Gang Shi

发表

Mining gold dust under the genome wide significance level: a two‐stage approach to analysis of GWAS

E. Boerwinkle, A. Chakravarti, D. Rao, 2011, Genetic epidemiology.

Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease

Tom R. Gaunt, Scott M. Williams, Andrew D. Johnson, 2017, Journal of the American Heart Association.

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Christian Gieger, Jingyuan Fu, Thomas Meitinger, 2011, Nature Genetics.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Christian Gieger, Xiaofeng Zhu, Paolo Vineis, 2011, Nature.

Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci.

D. Rao, S. Hunt, D. Arnett, 2011, American journal of hypertension.

Epistatic effects of ACE I/D and AGT gene variants on left ventricular mass in hypertensive patients: The HyperGEN Study

R. Devereux, D. Arnett, J. Eckfeldt, 2011, Journal of Human Hypertension.

On rare variants in principal component analysis of population stratification

Gang Shi, Shengqing Ma, 2019, BMC Genetics.

Genome-wide variance quantitative trait locus analysis suggests small interaction effects in blood pressure traits

Gang Shi, 2022, Scientific reports.

Kernel-based gene–environment interaction tests for rare variants with multiple quantitative phenotypes

Gang Shi, Xiaoqin Jin, 2022, PloS one.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Tom R. Gaunt, Yan V. Sun, S. R. Kulkarni, 2011, Nature.

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.

Andrew D. Johnson, M. Fornage, C. Gieger, 2014, American journal of human genetics.

An update on genome-wide association studies of hypertension

Jie Zheng, Gang Shi, Dabeeru C. Rao, 2015, Applied Informatics.

Variants on Chromosome 6 p 22 . 3 Associated With Blood Pressure in the HyperGEN Study : Follow-Up of FBPP Quantitative Trait Loci

D. Rao, S. Hunt, D. Arnett, 2011 .

Edinburgh Research Explorer Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2022 .

Optimum designs for next‐generation sequencing to discover rare variants for common complex disease

Gang Shi, D C Rao, Gang Shi, 2011, Genetic epidemiology.

Genome-wide association analysis of Framingham Heart Study data for the Genetics Analysis Workshop 16: effects due to medication use

T. Rice, C. Gu, Y. Sung, 2009, BMC proceedings.

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2011, Human molecular genetics.

Meta-Analysis of Joint Test of SNP and SNP-Environment Interaction with Heterogeneity

Gang Shi, Qinqin Jin, 2021, Human Heredity.

Meta-Analysis of SNP-Environment Interaction with Heterogeneity

Gang Shi, Qinqin Jin, 2019, Human Heredity.

Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program.

R. Olshen, E. Boerwinkle, A. Chakravarti, 2010, American journal of hypertension.

Genetic Effect on Blood Pressure Is Modulated by Age: The Hypertension Genetic Epidemiology Network Study

J. Pankow, A. Kraja, D. Rao, 2009, Hypertension.

Robustness of meta-analyses in finding gene × environment interactions

Arye Nehorai, Gang Shi, A. Nehorai, 2017, PloS one.

Variance-component-based meta-analysis of gene–environment interactions for rare variants

Gang Shi, Xiaoqin Jin, 2021, G3.

Detecting gene‐environment interactions in genome‐wide association data

Bonnie R. Joubert, W. Gauderman, C. Engelman, 2009, Genetic epidemiology.

Body mass index modulates blood pressure heritability: the Family Blood Pressure Program.

E. Boerwinkle, D. Rao, S. Hunt, 2014, American journal of hypertension.

Application of three-level linear mixed-effects model incorporating gene-age interactions for association analysis of longitudinal family data

T. Rice, C. Gu, D. Rao, 2009, BMC proceedings.

Nitric Oxide Synthase and Causes Hypertension and Vascular Dysfunction Loss of Collectrin, an Angiotensin-Converting Enzyme 2 Homolog, Uncouples Endothelial

J. Pankow, A. Kraja, D. Arnett, 2015 .

Meta-analysis of SNP-environment interaction with heterogeneity for overlapping data

Gang Shi, Qinqin Jin, 2021, Scientific Reports.

Meta-Analysis of SNP-Environment Interaction With Overlapping Data

Gang Shi, Qinqin Jin, Gang Shi, 2020, Frontiers in Genetics.

Cauchy combination methods for the detection of gene–environment interactions for rare variants related to quantitative phenotypes

Gang Shi, Xiaoqin Jin, 2023, Heredity.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2011, Nature.

Genome-wide association analysis of Framingham Heart Study data for the Genetics Analysis Workshop 16: effects due to medication use.

T. Rice, C. Gu, Y. Sung, 2009, BMC Proceedings.

Ignoring temporal trends in genetic effects substantially reduces power of quantitative trait linkage analysis

Gang Shi, D. Rao, 2008, Genetic epidemiology.

Comparison between single-marker analysis using Merlin and multi-marker analysis using LASSO for Framingham simulated data

T. Rice, C. Gu, Y. Sung, 2009, BMC proceedings.

Ancestral Spectrum Analysis With Population-Specific Variants

Gang Shi, Qin Kuang, 2021, Frontiers in Genetics.

Genome-wide association analysis of Framingham Heart Study data for the Genetics Analysis Workshop 16: effects due to medication use

T. Rice, Y. Sung, Gang Shi, 2009, BMC proceedings.

Enriching rare variants using family-specific linkage information

Gang Shi, J. Simino, D. Rao, 2011, BMC proceedings.

rare variants using family-specific linkage information

Gang Shi, 2019 .