Corrigendum: Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example is a research paper published in Frontiers in Genetics (2015). On theSindex it has a DataRank of 0.
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.
National Institutes of Health
Grant: 5K25DK097279-02
Understanding and predicting cardiac events in HD using real-time EHRs
National Institutes of Health
Grant: 1K23DK088942-01A1
Determinants of Insulin Mediated Glucose uptake in South Asians
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