相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Single nucleotide polymorphism on chromosome 9p21 and endothelial progenitor cells in a general population cohort
Shu Ye et al.
ATHEROSCLEROSIS (2010)
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease
Patrick Linsel-Nitschke et al.
ATHEROSCLEROSIS (2010)
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
Axel Visel et al.
NATURE (2010)
Value of genetic profiling for the prediction of coronary heart disease
Jeroen B. van der Net et al.
AMERICAN HEART JOURNAL (2009)
Rapid DNA Methylation Changes after Exposure to Traffic Particles
Andrea Baccarelli et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2009)
Cardiovascular Disease Risk Prediction With and Without Knowledge of Genetic Variation at Chromosome 9p21.3
Nina P. Paynter et al.
ANNALS OF INTERNAL MEDICINE (2009)
Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease
Philippe Amouyel et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2009)
Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease
Axel Muendlein et al.
ATHEROSCLEROSIS (2009)
A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study
Kazumasa Yamagishi et al.
EUROPEAN HEART JOURNAL (2009)
The Impact of Newly Identified Loci on Coronary Heart Disease, Stroke and Total Mortality in the MORGAM Prospective Cohorts
Juha Karvanen et al.
GENETIC EPIDEMIOLOGY (2009)
Hepatic Lipase, Genetically Elevated High-Density Lipoprotein, and Risk of Ischemic Cardiovascular Disease
Trine Holm Johannsen et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
Cohort studies and the genetics of complex disease
Teri A. Manolio
NATURE GENETICS (2009)
New susceptibility locus for coronary artery disease on chromosome 3q22.3
Jeanette Erdmann et al.
NATURE GENETICS (2009)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Sekar Kathiresan et al.
NATURE GENETICS (2009)
Common Genetic Variation and Human Traits
David B. Goldstein
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Identification of a Shared Genetic Susceptibility Locus for Coronary Heart Disease and Periodontitis
Arne S. Schaefer et al.
PLOS GENETICS (2009)
Update and analysis of the University College London Low Density Lipoprotein receptor familial hypercholesterolemia database
S. E. A. Leigh et al.
ANNALS OF HUMAN GENETICS (2008)
Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest)
K. G. Abdullah et al.
ANNALS OF HUMAN GENETICS (2008)
Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study
Abbas Dehghan et al.
BMC MEDICINE (2008)
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
Heribert Schunkert et al.
CIRCULATION (2008)
Prevalence, predictors, and outcomes of primary nonadherence after acute myocardial infarction
Cynthia A. Jackevicius et al.
CIRCULATION (2008)
Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men
Philippa J. Talmud et al.
CLINICAL CHEMISTRY (2008)
Development of sensitive and specific age- and gender-specific low-density lipoprotein cholesterol cutoffs for diagnosis of first-degree relatives with familial hypercholesterolaemia in cascade testing
Brian Starr et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2008)
Maternal transmission of risk for atherosclerosis
Marco C. DeRuiter et al.
CURRENT OPINION IN LIPIDOLOGY (2008)
Chromosome 9p21.3 is associated with early-onset coronary heart disease in the Irish population
Weihua Meng et al.
DISEASE MARKERS (2008)
Detection of altered global DNA methylation in coronary artery disease patients
Priyanka Sharma et al.
DNA AND CELL BIOLOGY (2008)
Blood leucocyte telomere DNA content predicts vascular telomere DNA content in humans with and without vascular disease
W. Richard W. Wilson et al.
EUROPEAN HEART JOURNAL (2008)
Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia
Jeroen B. van der Net et al.
EUROPEAN HEART JOURNAL (2008)
Functional characterization of genetic variants in NPC1L1 supports the sequencing extremes strategy to identify complex trait genes
Saleemah Fahmi et al.
HUMAN MOLECULAR GENETICS (2008)
Association of loss-of-function mutations in the ABCA1 gene with high-density lipoprotein cholesterol levels and risk of ischemic heart disease
Ruth Frikke-Schmidt et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2008)
The association of telomere length with paternal history of premature myocardial infarction in the European Atherosclerosis Research Study II
Klelia D. Salpea et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2008)
LDL-cholesterol concentrations:: a genome-wide association study
Manjinder S. Sandhu et al.
LANCET (2008)
Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation
Kristi Kerkel et al.
NATURE GENETICS (2008)
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Anna Helgadottir et al.
NATURE GENETICS (2008)
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Cristen J. Willer et al.
NATURE GENETICS (2008)
Polymorphisms associated with cholesterol and risk of cardiovascular events
Sekar Kathiresan et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies
Brendan J. Keating et al.
