Hanna Julienne, Vincent Laville, Zachary R McCaw, Zihuai He, Vincent Guillemot, Carla Lasry, Andrey Ziyatdinov, Cyril Nerin, Amaury Vaysse, Pierre Lechat, Hervé Ménager, Wilfried Le Goff, Marie-Pierre Dube, Peter Kraft, Iuliana Ionita-Laza, Bjarni J Vilhjálmsson, Hugues Aschard. PLoS Genet 2021
Times Cited: 3
Times Cited: 3
Times Cited
Times Co-cited
Similarity
Mixed-model association for biobank-scale datasets.
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10 Years of GWAS Discovery: Biology, Function, and Translation.
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The UK Biobank resource with deep phenotyping and genomic data.
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Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
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A catalog of genetic loci associated with kidney function from analyses of a million individuals.
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Case-control association mapping by proxy using family history of disease.
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Mixed model with correction for case-control ascertainment increases association power.
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Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
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The Heritability of Autism Spectrum Disorder.
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Efficient toolkit implementing best practices for principal component analysis of population genetic data.
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Analysis of time-to-event for observational studies: Guidance to the use of intensity models.
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Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr.
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Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status.
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
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Genetic associations with human longevity at the APOE and ACE loci.
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The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.
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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
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Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
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A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.
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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
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Fast Algorithms for Conducting Large-Scale GWAS of Age-at-Onset Traits Using Cox Mixed-Effects Models.
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Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS).
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A mixed-model approach for genome-wide association studies of correlated traits in structured populations.
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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
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The Danish Psychiatric Central Research Register.
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
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Polygenic Risk and Progression to Bipolar or Psychotic Disorders Among Individuals Diagnosed With Unipolar Depression in Early Life.
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Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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Liability threshold modeling of case-control status and family history of disease increases association power.
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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
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Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture.
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A resource-efficient tool for mixed model association analysis of large-scale data.
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
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Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.