Evidence map›Paper›PMID 33098324›Full record

ArticleAnnals of neurology2021

Reply to "PPP2R5D Genetic Mutations and Early Onset Parkinsonism".

Christine Y Kim, Thomas Wirth, Cécile Hubsch, Andrea H Németh, Volkan Okur, Mathieu Anheim, Nathalie Drouot, Christine Tranchant, Gabrielle Rudolf, Jamel Chelly and 6 more

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Annals of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Thirteen New Patients ofChildren (Basel, Switzerland) · 2024
    Article
  2. A Practical Approach to Early-Onset Parkinsonism.Journal of Parkinson's disease · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 3 countries.

Christine Y KimDepartment of Neurology, Yale School of Medicine, Yale University, New Haven, CT, USA.ORCID 0000-0002-1424-4263
Thomas WirthUnit of Functional Neurosurgery, National Hospital for Neurology and Neurosurgery, University College London Hospital, London, UK.ORCID 0000-0002-4427-5765
Cécile HubschA. de Rothschild Ophthalmological Foundation, Paris, France.
Andrea H NémethOxford University Hospitals National Health Service Trust and University of Oxford, Oxford, UK.
Volkan OkurDepartment of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Mathieu AnheimNeurology Department, Strasbourg University Hospitals, Strasbourg, France.
Nathalie DrouotInstitute of Genetics and Molecular and Cellular Biology, INSERM-U964/CNRS-UMR7104/University of Strasbourg, Illkirch-Graffenstaden, France.
Christine TranchantNeurology Department, Strasbourg University Hospitals, Strasbourg, France.
Gabrielle RudolfNeurology Department, Strasbourg University Hospitals, Strasbourg, France.ORCID 0000-0002-2050-3911
Jamel ChellyNeurology Department, Strasbourg University Hospitals, Strasbourg, France.
Katrina Tatton-BrownSt George's University Hospitals National Health Service Foundation Trust, London, UK.
Cornelis BlauwendraatLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Jean Paul G VonsattelDepartment of Pathology and Cell Biology, Columbia University Medical Center and the New York Presbyterian Hospital, New York, NY, USA.
Etty CortesDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Roy N AlcalayDepartment of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Wendy K ChungDepartment of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Centre National de la Recherche Scientifique · FRColumbia University · USNational Health Service · GBFondation de Rothschild · FRIcahn School of Medicine at Mount Sinai · USNational Institutes of Health · USNewYork–Presbyterian Hospital · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Parkinsonian DisordersHumansMutationProtein Phosphatase 2PPP2R5D protein, humanProtein Phosphatase 2

Identifiers

PMID33098324
OpenAlexW3094406415

What OpenQuestion holds

Textmetadata
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.