MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations is a dataset published in Nucleic Acids Research (2020). On theSindex it has a DataRank of 6.0, placing it in the top 3.3% of the data-sharing corpus. It has been cited 2,013 times, with 100 citing works in its 1-hop citation network. Its calibrated FAIR score is 65/100.
Ranks in the top 3% for downstream scientific impact
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
Full FAIR picture · advisory
This score predates the current agent — it came from the earlier rubric, which blended repository metadata into the number and asked the model for a rating rather than an evidenced verdict. Re-evaluate the paper to score it against the current standards-anchored criteria, where every verdict is backed by a quote from the full text.
DOI present
datacite=25, pmcid=True, pmid=True
OpenAlex id present
files/OA location present but not flagged OA
16 OA location(s)
linked_datasets=25, datacite=25
accessions=0, trials=0
license present (other-oa)
downloads=0
no version chain
is_dataset
Calibrated FAIR score — a parallel quality metric, independent of the DataRank citation score. See the full evaluation →
Base Score Contribution
1.1
From this paper's citation signal
Citation Network Contribution
4.8
From 100 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 100 citers.
National Institutes of Health
Grant: K00CA212468
National Institutes of Health
Grant: T32AG000222
National Institutes of Health
Grant: K08DK115881
National Institutes of Health
Grant: R01AR071942
National Institutes of Health
Grant: F32GM128259
National Institutes of Health
Grant: F32GM133047
National Institutes of Health
Grant: T32DK007028
National Institutes of Health
Grant: R35GM122455
Deutsche Forschungsgemeinschaft
Grant: 431313887
National Institutes of Health
Grant: 5K00CA212468-05
Molecular Determinants of Mitochondrial Genome Abundance and Integrity
Fundação para a Ciência e a Tecnologia, I.P.
Grant: ARTEMIS/0003/2013
Embedded Multi-core Systems for Mixed Criticality Applications inDynamic and Changeable Real-Time Environments
National Institutes of Health
Grant: 3T32DK007028-48S1
Training Program in Endocrinology
National Institutes of Health
Grant: 2R01AR071942-06A1
Biochemistry and molecular physiology of the mitochondrial calcium uniporter
National Institutes of Health
Grant: 5R35GM122455-05
Mitochondrial Parts, Pathways, and Pathogenesis
National Institutes of Health
Grant: 5K08DK115881-04
A METABOLIC BIOMARKER OF HEPATIC NADH/NAD+ RATIO
National Institutes of Health
Grant: 5T32AG000222-02
TRAINING IN THE MOLECULAR BIOLOGY OF NEURODEGENERATION
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
Fundação para a Ciência e a Tecnologia, I.P.
Grant: ARTEMIS/0002/2013
Embedded multi-core systems for mixed criticality applications in dynamic and changeable real-time environments
National Institutes of Health
Grant: 1F32GM128259-01
Elucidating the mechanism of hypoxia rescue of mitochondrial dysfunction
National Institutes of Health
Grant: 5F32GM133047-02
Characterizing the biochemical regulation of mitochondrial one-carbon metabolism
Fundação para a Ciência e a Tecnologia, I.P.
Grant: ARTEMIS/0001/2013
Embedded multi-core systems for mixed criticality applications in dynamic and changeable real-time environments
Dollis Huntington Endowment Fund for Cancer Research
Massachusetts General Hospital Department of Neurology
Howard Hughes Medical Institute
Jane Coffin Childs
FWCI
63.23
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 2 of Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients
Additional file 2 of Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients
Additional file 12 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 12 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 13 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 13 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 15 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 15 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 16 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 16 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 1 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 1 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 20 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 20 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 4 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 4 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 5 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 5 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 6 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins
Additional file 6 of The interactome of CLUH reveals its association to SPAG5 and its co-translational proximity to mitochondrial proteins