Evidence map›Paper›PMID 42326775›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Multi-ancestry analysis of

Yi Wen Tay, Inas Elsayed, Dennis Yeow, Mikayla James, Pin-Jui Kung, Laurel Screven, Allison A Dilliott, Roy N Alcalay, Zih-Hua Fang, Ai Huey Tan 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.

Yi Wen TayDepartment of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Inas ElsayedFaculty of Pharmacy, University of Gezira, Wad Medani, Sudan.
Dennis YeowNeuroscience Research Australia, Randwick, New South Wales, Australia.ORCID 0000-0001-7534-7007
Mikayla JamesCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Pin-Jui KungDivision of Plastic Surgery, Department of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Laurel ScrevenThe Global Parkinson's Genetics Program (GP2), Bethesda, USA.
Allison A DilliottParkinson's Foundation, NewYork, NY 10018, USA.ORCID 0000-0003-3863-9304
Roy N AlcalayNeurological Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Zih-Hua FangDataTecnica LLC, Washington, DC 20037, USA.
Ai Huey TanDivision of Neurology, Department of Medicine, and The Mah Pooi Soo & Tan Chin Nam Centre for Parkinson's & Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Global Parkinson’s Genetics Program (GP2)
Carolyn M SueNeuroscience Research Australia, Randwick, New South Wales, Australia.
Lara M LangeLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Maria Teresa PeriñanCentre for Preventive Neurology, Wolfson Institute of Population Health, Queen Mary University of London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Variants in the Objectives: To investigate the genetic spectrum and prevalence of Methods: We leveraged multi-ancestry genetic data from the Global Parkinson's Genetics Program (GP2), including genotyping data from 98,589 and short-read sequencing data from 36,022 individuals. We performed a Results: Five PD cases carried potentially biallelic rare pathogenic/likely pathogenic Conclusions:

Indexed as

geneticsmulti-ancestry analysisParkinson’s diseasePOLG

Identifiers

PMID42326775
PMCPMC13278229

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.