Evidence map›Paper›PMID 31940124›Full record

ArticleCerebellum (London, England)2020

Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

Mario Cornejo-Olivas, Miguel Inca-Martinez, Raphael Machado Castilhos, Gabriel Vasata Furtado, Eduardo Preusser Mattos, Giovana Bavia Bampi, Sandra Leistner-Segal, Victoria Marca, Pilar Mazzetti, Maria Luiza Saraiva-Pereira and 2 more

Open access · bronzeAbstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2020. 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
–field-weighted citation impact, top 99% 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 3 countries.

Mario Cornejo-OlivasNeurogenetics Research Center, Instituto Nacional de Ciencias, Neurológicas, 1271 Ancash St, Barrios Altos, 15003, Lima, Peru. mario.cornejo.o@incngen.org.pe.ORCID 0000-0001-6313-5680
Miguel Inca-MartinezNeurogenetics Research Center, Instituto Nacional de Ciencias, Neurológicas, 1271 Ancash St, Barrios Altos, 15003, Lima, Peru.
Raphael Machado CastilhosPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Gabriel Vasata FurtadoPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Eduardo Preusser MattosPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Giovana Bavia BampiPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Sandra Leistner-SegalServiço de Genética Médica, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Victoria MarcaNeurogenetics Research Center, Instituto Nacional de Ciencias, Neurológicas, 1271 Ancash St, Barrios Altos, 15003, Lima, Peru.
Pilar MazzettiNeurogenetics Research Center, Instituto Nacional de Ciencias, Neurológicas, 1271 Ancash St, Barrios Altos, 15003, Lima, Peru.
Maria Luiza Saraiva-PereiraPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Laura Bannach JardimPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Rede Neurogenetica
Universidade Federal do Rio Grande do Sul · BRInstituto Nacional de Ciencias NeurológicasHospital de Clínicas de Porto Alegre · BRUniversidad Peruana Cayetano Heredia · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The original version of this article unfortunately contained some mistakes in Table 2. The additional row (just above SCA2) with the following information "SCA1, 1(1), 1, 50, 74, 24, 46 and 0/1" should be inserted.

Identifiers

PMID31940124
OpenAlexW3000744643

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.