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Author Details

Bruce S Weir
University of Washington
1968
210
59
PMIDPaper TitleJournal TitlePublished Year
37325613Perceptions of forensic scientists on statistical models, sequence data, and ethical implications for DNA evidence evaluations: A qualitative assessment.Forensic Sci Int Synerg2023
38011288An allele-sharing, moment-based estimator of global, population-specific and population-pair FST under a general model of population structure.PLoS Genet2023
34824382Rank-invariant estimation of inbreeding coefficients.Heredity (Edinb)2022
35430892How HLA diversity is apportioned: influence of selection and relevance to transplantation.Philos Trans R Soc Lond B Biol Sci2022
35817969From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill.Nat Genet2022
35869320Author Correction: From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill.Nat Genet2022
34937905Author Correction: Genetic relatedness analysis: modern data and new challenges.Nat Rev Genet2022
35165434Elephant genotypes reveal the size and connectivity of transnational ivory traffickers.Nat Hum Behav2022
33240273How Ancestry Influences the Chances of Finding Unrelated Donors: An Investigation in Admixed Brazilians.Front Immunol2020
31145877Stationary distribution of the linkage disequilibrium coefficient r<sup>2</sup>.Theor Popul Biol2019
31405996The Summer Institute in Statistical Genetics.Genetics2019
29288525Multi-allelic exact tests for Hardy-Weinberg equilibrium that account for gender.Mol Ecol Resour2018
30107060How to estimate kinship.Mol Ecol2018
29857959A response to "Likelihood ratio as weight of evidence: A closer look" by Lund and Iyer.Forensic Sci Int2018
30255141Combating transnational organized crime by linking multiple large ivory seizures to the same dealer.Sci Adv2018
30571773Doubling down on forensic twin studies.PLoS Genet2018
29467293Reply to Kardos et al.: Estimation of inbreeding depression from SNP data.Proc Natl Acad Sci U S A2018
29071737On the testing of Hardy-Weinberg proportions and equality of allele frequencies in males and females at biallelic genetic markers.Genet Epidemiol2018
28550018A Unified Characterization of Population Structure and Relatedness.Genetics2017
30345411New Method Application for Marker-Trait Association Studies in Plants: Partial Least Square Regression Aids Detection of Simultaneous Correlations.Agric Res Technol2017
28334390SeqArray-a storage-efficient high-performance data format for WGS variant calls.Bioinformatics2017
28273509The factor of 10 in forensic DNA match probabilities.Forensic Sci Int Genet2017
28374190A genome-wide study of Hardy-Weinberg equilibrium with next generation sequence data.Hum Genet2017
28747529Detection and quantification of inbreeding depression for complex traits from SNP data.Proc Natl Acad Sci U S A2017
27082756Population-specific FST values for forensic STR markers: A worldwide survey.Forensic Sci Int Genet2016
26482676Eigenanalysis of SNP data with an identity by descent interpretation.Theor Popul Biol2016
27071844Testing for Hardy-Weinberg equilibrium at biallelic genetic markers on the X chromosome.Heredity (Edinb)2016
26748518Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.Am J Hum Genet2016
26748516Model-free Estimation of Recent Genetic Relatedness.Am J Hum Genet2016
26805783Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.Am J Hum Genet2016
25683123Dominance genetic variation contributes little to the missing heritability for human complex traits.Am J Hum Genet2015
28794809SNPs and SNVs in forensic science.Forensic Sci Int Genet Suppl Ser2015
26377959Exact Inference for Hardy-Weinberg Proportions with Missing Genotypes: Single and Multiple Imputation.G3 (Bethesda)2015
26089357CONSERVATION. Genetic assignment of large seizures of elephant ivory reveals Africa's major poaching hotspots.Science2015
23712092HIBAG--HLA genotype imputation with attribute bagging.Pharmacogenomics J2014
25498943Letter to editor in response to editorial by Risinger et al.Sci Justice2014
23979933Imputation-based genomic coverage assessments of current human genotyping arrays.G3 (Bethesda)2013
24275226Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study.J Pain2013
24273615Interpreting Whole-Genome Marker Data.Stat Biosci2013
22346758Familial identification: population structure and relationship distinguishability.PLoS Genet2012
26405363Estimating F-statistics: A historical view.Philos Sci2012
23298449Variation in actual relationship among descendants of inbred individuals.Genet Res (Camb)2012
23060615A high-performance computing toolset for relatedness and principal component analysis of SNP data.Bioinformatics2012
23052040GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies.Bioinformatics2012
22864188DNA commission of the International Society of Forensic Genetics: Recommendations on the evaluation of STR typing results that may include drop-out and/or drop-in using probabilistic methods.Forensic Sci Int Genet2012
22901090A novel method to identify high order gene-gene interactions in genome-wide association studies: gene-based MDR.BMC Bioinformatics2012
22561516Detectable clonal mosaicism from birth to old age and its relationship to cancer.Nat Genet2012
22268511A population genetic database of cat breeds developed in coordination with a domestic cat STR multiplex.J Forensic Sci2012
21226974Variation in actual relationship as a consequence of Mendelian sampling and linkage.Genet Res (Camb)2011
22784568SNP-PRAGE: SNP-based parametric robust analysis of gene set enrichment.BMC Syst Biol2011
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University of Florida
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National Human Genome Research Institute, National Institutes of Health
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Institute of Molecular Bioscience, The University of Queensland
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National Human Genome Research Institute
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Chongqing Center for Disease Control and Prevention.
Co-authored papers 3
National Cancer Institute
Co-authored papers 3
National Cancer Institute, National Institutes of Health
Co-authored papers 3
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Center for Inherited Disease Research, Johns Hopkins School of Medicine
Co-authored papers 3
Broad Institute of MIT and Harvard
Co-authored papers 3
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Adaptive Biotechnologies
Co-authored papers 2
Fudan University
Co-authored papers 2
Wellcome Trust Sanger Institute
Co-authored papers 2
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
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