Bruce S. Weir
Genetics · 2002–2019
A researcher in the Science corpus: 10 papers; trusts 16 researchers and is trusted by 28 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 168 citations into it; #412 of 6,854 by trust here, #300 by citations
- Molecular Biology — 88 citations into it
- Statistics and Probability — 11 citations into it
- Ecology — 7 citations into it
- Evaluation & Benchmarks — 6 citations into it
Whom Bruce S. Weir trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Kent E. Holsinger
- François Rousset
- Thorsten B. H. Reusch
- James O. Berger
- Christian P. Robert
- A. Gómez
- Laurent Excoffier
- Alan E. Gelfand
- François Balloux
- J. Sévigny
Who trusts Bruce S. Weir overall
- J. Arnaud
- Devon E. Pearse
- Robin S. Waples
- Peter Beerli
- Eric Bazin
- A. Machordom
- S. Arnaud-Haond
- Patricio S. La Rosa
- P. Meirmans
- Michael Palczewski
Papers from Bruce S. Weir's perspective
Ordered by how strongly the researchers Bruce S. Weir trusts endorse each paper. Same corpus, a different order for every researcher.
- Sampling-Based Approaches to Calculating Marginal Densities
- A Human Genome Diversity Cell Line Panel (Science)
- A Genome-Scan Method to Identify Selected Loci Appropriate for Both Dominant and Codominant Markers: A Bayesian Perspective (Genetics)
- Inferences from Spatial Population Genetics
- Statistical Decision Theory and Bayesian Analysis, Second Edition
- Adaptive population divergence: markers, QTL and traits
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- The estimation of population differentiation with microsatellite markers (Molecular Ecology)
- The Bayesian choice : from decision-theoretic foundations to computational implementation
- Microsatellites reveal high population connectivity in eelgrass (Zostera marina) in two contrasting coastal areas
Their papers
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Recovery of trait heritability from whole genome sequence data (2019) — 222 citations
- Dominance genetic variation contributes little to the missing heritability for human complex traits. (2015) — 200 citations
- HIBAG – HLA Genotype Imputation with Attribute Bagging (2013) — 420 citations
- A high-performance computing toolset for relatedness and principal component analysis of SNP data (2012) — 2,314 citations
- Genome-partitioning of genetic variation for complex traits using common SNPs (2011) — 950 citations
- Genetics in geographically structured populations: defining, estimating and interpreting FST (2009) — 1,360 citations
- Truncated product method for combining P‐values (2002) — 555 citations
- Estimating F-statistics. (2002) — 1,000 citations