Evidence map›Paper›PMID 38397401›Full record

ArticleBiomolecules2024

Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease.

Helena Lucena-Padros, Nereida Bravo-Gil, Cristina Tous, Elena Rojano, Pedro Seoane-Zonjic, Raquel María Fernández, Juan A G Ranea, Guillermo Antiñolo, Salud Borrego

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2024. 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
1.7field-weighted citation impact, top 18% 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, 3 citations in OpenAlex.

  1. Review
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

9 authors at 4 institutions in 1 country.

Helena Lucena-PadrosDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Nereida Bravo-GilDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Cristina TousDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Elena RojanoDepartment of Molecular Biology and Biochemistry, University of Malaga, 29010 Malaga, Spain.ORCID 0000-0002-2678-710X
Pedro Seoane-ZonjicDepartment of Molecular Biology and Biochemistry, University of Malaga, 29010 Malaga, Spain.ORCID 0000-0002-3020-1415
Raquel María FernándezDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Juan A G RaneaDepartment of Molecular Biology and Biochemistry, University of Malaga, 29010 Malaga, Spain.
Guillermo AntiñoloDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Salud BorregoDepartment of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESInstituto de Biomedicina de Sevilla · ESInstituto de Investigación Biomédica de Málaga · ESInstituto de Salud Carlos III · ES

Funding

Instituto de Salud Carlos III IMP-0009Instituto de Salud Carlos III PI19-01550Instituto de Salud Carlos III PI22-01428Regional Government of Andalusia PEER-0470-2019
6 · The paper itself

Abstract

Hirschsprung's disease (HSCR) is a rare developmental disorder in which enteric ganglia are missing along a portion of the intestine. HSCR has a complex inheritance, with

Indexed as

Hirschsprung DiseaseMicroRNAsBiomarkersComputational BiologyHumansMultiomicsBiomarkersMicroRNAsenteric neuropathyHirschsprung’s diseasenetworks analysisomics expression datasystem biology

Identifiers

PMID38397401
PMCPMC10886964
OpenAlexW4391347874

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.