Evidence map›Paper›PMID 40631485›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across Ancestries.

Joshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, Chin-Hsien Lin, Kajsa Atterling Brolin, Björn-Hergen Laabs, Sebastian Sendel, Inke R König, Amke Caliebe, Carolin Gabbert and 9 more

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2025. 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

5 · Who and what money

Authors and funding

19 authors.

Joshua Chin Ern OoiNeurology Unit, Queen Elizabeth Hospital, Kota Kinabalu, Malaysia.ORCID https://orcid.org/0000-0002-6235-3712
Yi Wen TayDepartment of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID https://orcid.org/0000-0002-9319-0768
Ai Huey TanDivision of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID https://orcid.org/0000-0002-2979-3839
Chin-Hsien LinDepartment of Neurology, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-8566-7573
Kajsa Atterling BrolinTranslational Neurogenetics Unit, Wallenberg Neuroscience Center, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Björn-Hergen LaabsInstitute of Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany.
Sebastian SendelInstitute of Medical Informatics and Statistics, Kiel University and University Hospital Schleswig-Holstein, Kiel, Germany.
Inke R KönigInstitute of Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany.
Amke CaliebeInstitute of Medical Informatics and Statistics, Kiel University and University Hospital Schleswig-Holstein, Kiel, Germany.
Carolin GabbertInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.ORCID https://orcid.org/0000-0002-2308-9330
Katherine M AndershCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Lietsel JonesCenter for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Lara M LangeInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Brian FiskeThe Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.
Carolyn SueNeuroscience Research Australia (NeuRA), Randwick, New South Wales, Australia.
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Joanne TrinhInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Theresa LüthInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Global Parkinson's Genetics Program (GP2)

Funding

Genome wide SNP analysis in Parkinson's diseaseZIAAG000949 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW · 2009 to 2024
$12.6M
Aligning Science Across Parkinson'sIntramural NIH HHS ZIA AG000949
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

LRRK2mitochondriamitochondrial polygenic scoreParkinson's diseasepolygenic score

Identifiers

PMID40631485
PMCPMC12485575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.