Olivier Delaneau
Reproducibility track record
1
assessed papers
100/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
139
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
Eleonora Porcu 1Stefania Bandinelli 1Chiara Auwerx 1Uwe Völker 1Federico Santoni 1Alexander Teumer 1Andres Metspalu 1Toshiko Tanaka 1Zoltán Kutalik 1Antoine Weihs 1
Institutions
SIB Swiss Institute of Bioinformatics 1University of Lausanne 1University of Tartu 1University of Exeter 1Universitätsmedizin Greifswald 1École Polytechnique Fédérale de Lausanne 1
Geography (author institutions)
CH 1EE 1GB 1DE 1IT 1US 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (193)
Request a reproduction →1 assessed by us (1 reproduced) · 192 not yet assessed — every PubMed paper on record, linked below.
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Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource ↗Nature · 2026 · PMID 42310464not yet assessed
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Population-scale repeat expansions elucidate disease risk and brain atrophy ↗Nature · 2026 · PMID 41951733not yet assessed
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Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries ↗Nature Communications · 2026 · PMID 41735279not yet assessed
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Germline Variants in Chronic Pancreatitis-Associated Genes and Risk of Pancreatic Ductal Adenocarcinoma ↗Clinical Gastroenterology and Hepatology · 2026 · PMID 42019862not yet assessed
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Polygenic scores for risk of pancreatic ductal adenocarcinoma: evaluation of novel and published models ↗npj Precision Oncology · 2026 · PMID 42203843not yet assessed
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Separating direct, indirect, and parent-of-origin genetic effects in the human population ↗Cell Genomics · 2026 · PMID 42263682not yet assessed
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Benchmarking imputation accuracy in the presence or absence of a reference panel ↗Molecular Biology and Evolution · 2026 · PMID 41967458not yet assessed
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Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants ↗Science · 2025 · PMID 39913582not yet assessed
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Parent-of-origin effects on complex traits in up to 236,781 individuals ↗Nature · 2025 · PMID 40770099not yet assessed
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Noncoding rare variant associations with blood traits in 166,740 UK Biobank genomes ↗Nature Genetics · 2025 · PMID 40770577not yet assessed
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Genomic Ascertainment of <i>CHEK2</i> -Related Cancer Predisposition ↗JAMA Network Open · 2025 · PMID 41396600not yet assessed
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Polygenic risk score prediction accuracy convergence ↗Human Genetics and Genomics Advances · 2025 · PMID 40375557not yet assessed
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Variant Classification Using Proteomics‐Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target Discovery ↗Genetic Epidemiology · 2025 · PMID 41178319not yet assessed
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Separating direct, indirect and parent-of-origin genetic effects in the human population ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025 · PMID 40909755not yet assessed
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Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals ↗Nature · 2025 · PMID 39779867not yet assessed
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Parent-of-Origin inference and its role in the genetic architecture of complex traits: evidence from ~265,000 individuals ↗Research Square · 2025not yet assessed
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Variant Classification Using Proteomics-Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target Discovery ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025not yet assessed
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Population genomics of post-glacial western Eurasia ↗Nature · 2024 · PMID 38200295not yet assessed
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100 ancient genomes show repeated population turnovers in Neolithic Denmark ↗Nature · 2024 · PMID 38200294not yet assessed
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A deep catalogue of protein-coding variation in 983,578 individuals ↗Nature · 2024 · PMID 38768635not yet assessed
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Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk ↗JAMA Cardiology · 2024 · PMID 38922602not yet assessed
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Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank ↗Nature Genetics · 2024 · PMID 39322778not yet assessed
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Ancient Rapanui genomes reveal resilience and pre-European contact with the Americas ↗Nature · 2024 · PMID 39261618not yet assessed
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Assessing the impact of post-mortem damage and contamination on imputation performance in ancient DNA ↗Scientific Reports · 2024 · PMID 38486065not yet assessed
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Improving population scale statistical phasing with whole-genome sequencing data ↗PLoS Genetics · 2024 · PMID 38959269not yet assessed
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A resampling-based approach to share reference panels ↗Nature Computational Science · 2024 · PMID 38745108not yet assessed
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SURFBAT: a surrogate family based association test building on large imputation reference panels ↗G3 Genes Genomes Genetics · 2024 · PMID 39657733not yet assessed
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Parent-of-Origin inference and its role in the genetic architecture of complex traits: evidence from ∼265,000 individuals ↗medRxiv · 2024not yet assessed
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Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City ↗Nature · 2024 · PMID 38332034not yet assessed
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Publisher Correction: Population genomics of post-glacial western Eurasia ↗Nature · 2024 · PMID 38238538not yet assessed
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Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank ↗Nature Genetics · 2023 · PMID 37386248not yet assessed
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Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes ↗Nature Genetics · 2023 · PMID 37386250not yet assessed
