Evidence map›Paper›PMID 42396329›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Sex-biased Genetic Risk Loci and Causal Brain Proteins in Parkinson's Disease.

Noah Cook, Youjie Zeng, Tianyi Fu, Chenyu Yang, Sathesh K Sivasankaran, Phuc Nguyen, FinnGen, Aliza P Wingo, Thomas S Wingo, Jia Nee Foo and 4 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

14 authors.

Noah CookDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0009-0006-7906-5924
Youjie ZengDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-3842-1815
Tianyi FuDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Chenyu YangDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0009-0003-2017-6134
Sathesh K SivasankaranDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-3037-6001
Phuc NguyenDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
FinnGenDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Aliza P WingoDepartment of Psychiatry, University of California, Davis, Sacramento, CA, USA.ORCID 0000-0002-6360-6726
Thomas S WingoDepartment of Neurology, University of California, Davis, Sacramento, CA, USA.ORCID 0000-0002-7679-6282
Jia Nee FooLee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.ORCID 0000-0001-9899-2308
Albert A DavisDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-2042-8445
Laura IbanezDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-2381-7059
Carlos CruchagaNeuroGenomics and Informatics Center, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0002-0276-2899
Michael E BelloyDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0001-7748-9033

Funding

Elucidating sex-specific risk for Alzheimer's disease through state-of-the-art genetics and multi-omicsR00AG075238 · NIA · WASHINGTON UNIVERSITY · PI BELLOY, MICHAEL · 2024 to 2025
$727k
NIA NIH HHS R00 AG075238
6 · The paper itself

Abstract

Parkinson's disease (PD) exhibits pronounced sex differences, yet the underlying genetic and molecular mechanisms remain poorly understood. We performed the largest-to-date meta-analysis of sex-stratified genome-wide association studies of PD followed by brain proteogenomics-based causal inference analyses. We nominated 10 candidate proteins that appear important to sex-biased PD risk, of which 2 female-biased, GALC and PSMG1, and 3 male-biased, ACTR1B, WDR41, and CD151, were most robustly prioritized. Together, our findings provide evidence for genetic sex differences in PD, prioritizing sex-biased proteins implicated in lysosomal regulation, neuroinflammation, lipid biology, and other PD-relevant mechanisms, and highlighting potential sex-informed therapeutic opportunities.

Identifiers

PMID42396329
PMCPMC13321186

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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.