Automated Author ProfileKim, Michelle
Kim, Michelle
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 6.2 (sum of 4 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Table S3. Curated set of 3036 disease-associated loci from the NHGRI-EBI GWAS Catalog. (TXT 798 kb)
Authors
- Kim, Michelle ;
- Patel, Kane ;
- Teng, Andrew ;
- Berens, Ali ;
- Lachance, Joseph
Table S3. Curated set of 3036 disease-associated loci from the NHGRI-EBI GWAS Catalog. (TXT 798 kb)
Authors
- Kim, Michelle ;
- Patel, Kane ;
- Teng, Andrew ;
- Berens, Ali ;
- Lachance, Joseph
: Table S4. Representative set of loci from GWAS simulations. Simulation parameters: technology = Affymetrix Genome-Wide Human SNP Array 6.0, sample size = 3500 cases and 3500 controls, mode of inheritance = additive genetic effects, p value cutoff = 10-5, prevalence = 10%, study cohort = EUR, genotype relative risks vary symmetrically across populations. (TXT 245 kb)
Authors
- Kim, Michelle ;
- Patel, Kane ;
- Teng, Andrew ;
- Berens, Ali ;
- Lachance, Joseph
: Table S4. Representative set of loci from GWAS simulations. Simulation parameters: technology = Affymetrix Genome-Wide Human SNP Array 6.0, sample size = 3500 cases and 3500 controls, mode of inheritance = additive genetic effects, p value cutoff = 10-5, prevalence = 10%, study cohort = EUR, genotype relative risks vary symmetrically across populations. (TXT 245 kb)
Authors
- Kim, Michelle ;
- Patel, Kane ;
- Teng, Andrew ;
- Berens, Ali ;
- Lachance, Joseph