Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases
暂无分享,去创建一个
[1] Kyle J. Gaulton,et al. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations , 2018, PLoS Genetics.
[2] Dajiang J. Liu,et al. Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants contributing to lipid levels and coronary artery disease , 2017, Nature Genetics.
[3] Henry J. Lin,et al. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk , 2017, Nature Communications.
[4] Andrew D. Johnson,et al. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney , 2017, Hypertension.
[5] J. Danesh,et al. Association analyses based on false discovery rate implicate new loci for coronary artery disease , 2017, Nature Genetics.
[6] Kathleen F. Kerr,et al. Genetic loci associated with heart rate variability and their effects on cardiac disease risk , 2017, Nature Communications.
[7] Xiaofeng Zhu,et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations , 2017, PLoS genetics.
[8] Y. Kamatani,et al. Identification of six new genetic loci associated with atrial fibrillation in the Japanese population , 2017, Nature Genetics.
[9] Y. Teo,et al. Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians , 2017, Circulation. Cardiovascular genetics.
[10] Archie Campbell,et al. Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants , 2017, Genome Medicine.
[11] He Gao,et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk , 2017, Nature Genetics.
[12] E. Boerwinkle,et al. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. , 2016, The New England journal of medicine.
[13] A. Yashin,et al. Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases , 2016, Front. Genet..
[14] Shuohua Chen,et al. Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension , 2016, Scientific Reports.
[15] M. Jarvelin,et al. International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents , 2016, Circulation. Cardiovascular genetics.
[16] Ruth McPherson,et al. Genetics of Coronary Artery Disease. , 2016, Circulation research.
[17] Munish Mehta,et al. A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. , 2016, Atherosclerosis.
[18] Jing He,et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation , 2015, Nature Genetics.
[19] J. Danesh,et al. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease , 2016 .
[20] Sara M. Willems,et al. The impact of low-frequency and rare variants on lipid levels , 2015, Nature Genetics.
[21] D. Rao,et al. Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study. , 2015, American journal of hypertension.
[22] Xueli Yang,et al. Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. , 2015, Human molecular genetics.
[23] A. Stewart,et al. Functional Genomics of the 9p21.3 Locus for Atherosclerosis: Clarity or Confusion? , 2014, Current Cardiology Reports.
[24] Markus Perola,et al. Amerindian-specific regions under positive selection harbour new lipid variants in Latinos , 2014, Nature Communications.
[25] Michael J Ackerman,et al. Nature Genetics Advance Online Publication Genetic Association Study of Qt Interval Highlights Role for Calcium Signaling Pathways in Myocardial Repolarization , 2022 .
[26] D. Rao,et al. Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9 , 2013, Front. Genet..
[27] Tanya M. Teslovich,et al. Discovery and refinement of loci associated with lipid levels , 2013, Nature Genetics.
[28] Matteo Trudu,et al. Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression , 2013, Nature Medicine.
[29] Xiaofeng Zhu,et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. , 2013, American journal of human genetics.
[30] Peter F. Stadler,et al. Alu Elements in ANRIL Non-Coding RNA at Chromosome 9p21 Modulate Atherogenic Cell Functions through Trans-Regulation of Gene Networks , 2013, PLoS genetics.
[31] Arcadi Navarro,et al. High Trans-ethnic Replicability of GWAS Results Implies Common Causal Variants , 2013, PLoS genetics.
[32] Claude Bouchard,et al. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders , 2014 .
[33] T. Assimes,et al. Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. , 2013, Journal of the American College of Cardiology.
[34] Juyoung Lee,et al. A genome-wide association study of a coronary artery disease risk variant , 2013, Journal of Human Genetics.
[35] Jason H. Moore,et al. Chapter 11: Genome-Wide Association Studies , 2012, PLoS Comput. Biol..
[36] Chong Shen,et al. Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease , 2012, Nature Genetics.
[37] Jean-Baptiste Cazier,et al. Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis , 2012, PloS one.
[38] K. Lunetta,et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation , 2012, Nature Genetics.
[39] T. Ogihara,et al. Genome-wide association study of coronary artery disease in the Japanese , 2011, European Journal of Human Genetics.
[40] Taesung Park,et al. Large-scale genome-wide association studies in east Asians identify new genetic loci influencing metabolic traits , 2011, Nature Genetics.
[41] Christian Gieger,et al. Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk , 2011, Nature.
[42] Christian Gieger,et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure , 2011, Nature Genetics.
[43] N. Mehta. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. , 2011, Circulation. Cardiovascular genetics.