PLOS ONE (2008)
The methylome: approaches for global DNA methylation profiling
Stephan Beck et al.
TRENDS IN GENETICS (2008)
Psychological and behavioural impact of genetic testing smokers for lung cancer risk - A phase II exploratory trial
Saskia C. Sanderson et al.
JOURNAL OF HEALTH PSYCHOLOGY (2008)
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
Helen M. Broadbent et al.
HUMAN MOLECULAR GENETICS (2008)
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
Gong-Qing Shen et al.
JOURNAL OF HUMAN GENETICS (2008)
Resequencing genomic DNA of patients with severe Hypertriglyceridemia (MIM 144650)
Jian Wang et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2007)
Direct selection of human genomic loci by microarray hybridization
Thomas J. Albert et al.
NATURE METHODS (2007)
Association of apolipoprotein E genotypes with lipid levels and coronary risk
Anna M. Bennet et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2007)
The use of meta-analysis risk estimates for candidate genes in combination to predict coronary heart disease risk
F. Drenos et al.
ANNALS OF HUMAN GENETICS (2007)
Genomewide association analysis of coronary artery disease
Nilesh J. Samani et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Copy-number variation and association studies of human disease
Steven A. McCarroll et al.
NATURE GENETICS (2007)
A common variant on chromosome 9p21 affects the risk of myocardial infarction
Anna Helgadottir et al.
SCIENCE (2007)
A common allele on chromosome 9 associated with coronary heart disease
Ruth McPherson et al.
SCIENCE (2007)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
Richa Saxena et al.
SCIENCE (2007)
Genetic testing for heart disease susceptibility: potential impact on motivation to quit smoking
S. C. Sanderson et al.
CLINICAL GENETICS (2007)
Impact of inflammation on epigenetic DNA methylation -: a novel risk factor for cardiovascular disease?
P. Stenvinkel et al.
JOURNAL OF INTERNAL MEDICINE (2007)
Genetic effects versus bias for candidate polymorphisms in myocardial infarction: Case study and overview of large-scale evidence
Evangelia E. Ntzani et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2007)
Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family:: Identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF
Eric Pasmant et al.
CANCER RESEARCH (2007)
Use and misuse of the receiver operating characteristic curve in risk prediction
Nancy R. Cook
CIRCULATION (2007)
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
Stefano Romeo et al.
NATURE GENETICS (2007)
To know or not to know: A review of behaviour and suicidal ideation in preclinical Huntington's disease
Tarja-Brita Robins Wahlin
PATIENT EDUCATION AND COUNSELING (2007)
Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
S. E. Humphries et al.
JOURNAL OF MEDICAL GENETICS (2006)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
Short term psychological distress in patients actively approached for genetic counselling after diagnosis of breast cancer
Kathryn J. Schlich-Bakker et al.
EUROPEAN JOURNAL OF CANCER (2006)
Vascular smooth muscle cells undergo telomere-based senescence in human atherosclerosis - Effects of telomerase and oxidative stress
Charles Matthews et al.
CIRCULATION RESEARCH (2006)
Predictive testing for complex diseases using multiple genes: Fact or fiction?
A. Cecile J. W. Janssens et al.
GENETICS IN MEDICINE (2006)
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
JC Cohen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Investigating the genetic determinants of cardiovascular disease using candidate genes and meta-analysis of association studies
JP Casas et al.
ANNALS OF HUMAN GENETICS (2006)
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels
JC Cohen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
The efficacy of combining several risk factors as a screening test
NJ Wald et al.
JOURNAL OF MEDICAL SCREENING (2005)
Detection of large-scale variation in the human genome
AJ Iafrate et al.
NATURE GENETICS (2004)
Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
JC Cohen et al.
SCIENCE (2004)
ESEfinder: a web resource to identify exonic splicing enhancers
L Cartegni et al.
NUCLEIC ACIDS RESEARCH (2003)
White cell telomere length and risk of premature myocardial infarction
S Brouilette et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2003)
Prediction of risk of coronary events in middle-aged men in the Prospective Cardiovascular Munster Study (PROCAM) using neural networks
R Voss et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2002)
MTHFR 677C→T polymorphism and risk of coronary heart disease -: A meta-analysis
M Klerk et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2002)
Long-term persistence in use of statin therapy in elderly patients
JS Benner et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2002)
Telomere lengths are characteristic in each human individual
K Takubo et al.
EXPERIMENTAL GERONTOLOGY (2002)
BRENDA, enzyme data and metabolic information
I Schomburg et al.
NUCLEIC ACIDS RESEARCH (2002)
分享论文
