Evidence map›Paper›PMID 37061878›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2023

Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism".

Nikola Kresojević, Vladana Marković, Valerija Dobričić, Iva Stanković, Tanja Stojković, Aleksandra Tomić, MIlica Ječmenica Lukić, Milena Janković, Ana Marjanović, Marija Branković and 5 more

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review.Movement disorders : official journal of the Movement Disorder Society · 2025
    Pooled it
  2. Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  3. Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.Movement disorders : official journal of the Movement Disorder Society · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Nikola KresojevićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.ORCID 0000-0002-2788-506X
Vladana MarkovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Valerija DobričićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Iva StankovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.ORCID 0000-0003-1484-4717
Tanja StojkovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Aleksandra TomićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
MIlica Ječmenica LukićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Milena JankovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Ana MarjanovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Marija BrankovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Ivana NovakovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Igor PetrovićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Nataša DragaševićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Marina SvetelNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Vladimir KostićNeurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Gaucher DiseaseParkinsonian DisordersFemaleGlucosylceramidaseHeterozygoteHumansMaleMutationGlucosylceramidase

Identifiers

PMID37061878

What Socratic 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 Socratic graph.