Published in Int J Mol Sci on September 29, 2014
Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population. Int J Mol Sci (2016) 0.79
Association between VEGF polymorphisms (936c/t, -460t/c and -634g/c) with haplotypes and coronary heart disease susceptibility. Int J Clin Exp Pathol (2015) 0.78
Association study of BUD13-ZNF259 gene rs964184 polymorphism and hemorrhagic stroke risk. Int J Clin Exp Med (2015) 0.77
Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease. Medicine (Baltimore) (2016) 0.76
CDKN2BAS polymorphisms: are associated with coronary heart disease risk a Han Chinese population. Oncotarget (2016) 0.75
Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis. Clin Psychopharmacol Neurosci (2017) 0.75
Chemotherapy-induced hypomethylation of N-myc downstream-regulated gene 4 in the bone marrow of patients with acute myeloid leukemia. Oncol Lett (2017) 0.75
Bias in meta-analysis detected by a simple, graphical test. BMJ (1997) 122.24
Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA (2000) 55.37
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science (2007) 43.16
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour (2010) 42.87
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science (2007) 32.97
Genomewide association analysis of coronary artery disease. N Engl J Med (2007) 24.38
A common allele on chromosome 9 associated with coronary heart disease. Science (2007) 20.37
Long non-coding RNAs: insights into functions. Nat Rev Genet (2009) 19.61
A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science (2007) 18.96
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
Power and sample size calculations. A review and computer program. Control Clin Trials (1990) 9.58
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ Cardiovasc Genet (2009) 8.42
Monte Carlo tests for associations between disease and alleles at highly polymorphic loci. Ann Hum Genet (1995) 8.09
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response. Nature (2011) 6.25
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet (2011) 5.23
New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet (2009) 5.12
SNP genotyping using the Sequenom MassARRAY iPLEX platform. Curr Protoc Hum Genet (2009) 5.01
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet (2007) 4.09
Sex-specific genetic architecture of human disease. Nat Rev Genet (2008) 4.01
Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk. PLoS Genet (2010) 3.89
Association of race and sex with risk of incident acute coronary heart disease events. JAMA (2012) 3.07
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus. Arterioscler Thromb Vasc Biol (2009) 2.79
INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis. PLoS One (2009) 2.77
ANRIL, a long, noncoding RNA, is an unexpected major hotspot in GWAS. FASEB J (2010) 2.73
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet (2008) 2.71
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression. PLoS Genet (2010) 2.39
Genetic--epidemiologic study of early-onset ischemic heart disease. Circulation (1980) 2.36
Expression of p16(INK4a) in peripheral blood T-cells is a biomarker of human aging. Aging Cell (2009) 2.21
Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke (2008) 2.19
Role of angiogenesis in cardiovascular disease: a critical appraisal. Circulation (2005) 2.13
ANRIL expression is associated with atherosclerosis risk at chromosome 9p21. Arterioscler Thromb Vasc Biol (2010) 1.87
Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis. Circ Cardiovasc Genet (2013) 1.47
Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort. PLoS One (2010) 1.46
Contemporary use of adjunctive thrombectomy during primary percutaneous coronary intervention for ST-elevation myocardial infarction in the United States. Catheter Cardiovasc Interv (2012) 1.45
Gender differences in genetic risk profiles for cardiovascular disease. PLoS One (2008) 1.31
Genetic risk score and risk of myocardial infarction in Hispanics. Circulation (2011) 1.30
The Seldinger technique: 50 years on. Lancet (2005) 1.29
Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies. J Am Coll Cardiol (2011) 1.26
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur Heart J (2010) 1.25
Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population. BMC Med Genet (2010) 1.24
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies. Circ Cardiovasc Genet (2010) 1.23
A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease. Mol Biol Rep (2008) 1.22
Inflammatory markers in coronary heart disease. Br Med Bull (2011) 1.14
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PLoS One (2011) 1.07
Lack of association between apolipoprotein C3 gene polymorphisms and risk of coronary heart disease in a Han population in East China. Lipids Health Dis (2011) 1.02
Japanese dietary lifestyle and cardiovascular disease. J Atheroscler Thromb (2011) 1.02
A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect. Thromb Res (2012) 0.98
Genetic variants on chromosome 9p21 and ischemic stroke in Chinese. Brain Res Bull (2009) 0.95
Genome-wide association studies in atherothrombosis. Eur J Intern Med (2009) 0.94
Variants on chromosome 9p21.3 correlated with ANRIL expression contribute to stroke risk and recurrence in a large prospective stroke population. Stroke (2011) 0.92
Meta-analyses of KIF6 Trp719Arg in coronary heart disease and statin therapeutic effect. PLoS One (2012) 0.92
An association study between genetic polymorphisms related to lipoprotein-associated phospholipase A(2) and coronary heart disease. Exp Ther Med (2013) 0.92
Chromosome 9p21 genetic variants are associated with myocardial infarction but not with ischemic stroke in a Taiwanese population. J Investig Med (2011) 0.89
Genetic and environmental determinants of total and high-molecular weight adiponectin in families with low HDL-cholesterol and early onset coronary heart disease. Atherosclerosis (2009) 0.87
Angiogenesis gene therapy to rescue ischaemic tissues: achievements and future directions. Br J Pharmacol (2001) 0.86
Meta-analyses of four eosinophil related gene variants in coronary heart disease. J Thromb Thrombolysis (2013) 0.86
Constructing a point-based prediction model for the risk of coronary artery disease in a Chinese community: a report from a cohort study in Taiwan. Int J Cardiol (2012) 0.86
The relationship between polymorphisms on chromosome 9p21 and age of onset of coronary heart disease in black and white women. Genet Test Mol Biomarkers (2011) 0.85
CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection. J Med Genet (2010) 0.85
MTAP and CDKN2B genes are associated with myocardial infarction in Chinese Hans. Clin Biochem (2009) 0.85
Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese. Genet Test Mol Biomarkers (2012) 0.84
Searching for the optimal strategy for the diagnosis of stable coronary artery disease. Cost-effectiveness of the new algorithm. Cardiol J (2007) 0.83
Four genetic polymorphisms of lymphotoxin-alpha gene and cancer risk: a systematic review and meta-analysis. PLoS One (2013) 0.83
Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: case-control study and meta-analysis. Clin Biochem (2013) 0.82
Sex differences in the prevalence and clinical outcomes of subclinical peripheral artery disease in the Health, Aging, and Body Composition (Health ABC) study. Vascular (2013) 0.79
Association of CD36 gene polymorphisms with echo- and electrocardiographic parameters in patients with early onset coronary artery disease. Arch Med Sci (2012) 0.79
Meta-analysis of genetic association of chromosome 9p21 with early-onset coronary artery disease. Gene (2012) 0.78
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. Circ Cardiovasc Genet (2014) 0.77
Genome-wide linkage approach yields novel early onset myocardial infarction locus in East Asians. Circ Cardiovasc Genet (2013) 0.76