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Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing

Human Molecular Genetics(2024)10.1093/hmg/ddae105Source: DataRank Database

Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing is a research paper published in Human Molecular Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 1 time.

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0DataRank · unranked

Scored on demand from live citation data

Open Access1 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 0.30)OA: greenTopics (33)IDs (PubMed, PMC, OpenAlex)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 (11)

Shamika Ketkar ORCID,Taotao Tan ORCID,Elizabeth G. Atkinson ORCID,Lindsay C. Burrage ORCID,Kim C. Worley ORCID

Live enrichment

PubMed:38970828 PMC:PMC11413644 OpenAlex:https://openalex.org/W4400380420

Department of Defense

Grant: W81XWH-18-1-0499

National Institute of Mental Health

Grant: K01MH121659

NIH/NIAMS

Grant: R01AR073284

NHGRI NIH HHS

Grant: R01 HG012869

Caroline Wiess Law Fund for Research in Molecular Medicine

ARCO Foundation Young Teacher-Investigator Fund at Baylor College of Medicine

FWCI

0.30

Citation Percentile

0.6%

Citation Trend

2025

greenLicense: https://academic.oup.com/pages/standard-publication-reuse-rights

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11413644/pdf/ddae105.pdf

publisherhttps://academic.oup.com/hmg/article-pdf/33/19/1643/59194269/ddae105.pdf

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11413644

journalhttps://doi.org/10.1093/hmg/ddae105

Fields of Study

Systemic Sclerosis and Related DiseasesRenal Diseases and GlomerulopathiesCeliac Disease Research and Management

MeSH Terms

NIMA-Related KinasesWhole Genome SequencingAdultFemaleFibroblastsHumansMaleMiddle AgedScleroderma, SystemicGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenome-Wide Association StudyDNA Copy Number Variations

Keywords

Candidate geneGenome-wide association studyGeneticsBiologyGeneCopy-number variationGenetic associationGenomeTranscriptomeSingle-nucleotide polymorphismMultiple sclerosisGenotypeImmunologyGene expressionSystemic SclerosisRare VariantsWhole Genome Sequencing

Sustainable Development Goals

SDG 0: Good health and well-being