Evidence map›Paper›PMID 35531120›Full record

ArticleTremor and other hyperkinetic movements (New York, N.Y.)2022

Genetic Diagnosis in Movement Disorders. Use of Whole-Exome Sequencing in Clinical Practice.

Patricio Millar Vernetti, María Agustina Ruiz Yanzi, Malco Rossi, Marcelo Merello

Open access · goldAbstract readLetter
In one paragraph

Article in Tremor and other hyperkinetic movements (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.1field-weighted citation impact, top 21% 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, 6 citations in OpenAlex.

  1. Late-Onset Dystonia WithJournal of clinical neurology (Seoul, Korea) · 2023
    Article
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 at 2 institutions in 3 countries.

Patricio Millar VernettiMovement Disorders Clinic, Neurology Department, Fleni, Buenos Aires, Argentina.ORCID 0000-0002-1330-3321
María Agustina Ruiz YanziNeurology Department, Fleni, Buenos Aires, Argentina.ORCID 0000-0002-3385-9730
Malco RossiMovement Disorders Clinic, Neurology Department, Fleni, Buenos Aires, Argentina.ORCID 0000-0003-3383-8566
Marcelo MerelloMovement Disorders Clinic, Neurology Department, Fleni, Buenos Aires, Argentina.ORCID 0000-0001-6898-7823
Consejo Nacional de Investigaciones Científicas y Técnicas · ARFundación para la Lucha contra las Enfermedades Neurológicas de la Infancia · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic TestingMovement DisordersExome SequencingHumansMutationcontroversiesdiagnosisgeneticsWESwhole-exome sequencing

Identifiers

PMID35531120
PMCPMC9029674
OpenAlexW4225893775

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.