Lista de obras - Peng Wei - Dominio Público Uruguay

A Powerful Framework for Integrating eQTL and GWAS Summary Data.

artículo científico publicado en 2017

A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants.

artículo científico publicado en 2015

A family-based joint test for mean and variance heterogeneity for quantitative traits

artículo científico publicado en 2014

A powerful and adaptive association test for rare variants

artículo científico publicado en 2014

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

article

A semiparametric model for vQTL mapping

artículo científico publicado en 2016

A versatile omnibus test for detecting mean and variance heterogeneity.

artículo científico publicado en 2014

Activation of endothelial and coagulation systems in left ventricular assist device recipients.

artículo científico publicado en 2009

An adaptive two-sample test for high-dimensional means

artículo científico

Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease

artículo científico publicado en 2015

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

artículo científico publicado en 2014

Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data.

artículo científico publicado en 2014

Bayesian Joint Modeling of Multiple Gene Networks and Diverse Genomic Data to Identify Target Genes of a Transcription Factor

artículo científico publicado en 2012

Bayesian inference on risk differences: an application to multivariate meta-analysis of adverse events in clinical trials

artículo científico publicado en 2013

Caffeine, creatine, GRIN2A and Parkinson's disease progression

artículo científico publicado en 2017

Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features

scientific article published on 26 August 2020

Combining gene annotations and gene expression data in model-based clustering: weighted method.

artículo científico publicado en 2006

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

artículo científico publicado en 2013

Differential endothelial cell gene expression by African Americans versus Caucasian Americans: a possible contribution to health disparity in vascular disease and cancer.

artículo científico publicado en 2011

Differentially regulated gene expression associated with hepatitis C virus clearance

artículo científico publicado en 2012

Dysregulation of EMT Drives the Progression to Clinically Aggressive Sarcomatoid Bladder Cancer.

artículo científico publicado en 2019

FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.

artículo científico publicado en 2016

FunSPU: A versatile and adaptive multiple functional annotation-based association test of whole-genome sequencing data

artículo científico publicado en 2019

Functional logistic regression approach to detecting gene by longitudinal environmental exposure interaction in a case-control study.

artículo científico publicado en 2014

Functional principal component based landmark analysis for the effects of longitudinal cholesterol profiles on the risk of coronary heart disease

artículo científico publicado en 2020

Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.

artículo científico publicado en 2013

Genetic endothelial systems biology of sickle stroke risk

artículo científico publicado en 2007

Genetic polymorphisms associated with pancreatic cancer survival: a genome-wide association study.

artículo científico publicado en 2017

Genetic variants in TNF-α promoter are predictors of recurrence in patients with squamous cell carcinoma of oropharynx after definitive radiotherapy

artículo científico publicado en 2013

Genome-wide association study identifies common genetic variants associated with salivary gland carcinoma and its subtypes

artículo científico publicado en 2015

Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority tria

artículo científico publicado en 2015

Identification of an Association of TNFAIP3 Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors

artículo científico publicado en 2015

Incorporating ENCODE information into association analysis of whole genome sequencing data.

artículo científico publicado en 2016

Incorporating biological information into association studies of sequencing data.

artículo científico publicado en 2011

Incorporating gene functions into regression analysis of DNA-protein binding data and gene expression data to construct transcriptional networks

artículo científico publicado en 2008

Incorporating gene networks into statistical tests for genomic data via a spatially correlated mixture model

artículo científico publicado en 2007

Incorporating multiple sets of eQTL weights into gene-by-environment interaction analysis identifies novel susceptibility loci for pancreatic cancer

artículo científico publicado en 2020

Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative study

artículo científico publicado en 2011

Insights into pancreatic cancer etiology from pathway analysis of genome-wide association study data

artículo científico publicado en 2012

Long-term Expression of Apolipoprotein B mRNA-specific Hammerhead Ribozyme via scAAV8.2 Vector Inhibits Atherosclerosis in Mice

artículo científico publicado en 2013

Mendelian randomization analysis of a time-varying exposure for binary disease outcomes using functional data analysis methods

artículo científico publicado en 2016

Network-based genomic discovery: application and comparison of Markov random field models

artículo científico publicado en 2010

On Robust Association Testing for Quantitative Traits and Rare Variants.

artículo científico publicado en 2016

Overexpression of miRNA 4451 is Associated With a Poor Survival of Patients With Hypopharyngeal Cancer After Surgery With Postoperative Radiotherapy

Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions

artículo científico publicado en 2015

Proinflammatory phenotype with imbalance of KLF2 and RelA: risk of childhood stroke with sickle cell anemia.

artículo científico publicado en 2010

Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma.