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Imputation of ancient human genomes ↗Nature Communications · 2023 · PMID 37339987not yet assessed
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Genotyping, sequencing and analysis of 140,000 adults from Mexico City ↗Nature · 2023 · PMID 37821707not yet assessed
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A large meta-analysis identifies genes associated with anterior uveitis ↗Nature Communications · 2023 · PMID 37949852not yet assessed
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Mapache: a flexible pipeline to map ancient DNA ↗Bioinformatics · 2023 · PMID 36637197not yet assessed
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Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks ↗Communications Biology · 2023 · PMID 36697501not yet assessed
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The HLA-B*57:01 allele corresponds to a very large MHC haploblock likely explaining its massive effect for HIV-1 elite control ↗Frontiers in Immunology · 2023 · PMID 38146367not yet assessed
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Genetic variation in cis-regulatory domains suggests cell type-specific regulatory mechanisms in immunity ↗Communications Biology · 2023 · PMID 36977773not yet assessed
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Multimodal single cell analysis infers widespread enhancer co-activity in a lymphoblastoid cell line ↗Communications Biology · 2023 · PMID 37237005not yet assessed
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Exploiting parallelization in positional Burrows–Wheeler transform (PBWT) algorithms for efficient haplotype matching and compression ↗Bioinformatics Advances · 2023 · PMID 36908398not yet assessed
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Author Correction: Pan-cancer analysis of whole genomes ↗Nature · 2023 · PMID 36697834not yet assessed
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Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes ↗Nature · 2023 · PMID 36697832not yet assessed
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Author Correction: The repertoire of mutational signatures in human cancer ↗Nature · 2023 · PMID 36697836not yet assessed
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Non-coding rare variant associations with blood traits on 166 740 UK Biobank genomes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Author Correction: The evolutionary history of 2,658 cancers ↗Nature · 2023 · PMID 36697833not yet assessed
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Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing ↗Nature Genetics · 2023 · PMID 36944733not yet assessed
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Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition ↗Nature Genetics · 2023 · PMID 36944736not yet assessed
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Author Correction: Patterns of somatic structural variation in human cancer genomes ↗Nature · 2023 · PMID 36697835not yet assessed
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Polygenic risk score prediction accuracy convergence ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers ↗Nature Genetics · 2023 · PMID 36944732not yet assessed
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A resampling-based approach to share reference panels ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Author Correction: Genomic basis for RNA alterations in cancer ↗Nature · 2023 · PMID 36697831not yet assessed
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Author Correction: The landscape of viral associations in human cancers ↗Nature Genetics · 2023 · PMID 36944734not yet assessed
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Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer ↗Nature Genetics · 2023 · PMID 36944735not yet assessed
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SURFBAT: a surrogate family-based association test building on large imputation reference panels ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Author Correction: Butler enables rapid cloud-based analysis of thousands of human genomes ↗Nature Biotechnology · 2023 · PMID 36944844not yet assessed
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42 imputed downsampled ancient human genomes ↗Zenodo (CERN European Organization for Nuclear Research) · 2023not yet assessed
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Improving population scale statistical phasing with whole-genome sequencing data ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Assessing the impact of post-mortem damage and contamination on imputation performance in ancient DNA ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Parent-of-Origin inference for biobanks ↗Nature Communications · 2022 · PMID 36335127not yet assessed
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Shared regulation and functional relevance of local gene co-expression revealed by single cell analysis ↗Communications Biology · 2022 · PMID 36028576not yet assessed
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XSI—a genotype compression tool for compressive genomics in large biobanks ↗Bioinformatics · 2022 · PMID 35748697not yet assessed
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GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing ↗Nucleic Acids Research · 2022 · PMID 35176773not yet assessed
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Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy ↗Nature Communications · 2022 · PMID 36042219not yet assessed
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Population genomics of postglacial western eurasia ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Imputation of ancient genomes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Author Correction: Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis ↗Communications Biology · 2022 · PMID 36482178not yet assessed
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Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank ↗Research Square · 2022not yet assessed
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Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns ↗Nature Communications · 2022 · PMID 36481665not yet assessed
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Genetic variation in correlated regulatory region of Immunity ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Author Correction: Pathway and network analysis of more than 2500 whole cancer genomes ↗Nature Communications · 2022 · PMID 36481610not yet assessed
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Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours ↗Nature Communications · 2022 · PMID 36481612not yet assessed
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Genetic variation in correlated regulatory regions of immunity ↗Research Square · 2022not yet assessed
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Mapache: a flexible pipeline to map ancient DNA ↗arXiv (Cornell University) · 2022not yet assessed
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Widespread enhancer co-activity identified by multimodal single cell analysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer ↗Nature Communications · 2022 · PMID 36481818not yet assessed
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Author Correction: High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations ↗Nature Communications · 2022 · PMID 36481652not yet assessed
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Author Correction: Integrative pathway enrichment analysis of multivariate omics data ↗Nature Communications · 2022 · PMID 36481658not yet assessed
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Author Correction: Inferring structural variant cancer cell fraction ↗Nature Communications · 2022 · PMID 36481724not yet assessed
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Author Correction: Combined burden and functional impact tests for cancer driver discovery using DriverPower ↗Nature Communications · 2022 · PMID 36481739not yet assessed
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Author Correction: Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig ↗Nature Communications · 2022 · PMID 36482170not yet assessed
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Mapping the human genetic architecture of COVID-19 ↗Nature · 2021 · PMID 34237774not yet assessed
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Efficient phasing and imputation of low-coverage sequencing data using large reference panels ↗Nature Genetics · 2021 · PMID 33414550not yet assessed
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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptomeNature Communications · 2021 · PMID 34561431L1 100/100
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The genomic history of the Aegean palatial civilizations ↗Cell · 2021 · PMID 33930288not yet assessed
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The molecular basis, genetic control and pleiotropic effects of local gene co-expression ↗Nature Communications · 2021 · PMID 34376650not yet assessed
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Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studies ↗Scientific Reports · 2021 · PMID 33542415not yet assessed
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Publisher Correction: Efficient phasing and imputation of low-coverage sequencing data using large reference panels ↗Nature Genetics · 2021 · PMID 33473199not yet assessed
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Parent-of-origin effects in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Shared regulation and functional relevance of local gene co-expression revealed by single cell analysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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not yet assessed
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Parent-of-origin effects in the UK Biobank ↗Research Square · 2021not yet assessed
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The repertoire of mutational signatures in human cancer ↗Nature · 2020 · PMID 32025018not yet assessed
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Pan-cancer analysis of whole genomes ↗Nature · 2020 · PMID 32025007not yet assessed
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The evolutionary history of 2,658 cancers ↗Nature · 2020 · PMID 32025013not yet assessed
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Patterns of somatic structural variation in human cancer genomes ↗Nature · 2020 · PMID 32025012not yet assessed
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Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing ↗Nature Genetics · 2020 · PMID 32025003not yet assessed
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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes ↗Nature · 2020 · PMID 32025015not yet assessed
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Comprehensive molecular characterization of mitochondrial genomes in human cancers ↗Nature Genetics · 2020 · PMID 32024997not yet assessed
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Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition ↗Nature Genetics · 2020 · PMID 32024998not yet assessed
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Genomic basis for RNA alterations in cancer ↗Nature · 2020 · PMID 32025019not yet assessed
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The landscape of viral associations in human cancers ↗Nature Genetics · 2020 · PMID 32025001not yet assessed
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Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer ↗Nature Genetics · 2020 · PMID 32024999not yet assessed
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A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns ↗Nature Communications · 2020 · PMID 32024849not yet assessed
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Integrative pathway enrichment analysis of multivariate omics data ↗Nature Communications · 2020 · PMID 32024846not yet assessed
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Genotype imputation using the Positional Burrows Wheeler Transform ↗PLoS Genetics · 2020 · PMID 33196638not yet assessed
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Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis ↗Communications Biology · 2020 · PMID 32024996not yet assessed
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Divergent mutational processes distinguish hypoxic and normoxic tumours ↗Nature Communications · 2020 · PMID 32024819not yet assessed
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Genomic footprints of activated telomere maintenance mechanisms in cancer ↗Nature Communications · 2020 · PMID 32024817not yet assessed
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Sex differences in oncogenic mutational processes ↗Nature Communications · 2020 · PMID 32859912not yet assessed
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Pathway and network analysis of more than 2500 whole cancer genomes ↗Nature Communications · 2020 · PMID 32024854not yet assessed
