Hilary K Finucane
Genetics · 2011–2023
A researcher in the Science corpus: 19 papers; trusts 9 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 477 citations into it; #4,648 of 6,854 by trust here, #154 by citations
- Molecular Biology — 258 citations into it
- Statistics and Probability — 20 citations into it
Whom Hilary K Finucane trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Joseph K. Pickrell
- Jian Yang
- Brendan K. Bulik-Sullivan
- George Davey Smith
- Po-Ru Loh
- Frank Dudbridge
- J. Stockman
- Alkes L Price
- Michael E. Goddard
- Matthew Stephens
Who trusts Hilary K Finucane overall
- Po-Ru Loh
- Evan A. Boyle
- Steven Gazal
- Yang I Li
- Gleb Kichaev
- Tian Ge
- Chia-Yen Chen
- Alicia R. Martin
- Florian Privé
- Brendan K. Bulik-Sullivan
Papers from Hilary K Finucane's perspective
Ordered by how strongly the researchers Hilary K Finucane 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)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Regression Shrinkage and Selection via the Lasso
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Accuracy of Predicting the Genetic Risk of Disease Using a Genome-Wide Approach (PLoS ONE)
- The Elements of Statistical Learning
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (Human Molecular Genetics)
- The human genome browser at UCSC.
Their papers
- Detecting Novel Associations in Large Datasets (2011) — 3,212 citations
- Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
- Genome-wide enhancer maps link risk variants to disease genes (2021) — 541 citations
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 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
- FinnGen provides genetic insights from a well-phenotyped isolated population (2023) — 3,553 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases (2020) — 305 citations
- Functionally-informed fine-mapping and polygenic localization of complex trait heritability (2019) — 341 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 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
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (2016) — 890 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
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 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