Genetics of cardiovascular disease: Importance of sex and ethnicity.
暂无分享,去创建一个
[1] D. Mozaffarian,et al. Heart disease and stroke statistics--2014 update: a report from the American Heart Association. , 2014, Circulation.
[2] I-Min Lee,et al. A randomized trial of low-dose aspirin in the primary prevention of cardiovascular disease in women , 2005 .
[3] K. Taylor,et al. Association of androgen receptor CAG repeat polymorphism and polycystic ovary syndrome. , 2008, The Journal of clinical endocrinology and metabolism.
[4] Tanya M. Teslovich,et al. Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids , 2010, Nature.
[5] Jennifer F. Hughes,et al. Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators , 2014, Nature.
[6] Maria Gutierrez-Arcelus,et al. Sex-biased genetic effects on gene regulation in humans , 2012, Genome research.
[7] James M. Eales,et al. Male-Specific Region of the Y Chromosome and Cardiovascular Risk: Phylogenetic Analysis and Gene Expression Studies , 2013, Arteriosclerosis, thrombosis, and vascular biology.
[8] Barry J. Davis,et al. Efficacy and safety of LDL-lowering therapy among men and women: meta-analysis of individual data from 174 000 participants in 27 randomised trials , 2015, The Lancet.
[9] F. Collins,et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.
[10] C. Langefeld,et al. Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS). , 2006, American heart journal.
[11] Tom R. Gaunt,et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. , 2012, American journal of human genetics.
[12] S. Moon,et al. Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome. , 2008, Fertility and sterility.
[13] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[14] S. Schwartz,et al. Clonal architecture of normal and atherosclerotic aorta: implications for atherogenesis and vascular development. , 1998, The American journal of pathology.
[15] B. Ning,et al. Common genetic polymorphisms in the 5′-flanking Region of the SULT1A1 gene: haplotypes and their association with platelet enzymatic activity , 2005, Pharmacogenetics and genomics.
[16] K. Taylor,et al. Association of the diabetes gene calpain-10 with subclinical atherosclerosis: the Mexican-American Coronary Artery Disease Study. , 2005, Diabetes.
[17] D. Levy,et al. Vascular Stiffness and Genetic Variation at the Endothelial Nitric Oxide Synthase Locus: The Framingham Heart Study , 2007, Hypertension.
[18] T. Buchanan,et al. Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families. , 2008, Atherosclerosis.
[19] S. Kardia,et al. Sex steroid hormone polymorphisms, high-density lipoprotein cholesterol, and apolipoprotein A-1 from the Study of Women's Health Across the Nation (SWAN). , 2006, The American journal of medicine.
[20] Z. Rahimi,et al. AT2R -1332 G:A polymorphism and its interaction with AT1R 1166 A:C, ACE I/D and MMP-9 -1562 C:T polymorphisms: risk factors for susceptibility to preeclampsia. , 2014, Gene.
[21] P. Donnelly,et al. Inference of population structure using multilocus genotype data. , 2000, Genetics.
[22] Y. Gong,et al. β‐Adrenergic Receptor Gene Polymorphisms and β‐Blocker Treatment Outcomes in Hypertension , 2008, Clinical pharmacology and therapeutics.
[23] M. Link,et al. Gender-related differences in the clinical presentation and outcome of hypertrophic cardiomyopathy. , 2005, Journal of the American College of Cardiology.
[24] S. Juo. Genetics of carotid atherosclerosis. , 2009, Frontiers in bioscience.
[25] Louis Richer,et al. Functional Variation in the Androgen-Receptor Gene Is Associated With Visceral Adiposity and Blood Pressure in Male Adolescents , 2010, Hypertension.
[26] B. Horne,et al. Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids. , 2011, Journal of clinical & experimental cardiology.
[27] J. Nathans,et al. Cellular Resolution Maps of X Chromosome Inactivation: Implications for Neural Development, Function, and Disease , 2014, Neuron.
[28] C. Albert,et al. Epidemiology and genetics of sudden cardiac death. , 2012, Circulation.
[29] D. Page,et al. Functional coherence of the human Y chromosome. , 1997, Science.
[30] K. Korach,et al. Endothelial dysfunction in a man with disruptive mutation in oestrogen-receptor gene , 1997, The Lancet.
