Evidence map›Paper›PMID 30046498›Full record

ArticleCase reports in genetics2018

A Novel c.91dupG

Alejandra Del Pilar Reyes-de la Rosa, Gustavo Varela-Fascinetto, Constanza García-Delgado, Edgar Ricardo Vázquez-Martínez, Pedro Valencia-Mayoral, Marco Cerbón, Verónica Fabiola Morán-Barroso

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

Article in Case reports in genetics, 2018. 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
0.2field-weighted citation impact, top 41% 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, 3 citations in OpenAlex.

  1. Article
  2. Alagille Syndrome: A Novel Mutation inFrontiers in pediatrics · 2019
    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

7 authors at 2 institutions in 1 country.

Alejandra Del Pilar Reyes-de la RosaDepartment of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Gustavo Varela-FascinettoDepartment of Transplantation, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Constanza García-DelgadoDepartment of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Edgar Ricardo Vázquez-MartínezUnidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología Isidro Espinosa de los Reyes-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Pedro Valencia-MayoralDepartment of Pathology, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Marco CerbónUnidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología Isidro Espinosa de los Reyes-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Verónica Fabiola Morán-BarrosoDepartment of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.ORCID 0000-0001-8256-7729
Hospital Infantil de México Federico Gómez · MXInstituto Nacional de Perinatología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alagille syndrome (MIM 118450) is an autosomal dominant disorder characterized by paucity of intrahepatic bile ducts, chronic cholestasis, pulmonary stenosis, butterfly-like vertebrae, posterior embryotoxon, and dysmorphic facial features. Most cases are caused by

Identifiers

PMID30046498
PMCPMC6036836
OpenAlexW2810818672

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.