[44] Tien Yin Wong,et al. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians , 2011, Nature Genetics.
[45] R. Elston,et al. Two-marker association tests yield new disease associations for coronary artery disease and hypertension , 2011, Human Genetics.
[46] L. Fauchier,et al. A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. , 2011, European heart journal.
[47] Raymond K. Auerbach,et al. A User's Guide to the Encyclopedia of DNA Elements (ENCODE) , 2011, PLoS biology.
[48] Thomas W. Mühleisen,et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease , 2011, Nature Genetics.
[49] Donald W. Bowden,et al. Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project , 2011, PLoS genetics.
[50] Mark I. McCarthy,et al. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease , 2011, Nature Genetics.
[51] 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.
[52] Jingyuan Fu,et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction , 2010, Nature Genetics.
[53] L. Peltonen,et al. A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses , 2010, The Lancet.
[54] J. Pell,et al. Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension , 2010, PLoS genetics.
[55] P. Madsen,et al. Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export. , 2010, Cell metabolism.
[56] Olle Melander,et al. From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus , 2010, Nature.
[57] Tanya M. Teslovich,et al. Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids , 2010, Nature.
[58] Eric Boerwinkle,et al. 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 , 2010, Circulation. Cardiovascular genetics.
[59] Thomas Meitinger,et al. Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation , 2010, Nature Genetics.
[60] Mark N. Wass,et al. Genetic variation in SCN10A influences cardiac conduction , 2010, Nature Genetics.
[61] Christian Gieger,et al. Genome-wide association study of PR interval , 2010, Nature Genetics.
[62] H. Boezen,et al. Genome-wide association studies: what do they teach us about asthma and chronic obstructive pulmonary disease? , 2009, Proceedings of the American Thoracic Society.
[63] P. Park. ChIP–seq: advantages and challenges of a maturing technology , 2009, Nature Reviews Genetics.
[64] C. Gieger,et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke , 2009, Nature Genetics.
[65] P. O’Reilly,et al. Genome-wide association study identifies eight loci associated with blood pressure , 2009, Nature Genetics.
[66] Andrew D. Johnson,et al. Genome-wide association study of blood pressure and hypertension , 2009, Nature Genetics.
[67] Thomas Lumley,et al. Common variants at ten loci influence QT interval duration in the QTGEN Study , 2009, Nature Genetics.
[68] Daniel F. Schwarz,et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3 , 2009, Nature Genetics.
[69] Benjamin J. Wright,et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease , 2009, Nature Genetics.
[70] M. Daly,et al. Estimation of the multiple testing burden for genomewide association studies of nearly all common variants , 2008, Genetic epidemiology.
[71] T. Manolio,et al. How to Interpret a Genome-wide Association Study Topic Collections , 2022 .
[72] D. Strachan,et al. LDL-cholesterol concentrations: a genome-wide association study , 2008, The Lancet.
[73] P. Elliott,et al. Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides , 2008, Nature Genetics.
[74] Dolores Corella,et al. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans , 2008, Nature Genetics.
[75] Daniel Levy,et al. Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness , 2007, BMC Medical Genetics.
[76] Kari Stefansson,et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. , 2007, Science.
[77] C. Gieger,et al. Genomewide association analysis of coronary artery disease. , 2007, The New England journal of medicine.
[78] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[79] Marcia M. Nizzari,et al. Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels , 2007, Science.
[80] S. Hiramitsu,et al. [Heart failure due to dilated cardiomyopathy]. , 2007, Nihon rinsho. Japanese journal of clinical medicine.
[81] Jonathan C. Cohen,et al. A Common Allele on Chromosome 9 Associated with Coronary Heart Disease , 2007, Science.
[82] Christian Gieger,et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization , 2006, Nature Genetics.
[83] Martin Farrall,et al. Genetic susceptibility to coronary artery disease: from promise to progress , 2006, Nature Reviews Genetics.
[84] N. Tommerup,et al. Molecular Identification of a Novel Candidate Sorting Receptor Purified from Human Brain by Receptor-associated Protein Affinity Chromatography* , 1997, The Journal of Biological Chemistry.
[85] T. Takeshita,et al. Phenotypic differences in low Km aldehyde dehydrogenase in Japanese workers , 1993, The Lancet.
[86] P. D. Oldham,et al. The Hereditary Factor in Arterial Blood-pressure , 1963, British medical journal.
[87] Camilla,et al. A sequence variant in ZFHX 3 on 16 q 22 associates with atrial fibrillation and ischemic stroke , 2009 .