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The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria

Human Molecular Genetics(2024)10.1093/hmg/ddae014Source: DataRank Database

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria is a research paper published in Human Molecular Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 12 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access12 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (9 grants)Impact (FWCI 3.43)OA: hybridTopics (65)IDs (PubMed, OpenAlex)SDGs (2)

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 (35)

Titilope A. Adeyemo ORCID,Ajoke Idayat Oyetunji,Bassey Inyang,Afolashade Akinrindoye,Baraka Stewart Mkumbe ORCID

Live enrichment

PubMed:38339995 OpenAlex:https://openalex.org/W4391727425

MRC

Grant: MR/T013389/1

Identification of novel mechanisms of fetal-haemoglobin induction by common genetic variation in patients with sickle cell disease

EPSRC

Grant: EP/X527920/1

GCRF and Newton Consolidation Accounts King's College London

Wellcome Trust Core

Grant: 203141/Z/16/Z

UCL Global Engagement Funds

Grant: 2016/17

Sickle Pan-Africa Research Consortium Nigeria NEtwork

Grant: 1U01HL156942–01-02

National Institutes of Health

Grant: 5U01HL156942-05

Sickle Pan African Research Consortium Nigeria (SPARC-NEt)

Wellcome Trust

Grant: 203141

Human Genetics and Disease Biology: Core Renewal for the Wellcome Trust Centre for Human Genetics

NHLBI NIH HHS

Grant: U01 HL156942

Wellcome Trust

FWCI

3.43

Citation Percentile

0.9%

Citation Trend

2024

2025

2026

hybridLicense: cc-by

journalhttps://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddae014/56647628/ddae014.pdf

publisherhttps://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddae014/56647628/ddae014.pdf

publisherhttps://academic.oup.com/hmg/article-pdf/33/10/919/57401279/ddae014.pdf

journalhttps://doi.org/10.1093/hmg/ddae014

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38339995

Fields of Study

Hemoglobinopathies and Related DisordersIron Metabolism and DisordersBlood groups and transfusion0301 basic medicine0303 health sciences03 medical and health sciencesFemaleHumansMaleAllelesAnemia, Sickle CellGenetic Predisposition to DiseaseGenome-Wide Association StudyGTP-Binding ProteinsHaplotypesNigeriaNuclear ProteinsPolymorphism, Single NucleotideRepressor Proteins

MeSH Terms

AdolescentAdultAllelesAnemia, Sickle CellCarrier ProteinsFemaleFetal HemoglobinHaplotypesHumansMaleNigeriaNuclear ProteinsRepressor ProteinsGTP-Binding ProteinsGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenome-Wide Association Study

Keywords

BiologyPersistence (discontinuity)FetusDiseaseFetal hemoglobinGeneticsDissection (medical)PregnancyInternal medicineAnatomyMedicineMaleNigeriaNuclear ProteinsAnemia, Sickle CellPolymorphism, Single NucleotideRepressor ProteinsHaplotypesGTP-Binding ProteinsHumansFemaleGenetic Predisposition to DiseaseAssociation Studies ArticleAllelesGenome-Wide Association Studyfetal haemoglobinhaplotype analysisheritabilitysickle cell disease

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being