[31] T. Graves,et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes , 2003, Nature.
[32] N. Woods,et al. Polymorphisms in the estrogen synthesis and metabolism pathways and symptoms during the menopausal transition: observations from the Seattle Midlife Women's Health Study , 2006, Menopause.
[33] R. Weinshilboum,et al. Human phenol sulfotransferases SULT1A2 and SULT1A1: genetic polymorphisms, allozyme properties, and human liver genotype-phenotype correlations. , 1999, Biochemical pharmacology.
[34] C. Rajkumar. Effectiveness of intermittent pneumatic compression in reduction of risk of deep vein thrombosis in patients who have had a stroke (CLOTS 3): a multicentre randomised controlled trial , 2013 .
[35] Xu Li. Sex chromosomes and sex chromosome abnormalities. , 2011, Clinics in laboratory medicine.
[36] J. Gimble,et al. Bisphenol A enhances adipogenic differentiation of human adipose stromal/stem cells. , 2014, Journal of molecular endocrinology.
[37] Shane J. Neph,et al. A comparative encyclopedia of DNA elements in the mouse genome , 2014, Nature.
[38] K. Korach,et al. Premature coronary artery disease associated with a disruptive mutation in the estrogen receptor gene in a man. , 1997, Circulation.
[39] R. Collins,et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease , 2008, Nature Genetics.
[40] A. Folsom,et al. Carotid wall thickness is predictive of incident clinical stroke: the Atherosclerosis Risk in Communities (ARIC) study. , 2000, American journal of epidemiology.
[41] Tanya M. Teslovich,et al. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes , 2012, Nature Genetics.
[42] Tomas W. Fitzgerald,et al. Genetic basis of Y-linked hearing impairment. , 2013, American journal of human genetics.
[43] D. Schaid,et al. Human SULT1A1 gene: copy number differences and functional implications. , 2007, Human molecular genetics.
[44] P. Wolf,et al. Genetic and Environmental Contributions to Atherosclerosis Phenotypes in Men and Women: Heritability of Carotid Intima-Media Thickness in the Framingham Heart Study , 2003, Stroke.
[45] C. Disteche,et al. Genes that escape from X inactivation , 2011, Human Genetics.
[46] H. Markus,et al. The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis , 2006, Journal of Medical Genetics.
[47] S. Teutsch,et al. NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older. , 2003, Diabetes.
[48] J. Marchini,et al. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing , 2012, Nature Genetics.
[49] Vera Regitz-Zagrosek,et al. Gender differences in the metabolic syndrome and their role for cardiovascular disease , 2006, Clinical Research in Cardiology.
[50] J. Manson,et al. Estrogen therapy and coronary-artery calcification. , 2007, The New England journal of medicine.
[51] Paul M Ridker,et al. Inflammation in atherosclerosis: from pathophysiology to practice. , 2009, Journal of the American College of Cardiology.
[52] Mark D. Huffman,et al. AHA Statistical Update Heart Disease and Stroke Statistics — 2012 Update A Report From the American Heart Association WRITING GROUP MEMBERS , 2010 .
[53] Ross M. Fraser,et al. Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits , 2013, PLoS genetics.
[54] K. Kohara,et al. Association Between Risk Factors for Atherosclerosis and Mechanical Forces in Carotid Artery , 2000, Stroke.
[55] J. Murabito,et al. Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study , 2007, BMC Medical Genetics.
[56] L. Mosca. Sex, statins, and statistics , 2015, The Lancet.
[57] R. Sacco,et al. Segment-Specific Genetic Effects on Carotid Intima-Media Thickness: The Northern Manhattan Study , 2008, Stroke.
[58] R. Krauss,et al. Relationship of Sex to Diabetes Risk in Statin Trials , 2013, Diabetes Care.
[59] M. Fornage,et al. Matrix Gla protein and osteopontin genetic associations with coronary artery calcification and bone density: the CARDIA study , 2005, Human Genetics.
[60] Chong Shen,et al. Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease , 2012, Nature Genetics.
[61] C. Kooperberg,et al. Estrogen Receptor Polymorphisms and the Vascular Effects of Hormone Therapy , 2011, Arteriosclerosis, thrombosis, and vascular biology.
[62] A. Dominiczak,et al. Y is there a risk to being male? , 2003, Trends in Endocrinology & Metabolism.
