Evidence map›Paper›PMID 35884678›Full record

ArticleBrain sciences2022

Structural Protein Effects Underpinning Cognitive Developmental Delay of the

Juan Javier López-Rivera, Luna Rodríguez-Salazar, Alejandro Soto-Ospina, Carlos Estrada-Serrato, David Serrano, Henry Mauricio Chaparro-Solano, Olga Londoño, Paula A Rueda, Geraldine Ardila, Andrés Villegas-Lanau and 6 more

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2022. 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
1.2field-weighted citation impact, top 22% 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, 16 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

16 authors at 4 institutions in 1 country.

Juan Javier López-RiveraINPAC Research Group, Fundación Universitaria Sanitas, Bogotá 111321, Colombia.ORCID 0000-0003-4989-4853
Luna Rodríguez-SalazarGrupo de Bioinformática, Laboratorio de Clínica Colsanitas, Bogotá 110221, Colombia.
Alejandro Soto-OspinaGenética Molecular (GenMol), Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medellín 050012, Colombia.ORCID 0000-0003-2382-7038
Carlos Estrada-SerratoGrupo de Genética Médica, Clínica Universitaria Colombia y Clínica Pediátrica Colsanitas, Bogotá 111321, Colombia.
David SerranoGrupo de Genética Médica, Clínica Universitaria Colombia y Clínica Pediátrica Colsanitas, Bogotá 111321, Colombia.
Henry Mauricio Chaparro-SolanoGrupo de Genética Médica, Clínica Universitaria Colombia y Clínica Pediátrica Colsanitas, Bogotá 111321, Colombia.ORCID 0000-0002-1649-7854
Olga LondoñoGrupo de Genética Médica, Clínica Universitaria Colombia y Clínica Pediátrica Colsanitas, Bogotá 111321, Colombia.
Paula A RuedaGrupo de Bioinformática, Laboratorio de Clínica Colsanitas, Bogotá 110221, Colombia.
Geraldine ArdilaGrupo de Bioinformática, Laboratorio de Clínica Colsanitas, Bogotá 110221, Colombia.
Andrés Villegas-LanauGenética Molecular (GenMol), Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medellín 050012, Colombia.
Marcela Godoy-CorredorLaboratorio Clínico y de Patología, Clínica Colsanitas, Bogotá 110221, Colombia.
Mauricio CuartasGrupo de Investigación Estudios en Psicología, Departamento de Psicología, Escuela de Humanidades, Universidad EAFIT, Medellín 050022, Colombia.
Jorge I VélezUniversidad del Norte, Barranquilla 080001, Colombia.ORCID 0000-0002-3146-7899
Oscar M VidalUniversidad del Norte, Barranquilla 080001, Colombia.ORCID 0000-0002-7807-1242
Mario A Isaza-RugetINPAC Research Group, Fundación Universitaria Sanitas, Bogotá 111321, Colombia.
Mauricio Arcos-BurgosGrupo de Investigación en Psiquiatría (GIPSI), Departamento de Psiquiatría, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia, Medellín 050012, Colombia.ORCID 0000-0002-8529-0574
Fundación Universitaria Sanitas · COUniversidad de Antioquia · COUniversidad del Norte · COUniversidad EAFIT · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A whole-exome capture and next-generation sequencing was applied to an 11 y/o patient with a clinical history of congenital hypotonia, generalized motor and cognitive neurodevelopmental delay, and severe cognitive deficit, and without any identifiable Syndromic pattern, and to her parents, we disclosed a de novo heterozygous pathogenic mutation, c.697_699del p.Phe233del (rs786204835)(ACMG classification PS2, PM1, PM2, PP5), harbored in the

Indexed as

cognitive developmental delaymental retardationMutation c.697_699del p.Phe233delPURAPurine-rich element binding protein A genetranscriptional activator protein Pur-alpha

Identifiers

PMID35884678
PMCPMC9313109
OpenAlexW4283757303

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.