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High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations ↗Nature Communications · 2020 · PMID 32024823not yet assessed
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Combined burden and functional impact tests for cancer driver discovery using DriverPower ↗Nature Communications · 2020 · PMID 32024818not yet assessed
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Genetic effects on gene expression across human tissues ↗UNC Libraries · 2020not yet assessed
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Inferring structural variant cancer cell fraction ↗Nature Communications · 2020 · PMID 32024845not yet assessed
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples ↗Nature Communications · 2020 · PMID 32958763not yet assessed
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Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig ↗Nature Communications · 2020 · PMID 32024834not yet assessed
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Butler enables rapid cloud-based analysis of thousands of human genomes ↗Nature Biotechnology · 2020 · PMID 32024987not yet assessed
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Efficient phasing and imputation of low-coverage sequencing data using large reference panels ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs ↗medRxiv · 2020 · PMID 32766602not yet assessed
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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome ↗medRxiv · 2020not yet assessed
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The molecular basis, genetic control and pleiotropic effects of local gene co-expression ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples ↗Nature Communications · 2020 · PMID 33257764not yet assessed
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not yet assessed
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A reference panel of 64,976 haplotypes for genotype imputation ↗UNC Libraries · 2020not yet assessed
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Accurate, scalable and integrative haplotype estimation ↗Nature Communications · 2019 · PMID 31780650not yet assessed
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Chromatin three-dimensional interactions mediate genetic effects on gene expression ↗Science · 2019 · PMID 31048460not yet assessed
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A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment ↗Nature Neuroscience · 2019 · PMID 30692689not yet assessed
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Expression estimation and eQTL mapping for HLA genes with a personalized pipeline ↗PLoS Genetics · 2019 · PMID 31009447not yet assessed
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Genotype imputation using the Positional Burrows Wheeler Transform ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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odelaneau/clomics: Clomics ↗Zenodo (CERN European Organization for Nuclear Research) · 2019not yet assessed
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Processed data for the study on "Chromatin 3D interactions mediate genetic effects on gene expression" ↗Figshare · 2019not yet assessed
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Processed data for the study on "Chromatin 3D interactions mediate genetic effects on gene expression" ↗Zenodo (CERN European Organization for Nuclear Research) · 2019not yet assessed
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The UK Biobank resource with deep phenotyping and genomic data ↗Nature · 2018 · PMID 30305743not yet assessed
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Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics ↗Nature Communications · 2018 · PMID 29739930not yet assessed
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Integrative haplotype estimation with sub-linear complexity ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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Expression estimation and eQTL mapping for HLA genes with a personalized pipeline ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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Genetic effects on gene expression across human tissues ↗Nature · 2017 · PMID 29022597not yet assessed
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A complete tool set for molecular QTL discovery and analysis ↗Nature Communications · 2017 · PMID 28516912not yet assessed
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Estimating the causal tissues for complex traits and diseases ↗Nature Genetics · 2017 · PMID 29058715not yet assessed
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Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues ↗Nature Genetics · 2017 · PMID 29058714not yet assessed
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The effect of genetic variation on promoter usage and enhancer activity ↗Nature Communications · 2017 · PMID 29116076not yet assessed
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<i>MBV</i>: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets ↗Bioinformatics · 2017 · PMID 28186259not yet assessed
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Genome-wide genetic data on ~500,000 UK Biobank participants ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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Germline determinants of the somatic mutation landscape in 2,642 cancer genomes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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Intra- and inter-chromosomal chromatin interactions mediate genetic effects on regulatory networks ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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Narrow-sense heritability estimation of complex traits using identity-by-descent information ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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Hundreds of Putative Non-Coding Cis-Regulatory Drivers in Chronic Lymphocytic Leukaemia and Skin Cancer ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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A reference panel of 64,976 haplotypes for genotype imputation ↗Nature Genetics · 2016 · PMID 27548312not yet assessed
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The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease ↗Cell · 2016 · PMID 27863252not yet assessed
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Haplotype estimation for biobank-scale data sets ↗Nature Genetics · 2016 · PMID 27270105not yet assessed