artículo científico publicado en 2019

Retracted: Genetic Variants in DNA Double-Strand Break Repair Genes and Risk of Salivary Gland Carcinoma: A Case-Control Study

artículo científico publicado en 2015

Site disparities in apoptotic variants as predictors of risk for second primary malignancy in patients with squamous cell carcinoma of the head and neck

artículo científico publicado en 2015

Testing for polygenic effects in genome-wide association studies.

artículo científico publicado en 2015

The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study

artículo científico publicado en 2016

Vitamin C and Vitamin E Mitigate the Risk of Pancreatic Ductal Adenocarcinoma from Meat-Derived Mutagen Exposure in Adults in a Case-Control Study

artículo científico publicado en 2019

WGSA: an annotation pipeline for human genome sequencing studies.

artículo científico publicado en 2015

Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis

scientific article published on 01 February 2019

Lista de obras de Peng Wei

A Powerful Framework for Integrating eQTL and GWAS Summary Data.

A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants.

A family-based joint test for mean and variance heterogeneity for quantitative traits

A powerful and adaptive association test for rare variants

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

A semiparametric model for vQTL mapping

A versatile omnibus test for detecting mean and variance heterogeneity.

Activation of endothelial and coagulation systems in left ventricular assist device recipients.

An adaptive two-sample test for high-dimensional means

Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data.

Bayesian Joint Modeling of Multiple Gene Networks and Diverse Genomic Data to Identify Target Genes of a Transcription Factor

Bayesian inference on risk differences: an application to multivariate meta-analysis of adverse events in clinical trials

Caffeine, creatine, GRIN2A and Parkinson's disease progression

Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features

Combining gene annotations and gene expression data in model-based clustering: weighted method.

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

Differential endothelial cell gene expression by African Americans versus Caucasian Americans: a possible contribution to health disparity in vascular disease and cancer.

Differentially regulated gene expression associated with hepatitis C virus clearance

Dysregulation of EMT Drives the Progression to Clinically Aggressive Sarcomatoid Bladder Cancer.

FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.

FunSPU: A versatile and adaptive multiple functional annotation-based association test of whole-genome sequencing data

Functional logistic regression approach to detecting gene by longitudinal environmental exposure interaction in a case-control study.

Functional principal component based landmark analysis for the effects of longitudinal cholesterol profiles on the risk of coronary heart disease

Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.

Genetic endothelial systems biology of sickle stroke risk

Genetic polymorphisms associated with pancreatic cancer survival: a genome-wide association study.

Genetic variants in TNF-α promoter are predictors of recurrence in patients with squamous cell carcinoma of oropharynx after definitive radiotherapy

Genome-wide association study identifies common genetic variants associated with salivary gland carcinoma and its subtypes

Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority tria

Identification of an Association of TNFAIP3 Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors

Incorporating ENCODE information into association analysis of whole genome sequencing data.

Incorporating biological information into association studies of sequencing data.

Incorporating gene functions into regression analysis of DNA-protein binding data and gene expression data to construct transcriptional networks

Incorporating gene networks into statistical tests for genomic data via a spatially correlated mixture model

Incorporating multiple sets of eQTL weights into gene-by-environment interaction analysis identifies novel susceptibility loci for pancreatic cancer

Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative study

Insights into pancreatic cancer etiology from pathway analysis of genome-wide association study data

Long-term Expression of Apolipoprotein B mRNA-specific Hammerhead Ribozyme via scAAV8.2 Vector Inhibits Atherosclerosis in Mice

Mendelian randomization analysis of a time-varying exposure for binary disease outcomes using functional data analysis methods

Network-based genomic discovery: application and comparison of Markov random field models

On Robust Association Testing for Quantitative Traits and Rare Variants.

Overexpression of miRNA 4451 is Associated With a Poor Survival of Patients With Hypopharyngeal Cancer After Surgery With Postoperative Radiotherapy

Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions

Proinflammatory phenotype with imbalance of KLF2 and RelA: risk of childhood stroke with sickle cell anemia.

Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma.

Retracted: Genetic Variants in DNA Double-Strand Break Repair Genes and Risk of Salivary Gland Carcinoma: A Case-Control Study

Site disparities in apoptotic variants as predictors of risk for second primary malignancy in patients with squamous cell carcinoma of the head and neck

Testing for polygenic effects in genome-wide association studies.

The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study

Vitamin C and Vitamin E Mitigate the Risk of Pancreatic Ductal Adenocarcinoma from Meat-Derived Mutagen Exposure in Adults in a Case-Control Study

WGSA: an annotation pipeline for human genome sequencing studies.

Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis