List of works - Haiqing Shen

A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro

scientific article

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection

scientific article published on December 2008

Aspirin Resistance in healthy drug-naive men versus women (from the Heredity and Phenotype Intervention Heart Study).

scientific article published on 21 June 2009

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

scientific article

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

scientific article

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

scientific article

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

scientific article published on 30 May 2013

Common variants in the GDF5-UQCC region are associated with variation in human height

scientific article

Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100.

scientific article published on 08 October 2013

Determinants of coronary artery and aortic calcification in the Old Order Amish

scientific article

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Extent and distribution of linkage disequilibrium in the Old Order Amish

scientific article

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

scientific article published on November 2010

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

scientific article

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

scientific article published on 20 February 2014

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels

scientific article

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

scientific article

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

scientific article

Hundreds of variants clustered in genomic loci and biological pathways affect human height

scientific article

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

scientific article

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

scientific article

Loci influencing blood pressure identified using a cardiovascular gene-centric array

scientific article published on 8 January 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

scientific article

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

scientific article

Physical activity and the association of common FTO gene variants with body mass index and obesity

scientific article

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance

scientific article

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

scientific article published on 19 September 2008

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

scientific article published on 5 March 2008

Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women

scientific article

Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels

scientific article

List of works by Haiqing Shen

A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection

Aspirin Resistance in healthy drug-naive men versus women (from the Heredity and Phenotype Intervention Heart Study).

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

Common variants in the GDF5-UQCC region are associated with variation in human height

Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100.

Determinants of coronary artery and aortic calcification in the Old Order Amish

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Extent and distribution of linkage disequilibrium in the Old Order Amish

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Physical activity and the association of common FTO gene variants with body mass index and obesity

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women

Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels