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The role of complement factor I rare genetic variants in age related macular degeneration in Finland

Human Molecular Genetics(2024)10.1093/hmg/ddae165Source: DataRank Database

The role of complement factor I rare genetic variants in age related macular degeneration in Finland is a research paper published in Human Molecular Genetics (2024). On theSindex it has a DataRank of 0.165. It has been cited 2 times.

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0.165DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (14 grants)Impact (FWCI 0.81)OA: hybridTopics (68)IDs (PubMed, PMC, OpenAlex)Annotations (2)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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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.165

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (13)

Thomas M Hallam ORCID,Vicky Brocklebank,Scott J Sharp,Patrick R. Walsh ORCID,Tom Southerington ORCID

Live enrichment

PubMed:39584280 PMC:PMC11792236 OpenAlex:https://openalex.org/W4404701478

US National Institutes of Health

Grant: R01-EY028602

US National Institutes of Health

Grant: R01-EY011309

Wellcome Trust: 4Ward North Academy

Grant: RES/0248/7836

Medical Research Council

Grant: MR/X020975/1

ICF: Using mouse models to establish the effectiveness of gene therapy in the treatment of renal diseases.

Medical Research Council/Kidney Research UK Clinical Research Training Fellow

Grant: MR/R000913/1

Personalised management of atypical haemolytic uraemic syndrome

NEI NIH HHS

Grant: R01 EY011309

NEI NIH HHS

Grant: R01 EY028602

National Institutes of Health

Grant: 5R01EY011309-09

Etiologic Studies of Age-Related Macular Degeneration

National Institutes of Health

Grant: 5R01EY028602-03

Rare Genetic Variation in Macular Degeneration

Wellcome Trust

Grant: unidentified

unidentified

NIHR Newcastle Biomedical Research Centre at Newcastle upon Tyne Hospitals NHS Foundation Trust

Wellcome Trust

NIHR Newcastle Biomedical Research Centre at Newcastle upon Tyne Hospitals NHS Foundation Trust

Wellcome Trust

FWCI

0.81

Citation Percentile

0.7%

Citation Trend

2025

2026

hybridLicense: cc-by

journalhttps://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddae165/60807409/ddae165.pdf

publisherhttps://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddae165/60807409/ddae165.pdf

publisherhttps://academic.oup.com/hmg/article-pdf/34/3/218/60807409/ddae165.pdf

journalhttps://doi.org/10.1093/hmg/ddae165

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39584280

Fields of Study

Retinal Diseases and TreatmentsComplement system in diseasesMosquito-borne diseases and control0301 basic medicine0303 health sciences03 medical and health sciencesHumansFinlandMacular DegenerationComplement Factor IFemaleGenetic Predisposition to DiseaseMaleAgedGene FrequencyPolymorphism, Single NucleotideGenetic VariationGenotypeMiddle AgedComplement Pathway, Alternative

MeSH Terms

AgedComplement Pathway, AlternativeFemaleFinlandGene FrequencyGenotypeHumansMacular DegenerationMaleMiddle AgedGenetic VariationComplement Factor IGenetic Predisposition to DiseasePolymorphism, Single Nucleotide

Keywords

BiologyMacular degenerationGeneticsFactor HAlleleGenotypePopulationExonDiseaseComplement systemGeneInternal medicineMedicineComplementFinlandAge Related Macular DegenerationAhusFactor IRare Genetic VariantsFinbbMale570Complement Pathway, Alternative610Genetic VariationMiddle AgedPolymorphism, Single NucleotideGene FrequencyComplement Factor IHumansOriginal ArticleFemaleGenetic Predisposition to DiseaseAged

Sustainable Development Goals

SDG 0: Partnerships for the goals