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Author Details

Xin Li
Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences
2013
16
13
PMIDPaper TitleJournal TitlePublished Year
35588732Integration of rare expression outlier-associated variants improves polygenic risk prediction.Am J Hum Genet2022
31123710Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms.Commun Biol2019
31684996Genetic regulation of gene expression and splicing during a 10-year period of human aging.Genome Biol2019
28719597Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.Pharmacogenomics J2018
27799337Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active Export.G3 (Bethesda)2017
28394350Population- and individual-specific regulatory variation in Sardinia.Nat Genet2017
28369037The impact of structural variation on human gene expression.Nat Genet2017
29022581The impact of rare variation on gene expression across tissues.Nature2017
27569549DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.Am J Hum Genet2016
27197214Impact of the X Chromosome and sex on regulatory variation.Genome Res2016
25848752Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse.Nat Genet2015
24270603Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.Nat Methods2014
25251678High-resolution transcriptome analysis with long-read RNA sequencing.PLoS One2014
25192044Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants.Am J Hum Genet2014
24786518Allelic expression of deleterious protein-coding variants across human tissues.PLoS Genet2014
23755067Detection and impact of rare regulatory variants in human disease.Front Genet2013
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