about
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesStrategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityThe genetic architecture of type 2 diabetesTesting genetic association with rare and common variants in family data.Sequence kernel association test for survival traits.Comparison of statistical approaches to rare variant analysis for quantitative traits.Incorporating gene-environment interaction in testing for association with rare genetic variantsGenetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociRare genetic variant analysis on blood pressure in related samplesNo interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels.Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.Test for rare variants by environment interactions in sequencing association studiesA genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistanceControl for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed ModelsSequence kernel association test for quantitative traits in family samplesExome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary DiseaseTransancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses.Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.A method of moments estimator for random effect multivariate meta-analysisGenetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment.Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.Rare Variant Association Analysis: Beyond Collapsing ApproachesAdmixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americansAssociations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepA powerful and data-adaptive test for rare-variant-based gene-environment interaction analysisWhole exome sequencing analysis in severe chronic obstructive pulmonary diseaseSequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation LevelEfficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesMulti-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep durationManagement and reproductive counseling in cervical, caesarean scar and interstitial ectopic pregnancies over 11 years: identifying the need for a modern management algorithmA unified method for rare variant analysis of gene-environment interactionsCo-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registriesGenetic association testing using the GENESIS R/Bioconductor package
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P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Han Chen
@ast
Han Chen
@en
Han Chen
@es
Han Chen
@nl
Han Chen
@sl
type
label
Han Chen
@ast
Han Chen
@en
Han Chen
@es
Han Chen
@nl
Han Chen
@sl
prefLabel
Han Chen
@ast
Han Chen
@en
Han Chen
@es
Han Chen
@nl
Han Chen
@sl
P214
P106
P21
P214
P31
P496
0000-0002-9510-4923
P569
2000-01-01T00:00:00Z
P735
P7859
lccn-n2009017023