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Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

Molecular Therapy(2020)10.1016/j.ymthe.2020.06.001Source: DataRank Database

Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B is a research paper published in Molecular Therapy (2020). On theSindex it has a DataRank of 0. It has been cited 210 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access210 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 19.43)OA: greenTopics (68)Linked Datasets (8)DataCite Reuse (8)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

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Authors (15)

Margaret V. Ragni ORCID,John E.J. Rasko ORCID,Leslie Raffini ORCID,Benjamin J. Samelson‐Jones ORCID,Margareth C. Ozelo ORCID

Live enrichment

PubMed:32559433 OpenAlex:https://openalex.org/W3035047148

National Institutes of Health

Grant: P01 HL64190

National Institutes of Health

Grant: K08 HL 146991-01

NHLBI NIH HHS

Grant: K08 HL140078

NHLBI NIH HHS

Grant: K08 HL146991

NHLBI NIH HHS

Grant: P01 HL064190

FWCI

19.43

Citation Percentile

1.0%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

greenLicense: http://creativecommons.org/licenses/by-nc-nd/4.0/

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7474338

publisherhttps://api.elsevier.com/content/article/PII:S1525001620302914?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1525001620302914?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.ymthe.2020.06.001

Fields of Study

Virus-based gene therapy researchCAR-T cell therapy researchCRISPR and Genetic EngineeringAdultAntibodies, NeutralizingAntibodies, ViralCapsidCross ReactionsDependovirusFactor IXFollow-Up StudiesGene Transfer TechniquesGenetic TherapyGenetic VectorsHemophilia BHepatocytesHumansInfusions, Intra-ArterialLiverLongitudinal StudiesMaleMiddle AgedSignal TransductionTreatment OutcomeYoung AdultAdeno-associated virus-2

MeSH Terms

DependovirusAdultAntibodies, ViralCapsidHemophilia BCross ReactionsFactor IXFollow-Up StudiesGenetic VectorsHumansInfusions, Intra-ArterialLiverLongitudinal StudiesMaleMiddle AgedGenetic TherapySignal TransductionTreatment OutcomeGene Transfer TechniquesHepatocytesYoung AdultAntibodies, Neutralizing

Keywords

Genetic enhancementMedicineFactor IXGene deliveryVirologyVector (molecular biology)Adeno-associated virusSerotypeVirusImmunologyCoagulationBiologyGeneInternal medicineRecombinant DNAAAVclinical gene therapygene therapyhemophilianeutralizing antibody

Sustainable Development Goals

SDG 0: Good health and well-being

Additional file 2 of In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin

10.6084/m9.figshare.25893966.v1figshare

Additional file 2 of In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin

10.6084/m9.figshare.25893966figshare

Additional file 1 of In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin

10.6084/m9.figshare.25893815.v1figshare

Additional file 1 of In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin

10.6084/m9.figshare.25893815figshare

Additional file 4 of In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin

10.6084/m9.figshare.26724665.v1figshare