Screening of Candidate Coronary Artery Disease Genes in Pakistani Population
暂无分享,去创建一个
[1] P. Armitage. Tests for Linear Trends in Proportions and Frequencies , 1955 .
[2] V. Froelicher,et al. Analysis of epidemiologic studies of physical inactivity as risk factor for coronary artery disease , 1973 .
[3] A. Copley,et al. The physiological significance of the endoendothelial fibrin lining (EEFL) as the critical interface in the "vessel-blood organ' and the importance of in vivo "fibrinogenin formation' in health and disease. , 1983, Thrombosis research.
[4] J. Walker,et al. The delta-subunit of ATP synthase from bovine heart mitochondria. Complementary DNA sequence of its import precursor cloned with the aid of the polymerase chain reaction. , 1990, The Biochemical journal.
[5] G. Jansen,et al. Who Are Guidelines For , 1990 .
[6] D. Levy,et al. Lipids and risk of coronary heart disease. The Framingham Study. , 1992, Annals of epidemiology.
[7] G. Watts,et al. Effects on coronary artery disease of lipid-lowering diet, or diet plus cholestyramine, in the St Thomas' Atherosclerosis Regression Study (STARS) , 1992, The Lancet.
[8] Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S) , 1994, The Lancet.
[9] L. Berkman,et al. Genetic susceptibility to death from coronary heart disease in a study of twins. , 1994, The New England journal of medicine.
[10] P. Wilson,et al. Established risk factors and coronary artery disease: the Framingham Study. , 1994, American journal of hypertension.
[11] D. Wilcken,et al. Polymorphisms of the apolipoprotein E gene and severity of coronary artery disease defined by angiography. , 1995, Arteriosclerosis, thrombosis, and vascular biology.
[12] T. Mazzone. Apolipoprotein E secretion by macrophages: its potential physiological functions , 1996, Current opinion in lipidology.
[13] Jonathan D. Smith,et al. Apolipoprotein E allele–specific antioxidant activity and effects on cytotoxicity by oxidative insults and β–amyloid peptides , 1996, Nature Genetics.
[14] K. Marder,et al. The APOE- (cid:101) 4 Allele and the Risk of Alzheimer Disease Among African Americans, Whites, and Hispanics , 2001 .
[15] A. Gotto. Triglyceride as a risk factor for coronary artery disease. , 1998, The American journal of cardiology.
[16] S. Yusuf,et al. Cardiovascular and cancer mortality among Canadians of European, south Asian and Chinese origin from 1979 to 1993: an analysis of 1.2 million deaths. , 1999, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.
[17] A. Vaughan,et al. The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway. , 1999, The Journal of clinical investigation.
[18] M. Daly,et al. Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. , 2000, American journal of human genetics.
[19] J. Pritchard,et al. Linkage disequilibrium in humans: models and data. , 2001, American journal of human genetics.
[20] S. Yusuf,et al. Global burden of cardiovascular diseases: part I: general considerations, the epidemiologic transition, risk factors, and impact of urbanization. , 2001, Circulation.
[21] A. Sharrett,et al. Coronary Heart Disease Prediction From Lipoprotein Cholesterol Levels, Triglycerides, Lipoprotein(a), Apolipoproteins A-I and B, and HDL Density Subfractions: The Atherosclerosis Risk in Communities (ARIC) Study , 2001, Circulation.
[22] C. Dina,et al. A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27. , 2001, Human molecular genetics.
[23] Y. Zhi. Apolipoprotein E Alleles, Dyslipidemia,and Coronary Heart Disease , 2001 .
[24] Pardis C Sabeti,et al. Linkage disequilibrium in the human genome , 2001, Nature.
[25] A. Tonkin,et al. Genome-Wide Linkage Analysis of the Acute Coronary Syndrome Suggests a Locus on Chromosome 2 , 2002, Arteriosclerosis, thrombosis, and vascular biology.
[26] T. Henry,et al. Pharmacological Treatment of Coronary Artery Disease With Recombinant Fibroblast Growth Factor-2: Double-Blind, Randomized, Controlled Clinical Trial , 2002, Circulation.
[27] R. Collins,et al. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies , 2002, The Lancet.
[28] B. Sobel. Effects of glycemic control and other determinants on vascular disease in type 2 diabetes. , 2002, The American journal of medicine.
[29] S. Liu-Cordero. Patterns of linkage disequilibrium in the human genome , 2002 .
[30] A. Simon,et al. Intima–media thickness: a new tool for diagnosis and treatment of cardiovascular risk , 2002, Journal of hypertension.
[31] Lisa J. Martin,et al. A comprehensive linkage analysis for myocardial infarction and its related risk factors , 2002, Nature Genetics.
[32] W. Dietz,et al. Prevalence of the metabolic syndrome among US adults: findings from the third National Health and Nutrition Examination Survey. , 2002, JAMA.
[33] A. Yashin,et al. Heritability of death from coronary heart disease: a 36‐year follow‐up of 20 966 Swedish twins , 2002, Journal of internal medicine.
[34] Berrit C Stroehla,et al. Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review. , 2002, American journal of epidemiology.
[35] A. Lakkaraju,et al. Low-density Lipoprotein Receptor-related Protein Mediates the Endocytosis of Anionic Liposomes in Neurons* 210 , 2002, The Journal of Biological Chemistry.
[36] H. Izawa,et al. Prediction of the risk of myocardial infarction from polymorphisms in candidate genes. , 2002 .
[37] T. Langmann,et al. Mutations in the human ATP‐binding cassette transporters ABCG5 and ABCG8 in sitosterolemia , 2002, Human mutation.
[38] S. Reis,et al. APOE polymorphism and angiographic coronary artery disease severity in the Women's Ischemia Syndrome Evaluation (WISE) study. , 2003, Atherosclerosis.
[39] E. Topol,et al. Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease , 2003, Science.
[40] Daniel W. Jones,et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. , 2003, JAMA.
[41] E. Topol,et al. Thrombospondin-4 and Its Variants: Expression and Differential Effects on Endothelial Cells , 2003, Circulation.
[42] A. Marais. Familial hypercholesterolaemia. , 2004, The Clinical biochemist. Reviews.
[43] I. Fearnley,et al. The Phosphorylation of Subunits of Complex I from Bovine Heart Mitochondria* , 2004, Journal of Biological Chemistry.
[44] A. Lusis,et al. Effect of macrophage-derived apolipoprotein E on hyperlipidemia and atherosclerosis of LDLR-deficient mice. , 2004, Biochemical and biophysical research communications.
[45] E. Topol,et al. Transcription factor MEF2A mutations in patients with coronary artery disease. , 2004, Human molecular genetics.
[46] Yusuke Nakamura,et al. Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro , 2004, Nature.
[47] T. Hirao. Disability‐adjusted life expectancy: Is it useful? , 2004 .
[48] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[49] P. Poole‐Wilson,et al. 5-year outcome of an interventional strategy in non-ST-elevation acute coronary syndrome: the British Heart Foundation RITA 3 randomised trial , 2005, The Lancet.
[50] E. Topol,et al. Identification of four gene variants associated with myocardial infarction. , 2005, American journal of human genetics.
[51] P. Libby,et al. Pathophysiology of Coronary Artery Disease , 2005, Circulation.
[52] N. Chaturvedi,et al. Heart disease epidemic in Pakistan: women and men at equal risk. , 2005, American heart journal.
[53] U. Thorsteinsdóttir,et al. Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population. , 2005, American journal of human genetics.
[54] P. Burton,et al. A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study. , 2005, American journal of human genetics.
[55] William Stafford Noble,et al. Quantifying similarity between motifs , 2007, Genome Biology.
[56] Alan D. Lopez,et al. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data , 2006, The Lancet.
[57] Jonathan C. Cohen,et al. Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. , 2006, The New England journal of medicine.
[58] R. Collins,et al. Genome-Wide Mapping of Susceptibility to Coronary Artery Disease Identifies a Novel Replicated Locus on Chromosome 17 , 2006, PLoS genetics.
[59] G. Abecasis,et al. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies , 2006, Nature Genetics.
[60] T. Hudson,et al. Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol. , 2007, American journal of human genetics.
[61] C. Gieger,et al. Genomewide association analysis of coronary artery disease. , 2007, The New England journal of medicine.
[62] N. Pedersen,et al. Genetic influences on angina pectoris and its impact on coronary heart disease , 2007, European Journal of Human Genetics.
[63] Inna Dubchak,et al. VISTA Enhancer Browser—a database of tissue-specific human enhancers , 2006, Nucleic Acids Res..
[64] R. Luben,et al. Apolipoprotein E polymorphisms, dietary fat and fibre, and serum lipids: the EPIC Norfolk study. , 2007, European heart journal.
[65] E. Enas,et al. Dyslipidemia in South Asian patients , 2007, Current atherosclerosis reports.
[66] P. Grant. Diabetes mellitus as a prothrombotic condition , 2007, Journal of internal medicine.
[67] A. Gylfason,et al. A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction , 2007, Science.
[68] S. Yusuf,et al. Global burden of cardiovascular disease , 2007, Heart.
[69] T. Jafar,et al. Coronary artery disease epidemic in Pakistan: more electrocardiographic evidence of ischaemia in women than in men , 2007, Heart.
[70] M. McCarthy,et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges , 2008, Nature Reviews Genetics.
[71] T. Furey,et al. A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease , 2009, Human Genomics.
[72] Brad T. Sherman,et al. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.
[73] P. Huber,et al. Endothelial adherens and tight junctions in vascular homeostasis, inflammation and angiogenesis. , 2008, Biochimica et biophysica acta.
[74] Andrew D. Johnson,et al. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap , 2008, Bioinform..
[75] M. Bodén,et al. Associating transcription factor-binding site motifs with target GO terms and target genes , 2008, Nucleic acids research.
[76] K. Furie,et al. Heart disease and stroke statistics--2008 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. , 2007, Circulation.
[77] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[78] R. Collins,et al. Body-mass index and cause-specific mortality in 900 000 adults: collaborative analyses of 57 prospective studies , 2009, The Lancet.
[79] Daniel F. Schwarz,et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3 , 2009, Nature Genetics.
[80] T. Hudson,et al. Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups: The INTERHEART Genetics Study , 2009, Circulation. Cardiovascular genetics.
[81] P. Greenland. Time for the medical profession to act: new policies needed now on interactions between pharmaceutical companies and physicians. , 2009, Archives of internal medicine.
[82] Anping Chen,et al. Curcumin suppresses expression of low‐density lipoprotein (LDL) receptor, leading to the inhibition of LDL‐induced activation of hepatic stellate cells , 2009, British journal of pharmacology.
[83] D. Postma,et al. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction , 2009, Nature Genetics.
[84] R. Collins,et al. Common variants at 30 loci contribute to polygenic dyslipidemia , 2009, Nature Genetics.
[85] S. Yusuf,et al. Relationship of the ApoE polymorphism to plasma lipid traits among South Asians, Chinese, and Europeans living in Canada. , 2009, Atherosclerosis.
[86] R. Collins,et al. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. , 2009, The New England journal of medicine.
[87] P. Deloukas,et al. Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease , 2009, Arteriosclerosis, thrombosis, and vascular biology.
[88] Mikael Bodén,et al. Assigning roles to DNA regulatory motifs using comparative genomics , 2010, Bioinform..
[89] Jason H. Moore,et al. Missing heritability and strategies for finding the underlying causes of complex disease , 2010, Nature Reviews Genetics.
[90] G. Bakris,et al. Tight blood pressure control and cardiovascular outcomes among hypertensive patients with diabetes and coronary artery disease. , 2010, JAMA.
[91] L. Lloyd,et al. Childhood obesity and adult cardiovascular disease risk: a systematic review , 2010, International Journal of Obesity.
[92] K. Siddiqi,et al. Local Determinants of Tobacco Use in Pakistan and the Importance of Context , 2010 .
[93] M. Pepe,et al. The Potential of Genes and Other Markers to Inform about Risk , 2010, Cancer Epidemiology, Biomarkers & Prevention.
[94] Nathaniel D. Heintzman,et al. 9p21 DNA variants associated with Coronary Artery Disease impair IFNγ signaling response , 2011, Nature.
[95] Y. Fujiwara,et al. Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. , 2011, Atherosclerosis.
[96] C. Gieger,et al. Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. , 2011, European heart journal.
[97] P. Libby,et al. Progress and challenges in translating the biology of atherosclerosis , 2011, Nature.
