Evidence map›Paper›PMID 37704671›Full record

ArticleNPJ Parkinson's disease2023

Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).

Lara M Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain and 14 more

Open access · goldAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in NPJ Parkinson's disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 41% of its field
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review.Movement disorders : official journal of the Movement Disorder Society · 2025
    Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 20 institutions in 47 countries.

Lara M LangeInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0002-7162-9821
Micol AvenaliIRCCS Mondino Foundation, Pavia, Italy.
Melina EllisNorthcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW, Australia.
Anastasia IllarionovaGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0000-0002-1711-7155
Ignacio J Keller SarmientoDepartment of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-0979-6001
Ai-Huey TanDivision of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID http://orcid.org/0000-0002-2979-3839
Harutyun MadoevInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Caterina GalandraIRCCS Mondino Foundation, Pavia, Italy.
Johanna JunkerInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Karisha RoopnarainInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Justin SolleDepartment of Clinical Research, Michael J. Fox Foundation for Parkinson's Research, New York City, NY, USA.
Claire WegelDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Zih-Hua FangGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0000-0002-0225-8772
Peter HeutinkGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.ORCID http://orcid.org/0000-0001-5218-1737
Kishore R KumarGarvan Institute of Medical Research, Darlinghurst, NSW, Australia.ORCID http://orcid.org/0000-0003-3482-6962
Shen-Yang LimDivision of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Enza Maria ValenteIRCCS Mondino Foundation, Pavia, Italy.ORCID http://orcid.org/0000-0002-0600-6820
Mike NallsData Tecnica International, Washington, DC, USA.
Cornelis BlauwendraatCenter 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.ORCID http://orcid.org/0000-0001-9358-8111
Andrew SingletonCenter 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.ORCID http://orcid.org/0000-0001-5606-700X
Niccolo MencacciDepartment of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Katja LohmannInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany. christine.klein@neuro.uni-luebeck.de.ORCID http://orcid.org/0000-0003-2102-3431
Global Parkinson’s Genetic Program (GP2)
National Institutes of Health · USUniversity College London · GBMichael J. Fox Foundation · USUniversity of Lübeck · DENorthwestern University · USUniversity of Malaya · MYGerman Center for Neurodegenerative Diseases · DEUniversity of Pavia · ITKoç University · TRCentral South University · CNHong Kong University of Science and Technology · HKThe University of Sydney · AUUniversidade Federal do Rio Grande do Sul · BRUniversity of Lagos · NGUniversity of Thessaly · GROslo University Hospital · NOParkinson's UK · GBQueen Mary University of London · GBStellenbosch University · ZAUniversity Kebangsaan Malaysia Medical Centre · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37704671
PMCPMC10499986
OpenAlexW4386710730

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.