Lista de obras - Han Chen - Dominio Público Uruguay

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A method of moments estimator for random effect multivariate meta-analysis

artículo científico publicado en 2012

A powerful and data-adaptive test for rare-variant-based gene-environment interaction analysis

article

A unified method for rare variant analysis of gene-environment interactions

scientific article published on 04 December 2019

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

scientific article published on 01 February 2019

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

artículo científico publicado en 2019

Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries

scientific article published on 16 July 2019

Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses

artículo científico publicado en 2016

Comparison of statistical approaches to rare variant analysis for quantitative traits.

artículo científico publicado en 2011

Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models

artículo científico publicado en 2016

Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies

artículo científico publicado en 2019

Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

scientific article published on 10 January 2019

Efficient gene-environment interaction tests for large biobank-scale sequencing studies

scientific article published on 30 August 2020

Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease

artículo científico publicado en 2016

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

artículo científico publicado en 2016

Genetic association testing using the GENESIS R/Bioconductor package

scientific article published on 01 December 2019

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

artículo científico publicado en 2016

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

artículo científico publicado en 2011

Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment

artículo científico publicado en 2017

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Incorporating gene-environment interaction in testing for association with rare genetic variants

artículo científico publicado en 2014

Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies

artículo científico publicado en 2017

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Management and reproductive counseling in cervical, caesarean scar and interstitial ectopic pregnancies over 11 years: identifying the need for a modern management algorithm

artículo científico publicado en 2019

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

artículo científico publicado en 2016

Metabolomic Associations of Asthma in the Hispanic Community Health Study/Study of Latinos

scientific article published in 2022

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

artículo científico publicado en 2019

Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.

artículo científico publicado en 2017

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

artículo científico publicado en 2012

Rare Variant Association Analysis: Beyond Collapsing Approaches

Rare genetic variant analysis on blood pressure in related samples

artículo científico publicado en 2014

Sequence kernel association test for quantitative traits in family samples

artículo científico publicado en 2012

Sequence kernel association test for survival traits.

artículo científico publicado en 2014

Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level

scientific article published on 24 October 2019

Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

artículo científico publicado en 2014

Test for rare variants by environment interactions in sequencing association studies

artículo científico publicado en 2015

Testing genetic association with rare and common variants in family data

artículo científico publicado en 2014

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

artículo científico publicado en 2016

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

artículo científico publicado en 2023

Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level

artículo científico publicado en 2016

Whole exome sequencing analysis in severe chronic obstructive pulmonary disease

scientific article published on 01 November 2018

Lista de obras de Han Chen

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

A method of moments estimator for random effect multivariate meta-analysis

A powerful and data-adaptive test for rare-variant-based gene-environment interaction analysis

A unified method for rare variant analysis of gene-environment interactions

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries

Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses

Comparison of statistical approaches to rare variant analysis for quantitative traits.

Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models

Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies

Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

Efficient gene-environment interaction tests for large biobank-scale sequencing studies

Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

Genetic association testing using the GENESIS R/Bioconductor package

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Incorporating gene-environment interaction in testing for association with rare genetic variants

Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Management and reproductive counseling in cervical, caesarean scar and interstitial ectopic pregnancies over 11 years: identifying the need for a modern management algorithm

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Metabolomic Associations of Asthma in the Hispanic Community Health Study/Study of Latinos

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

Rare Variant Association Analysis: Beyond Collapsing Approaches

Rare genetic variant analysis on blood pressure in related samples

Sequence kernel association test for quantitative traits in family samples

Sequence kernel association test for survival traits.

Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level

Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

Test for rare variants by environment interactions in sequencing association studies

Testing genetic association with rare and common variants in family data

The genetic architecture of type 2 diabetes

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level

Whole exome sequencing analysis in severe chronic obstructive pulmonary disease