[98] Simon C. Potter,et al. Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease , 2011, PLoS genetics.
[99] 明石 昌也. A coronary artery disease-associated gene product, JCAD/KIAA1462, is a novel component of endothelial cell-cell junctions , 2011 .
[100] Qing Yang,et al. Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population , 2011, Nature Genetics.
[101] E. Nabel,et al. Genomics of cardiovascular disease. , 2011, The New England journal of medicine.
[102] Masasuke Yoshida,et al. Knockdown of DAPIT (Diabetes-associated Protein in Insulin-sensitive Tissue) Results in Loss of ATP Synthase in Mitochondria , 2011, The Journal of Biological Chemistry.
[103] N. Mehta. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. , 2011, Circulation. Cardiovascular genetics.
[104] T. Assimes,et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies , 2011, The Lancet.
[105] L. F. A. Marrzoq,et al. Relationship between ApoE gene polymorphism and coronary heart disease in Gaza Strip , 2011, Journal of cardiovascular disease research.
[106] E. Topol,et al. Emerging genomic applications in coronary artery disease. , 2011, JACC. Cardiovascular interventions.
[107] Inna Dubchak,et al. VISTA Region Viewer (RViewer) - a computational system for prioritizing genomic intervals for biomedical studies , 2011, Bioinform..
[108] Jason H. Moore,et al. Chapter 11: Genome-Wide Association Studies , 2012, PLoS Comput. Biol..
[109] F. Ippoliti,et al. Cellular and molecular players in the atherosclerotic plaque progression , 2012, Annals of the New York Academy of Sciences.
[110] T. Ogihara,et al. Genome-wide association study of coronary artery disease in the Japanese , 2011, European Journal of Human Genetics.
[111] A. Marian. Molecular genetic studies of complex phenotypes. , 2012, Translational research : the journal of laboratory and clinical medicine.
[112] T. Lüscher,et al. Molecular mechanisms of vascular effects of High-density lipoprotein: alterations in cardiovascular disease , 2012, EMBO molecular medicine.
[113] Jake K. Byrnes,et al. Bayesian refinement of association signals for 14 loci in 3 common diseases , 2012, Nature Genetics.
[114] T. Spector,et al. Understanding coronary artery disease using twin studies , 2012, Heart.
[115] Natalie de Souza. The ENCODE project , 2012, Nature Methods.
[116] Rafael C. Jimenez,et al. The IntAct molecular interaction database in 2012 , 2011, Nucleic Acids Res..
[117] Andre Franke,et al. 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data , 2012, European Journal of Human Genetics.
[118] Eurie L. Hong,et al. Annotation of functional variation in personal genomes using RegulomeDB , 2012, Genome research.
[119] P. Malani. Harrison’s Principles of Internal Medicine , 2012 .
[120] D. Francis,et al. Mortality from ischaemic heart disease by country, region, and age: Statistics from World Health Organisation and United Nations , 2013, International journal of cardiology.
[121] J. Danesh,et al. Large-scale association analysis identifies new risk loci for coronary artery disease , 2013 .
[122] P. D. Zende,et al. Apolipoprotein e gene polymorphism and its effect on plasma lipids in arteriosclerosis. , 2013, Journal of clinical and diagnostic research : JCDR.
[123] V. Fuster,et al. Histopathologic characteristics of atherosclerotic coronary disease and implications of the findings for the invasive and noninvasive detection of vulnerable plaques. , 2013, Journal of the American College of Cardiology.
[124] Yan-wei Yin,et al. Association between Apolipoprotein E Gene Polymorphism and the Risk of Coronary Artery Disease in Chinese Population: Evidence from a Meta-Analysis of 40 Studies , 2013, PloS one.
[125] Ruoling Chen,et al. South Asians and coronary disease: is there discordance between effects on incidence and prognosis? , 2013, Heart.
[126] M. Budoff,et al. Mediators of Atherosclerosis in South Asians Living in America (MASALA) Study: Objectives, Methods, and Cohort Description , 2013, Clinical cardiology.
[127] Mark D. Huffman,et al. Executive summary: heart disease and stroke statistics--2013 update: a report from the American Heart Association. , 2013, Circulation.
