlin, Germany. kheilbro@broadinstitute.org.

Funding

5/7 Psychiatric Genomics Consortium: Advancing Discovery and ImpactR01MH124873 · NIMH · CARDIFF UNIVERSITY · PI LEWIS, CATHRYN, O'DONOVAN, MICHAEL · 2021 to 2025
$2.6M
European Union's Horizon program 101057454, "PsychSTRATA"National Institute Of Mental Health of the National Institutes of Health R01MH124873NIMH NIH HHS R01 MH124873The European Research Council ERC-2018-AdG GWAS2FUNC 834057The European Union's Horizon program 964874, "REALMENT"The German Research Foundation 402170461 "TRR265"The Netherlands Organization for Scientific Research 024.004.012
6 · The paper itself

Abstract

Many drug targets in ongoing Parkinson's disease (PD) clinical trials have strong genetic links. While genome-wide association studies (GWAS) nominate regions associated with disease, pinpointing causal genes is challenging. Our aim was to prioritize additional druggable genes underlying PD GWAS signals. The polygenic priority score (PoPS) integrates genome-wide information from MAGMA gene-level associations and over 57,000 gene-level features. We applied PoPS to East Asian and European PD GWAS data and prioritized genes based on PoPS, distance to the GWAS signal, and non-synonymous credible set variants. We prioritized 46 genes, including well-established PD genes (SNCA, LRRK2, GBA1, TMEM175, VPS13C), genes with strong literature evidence supporting a mechanistic link to PD (RIT2, BAG3, SCARB2, FYN, DYRK1A, NOD2, CTSB, SV2C, ITPKB), and genes relatively unexplored in PD. Many hold potential for drug repurposing or development. We prioritized high-confidence genes with strong links to PD pathogenesis that may represent our next-best candidates for developing disease-modifying therapeutics.

Identifiers

PMID40240380
PMCPMC12003903

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.