4.7 Review

Genetics of Cardiovascular Disease: How Far Are We from Personalized CVD Risk Prediction and Management?

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Association Analysis ofANRILPolymorphisms and Haplotypes with Autism Spectrum Disorders

Amin Safa et al.

Summary: The study did not find significant differences in SNP frequencies between children with ASD and normally developed children, but there were trends in the frequencies of two haplotypes associated with ASD risk. This suggests a potential causal variant in the mentioned haplotypes that could be further investigated in larger patient cohorts.

JOURNAL OF MOLECULAR NEUROSCIENCE (2021)

Article Biochemistry & Molecular Biology

The impact of epigenetics on cardiovascular disease

Dimple Prasher et al.

BIOCHEMISTRY AND CELL BIOLOGY (2020)

Article Cardiac & Cardiovascular Systems

European Society of Cardiology: Cardiovascular Disease Statistics 2019

Adam Timmis et al.

EUROPEAN HEART JOURNAL (2020)

Review Cardiac & Cardiovascular Systems

Genomics of Blood Pressure and Hypertension: Extending the Mosaic Toward Stratification

Stefanie Lip et al.

CANADIAN JOURNAL OF CARDIOLOGY (2020)

Review Biochemistry & Molecular Biology

Familial hypercholesterolemia: is it time to separate monogenic from polygenic familial hypercholesterolemia?

Julia Brandts et al.

CURRENT OPINION IN LIPIDOLOGY (2020)

Article Genetics & Heredity

Different prevalence of T2DM risk alleles in Roma population in comparison with the majority Czech population

Jaroslav A. Hubacek et al.

MOLECULAR GENETICS & GENOMIC MEDICINE (2020)

Review Nutrition & Dietetics

Genomics in Personalized Nutrition: Can You Eat for Your Genes?

Veronica A. Mullins et al.

NUTRIENTS (2020)

Review Genetics & Heredity

Genetics of Familial Hypercholesterolemia: New Insights

Michal Vrablik et al.

FRONTIERS IN GENETICS (2020)

Article Medicine, General & Internal

Association of Leukocyte Telomere Length With Mortality Among Adult Participants in 3 Longitudinal Studies

Konstantin G. Arbeev et al.

JAMA NETWORK OPEN (2020)

Article Genetics & Heredity

Genome-wide association analysis of common genetic variants of resistant hypertension

Nihal El Rouby et al.

PHARMACOGENOMICS JOURNAL (2019)

Review Biochemistry & Molecular Biology

Genetics of Common, Complex Coronary Artery Disease

Kiran Musunuru et al.

Review Cardiac & Cardiovascular Systems

Polygenic risk scores in coronary artery disease

Abhiram S. Rao et al.

CURRENT OPINION IN CARDIOLOGY (2019)

Article Cardiac & Cardiovascular Systems

Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia

Mark Trinder et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2019)

Article Genetics & Heredity

The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case-Control Study

Jaroslav A. Hubacek et al.

MOLECULAR DIAGNOSIS & THERAPY (2019)

Review Nutrition & Dietetics

Role of Personalized Nutrition in Chronic-Degenerative Diseases

Laura Di Renzo et al.

NUTRIENTS (2019)

Article Biochemistry & Molecular Biology

Relative Telomere Length and Cardiovascular Risk Factors

Moritz Koriath et al.

BIOMOLECULES (2019)

Article Cardiac & Cardiovascular Systems

2019 ESC/EAS guidelines for the management of dyslipidaemias: Lipid modification to reduce cardiovascular risk

Francois Mach et al.

ATHEROSCLEROSIS (2019)

Article Endocrinology & Metabolism

The TCF7L2 Locus: A Genetic Window Into the Pathogenesis of Type 1 and Type 2 Diabetes

Struan F. A. Grant

DIABETES CARE (2019)

Review Biochemistry & Molecular Biology

Towards clinical utility of polygenic risk scores

Samuel A. Lambert et al.

HUMAN MOLECULAR GENETICS (2019)

Review Pharmacology & Pharmacy

Role of flow-sensitive microRNAs and long noncoding RNAs in vascular dysfunction and atherosclerosis

Sandeep Kumar et al.

VASCULAR PHARMACOLOGY (2019)

Review Cardiac & Cardiovascular Systems

A decade of genome-wide association studies for coronary artery disease: the challenges ahead

Jeanette Erdmann et al.

CARDIOVASCULAR RESEARCH (2018)

Article Multidisciplinary Sciences

Telomere length and mortality in the Ludwigshafen Risk and Cardiovascular Health study

Irene Pusceddu et al.

PLOS ONE (2018)

Review Pharmacology & Pharmacy

Familial Hypercholesterolemia: New Horizons for Diagnosis and Effective Management

Maria Mytilinaiou et al.

FRONTIERS IN PHARMACOLOGY (2018)

Article Hematology

Impact of miRNA in Atherosclerosis

Yao Lu et al.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2018)

Article Pharmacology & Pharmacy

Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

Hayato Tada et al.

JOURNAL OF CLINICAL LIPIDOLOGY (2018)

Article Cardiac & Cardiovascular Systems

Clinical Genetic Testing for Familial Hypercholesterolemia

Amy C. Sturm et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)

Article Food Science & Technology

Dietary Intervention Modifies DNA Methylation Age Assessed by the Epigenetic Clock

Chanachai Sae-Lee et al.

MOLECULAR NUTRITION & FOOD RESEARCH (2018)

Letter Medicine, General & Internal

Worldwide Frequencies of APOL1 Renal Risk Variants

Girish N. Nadkarni et al.

NEW ENGLAND JOURNAL OF MEDICINE (2018)

Review Food Science & Technology

The future of nutrition: Nutrigenomics and nutrigenetics in obesity and cardiovascular diseases

Alicia Cristina Pena-Romero et al.

CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION (2018)

Article Hematology

MicroRNA-146a Induces Lineage-Negative Bone Marrow Cell Apoptosis and Senescence by Targeting Polo-Like Kinase 2 Expression

Shanming Deng et al.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2017)

Article Genetics & Heredity

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores

Kristi Laell et al.

GENETICS IN MEDICINE (2017)

Review Peripheral Vascular Disease

The impact of hypertension on leukocyte telomere length: a systematic review and meta-analysis of human studies

M. L. Tellechea et al.

JOURNAL OF HUMAN HYPERTENSION (2017)

Review Biochemistry & Molecular Biology

The Role of MicroRNAs in Myocardial Infarction: From Molecular Mechanism to Clinical Application

Teng Sun et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2017)

Article Cardiac & Cardiovascular Systems

Epigenetic Biomarkers and Cardiovascular Disease: Circulating MicroRNAs

David de Gonzalo-Calvo et al.

REVISTA ESPANOLA DE CARDIOLOGIA (2017)

Review Urology & Nephrology

The Expanding Role of APOL1 Risk in Chronic Kidney Disease and Cardiovascular Disease

Michelle M. Estrella et al.

SEMINARS IN NEPHROLOGY (2017)

Review Cardiac & Cardiovascular Systems

Genetic Architecture of Familial Hypercholesterolaemia

Mahtab Sharifi et al.

CURRENT CARDIOLOGY REPORTS (2017)

Article Peripheral Vascular Disease

Analysis of circulating miRNAs in patients with familial hypercholesterolaemia treated by LDL/Lp(a) apheresis

Dana Dlouha et al.

ATHEROSCLEROSIS SUPPLEMENTS (2017)

Review Cell Biology

FTO associations with obesity and telomere length

Yuling Zhou et al.

JOURNAL OF BIOMEDICAL SCIENCE (2017)

Review Cardiac & Cardiovascular Systems

MicroRNAs in the Pathobiology and Therapy of Atherosclerosis

Benoit Laffont et al.

CANADIAN JOURNAL OF CARDIOLOGY (2017)

Article Nutrition & Dietetics

Sugar-sweetened beverage intake, chromosome 9p21 variants, and risk of myocardial infarction in Hispanics

Yan Zheng et al.

AMERICAN JOURNAL OF CLINICAL NUTRITION (2016)

Review Cardiac & Cardiovascular Systems

microRNAs in lipoprotein metabolism and cardiometabolic disorders

Noemi Rotllan et al.

ATHEROSCLEROSIS (2016)

Article Cardiac & Cardiovascular Systems

Trends in Mortality From Ischemic Heart Disease and Cerebrovascular Disease in Europe: 1980 to 2009

Adam Hartley et al.

CIRCULATION (2016)

Review Medical Laboratory Technology

Sortilin: A novel regulator in lipid metabolism and atherogenesis

Li-yuan Zhong et al.

CLINICA CHIMICA ACTA (2016)

Article Cardiac & Cardiovascular Systems

Marginal role for 53 common genetic variants in cardiovascular disease prediction

Richard W. Morris et al.

HEART (2016)

Article Pharmacology & Pharmacy

Rare variants in known and novel candidate genes predisposing to statin-associated myopathy

Magdalena Neroldova et al.