[63] J. Graves. Review: Sex chromosome evolution and the expression of sex-specific genes in the placenta. , 2010, Placenta.
[64] Doris A Taylor,et al. Proceedings from the Scientific Symposium: Sex Differences in Cardiovascular Disease and Implications for Therapies , 2010 .
[65] J. Broderick,et al. The X-Chromosome Has a Different Pattern of Gene Expression in Women Compared With Men With Ischemic Stroke , 2012, Stroke.
[66] N. Samani,et al. Coronary artery disease predisposing haplogroup I of the Y chromosome, aggression and sex steroids--genetic association analysis. , 2014, Atherosclerosis.
[67] Christian Gieger,et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts , 2009, Nature Genetics.
[68] S. Kardia,et al. Sex steroid hormone pathway genes and health-related measures in women of 4 races/ethnicities: the Study of Women's Health Across the Nation (SWAN). , 2006, The American journal of medicine.
[69] Fabian J Theis,et al. Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers , 2011, PLoS genetics.
[70] Stacey J Winham,et al. Gene-environment interactions in genome-wide association studies: current approaches and new directions. , 2013, Journal of child psychology and psychiatry, and allied disciplines.
[71] A. Dyer,et al. Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat. , 2012, Journal of andrology.
[72] S. Juo,et al. Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis , 2010, BMC Medical Genetics.
[73] M. P. van den Berg,et al. Sex differences in cardiomyopathies , 2014, European journal of heart failure.
[74] Joseph B Hiatt,et al. Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster , 2011, Nature Genetics.
[75] Patrick Royston,et al. Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension , 2002, Arteriosclerosis, thrombosis, and vascular biology.
[76] R. Sacco,et al. Fine Mapping Study Reveals Novel Candidate Genes for Carotid Intima-Media Thickness in Dominican Republican Families , 2012, Circulation. Cardiovascular genetics.
[77] J. Manson,et al. Using Basic Science to Design a Clinical Trial: Baseline Characteristics of Women Enrolled in the Kronos Early Estrogen Prevention Study (KEEPS) , 2009, Journal of cardiovascular translational research.
[78] K. Bailey,et al. Alterations in Platelet Function and Cell-Derived Microvesicles in Recently Menopausal Women: Relationship to Metabolic Syndrome and Atherogenic Risk , 2011, Journal of cardiovascular translational research.
[79] Christian Gieger,et al. Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk , 2011, Nature.
[80] D. Clayton,et al. Testing for association on the X chromosome , 2008, Biostatistics.
[81] T. Graves,et al. Independent specialization of the human and mouse X chromosomes for the male germline , 2013, Nature Genetics.
[82] K. Matthews,et al. Symptoms, myocardial ischaemia and quality of life in women: results from the NHLBI-sponsored WISE Study. , 2003, European heart journal.
[83] I. Zineh,et al. Adrenergic gene polymorphisms and cardiovascular risk in the NHLBI-sponsored Women's Ischemia Syndrome Evaluation , 2008, Journal of Translational Medicine.
[84] Carolyn J. Brown,et al. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome , 1991, Nature.
[85] Takeshi Matsumura,et al. Statins Activate Peroxisome Proliferator-Activated Receptor γ Through Extracellular Signal-Regulated Kinase 1/2 and p38 Mitogen-Activated Protein Kinase–Dependent Cyclooxygenase-2 Expression in Macrophages , 2007, Circulation research.
[86] J. Stephens,et al. The structure of common genetic variation in United States populations. , 2007, American journal of human genetics.
[87] J. Mckinlay,et al. The androgen receptor gene CAG repeat polymorphism does not predict increased risk of heart disease: longitudinal results from the Massachusetts Male Ageing Study , 2006, Clinical endocrinology.
[88] R. Camerini-Otero,et al. The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation , 2004, Nature Genetics.
[89] Faha,et al. Aha Guideline Effectiveness-based Guidelines for the Prevention of Cardiovascular Disease in Women—2011 Update a Guideline from the American Heart Association Executive Writing Committee Expert Panel Members Cvd Risk Assessment Table 1. Class Iii Interventions (not Useful/effective and May Be Harmfu , 2022 .
[90] Q. Z. Li,et al. Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family , 2004, Journal of Medical Genetics.
