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A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease

PLoS Genetics(2020)10.1371/journal.pgen.1009106Source: DataRank Database

A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease is a research paper published in PLoS Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 11 times.

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Open Access11 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (8 grants)Impact (FWCI 1.37)OA: goldTopics (41)IDs (PubMed, PMC, OpenAlex)Annotations (3)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (34)

Stefanie Schmitteckert ORCID,Julia Volz,Cristina Martínez ORCID,Ralph Röth ORCID,Thomas Thumberger ORCID

Live enrichment

PubMed:33151932 PMC:PMC7643938 OpenAlex:https://openalex.org/W3095577566

Heinz and Heide Dürr Stiftung

Grant: 2017/2.2.1/04

Instituto de Salud Carlos III

Grant: CP18/00116

Instituto de Salud Carlos III

Grant: PI16/0142 and PI19/01550

Theme-Based Research Scheme

Grant: T12C-714/14-R

Medizinischen Fakultät Heidelberg, Universität Heidelberg

Studienstiftung des Deutschen Volkes

Heidelberg Stiftung Chirurgie

Dres. Majic/Majic Schlez Stiftung

FWCI

1.37

Citation Percentile

0.8%

Citation Trend

2021

2022

2023

2024

2025

2026

goldLicense: cc-by

journalhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009106&type=printable

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009106&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pgen.1009106

journalhttps://doi.org/10.1371/journal.pgen.1009106

repositoryhttps://pubmed.ncbi.nlm.nih.gov/33151932

Fields of Study

Congenital gastrointestinal and neural anomaliesIntestinal Malrotation and Obstruction DisordersCongenital Anomalies and Fetal Surgery

MeSH Terms

Exome SequencingCopper-Transporting ATPasesATP Binding Cassette Transporter, Subfamily D, Member 1AnimalsCell DifferentiationCell LineCell SurvivalComputer SimulationDisease Models, AnimalHirschsprung DiseaseHumansInfantMaleGene Expression ProfilingCell ProliferationProtein Inhibitors of Activated STATMiceSterol Regulatory Element Binding Protein 1Gene Knockout TechniquesCopper-transporting ATPases

Keywords

BiologyCandidate geneTranscriptomeIn silicoPhenotypeEnteric nervous systemGeneExome sequencingNeural crestGeneticsDiseaseZebrafishBioinformaticsComputational biologyGene expressionPathologyNeuroscienceMedicine

Sustainable Development Goals

SDG 0: Good health and well-being