[128] A. Aggarwal,et al. Cardiovascular Risk Factors in Young Patients of Coronary Artery Disease: Differences over a Decade , 2014, Journal of cardiovascular and thoracic research.
[129] David J. Arenillas,et al. JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles , 2013, Nucleic Acids Res..
[130] C. Murray,et al. Variations in ischemic heart disease burden by age, country, and income: the Global Burden of Diseases, Injuries, and Risk Factors 2010 study. , 2014, Global heart.
[131] Sonia S Anand,et al. Cardiovascular disease in Asian Americans: unmasking heterogeneity. , 2014, Journal of the American College of Cardiology.
[132] R. Roberts. Genetics of coronary artery disease: an update. , 2014, Methodist DeBakey cardiovascular journal.
[133] B. Snitz,et al. Association of APOE polymorphisms and stressful life events with dementia in a Pakistani population , 2014, Neuroscience Letters.
[134] S. Lerakis,et al. New and Emerging Risk Factors for Coronary Heart Disease , 2014, The American journal of the medical sciences.
[135] P. Scarborough,et al. Corrigendum to: cardiovascular disease in Europe 2014: epidemiological update. , 2015, European heart journal.
[136] J. Danesh,et al. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease , 2016 .
[137] Yusuke Nakamura,et al. A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese , 2022 .
[138] Coronary artery dimensions: Iranian population versus Indo-Asians and Caucasians , 2015, Asian cardiovascular & thoracic annals.
[139] Á. Avezum,et al. Cardiovascular Disease Burden: Evolving Knowledge of Risk Factors in Myocardial Infarction and Stroke through Population-Based Research and Perspectives in Global Prevention , 2015, Front. Cardiovasc. Med..
[140] Sonia S Anand,et al. Cardiovascular Disease in South Asian Migrants. , 2015, The Canadian journal of cardiology.
[141] B. Litschauer,et al. Physical inactivity increases endostatin and osteopontin in patients with coronary artery disease , 2016, Heart and Vessels.
[142] Asma N. Cheema,et al. APOE Gene Polymorphism and Risk of Coronary Stenosis in Pakistani Population , 2015, BioMed research international.
[143] C. Foster,et al. The physical activity profiles of South Asian ethnic groups in England , 2015, Journal of Epidemiology & Community Health.
[144] C. Fischbacher,et al. Ethnicity and risk of cardiovascular disease (CVD): 4.8 year follow-up of patients with type 2 diabetes living in Scotland , 2015, Diabetologia.
[145] Kengo Kinoshita,et al. COXPRESdb in 2015: coexpression database for animal species by DNA-microarray and RNAseq-based expression data with multiple quality assessment systems , 2014, Nucleic Acids Res..
[146] K. Bibbins-Domingo,et al. Global Overview of the Epidemiology of Atherosclerotic Cardiovascular Disease. , 2015, Archives of medical research.
[147] John E. Hall,et al. Guyton and Hall Textbook of Medical Physiology , 2015 .
[148] C. Gieger,et al. Genetic Evidence for PLASMINOGEN as a Shared Genetic Risk Factor of Coronary Artery Disease and Periodontitis , 2015, Circulation. Cardiovascular genetics.
[149] Tanya M. Teslovich,et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study , 2015, PLoS Genetics.
[150] R. Feldman. Heart Disease in Women: Unappreciated Challenges, GPER as a New Target , 2016, International journal of molecular sciences.
[151] R. Zweiker,et al. Hypertension and coronary artery disease: epidemiology, physiology, effects of treatment, and recommendations , 2016, Wiener klinische Wochenschrift.
[152] F. Dudbridge. Polygenic Epidemiology , 2016, Genetic epidemiology.
[153] C. Varma,et al. Epidemiology and pathogenesis of diffuse obstructive coronary artery disease: the role of arterial stiffness, shear stress, monocyte subsets and circulating microparticles , 2016, Annals of medicine.
[154] David J. Arenillas,et al. JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles , 2015, Nucleic Acids Res..
[155] Shu-guang Lin,et al. Ischemic heart disease deaths, disability-adjusted life years and risk factors in Fujian, China during 1990-2013: Data from the Global Burden of Disease Study 2013. , 2016, International journal of cardiology.