PubRank

Haiqing Shen

Author PubWeight™ 81.95‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 2008 25.83
2 Common variants in the GDF5-UQCC region are associated with variation in human height. Nat Genet 2008 7.31
3 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science 2008 4.50
4 Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. J Clin Invest 2008 3.51
5 From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proc Natl Acad Sci U S A 2008 3.39
6 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. Diabetes 2007 3.22
7 Physical activity and the association of common FTO gene variants with body mass index and obesity. Arch Intern Med 2008 3.15
8 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. Diabetes 2006 2.67
9 The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. Am Heart J 2008 2.61
10 Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am J Hum Genet 2012 2.53
11 Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish. Hum Hered 2007 2.26
12 Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. Am J Hum Genet 2010 2.15
13 Determinants of coronary artery and aortic calcification in the Old Order Amish. Circulation 2007 2.02
14 Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet 2012 1.96
15 Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 2011 1.96
16 Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease. Circ Cardiovasc Genet 2010 1.64
17 Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications. Am J Clin Nutr 2008 1.43
18 FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals. PLoS One 2010 1.34
19 Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet 2013 1.27
20 Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women. Hum Hered 2007 1.21
21 Gender-specific association of a perilipin gene haplotype with obesity risk in a white population. Obes Res 2004 1.17
22 Intragenic linkage disequilibrium structure of the human perilipin gene (PLIN) and haplotype association with increased obesity risk in a multiethnic Asian population. J Mol Med (Berl) 2005 1.13
23 The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults. Am J Epidemiol 2008 1.04
24 Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort). J Am Coll Cardiol 2013 0.88
25 Extent and distribution of linkage disequilibrium in the Old Order Amish. Genet Epidemiol 2010 0.86
26 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. Circ Cardiovasc Genet 2009 0.85
27 VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification. Hum Genet 2012 0.78
28 A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro. Bone 2010 0.77
29 Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100. J Clin Endocrinol Metab 2013 0.76
30 Is IL12B a potential genetic target for the prevention of type 1 diabetes through dietary intervention? Nutr Rev 2002 0.75
31 Pharmacogenetics of Lipid-lowering Therapies. Curr Atheroscler Rep 2002 0.75