Evidence map›Paper›PMID 37064331›Full record

ArticleMolecular syndromology2023

First Report of Mexican Patients with

Jorge Román Corona-Rivera, Juan Carlos Zenteno, Leopoldo Gildardo López-Pérez, Emiy Yokoyama-Rebollar, Camilo E Villarroel, Tania Barragán-Arévalo, Luis Ángel Montes-Almanza, Luz Consuelo Zepeda-Romero, Guadalupe Elena Morales-Domínguez, Christian Peña-Padilla and 2 more

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

Article in Molecular syndromology, 2023. 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
0.4field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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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

12 authors at 5 institutions in 1 country.

Jorge Román Corona-RiveraCenter for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Juan Carlos ZentenoDepartment of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico.
Leopoldo Gildardo López-PérezService of Genetics, Hospital of Pediatrics, UMAE, Western National Medical Center, Mexican Social Security Institute (IMSS), Guadalajara, Mexico.
Emiy Yokoyama-RebollarHuman Genetics Department, National Institute of Pediatrics, Mexico City, Mexico.
Camilo E VillarroelHuman Genetics Department, National Institute of Pediatrics, Mexico City, Mexico.
Tania Barragán-ArévaloDepartment of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico.
Luis Ángel Montes-AlmanzaDepartment of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico.
Luz Consuelo Zepeda-RomeroService of Ophthalmology, Division of Pediatrics, 'Fray Antonio Alcalde' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Guadalupe Elena Morales-DomínguezCenter for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Christian Peña-PadillaCenter for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Lucina Bobadilla-MoralesCenter for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Alfredo Corona-RiveraCenter for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Hospital Civil de Guadalajara · MXInstitute of Ophthalmology · MXUniversidad de Guadalajara · MXNational Institute of Genomic Medicine · MXMexican Social Security Institute · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Case Presentation: Here, we describe 4 individuals with Discussion: We reviewed the ocular phenotypes reported in 74 individuals with

Indexed as

ColobomaPACS1PACS2Peters anomalyWDR37

Identifiers

PMID37064331
PMCPMC10090972
OpenAlexW4313310839

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.