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。Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
Nadine Norton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
Eric Villard et al.
EUROPEAN HEART JOURNAL (2011)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret et al.
NATURE (2011)
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
Olivier Harismendy et al.
NATURE (2011)
Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome
Masayuki Yazawa et al.
NATURE (2011)
Modelling the long QT syndrome with induced pluripotent stem cells
Ilanit Itzhaki et al.
NATURE (2011)
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
Hilma Holm et al.
NATURE GENETICS (2011)
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
Joshua C. Bis et al.
NATURE GENETICS (2011)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Heribert Schunkert et al.
NATURE GENETICS (2011)
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
John F. Peden et al.
NATURE GENETICS (2011)
Acute Mesenteric Infarction Associated with Atrial Fibrillation
Jia-Ming Wang et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing
Callum J. Bell et al.
SCIENCE TRANSLATIONAL MEDICINE (2011)
Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals
Dan E. Arking et al.
PLOS GENETICS (2011)
Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data
Frances Wensley et al.
BRITISH MEDICAL JOURNAL (2011)
The Potential of Genes and Other Markers to Inform about Risk
Margaret S. Pepe et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2010)
2010 ACCF/AHA guideline for assessment of cardiovascular risk in asymptomatic adults: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Philip Greenland et al.
CIRCULATION (2010)
Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Nicholas L. Smith et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2010)
Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Alanna C. Morrison et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2010)
Use of genomic profiling to assess risk for cardiovascular disease and identify individualized prevention strategies-A targeted evidence-based review
Glenn E. Palomaki et al.
GENETICS IN MEDICINE (2010)
Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia
Jonathan Rios et al.
HUMAN MOLECULAR GENETICS (2010)
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
Maja Barbalic et al.
HUMAN MOLECULAR GENETICS (2010)
Identification of Evidence Suggestive of an Association with Peripheral Arterial Disease at the OSBPL10 Locus by Genome-Wide Investigation in the Japanese Population
Hiroshi Koriyama et al.
JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS (2010)
Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms
Koichi Akiyama et al.
JOURNAL OF HUMAN GENETICS (2010)
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
Samuli Ripatti et al.
LANCET (2010)
Clinical assessment incorporating a personal genome
Euan A. Ashley et al.
LANCET (2010)
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
Kiran Musunuru et al.
NATURE (2010)
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
Axel Visel et al.
NATURE (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich et al.
NATURE (2010)
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Solveig Gretarsdottir et al.
NATURE GENETICS (2010)
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
Helena Furberg et al.
NATURE GENETICS (2010)
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Christopher T. Johansen et al.
NATURE GENETICS (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes et al.
NATURE GENETICS (2010)
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Katsuhito Yasuno et al.
NATURE GENETICS (2010)
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction
Connie R. Bezzina et al.
NATURE GENETICS (2010)
Common variants in KCNN3 are associated with lone atrial fibrillation
Patrick T. Ellinor et al.
NATURE GENETICS (2010)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josee Dupuis et al.
NATURE GENETICS (2010)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight et al.
NATURE GENETICS (2010)
Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia
Kiran Musunuru et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Genome-Wide Association Study Identifies GPC5 as a Novel Genetic Locus Protective against Sudden Cardiac Arrest
Dan E. Arking et al.
PLOS ONE (2010)
Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
Jared C. Roach et al.
SCIENCE (2010)
Chromosome 9p21 in Ischemic Stroke Population Structure and Meta-Analysis
Christopher D. Anderson et al.
STROKE (2010)
Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level
Olivier Harismendy et al.
GENOME BIOLOGY (2010)
Hemostasis, Inflammation, and Fatal and Nonfatal Coronary Heart Disease Long-Term Follow-Up of the Atherosclerosis Risk in Communities (ARIC) Cohort
Anna M. Kucharska-Newton et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2009)
The LDL Receptor
Joseph L. Goldstein et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2009)
Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
Yoshiji Yamada et al.
ATHEROSCLEROSIS (2009)
Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study
Anders Malarstig et al.
BLOOD (2009)
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach
David-Alexandre Tregouet et al.
BLOOD (2009)
Association of Novel Genetic Loci With Circulating Fibrinogen Levels A Genome-Wide Association Study in 6 Population-Based Cohorts
Abbas Dehghan et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2009)
Genetically Elevated Lipoprotein(a) and Increased Risk of Myocardial Infarction
Pia R. Kamstrup et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2009)
Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease
Paul Elliott et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2009)
Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association
James R. Elmore et al.
JOURNAL OF VASCULAR SURGERY (2009)
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Santhi K. Ganesh et al.
NATURE GENETICS (2009)
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Emelia J. Benjamin 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)
Genomewide Association Studies of Stroke
M. Arfan Ikram et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Murim Choi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium
Nancy L. Heard-Costa et al.
PLOS GENETICS (2009)
Cardiovascular Genomics, Personalized Medicine, and the National Heart, Lung, and Blood Institute Part I: The Beginning of an Era
Christopher J. O'Donnell et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2008)
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeir E. Thorgeirsson et al.
NATURE (2008)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Weizhen Ji 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)
Susceptibility loci for intracranial aneurysm in European and Japanese populations
Kaya Bilguvar et al.
NATURE GENETICS (2008)
SLCO1B1Variants and Statin-Induced Myopathy — A Genomewide Study
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease-A Mendelian Randomisation Study
Patrick Linsel-Nitschke et al.
PLOS ONE (2008)
Parental occurrence of premature cardiovascular disease predicts increased coronary artery and abdominal aortic calcification in the Framingham Offspring and Third Generation cohorts
Nisha I. Parikh et al.
CIRCULATION (2007)
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daniel F. Gudbjartsson et al.
NATURE (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)
Assessment by cardiovascular magnetic resonance, electron beam computed tomography, and carotid ultrasonography of the distribution of subclinical atherosclerosis across Framingham risk strata
Sekar Kathiresan et al.
AMERICAN JOURNAL OF CARDIOLOGY (2007)
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
Stefano Romeo et al.
NATURE GENETICS (2007)
A polymorphism within a conserved β1-adrenergic receptor motif alters cardiac function and β-blocker response in human heart failure
Stephen B. Liggett et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Association of parental heart failure with risk of heart failure in offspring
Douglas S. Lee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
JC Cohen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
C Jonathan et al.
NATURE GENETICS (2005)
Cardiovascular disease
EG Nabel
NEW ENGLAND JOURNAL OF MEDICINE (2003)
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
KE Lohmueller et al.
NATURE GENETICS (2003)
Initial sequencing and analysis of the human genome
ES Lander et al.
NATURE (2001)