Evidence map›Paper›PMID 31155756›Full record

ArticleAnnals of neurology2019

Using global team science to identify genetic parkinson's disease worldwide.

Eva-Juliane Vollstedt, Meike Kasten, Christine Klein, MJFF Global Genetic Parkinson's Disease Study Group

Abstract readEditorial
In one paragraph

Article in Annals of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
–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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Genetic variants ofIBRO neuroscience reports · 2025
    Article
  6. Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  7. Understanding monogenic Parkinson's disease at a global scale.medRxiv : the preprint server for health sciences · 2024
    Article
  8. Article
  9. Article
  10. Research progress in the early diagnosis of Parkinson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Review
  11. Clinical relevance and translational impact of reduced penetrance in genetic movement disorders.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. GP2: The Global Parkinson's Genetics Program.Movement disorders : official journal of the Movement Disorder Society · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Long-Term Outcomes of Genetic Parkinson's Disease.Journal of movement disorders · 2020
    Article
  20. Review
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

4 authors.

Eva-Juliane VollstedtInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.ORCID 0000-0002-6898-9201
Meike KastenInstitute of Neurogenetics and Department of Psychiatry, University of Lübeck, Lübeck, Germany.
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
MJFF Global Genetic Parkinson's Disease Study Group

Funding

Dissecting Oligogenic Biomarkers in Ashkenazi Jews with Parkinson DiseaseU01NS107016 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI OZELIUS, LAURIE J., SAUNDERS-PULLMAN, RACHEL · 2019 to 2023
$6.6M
Targeting Lewy Body Specific Pathology Using BiomarkersU01NS100600 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HONIG, LAWRENCE S, MARDER, KAREN S · 2016 to 2020
$4.5M
Chief Scientist Office SCAF/18/01German Research Foundation FOR2488Medical Research Council G0701075Medical Research Council G0901254Medical Research Council MR/K01417X/1Medical Research Council MR/L501542/1Medical Research Council MR/N026004/1Michael J. Fox FoundationNINDS NIH HHS U01 NS100600NINDS NIH HHS U01 NS107016Parkinson's UK G-0907
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseaseGlobal HealthHumansInterdisciplinary ResearchParkinson Disease

Identifiers

PMID31155756
PMCPMC7410260

What OpenQuestion holds

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LicenceTDM
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.