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Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder

Genomics(2021)10.1016/j.ygeno.2021.04.020Source: DataRank Database

Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder is a research paper published in Genomics (2021). On theSindex it has a DataRank of 0. It has been cited 6 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access6 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (7 grants)Impact (FWCI 0.30)OA: hybridTopics (31)IDs (PubMed, PMC, OpenAlex)Annotations (3)

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 (6)

Hosei Nakajima,Colleen M. Carlston ORCID,Hakan Özadam ORCID,Can Cenik ORCID,Elif Sarinay Cenik ORCID

Live enrichment

PubMed:33862179 PMC:PMC8266734 OpenAlex:https://openalex.org/W3153161271

NCI NIH HHS

Grant: R00 CA204522

NIGMS NIH HHS

Grant: R35 GM138340

NCI NIH HHS

Grant: K99 CA204522

University of Texas at Austin

NIH

Welch Foundation

Cancer Prevention and Research Institute of Texas

FWCI

0.30

Citation Percentile

0.5%

Citation Trend

2024

2025

hybridLicense: cc-by-nc-nd

journalhttps://www.sciencedirect.com/science/article/pii/S0888754321001476/pdf

publisherhttps://www.sciencedirect.com/science/article/pii/S0888754321001476/pdf

publisherhttps://api.elsevier.com/content/article/PII:S0888754321001476?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0888754321001476?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.ygeno.2021.04.020

Fields of Study

RNA modifications and cancerRNA Research and SplicingRNA and protein synthesis mechanismsAnemia, Diamond-BlackfanGenes, MitochondrialHumansMutationRNA SplicingRare DiseasesRibosomal Proteins

MeSH Terms

HumansMutationRibosomal ProteinsRNA SplicingAnemia, Diamond-BlackfanRare DiseasesGenes, Mitochondrial

Keywords

BiologyGeneticsPenetranceMendelian inheritanceRNA splicingIntronExpressivityGeneExonNon-Mendelian inheritanceRibosomal RNAMitochondrial DNARNAPhenotype

Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder

FAIR Checklist

Authors (6)

Funding (7 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)