Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

Human Genetics(2022)10.1007/s00439-022-02444-xSource: DataRank Database

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene is a research paper published in Human Genetics (2022). On theSindex it has a DataRank of 0. It has been cited 26 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access26 citations

Download PDF

Cite:

Linked data & code

ensembl refsnp omim refseq

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)OA: hybridTopics (34)Linked Datasets (2)DataCite Reuse (2)IDs (PubMed, PMC)Annotations (4)

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)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (28)

Cindy Penney,Darren D. O’Rielly ORCID,Anne Griffin ORCID,Lara Kamal ORCID,Zippora Brownstein ORCID

Live enrichment

PubMed:35278131 PMC:PMC9035003

NIDCD NIH HHS

Grant: R01 DC011835

Canadian Institutes of Health Research

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5R01GM129325-08

ChimeraX -- Next Generation Visualization and Analysis Software for Multiscale Modeling

National Institutes of Health

Grant: 5R01DC011835-05

Gene Discovery for Hearing Loss in Middle East by Massively Parallel Sequencing

Genome Canada

Institute of Genetics

hybridLicense: CC BY

publisherhttps://link.springer.com/content/pdf/10.1007/s00439-022-02444-x.pdf

publisherhttps://link.springer.com/article/10.1007/s00439-022-02444-x/fulltext.html

Europe_PMChttps://europepmc.org/articles/PMC9035003

Europe_PMChttps://europepmc.org/articles/PMC9035003?pdf=render

https://doi.org/10.1007/s00439-022-02444-x

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciencesHumans3' Untranslated RegionsATP-Binding Cassette TransportersDeafnessHearing LossHearing Loss, SensorineuralMutationPedigreePhospholipidsRNA Splice Sites

MeSH Terms

HumansHearing LossDeafnessHearing Loss, SensorineuralPhospholipidsATP-Binding Cassette TransportersRNA Splice Sites3' Untranslated RegionsPedigreeMutation

Keywords

Hearing Loss, SensorineuralDeafnessPedigreeMutationHumansATP-Binding Cassette TransportersRNA Splice SitesHearing Loss3' Untranslated RegionsPhospholipidsOriginal Investigation

Additional file 1 of TMEM30A is essential for hair cell polarity maintenance in postnatal mouse cochlea

10.6084/m9.figshare.26577266.v1figshare

Additional file 1 of TMEM30A is essential for hair cell polarity maintenance in postnatal mouse cochlea

10.6084/m9.figshare.26577266figshare

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

FAIR Checklist

Authors (28)

Funding (6 grants)

Open Access

Topics

Linked Datasets (2)

Annotations (Europe PMC)