Evidence map›Paper›PMID 27896116›Full record

ArticleMolecular genetics and metabolism reports2014

Fabry disease: Evidence for a regional founder effect of the

Dayse Oliveira de Alencar, Cristina Netto, Patricia Ashton-Prolla, Roberto Giugliani, Ândrea Ribeiro-Dos-Santos, Fernanda Pereira, Ursula Matte, Ney Santos, Sidney Santos

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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. Article
  2. Article
  3. 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

9 authors.

Dayse Oliveira de AlencarLaboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.
Cristina NettoServiço de Genética Médica, Hospital de Clínicas de Porto Alegre, RS, Brazil.
Patricia Ashton-ProllaServiço de Genética Médica, Hospital de Clínicas de Porto Alegre, RS, Brazil; Programa de Pós-Graduação em Genética e Biologia Molecular, Departamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Roberto GiuglianiServiço de Genética Médica, Hospital de Clínicas de Porto Alegre, RS, Brazil; Programa de Pós-Graduação em Genética e Biologia Molecular, Departamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Ândrea Ribeiro-Dos-SantosLaboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil; Núcleo de Pesquisas em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.
Fernanda PereiraCentro de Terapia Gênica, UAMP, CPE, Hospital de Clínicas de Porto Alegre, RS, Brazil.
Ursula MattePrograma de Pós-Graduação em Genética e Biologia Molecular, Departamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Centro de Terapia Gênica, UAMP, CPE, Hospital de Clínicas de Porto Alegre, RS, Brazil.
Ney SantosLaboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil; Núcleo de Pesquisas em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.
Sidney SantosLaboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil; Núcleo de Pesquisas em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Fabry disease is caused by mutations in the gene (

Indexed as

30delG mutationBrazilFabry diseaseFounder effectGLA gene

Identifiers

PMID27896116
PMCPMC5121364

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.