M. Freund
Genetics · 2017
A researcher in the Science corpus: 2 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 44 citations into it
- Statistics and Probability — 5 citations into it
Whom M. Freund trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from M. Freund's perspective
Ordered by how strongly the researchers M. Freund trusts endorse each paper. Same corpus, a different order for every researcher.
- Regression Shrinkage and Selection via the Lasso
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (bioRxiv)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- False discovery control with p-value weighting
- Genotype imputation for genome-wide association studies (Nature reviews genetics)
- POSTERIOR PREDICTIVE ASSESSMENT OF MODEL FITNESS VIA REALIZED DISCREPANCIES
- UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age
- The Ensembl Variant Effect Predictor
Their papers
- Leveraging polygenic functional enrichment to improve GWAS power (2017) — 843 citations
- Probabilistic fine-mapping of transcriptome-wide association studies (2017) — 370 citations