Olivier Delaneau

Research interests

Publications

• Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank

  Nature Genetics · 2023 · https://doi.org/10.1038/s41588-023-01415-w

• Efficient phasing and imputation of low-coverage sequencing data using large reference panels

  Nature Genetics · 2021 · https://doi.org/10.1038/s41588-020-00756-0

• Genotype imputation using the Positional Burrows Wheeler Transform

  PLoS Genetics · 2020 · https://doi.org/10.1371/journal.pgen.1009049

• Accurate, scalable and integrative haplotype estimation

  Nature Communications · 2019 · https://doi.org/10.1038/s41467-019-13225-y

• Chromatin three-dimensional interactions mediate genetic effects on gene expression

  Science · 2019 · https://doi.org/10.1126/science.aat8266

• The UK Biobank resource with deep phenotyping and genomic data

  Nature · 2018 · https://doi.org/10.1038/s41586-018-0579-z

• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

  Nature Communications · 2018 · https://doi.org/10.1038/s41467-018-03621-1

• A complete tool set for molecular QTL discovery and analysis

  Nature Communications · 2017 · https://doi.org/10.1038/ncomms15452

• Estimating the causal tissues for complex traits and diseases

  Nature Genetics · 2017 · https://doi.org/10.1038/ng.3981

• Genetic effects on gene expression across human tissues

  Nature · 2017 · https://doi.org/10.1038/nature24277

• Genome-wide genetic data on ~500,000 UK Biobank participants

  bioRxiv (Cold Spring Harbor Laboratory) · 2017 · 10.1101/166298

• Haplotype estimation for biobank-scale data sets

  Nature Genetics · 2016 · https://doi.org/10.1038/ng.3583

• The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

  Cell · 2016 · https://doi.org/10.1016/j.cell.2016.10.042

• A reference panel of 64,976 haplotypes for genotype imputation

  Nature Genetics · 2016 · 10.1038/ng.3643

• Fast and efficient QTL mapper for thousands of molecular phenotypes

  Bioinformatics · 2015 · https://doi.org/10.1093/bioinformatics/btv722

• Population Variation and Genetic Control of Modular Chromatin Architecture in Humans

  Cell · 2015 · https://doi.org/10.1016/j.cell.2015.08.001

• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

  The Lancet Respiratory Medicine · 2015 · https://doi.org/10.1016/s2213-2600(15)00283-0

• A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

  PLoS Genetics · 2014 · https://doi.org/10.1371/journal.pgen.1004234

• Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

  Nature Communications · 2014 · https://doi.org/10.1038/ncomms4934

• Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

  Nature Communications · 2014 · https://doi.org/10.1038/ncomms4934

• Haplotype Estimation Using Sequencing Reads

  The American Journal of Human Genetics · 2013 · https://doi.org/10.1016/j.ajhg.2013.09.002

• Improved whole-chromosome phasing for disease and population genetic studies

  Nature Methods · 2012 · https://doi.org/10.1038/nmeth.2307

• An integrated map of genetic variation from 1,092 human genomes

  Nature · 2012 · 10.1038/nature11632

• A linear complexity phasing method for thousands of genomes

  Nature Methods · 2011 · https://doi.org/10.1038/nmeth.1785

• Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played byHLAGenes (ANRS Genomewide Association Study 02)

  The Journal of Infectious Diseases · 2008 · https://doi.org/10.1086/596067

Current projects

No projects listed.