PHARMACOGENOMICS (2016)

Article Obstetrics & Gynecology

An Introduction to Genome-Wide Association Studies: GWAS for Dummies

A. G. Uitterlinden

SEMINARS IN REPRODUCTIVE MEDICINE (2016)

Review Cardiac & Cardiovascular Systems

The role of microRNAs in coronary artery disease: From pathophysiology to diagnosis and treatment

Evangelos K. Economou et al.

ATHEROSCLEROSIS (2015)

Article Cardiac & Cardiovascular Systems

DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels

Liliane Pfeiffer et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2015)

Review Endocrinology & Metabolism

Effect of obesity on telomere length: Systematic review and meta-analysis

Eduardo Mundstock et al.

OBESITY (2015)

Article Multidisciplinary Sciences

Discordance of DNA Methylation Variance Between two Accessible Human Tissues

Ruiwei Jiang et al.

SCIENTIFIC REPORTS (2015)

Article Cardiac & Cardiovascular Systems

DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels

Liliane Pfeiffer et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2015)

Article Medicine, Research & Experimental

SLCO1B1 Polymorphism is not associated with Risk of Statin-Induced Myalgia/Myopathy in a Czech Population

Michal Vrablík

MEDICAL SCIENCE MONITOR (2015)

Article Endocrinology & Metabolism

Sixty-Five Common Genetic Variants and Prediction of Type 2 Diabetes

Philippa J. Talmud et al.

DIABETES (2015)

Article Genetics & Heredity

Genetic variability of microRNA regulome in human

Jana Obsteter et al.

MOLECULAR GENETICS & GENOMIC MEDICINE (2015)

Review Cell Biology

Obesity and FTO: Changing Focus at a Complex Locus

Y. C. Loraine Tung et al.

CELL METABOLISM (2014)

Review Genetics & Heredity

Genetic factors affecting statin concentrations and subsequent myopathy: a HuGENet systematic review

William J. Canestaro et al.

GENETICS IN MEDICINE (2014)

Review Endocrinology & Metabolism

The bigger picture of FTO-the first GWAS-identified obesity gene

Ruth J. F. Loos et al.

NATURE REVIEWS ENDOCRINOLOGY (2014)

Review Pharmacology & Pharmacy

The emerging role of epigenetics in cardiovascular disease

Charbel Abi Khalil

THERAPEUTIC ADVANCES IN CHRONIC DISEASE (2014)

Review Physiology

Statin-Associated Myopathy: From Genetic Predisposition to Clinical Management

M. Vrablik et al.

PHYSIOLOGICAL RESEARCH (2014)

Review Biochemistry & Molecular Biology

The Hallmarks of Aging

Carlos Lopez-Otin et al.

Article Peripheral Vascular Disease

Nutrigenetics and Nutrigenomics of Atherosclerosis

Aksam J. Merched et al.

CURRENT ATHEROSCLEROSIS REPORTS (2013)

Review Biochemistry & Molecular Biology

Oxidative stress in atherosclerosis: The role of microRNAs in arterial remodeling

Anna Zampetaki et al.

FREE RADICAL BIOLOGY AND MEDICINE (2013)

Review Pharmacology & Pharmacy

Pharmacogenetics and Cardiovascular Disease-Implications for Personalized Medicine

Julie A. Johnson et al.

PHARMACOLOGICAL REVIEWS (2013)

Article Cardiac & Cardiovascular Systems

Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia

Kristian Tveten et al.

ATHEROSCLEROSIS (2012)

Review Cardiac & Cardiovascular Systems

Profiling of circulating microRNAs: from single biomarkers to re-wired networks

Anna Zampetaki et al.

CARDIOVASCULAR RESEARCH (2012)

Article Medical Laboratory Technology

Association between FTO 1st intron tagging variant and telomere length in middle aged females. 3PMFs study

D. Dlouha et al.

CLINICA CHIMICA ACTA (2012)

Article Peripheral Vascular Disease

Sortilin as a Regulator of Lipoprotein Metabolism

Alanna Strong et al.

CURRENT ATHEROSCLEROSIS REPORTS (2012)

Article Public, Environmental & Occupational Health

Hypermethylation at loci sensitive to the prenatal environment is associated with increased incidence of myocardial infarction

Rudolf P. Talens et al.

INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2012)

Article Multidisciplinary Sciences

Genetic Variants in the Fat and Obesity Associated (FTO) Gene and Risk of Alzheimer's Disease

Christiane Reitz et al.

PLOS ONE (2012)

Review Hematology

From candidate gene to genome-wide association studies in cardiovascular disease

Francesco Gianfagna et al.

