Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction
暂无分享,去创建一个
Clara Albiñana | Jakob Grove | John J. McGrath | Esben Agerbo | Naomi R. Wray | Thomas Werge | Anders D. Børglum | Preben Bo Mortensen | Florian Privé | Bjarni J. Vilhjálmsson | N. Wray | T. Werge | B. Vilhjálmsson | P. Mortensen | A. Børglum | J. Grove | E. Agerbo | C. Albiñana | F. Privé | J. Mcgrath
[1] M. Blum,et al. Making the most of Clumping and Thresholding for polygenic scores , 2019, bioRxiv.
[2] Ross M. Fraser,et al. Genetic studies of body mass index yield new insights for obesity biology , 2015, Nature.
[3] Pak Chung Sham,et al. Polygenic scores via penalized regression on summary statistics , 2016, bioRxiv.
[4] Alicia R. Martin,et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder , 2018, Nature Genetics.
[5] Gary D Bader,et al. Association analysis identifies 65 new breast cancer risk loci , 2017, Nature.
[6] Po-Ru Loh,et al. Multi-ethnic polygenic risk scores improve risk prediction in diverse populations , 2016, bioRxiv.
[7] Zachary F. Gerring,et al. Unraveling the genetic architecture of major depressive disorder: merits and pitfalls of the approaches used in genome-wide association studies , 2019, Psychological Medicine.
[8] A. Shabalin,et al. Polygenic risk scoring and prediction of mental health outcomes. , 2019, Current opinion in psychology.
[9] Anorexia Nervosa Genetics Initiative. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa , 2019 .
[10] Po-Ru Loh,et al. Mixed-model association for biobank-scale datasets , 2018, Nature Genetics.
[11] Ross M. Fraser,et al. Defining the role of common variation in the genomic and biological architecture of adult human height , 2014, Nature Genetics.
[12] Doug Speed,et al. MultiBLUP: improved SNP-based prediction for complex traits , 2014, Genome research.
[13] B. Neale,et al. Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics. , 2020, American journal of human genetics.
[14] Mary E. Haas,et al. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations , 2018, Nature Genetics.
[15] John P. Rice,et al. Identification of common genetic risk variants for autism spectrum disorder , 2019, Nature Genetics.
[16] Yun Li,et al. METAL: fast and efficient meta-analysis of genomewide association scans , 2010, Bioinform..
[17] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[18] Naomi R. Wray,et al. Improved polygenic prediction by Bayesian multiple regression on summary statistics , 2019, Nature Communications.
[19] A. Janssens,et al. Reflection on modern methods: Revisiting the area under the ROC Curve. , 2020, International journal of epidemiology.
[20] Matthew Stephens,et al. Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes , 2018, Nature Communications.
[21] John J. McGrath,et al. Efficient toolkit implementing best practices for principal component analysis of population genetic data , 2019, bioRxiv.
[22] G. Breen,et al. Multi-polygenic score approach to trait prediction , 2017, Molecular Psychiatry.
[23] J. Danesh,et al. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease , 2016 .
[24] Hunna J. Watson,et al. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa , 2019, Nature Genetics.
[25] Helen E. Parkinson,et al. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 , 2018, Nucleic Acids Res..
[26] G. Breen,et al. Evaluation of polygenic prediction methodology within a reference-standardized framework , 2020, bioRxiv.
[27] N. Wray,et al. A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment , 2019, Nature Neuroscience.
[28] Tanya M. Teslovich,et al. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans , 2017, Diabetes.
[29] M Erbe,et al. Improving accuracy of genomic predictions within and between dairy cattle breeds with imputed high-density single nucleotide polymorphism panels. , 2012, Journal of dairy science.
[30] Bonnie Berger,et al. Efficient Bayesian mixed model analysis increases association power in large cohorts , 2014 .
[31] P. Donnelly,et al. The UK Biobank resource with deep phenotyping and genomic data , 2018, Nature.
[32] M. Goddard. Genomic selection: prediction of accuracy and maximisation of long term response , 2009, Genetica.
[33] Tanya M. Teslovich,et al. Genetic evidence of assortative mating in humans , 2017, Nature Human Behaviour.
[34] Tian Ge,et al. Polygenic Prediction via Bayesian Regression and Continuous Shrinkage Priors , 2018 .
[35] P. Visscher,et al. Estimating missing heritability for disease from genome-wide association studies. , 2011, American journal of human genetics.
[36] M. Blum,et al. Efficient Implementation of Penalized Regression for Genetic Risk Prediction , 2018, Genetics.
[37] Stephan Ripke,et al. Improving genetic prediction by leveraging genetic correlations among human diseases and traits , 2018, Nature Communications.
[38] Warren W. Kretzschmar,et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression , 2017, Nature Genetics.
[39] P. Visscher,et al. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores , 2015, bioRxiv.
[40] Justin Zobel,et al. SparSNP: Fast and memory-efficient analysis of all SNPs for phenotype prediction , 2012, BMC Bioinformatics.
[41] P. Visscher,et al. GCTA: a tool for genome-wide complex trait analysis. , 2011, American journal of human genetics.
[42] Benjamin Neale,et al. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults Implications for Primary Prevention , 2019 .
[43] Josyf Mychaleckyj,et al. Robust relationship inference in genome-wide association studies , 2010, Bioinform..
[44] M. Daly,et al. The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders , 2017, Molecular Psychiatry.
[45] Andrey Ziyatdinov,et al. Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr , 2018, Bioinform..
[46] Melissa J. Green,et al. Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder , 2017, bioRxiv.
[47] Xiang Zhou,et al. Polygenic Modeling with Bayesian Sparse Linear Mixed Models , 2012, PLoS genetics.
[48] P. Visscher,et al. A comprehensive evaluation of polygenic score methods across cohorts in psychiatric disorders , 2020, medRxiv.
[49] Alicia R. Martin,et al. Clinical use of current polygenic risk scores may exacerbate health disparities , 2019, Nature Genetics.
[50] R. Marioni,et al. Edinburgh Research Explorer Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways , 2022 .
[51] N. Wray,et al. Research review: Polygenic methods and their application to psychiatric traits. , 2014, Journal of child psychology and psychiatry, and allied disciplines.
[52] P. Visscher,et al. The Genetic Interpretation of Area under the ROC Curve in Genomic Profiling , 2010, PLoS genetics.
[53] C. Spencer,et al. Biological Insights From 108 Schizophrenia-Associated Genetic Loci , 2014, Nature.
[54] Xiang Zhou,et al. Accurate and Scalable Construction of Polygenic Scores in Large Biobank Data Sets. , 2020, American journal of human genetics.
[55] Jack Euesden,et al. PRSice: Polygenic Risk Score software , 2014, Bioinform..
[56] Robert Karlsson,et al. RICOPILI: Rapid Imputation for COnsortias PIpeLIne , 2019, bioRxiv.
[57] S. A. Lambert,et al. The Polygenic Score Catalog: an open database for reproducibility and systematic evaluation , 2020, medRxiv.