Gaurav Bhatia
Genetics · 2012–2017
A researcher in the Science corpus: 7 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 153 citations into it
- Statistics and Probability — 9 citations into it
Whom Gaurav Bhatia trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Gaurav Bhatia overall
Papers from Gaurav Bhatia's perspective
Ordered by how strongly the researchers Gaurav Bhatia trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Regression Shrinkage and Selection via the Lasso
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- The Ensembl Variant Effect Predictor
- The Elements of Statistical Learning
- Genomic selection: prediction of accuracy and maximisation of long term response (Genetica)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Integrative approaches for large-scale transcriptome-wide association studies (2015) — 2,212 citations
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
- Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia. (2016) — 370 citations
- Leveraging polygenic functional enrichment to improve GWAS power (2017) — 843 citations
- Estimating and interpreting FST: The impact of rare variants (2013) — 605 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations