Evidence map›Paper›PMID 38003344›Full record

ArticleInternational journal of molecular sciences2023

Uncovering the Genetic and Molecular Features of Huntington's Disease in Northern Colombia.

Mostapha Ahmad, Margarita R Ríos-Anillo, Johan E Acosta-López, Martha L Cervantes-Henríquez, Martha Martínez-Banfi, Wilmar Pineda-Alhucema, Pedro Puentes-Rozo, Cristian Sánchez-Barros, Andrés Pinzón, Hardip R Patel and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

15 authors at 8 institutions in 3 countries.

Mostapha AhmadFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Margarita R Ríos-AnilloFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Johan E Acosta-LópezLife Science Research Center, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Martha L Cervantes-HenríquezLife Science Research Center, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Martha Martínez-BanfiLife Science Research Center, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Wilmar Pineda-AlhucemaLife Science Research Center, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Pedro Puentes-RozoFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Cristian Sánchez-BarrosFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Andrés PinzónBioinformatics and Systems Biology Laboratory, Institute for Genetics, Universidad Nacional de Colombia, Bogota 111321, Colombia.
Hardip R PatelNational Centre for Indigenous Genomics, John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
Jorge I VélezDepartment of Industrial Engineering, Universidad del Norte, Barranquilla 081007, Colombia.ORCID 0000-0002-3146-7899
José Luis Villarreal-CamachoPrograma de Medicina, Facultad de Ciencias de la Salud, Universidad Libre Seccional Barranquilla, Barranquilla 081007, Colombia.ORCID 0000-0002-7240-7462
David A PinedaGrupo de Investigación en Neuropsicología y Conducta, Universidad de San Buenaventura, Medellin 050010, Colombia.ORCID 0000-0002-1080-4796
Mauricio Arcos-BurgosGrupo de Investigación en Psiquiatría (GIPSI), Departamento de Psiquiatría, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia, Medellin 050010, Colombia.ORCID 0000-0002-8529-0574
Manuel Sánchez-RojasFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Universidad Simón Bolívar · COUniversidad de Antioquia · COAustralian National University · AUHospital Costa del Sol · ESUniversidad del Norte · COUniversidad Libre de Colombia · COUniversidad Nacional de Colombia · COUniversity of Atlántico · CO

Funding

Miniciencias 777-2017
6 · The paper itself

Abstract

Huntington's disease (HD) is a genetic disorder caused by a CAG trinucleotide expansion in the huntingtin (

Indexed as

Huntington DiseaseAdultAllelesColombiaDNAFemaleHumansHuntingtin ProteinPedigreeTrinucleotide Repeat ExpansionDNAHuntingtin ProteinCAG repeatsHTTHuntington’s diseasemosaicismslippage

Identifiers

PMID38003344
PMCPMC10671691
OpenAlexW4388568990

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.