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Phasing for medical sequencing using rare variants and large haplotype reference panels ↗Bioinformatics · 2016 · PMID 27153703not yet assessed
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An integrated map of structural variation in 2,504 human genomes_supplement2016not yet assessed
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A complete tool set for molecular QTL discovery and analysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
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Estimating the causal tissues for complex traits and diseases ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
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Predicting causal variants affecting expression using whole genome sequence and RNA-seq from multiple human tissues ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
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A global reference for human genetic variation ↗Nature · 2015 · PMID 26432245not yet assessed
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Fast and efficient QTL mapper for thousands of molecular phenotypes ↗Bioinformatics · 2015 · PMID 26708335not yet assessed
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A global reference for human genetic variationCivil War Book Review · 2015not yet assessed
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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 · PMID 26423011not yet assessed
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Population Variation and Genetic Control of Modular Chromatin Architecture in Humans ↗Cell · 2015 · PMID 26300124not yet assessed
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Identification of Genes Whose Expression Profile Is Associated with Non-Progression towards AIDS Using eQTLs ↗PLoS ONE · 2015 · PMID 26367535not yet assessed
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Fast and efficient QTL mapper for thousands of molecular phenotypes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
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A reference panel of 64,976 haplotypes for genotype imputation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
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A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness ↗PLoS Genetics · 2014 · PMID 24743097not yet assessed
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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel ↗Nature Communications · 2014 · PMID 25653097not yet assessed
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Biased Allelic Expression in Human Primary Fibroblast Single Cells ↗The American Journal of Human Genetics · 2014 · PMID 25557783not yet assessed
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Evidence After Imputation for a Role of MICA Variants in Nonprogression and Elite Control of HIV Type 1 Infection ↗The Journal of Infectious Diseases · 2014 · PMID 24939907not yet assessed
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Haplotype Estimation Using Sequencing Reads ↗The American Journal of Human Genetics · 2013 · PMID 24094745not yet assessed
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Association Study of Common Genetic Variants and HIV-1 Acquisition in 6,300 Infected Cases and 7,200 Controls ↗PLoS Pathogens · 2013 · PMID 23935489not yet assessed
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An integrated map of genetic variation from 1,092 human genomes ↗Nature · 2012 · PMID 23128226not yet assessed
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Improved whole-chromosome phasing for disease and population genetic studies ↗Nature Methods · 2012 · PMID 23269371not yet assessed
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A Genome-Wide Association Study in Caucasian Women Points Out a Putative Role of the STXBP5L Gene in Facial Photoaging ↗Journal of Investigative Dermatology · 2012 · PMID 23223146not yet assessed
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Multicohort Genomewide Association Study Reveals a New Signal of Protection Against HIV-1 Acquisition ↗The Journal of Infectious Diseases · 2012 · PMID 22362864not yet assessed
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Haplotype Inference ↗Methods in molecular biology · 2012 · PMID 22665282not yet assessed
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A linear complexity phasing method for thousands of genomes ↗Nature Methods · 2011 · PMID 22138821not yet assessed
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CD39/Adenosine Pathway Is Involved in AIDS Progression ↗PLoS Pathogens · 2011 · PMID 21750674not yet assessed
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Genome-Wide Association Study Implicates PARD3B-Based AIDS Restriction ↗The Journal of Infectious Diseases · 2011 · PMID 21502085not yet assessed
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Genome-Wide Association Scan in HIV-1-Infected Individuals Identifying Variants Influencing Disease Course ↗PLoS ONE · 2011 · PMID 21811574not yet assessed
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Multiple‐Cohort Genetic Association Study Reveals CXCR6 as a New Chemokine Receptor Involved in Long‐Term Nonprogression to AIDS ↗The Journal of Infectious Diseases · 2010 · PMID 20704485not yet assessed
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Screening Low-Frequency SNPS From Genome-Wide Association Study Reveals a New Risk Allele for Progression to AIDS ↗JAIDS Journal of Acquired Immune Deficiency Syndromes · 2010 · PMID 21107268not yet assessed
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Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03) ↗The Journal of Infectious Diseases · 2009 · PMID 19754311not yet assessed
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Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played by<i>HLA</i>Genes (ANRS Genomewide Association Study 02) ↗The Journal of Infectious Diseases · 2008 · PMID 19115949not yet assessed
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Shape-IT: new rapid and accurate algorithm for haplotype inference ↗BMC Bioinformatics · 2008 · PMID 19087329not yet assessed
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Développement de logiciels d'halotypage et applications2008not yet assessed
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ISHAPE: new rapid and accurate software for haplotyping ↗BMC Bioinformatics · 2007 · PMID 17573965not yet assessed
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Computation of haplotypes on SNPs subsets: advantage of the "global method" ↗BMC Genetics · 2006 · PMID 17067372not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Delaneau O” paper on PubMed ↗