Han Chen
2000
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educated at: Boston University, Columbia University, Tsinghua University
occupation: researcher
Articles 43
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Metabolomic Associations of Asthma in the Hispanic Community Health Study/Study of Latinos
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Efficient gene-environment interaction tests for large biobank-scale sequencing studies
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Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans
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Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
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Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level
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Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies
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Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration
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Management and reproductive counseling in cervical, caesarean scar and interstitial ectopic pregnancies over 11 years: identifying the need for a modern management algorithm
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A unified method for rare variant analysis of gene-environment interactions
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Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries
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Genetic association testing using the GENESIS R/Bioconductor package
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Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies
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A powerful and data-adaptive test for rare-variant-based gene-environment interaction analysis
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Whole exome sequencing analysis in severe chronic obstructive pulmonary disease
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Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies
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Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment
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Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.
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The genetic architecture of type 2 diabetes
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Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models
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Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease
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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms
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Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses
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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
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Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci
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Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans
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Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
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Test for rare variants by environment interactions in sequencing association studies
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Rare Variant Association Analysis: Beyond Collapsing Approaches
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Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
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Testing genetic association with rare and common variants in family data
Human - wd:Q37632693