[91] C. H. Liu,et al. Heritability of Subclinical Atherosclerosis in Latino Families Ascertained Through a Hypertensive Parent , 2002, Arteriosclerosis, thrombosis, and vascular biology.
[92] Jennifer G. Robinson,et al. Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Disease Risk in Adults: Synopsis of the 2013 American College of Cardiology/American Heart Association Cholesterol Guideline , 2014, Annals of Internal Medicine.
[93] Robin Lovell-Badge,et al. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif , 1990, Nature.
[94] K. Taylor,et al. A Genome-Wide Scan for Carotid Artery Intima-Media Thickness: The Mexican-American Coronary Artery Disease Family Study , 2005, Stroke.
[95] Hynek Pikhart,et al. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials , 2015, The Lancet.
[96] R. Detrano,et al. Ethnic Differences in Coronary Calcification: The Multi-Ethnic Study of Atherosclerosis (MESA) , 2005, Circulation.
[97] R. Wild,et al. Characterizing Cardiovascular Risk in Women with Polycystic Ovary Syndrome: More than the Sum of Its Parts? , 2009, Seminars in reproductive medicine.
[98] D. Thomas,et al. Gene–environment-wide association studies: emerging approaches , 2010, Nature Reviews Genetics.
[99] David L. Steffen,et al. The DNA sequence of the human X chromosome , 2005, Nature.
[100] B. Lejeune,et al. Effects of beta1-adrenoceptor genetic polymorphisms on resting hemodynamics in patients undergoing diagnostic testing for ischemia. , 2001, The American journal of cardiology.
[101] S. Crawford,et al. Vasomotor symptom prevalence is associated with polymorphisms in sex steroid-metabolizing enzymes and receptors. , 2006, The American journal of medicine.
[102] E M Wijsman,et al. Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women. , 1996, American journal of human genetics.
[103] Nilesh J Samani,et al. Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome , 2012, The Lancet.
[104] H. Sprecher,et al. Estrogen-induced Production of a Peroxisome Proliferator-activated Receptor (PPAR) Ligand in a PPARγ-expressing Tissue* , 1998, The Journal of Biological Chemistry.
[105] T. Manolio,et al. eXclusion: toward integrating the X chromosome in genome-wide association analyses. , 2013, American journal of human genetics.
[106] E. Bleecker,et al. Common Estrogen Receptor Polymorphism Augments Effects of Hormone Replacement Therapy on E-Selectin but Not C-Reactive Protein , 2002, Circulation.
[107] C. Disteche. Dosage compensation of the sex chromosomes. , 2012, Annual review of genetics.
[108] Michael Zitzmann,et al. The CAG repeat polymorphism within the androgen receptor gene and maleness. , 2003, International journal of andrology.
[109] Michael Lehrke,et al. The Many Faces of PPARγ , 2005, Cell.
[110] C. Clancy,et al. Effects of Sex Hormones on Cardiac Repolarization , 2010, Journal of Cardiovascular Pharmacology.
[111] E. Bleecker,et al. Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease. , 2002, The New England journal of medicine.
[112] D. Page,et al. Four evolutionary strata on the human X chromosome. , 1999, Science.
[113] J. Hanover,et al. Chromosome Imbalance as a Driver of Sex Disparity in Disease , 2014, Journal of genomics.
[114] David N. Rider,et al. Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study. , 2013, Physiological genomics.
[115] H. Willard,et al. X-inactivation profile reveals extensive variability in X-linked gene expression in females , 2005, Nature.
[116] J. Blangero,et al. Effects of genotype‐by‐sex interaction on quantitative trait linkage analysis , 1997, Genetic epidemiology.
[117] Stephen R. Williams,et al. Genome-Wide Meta-Analysis of Homocysteine and Methionine Metabolism Identifies Five One Carbon Metabolism Loci and a Novel Association of ALDH1L1 with Ischemic Stroke , 2014, PLoS genetics.
[118] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[119] Thomas Meitinger,et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution , 2010, Nature Genetics.
[120] Kathleen F. Kerr,et al. Genetics of coronary artery calcification among African Americans, a meta-analysis , 2013, BMC Medical Genetics.
[121] M. Turner,et al. Which Sry Locus Is the Hypertensive Y Chromosome Locus? , 2009, Hypertension.