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Author Details
Full Name
Xin Li
Affiliation
Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences
ORCID
Career Start Year
2013
Papers
16
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35588732
Integration of rare expression outlier-associated variants improves polygenic risk prediction.
Am J Hum Genet
2022
31123710
Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms.
Commun Biol
2019
31684996
Genetic regulation of gene expression and splicing during a 10-year period of human aging.
Genome Biol
2019
28719597
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.
Pharmacogenomics J
2018
27799337
Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active Export.
G3 (Bethesda)
2017
28394350
Population- and individual-specific regulatory variation in Sardinia.
Nat Genet
2017
28369037
The impact of structural variation on human gene expression.
Nat Genet
2017
29022581
The impact of rare variation on gene expression across tissues.
Nature
2017
27569549
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.
Am J Hum Genet
2016
27197214
Impact of the X Chromosome and sex on regulatory variation.
Genome Res
2016
25848752
Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse.
Nat Genet
2015
24270603
Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.
Nat Methods
2014
25251678
High-resolution transcriptome analysis with long-read RNA sequencing.
PLoS One
2014
25192044
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants.
Am J Hum Genet
2014
24786518
Allelic expression of deleterious protein-coding variants across human tissues.
PLoS Genet
2014
23755067
Detection and impact of rare regulatory variants in human disease.
Front Genet
2013
1 - 16 of 16
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