Evidence map›Paper›PMID 31976146›Full record

ArticleJournal of pediatric genetics2020

Report of the Phenotype of a Patient with Roberts Syndrome and a Rare

Carla Bastos da Costa Almeida, Amanda Thum Welter, Gabriel Dotta Abech, Gabriela Rangel Brandão, José Antônio Monteiro Flores, Birgitt Schüle, Uta Francke, Marilu Fiegenbaum, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa

Open access · bronzeAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 2 institutions in 2 countries.

Carla Bastos da Costa AlmeidaDepartment of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.
Amanda Thum WelterDepartment of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.
Gabriel Dotta AbechDepartment of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.
Gabriela Rangel BrandãoDepartment of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.
José Antônio Monteiro FloresPediatric Radiology Service, Hospital da Criança Santo Antônio/Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil.
Birgitt SchüleDepartment of Genetics and Pediatrics, Stanford University School of Medicine, California, United States.
Uta FranckeDepartment of Genetics and Pediatrics, Stanford University School of Medicine, California, United States.
Marilu FiegenbaumDepartment of Human Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.
Paulo Ricardo Gazzola ZenDepartment of Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre and Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil.
Rafael Fabiano Machado RosaDepartment of Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre and Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil.
Universidade Federal de Ciências da Saúde de Porto Alegre · BRStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Roberts syndrome is a rare autosomal recessive genetic disease. In this report, we report a Brazilian patient with a rare

Indexed as

ESCO2 variantphocomeliaRoberts syndrome

Identifiers

PMID31976146
PMCPMC6976314
OpenAlexW2971723979

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.