Evidence map›Paper›PMID 36373941›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2022

Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts.

Marco Percetti, Edoardo Monfrini, Leonardo Caporali, Raffaella Minardi, Valerio Carelli, Enza Maria Valente, Alessio Di Fonzo

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2022. 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
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Marco PercettiDino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.ORCID 0000-0003-4679-3360
Edoardo MonfriniDino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.ORCID 0000-0003-4720-9234
Leonardo CaporaliIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Raffaella MinardiIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Valerio CarelliIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Enza Maria ValenteNeurogenetics Research Centes, IRCCS Mondino Foundation, Pavia, Italy.ORCID 0000-0002-0600-6820
Alessio Di FonzoDino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.ORCID 0000-0001-6478-026X
Istituto delle Scienze Neurologiche di Bologna · ITUniversity of Milan · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Parkinson DiseaseHumansMitochondrial ProteinsMutationMitochondrial ProteinsmtDNAparkinsonismParkinson's diseasetwinkleTWNK

Identifiers

PMID36373941
OpenAlexW4309020238

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.