Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation is a research paper published in Frontiers in Genetics (2020). On theSindex it has a DataRank of 0.470. It has been cited 22 times.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph β no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full β never from an abstract alone.
Base Score Contribution
0.470
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology βNational Cancer Institute
Grant: CA164944
National Cancer Institute
Grant: CA167551
National Cancer Institute
Grant: CA074800
National Cancer Institute
Grant: CA074783
National Cancer Institute
Grant: CA074794
National Health and Medical Research Council
Grant: ID1091211
National Health and Medical Research Council
Grant: ID1061779
NCI NIH HHS
Grant: U01 CA074783
NCI NIH HHS
Grant: U01 CA074794
NCI NIH HHS
Grant: UM1 CA167551
NCI NIH HHS
Grant: U24 CA074783
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Grant: R01 CA164944
NCI NIH HHS
Grant: U24 CA074800
NCI NIH HHS
Grant: U24 CA074794
NCI NIH HHS
Grant: U01 CA074800
NCI NIH HHS
Grant: U01 CA167551
National Institutes of Health
Grant: 5R01CA164944-03
Classifying DNA Mismatch Repair Gene Variants of Unknown Significance
National Health and Medical Research Council (NHMRC)
Grant: 1091211
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National Institutes of Health
Grant: 2U24CA074783-10
The Colon Cancer Family Registry: Ontario
National Institutes of Health
Grant: 5U01CA074800-08
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National Institutes of Health
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National Institutes of Health
Grant: 4UM1CA167551-04
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National Institutes of Health
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National Health and Medical Research Council (NHMRC)
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