Po-Ru Loh
Genetics · 2014–2019
A researcher in the Science corpus: 16 papers; trusts 20 researchers and is trusted by 14 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 361 citations into it; #1,308 of 6,854 by trust here, #159 by citations
- Molecular Biology — 161 citations into it; #17,737 of 17,773 by trust here, #2,516 by citations
- Statistics and Probability — 12 citations into it
Whom Po-Ru Loh trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Sharon R. Browning
- Matthew Stephens
- Brian L. Browning
- Jonathan Marchini
- Bryan N. Howie
- Brendan K. Bulik-Sullivan
- Jian Yang
- Alkes L Price
- Xiaoping Zhou
- Paul Scheet
Who trusts Po-Ru Loh overall
- Longda Jiang
- Brian L. Browning
- Olivier Delaneau
- Gleb Kichaev
- Zhili Zheng
- T. Richardson
- Tian Ge
- Chia-Yen Chen
- Siddhartha Jaiswal
- Xiaowen Tian
Papers from Po-Ru Loh's perspective
Ordered by how strongly the researchers Po-Ru Loh 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)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- Regression Shrinkage and Selection via the Lasso
- Fast and accurate long-range phasing in a UK Biobank cohort
- Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Their papers
- Fast, sensitive, and accurate integration of single cell data with Harmony (2019) — 8,178 citations
- Next-generation genotype imputation service and methods (2016) — 3,622 citations
- Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
- Fast and accurate long-range phasing in a UK Biobank cohort (2015) — 338 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
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (2017) — 984 citations
- Linkage disequilibrium dependent architecture of human complex traits reveals action of negative selection (2016) — 192 citations
- Insights about clonal hematopoiesis from 8,342 mosaic chromosomal alterations (2018) — 342 citations
- Estimating cross-population genetic correlations of causal effect sizes (2018) — 68 citations
- Mixed model association for biobank-scale data sets (2018) — 737 citations
- Leveraging polygenic functional enrichment to improve GWAS power (2017) — 843 citations
- Reference-based phasing using the Haplotype Reference Consortium panel (2016) — 1,643 citations
- An Atlas of Genetic Correlations across Human Diseases and Traits (2015) — 4,075 citations
- LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies (2014) — 5,156 citations
- Efficient Bayesian mixed model analysis increases association power in large cohorts (2014) — 1,384 citations