Olivier Delaneau

Genetics · 2011–2021

A researcher in the Science corpus: 19 papers; trusts 19 researchers and is trusted by 19 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 314 citations into it; #793 of 6,854 by trust here, #71 by citations
• Molecular Biology — 185 citations into it

Whom Olivier Delaneau trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Bryan N. Howie
2. Jonathan Marchini
3. Heng Li
4. Matthew Stephens
5. Brian L. Browning
6. Sharon R. Browning
7. Yun Li
8. Na Li
9. Jean-François Zagury
10. Po-Ru Loh

Who trusts Olivier Delaneau overall

1. Brian L. Browning
2. Marcel Martin
3. Murray Patterson
4. Xiaowen Tian
5. Jonathan Marchini
6. Po-Ru Loh
7. Peter Edge
8. Yingxiao Zhou
9. Matthew D. Rasmussen
10. Leo Speidel

Papers from Olivier Delaneau's perspective

Ordered by how strongly the researchers Olivier Delaneau trusts endorse each paper. Same corpus, a different order for every researcher.

1. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
2. MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
3. Detection of sharing by descent, long-range phasing and haplotype imputation (Nature Genetics)
4. Fast and accurate long-range phasing in a UK Biobank cohort
5. A comparison of bayesian methods for haplotype reconstruction from population genotype data. (American Journal of Human Genetics)
6. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
7. Exome sequencing as a tool for Mendelian disease gene discovery
8. Haplotype phasing: Existing methods and new developments (Nature reviews genetics)
9. Improved whole-chromosome phasing for disease and population genetic studies (Nature Methods)
10. Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)

Their papers

• A global reference for human genetic variation (2015) — 16,925 citations
• Genetic effects on gene expression across human tissues (2017) — 3,717 citations
• The UK Biobank resource with deep phenotyping and genomic data (2018) — 7,745 citations
• Genome-wide genetic data on ~500,000 UK Biobank participants (2017) — 696 citations
• Accurate, scalable and integrative haplotype estimation (2019) — 557 citations
• Haplotype estimation for biobank scale datasets (2016) — 226 citations
• Haplotype estimation using sequencing reads. (2013) — 388 citations
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
• Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
• Efficient phasing and imputation of low-coverage sequencing data using large reference panels (2020) — 374 citations
• A complete tool set for molecular QTL discovery and analysis (2016) — 326 citations
• Allelic Landscape of Human Blood Cell Trait Variation and Links (2016)
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) — 386 citations
• Fast and efficient QTL mapper for thousands of molecular phenotypes (2015) — 536 citations
• Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel (2014) — 415 citations
• A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness (2014) — 602 citations
• Improved whole-chromosome phasing for disease and population genetic studies (2013) — 535 citations
• An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
• A linear complexity phasing method for thousands of genomes (2011) — 1,855 citations