THROMBOSIS RESEARCH (2012)

Article Physiology

MicroRNA-126 contributes to renal microvascular heterogeneity of VCAM-1 protein expression in acute inflammation

S. A. Asgeirsdottir et al.

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2012)

Article Hematology

An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia

Christopher T. Johansen et al.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2011)

Review Cardiac & Cardiovascular Systems

Non-coding RNAs as regulators of gene expression and epigenetics

Minna U. Kaikkonen et al.

CARDIOVASCULAR RESEARCH (2011)

Article Pharmacology & Pharmacy

Pharmacogenetics: From Bench to Byte-An Update of Guidelines

J. J. Swen et al.

CLINICAL PHARMACOLOGY & THERAPEUTICS (2011)

Review Biochemistry & Molecular Biology

MicroRNAs in lipid metabolism

Carlos Fernandez-Hernando et al.

CURRENT OPINION IN LIPIDOLOGY (2011)

Review Pharmacology & Pharmacy

The genetic epidemiology of melanocortin 4 receptor variants

Ruth J. F. Loos

EUROPEAN JOURNAL OF PHARMACOLOGY (2011)

Article Multidisciplinary Sciences

Analysis of DNA Methylation in Various Swine Tissues

Chun Yang et al.

PLOS ONE (2011)

Article Biochemistry & Molecular Biology

The obesity-associated Fto gene is a transcriptional coactivator

Qiong Wu et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)

Article Medical Laboratory Technology

A FTO variant and risk of acute coronary syndrome

Jaroslav A. Hubacek et al.

CLINICA CHIMICA ACTA (2010)

Article Genetics & Heredity

Genetic markers in hypercholesterolemic and normocholesterolemic Czech children

Rudolf Poledne et al.

CLINICAL GENETICS (2010)

Review Medicine, General & Internal

Association Between 9p21 Genomic Markers and Heart Disease A Meta-analysis

Glenn E. Palomaki et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)

Article Multidisciplinary Sciences

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

Kiran Musunuru et al.

NATURE (2010)

Article Multidisciplinary Sciences

Biological, clinical and population relevance of 95 loci for blood lipids

Tanya M. Teslovich et al.

NATURE (2010)

Letter Genetics & Heredity

Distribution of the Alcohol Dehydrogenase ADH1B*47His Allele in Eurasia

Svetlana Borinskaya et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Article Genetics & Heredity

Multiple Distinct Risk Loci for Nicotine Dependence Identified by Dense Coverage of the Complete Family of Nicotinic Receptor Subunit (CHRN) Genes

Nancy L. Saccone et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)

Article Cardiac & Cardiovascular Systems

MicroRNA 217 Modulates Endothelial Cell Senescence via Silent Information Regulator 1

Rossella Menghini et al.

CIRCULATION (2009)

Article Cardiac & Cardiovascular Systems

The SLCO1B1*5 Genetic Variant Is Associated With Statin-Induced Side Effects

Deepak Voora et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)

Review Nutrition & Dietetics

Personalized nutrition for the prevention of cardiovascular disease: a future perspective

J. A. Lovegrove et al.

JOURNAL OF HUMAN NUTRITION AND DIETETICS (2008)

Review Genetics & Heredity

miRNAs at the heart of the matter

Zhiguo Wang et al.

JOURNAL OF MOLECULAR MEDICINE-JMM (2008)

Article Dentistry, Oral Surgery & Medicine

Epigenetic Regulation of Gene Expression in the Inflammatory Response and Relevance to Common Diseases

Anthony G. Wilson

JOURNAL OF PERIODONTOLOGY (2008)

Article Genetics & Heredity

Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

Jaspal S. Kooner et al.

NATURE GENETICS (2008)

Article Medicine, General & Internal

SLCO1B1Variants and Statin-Induced Myopathy — A Genomewide Study

NEW ENGLAND JOURNAL OF MEDICINE (2008)

Article Medicine, General & Internal

Genomewide association analysis of coronary artery disease

Nilesh J. Samani et al.

NEW ENGLAND JOURNAL OF MEDICINE (2007)

Article Genetics & Heredity

Variation in FTO contributes to childhood obesity and severe adult obesity

Christian Dina et al.

NATURE GENETICS (2007)

Article Genetics & Heredity

Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

Martin G. Larson et al.

BMC MEDICAL GENETICS (2007)

Article Genetics & Heredity

Role of cholesterol 7 alpha-hydroxylase (CYP7A1) in nutrigenetics and pharmacogenetics of cholesterol lowering

Jaroslav A. Hubacek et al.

MOLECULAR DIAGNOSIS & THERAPY (2006)

Article Multidisciplinary Sciences

Apolipoprotein L-I is the trypanosome lytic factor of human serum

L Vanhamme et al.

NATURE (2003)