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Severe anemia caused by dominant mutations in Krüppel-like factor 1 (KLF1)

Mutation Research/Reviews in Mutation Research(2020)10.1016/j.mrrev.2020.108336Source: DataRank Database

Severe anemia caused by dominant mutations in Krüppel-like factor 1 (KLF1) is a research paper published in Mutation Research/Reviews in Mutation Research (2020). On theSindex it has a DataRank of 0. It has been cited 18 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access18 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.90)OA: greenTopics (35)IDs (PubMed, PMC, OpenAlex)Annotations (1)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 (3)

James J. Bieker ORCID,Mirosława Siatecka ORCID,Klaudia Kulczyńska-Figurny ORCID

Live enrichment

PubMed:33339573 PMC:PMC10199782 OpenAlex:https://openalex.org/W3092568829

National Institutes of Health

Grant: DK046865

Narodowe Centrum Nauki

Grant: 2013/09/B/NZ1/01879

NIDDK NIH HHS

Grant: R01 DK046865

FWCI

0.90

Citation Percentile

0.7%

Citation Trend

2021

2022

2023

2024

2025

2026

greenLicense: https://doi.org/10.15223/policy-004

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10199782/pdf/nihms-1897047.pdf

publisherhttps://api.elsevier.com/content/article/PII:S1383574220300569?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1383574220300569?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/10199782

Fields of Study

Kruppel-like factors researchHemoglobinopathies and Related DisordersGenetic Syndromes and ImprintingAnemiaBinding SitesCell DifferentiationHumansKruppel-Like Transcription FactorsMutation, MissensePhenotype

MeSH Terms

AnemiaBinding SitesCell DifferentiationHumansPhenotypeMutation, MissenseKruppel-Like Transcription Factors

Keywords

GATA1Zinc fingerHaploinsufficiencyEctopic expressionBiologyGeneticsMutationTranscription factorMutantGeneHereditary spherocytosisPhenotypeCell biologyGene ExpressionKrüppel-like Factor 1 (Klf1)Congenital Dyserythropoietic AnemiaAberrant TranscriptionNan – Neonatal Anemia

Sustainable Development Goals

SDG 0: Good health and well-being