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Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus

Annals of the Rheumatic Diseases(2022)10.1136/ard-2022-222795Source: DataRank Database

Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus is a research paper published in Annals of the Rheumatic Diseases (2022). On theSindex it has a DataRank of 0. It has been cited 32 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access32 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 2.44)OA: greenTopics (38)Linked Datasets (4)DataCite Reuse (4)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 (25)

Jian Zhao ORCID,Qing Sun ORCID,Xue Xu ORCID,Lei Wang ORCID,Ting Liu ORCID

Live enrichment

PubMed:35977808 OpenAlex:https://openalex.org/W4292117620

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Grant: NIH R21074691

NIAMS NIH HHS

Grant: P30 AR072582

NIAMS NIH HHS

Grant: P60 AR062755

NIAMS NIH HHS

Grant: R21 AR074691

FWCI

2.44

Citation Percentile

0.9%

Citation Trend

2023

2024

2025

2026

greenLicense: https://www.elsevier.com/legal/tdmrep-license

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10394691/pdf/nihms-1829042.pdf

publisherhttps://api.elsevier.com/content/article/PII:S0003496724087387?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0003496724087387?httpAccept=text/plain

publisherhttps://syndication.highwire.org/content/doi/10.1136/ard-2022-222795

Fields of Study

Polyamine Metabolism and ApplicationsLysosomal Storage Disorders ResearchGenomics and Rare DiseasesAnimalsChildFemaleHumansMaleMiceGenetic Predisposition to DiseaseHomozygoteLupus Erythematosus, SystemicSpermineGenetic Diseases, X-LinkedAcetyltransferasesDiamine N-Acetyltransferase

MeSH Terms

Diamine N-AcetyltransferaseAcetyltransferasesAnimalsChildFemaleHomozygoteHumansLupus Erythematosus, SystemicMaleSpermineGenetic Predisposition to DiseaseGenetic Diseases, X-LinkedMice

Keywords

MedicineImmunologyLupus erythematosusSystemic lupus erythematosusInternal medicineDiseaseAutoimmune DiseasesImmune System DiseasesLupus Erythematosus, Systemic

Sustainable Development Goals

SDG 0: Good health and well-being

Additional file 2 of The landscape of transcriptional profiles in human oocytes with different chromatin configurations

10.6084/m9.figshare.25801120.v1figshare

Additional file 2 of The landscape of transcriptional profiles in human oocytes with different chromatin configurations

10.6084/m9.figshare.25801120figshare

Additional file 1 of The landscape of transcriptional profiles in human oocytes with different chromatin configurations

10.6084/m9.figshare.25800977figshare

Additional file 1 of The landscape of transcriptional profiles in human oocytes with different chromatin configurations

10.6084/m9.figshare.25800977.v1figshare