List of works - QiPing Feng

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

scientific article published on 13 April 2020

A phenome-wide association study to discover pleiotropic effects of , , and

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

scientific article published in Nature Communications

Amplification and up-regulation of microRNA-30b in oral squamous cell cancers ⬇️

scientific article published on April 26, 2012

Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry

scientific article published in 2021

ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms

scientific article published on 10 November 2020

Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins

scientific article published on 07 April 2014

ERBB2 gene amplification in oral squamous cell malignancies: a correlation with tumor progression and gene expression ⬇️

scientific article published on April 30, 2011

Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting

scientific article

Human S-adenosylhomocysteine hydrolase: common gene sequence variation and functional genomic characterization

scientific article

Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization

scientific article published on 23 May 2008

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

scientific article

Methionine adenosyltransferase 2A/2B and methylation: gene sequence variation and functional genomics

scientific article

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

scientific article published on 30 March 2020

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

scientific article

PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records

scientific article published on 24 September 2020

Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways

scientific article published on 17 February 2020

Phenotype risk scores identify patients with unrecognized Mendelian disease patterns

scientific article published in Science

Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records

scientific article published on 28 August 2018

The power of genetic diversity in genome-wide association studies of lipids

Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA)

scientific article published on 13 February 2019

List of works by QiPing Feng

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

A phenome-wide association study to discover pleiotropic effects of , , and

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

Amplification and up-regulation of microRNA-30b in oral squamous cell cancers ⬇️

Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry

ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms

Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins

ERBB2 gene amplification in oral squamous cell malignancies: a correlation with tumor progression and gene expression ⬇️

Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting

Human S-adenosylhomocysteine hydrolase: common gene sequence variation and functional genomic characterization

Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

Methionine adenosyltransferase 2A/2B and methylation: gene sequence variation and functional genomics

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records

Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways

Phenotype risk scores identify patients with unrecognized Mendelian disease patterns

Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records

The power of genetic diversity in genome-wide association studies of lipids

Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA)