Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits
暂无分享,去创建一个
Manuel A. R. Ferreira | Nicholas G Martin | Andrew C Heath | N. Martin | J. Whitfield | G. Montgomery | A. Heath | P. Madden | A. Henders | R. Middelberg | John B Whitfield | Grant W Montgomery | Anjali K Henders | Rita P. S. Middelberg | Rita PS Middelberg | Manuel AR Ferreira | Pamela AF Madden | M. Ferreira | N. Martin | N. Martin | N. Martin
[1] G. Poli,et al. Contribution of gamma glutamyl transpeptidase to oxidative damage of ischemic rat kidney. , 2000, Kidney international.
[2] Ayellet V. Segrè,et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis , 2010, Nature Genetics.
[3] G. Abecasis,et al. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees , 2002, Nature Genetics.
[4] Luigi Ferrucci,et al. Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham Heart Study data , 2010, BMC Medical Genetics.
[5] N. Martin,et al. Genetic covariation between serum gamma-glutamyltransferase activity and cardiovascular risk factors. , 2002, Clinical chemistry.
[6] N. Martin,et al. Genetic Covariation between Serum γ-Glutamyltransferase Activity and Cardiovascular Risk Factors , 2002 .
[7] E Budtz-Jørgensen,et al. Prenatal methylmercury exposure as a cardiovascular risk factor at seven years of age. , 1999, Epidemiology.
[8] P. Ridker,et al. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. , 2000, The New England journal of medicine.
[9] J. Vaupel,et al. Evidence for a substantial genetic influence on biochemical liver function tests: results from a population-based Danish twin study. , 2001, Clinical chemistry.
[10] N. Martin,et al. A Longitudinal Genetic Study of Plasma Lipids in Adolescent Twins , 2007, Twin Research and Human Genetics.
[11] K. Suzuki,et al. Serum γ‐glutamyltransferase and development of impaired fasting glucose or type 2 diabetes in middle‐aged Japanese men , 2003, Journal of internal medicine.
[12] 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.
[13] A. Döring,et al. Association of serum uric acid with all-cause and cardiovascular disease mortality and incident myocardial infarction in the MONICA Augsburg cohort. World Health Organization Monitoring Trends and Determinants in Cardiovascular Diseases. , 1999, Epidemiology.
[14] P. van Eerdewegh,et al. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. I. Likelihood formulation and simulation results. , 1999, American journal of human genetics.
[15] Manuel A. R. Ferreira,et al. Common variants in the trichohyalin gene are associated with straight hair in Europeans. , 2009, American journal of human genetics.
[16] Christian Gieger,et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts , 2009, Nature Genetics.
[17] J. Marchini,et al. Genotype imputation for genome-wide association studies , 2010, Nature Reviews Genetics.
[18] Inês Barroso,et al. Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease , 2010, Arteriosclerosis, thrombosis, and vascular biology.
[19] J. Aitken,et al. Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins , 1999, Genetic epidemiology.
[20] Daniel F. Schwarz,et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3 , 2009, Nature Genetics.
[21] P. Visscher,et al. Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis , 2010, Nature Genetics.
[22] C. V. van Duijn,et al. Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study , 2006, Human Heredity.
[23] Yongmei Liu,et al. Heritability and Expression of C‐Reactive Protein in Type 2 Diabetes in the Diabetes Heart Study , 2006, Annals of human genetics.
[24] L. Almasy,et al. Bivariate quantitative trait linkage analysis: Pleiotropy versus co‐incident linkages , 1997, Genetic epidemiology.
[25] Y. Friedlander,et al. Family resemblance for serum uric acid in a Jerusalem sample of families , 1988, Human Genetics.
[26] P. Elliott,et al. Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels , 2011, Circulation.
[27] Nicola J. Rinaldi,et al. Control of Pancreas and Liver Gene Expression by HNF Transcription Factors , 2004, Science.
[28] J. Whitfield. Gamma Glutamyl Transferase , 2001, Critical reviews in clinical laboratory sciences.
[29] G. Poli,et al. Contribution of γ glutamyl transpeptidase to oxidative damage of ischemic rat kidney , 2000 .
[30] Michael Krawczak,et al. A comprehensive evaluation of SNP genotype imputation , 2009, Human Genetics.
[31] D. O'Connor,et al. Butyrylcholinesterase: association with the metabolic syndrome and identification of 2 gene loci affecting activity. , 2006, Clinical chemistry.
[32] Yusuke Nakamura,et al. Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. , 2011, Human molecular genetics.
[33] R. Mahley,et al. Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. , 1988, Science.
[34] Harold Snieder,et al. Genetic and environmental influences on systemic markers of inflammation in middle-aged male twins. , 2008, Atherosclerosis.
[35] Christoph Lange,et al. A multivariate family-based association test using generalized estimating equations: FBAT-GEE. , 2003, Biostatistics.
[36] Margaret J. Wright,et al. Brisbane Adolescent Twin Study: Outline of study methods and research projects , 2004 .
[37] H. Yamanaka,et al. Does hyperuricemia affect mortality? A prospective cohort study of Japanese male workers. , 2000, Journal of epidemiology.
[38] Y. Terauchi,et al. Serum butyrylcholinesterase is strongly associated with adiposity, the serum lipid profile and insulin resistance. , 2007, Internal medicine.
[39] P. Heagerty,et al. Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease , 2009, Lipids in Health and Disease.
[40] Z B Zeng,et al. Multiple trait analysis of genetic mapping for quantitative trait loci. , 1995, Genetics.
[41] H. Brenner,et al. Elevated liver enzyme activity in construction workers: prevalence and impact on early retirement and all-cause mortality , 1998, International archives of occupational and environmental health.
[42] J F Aitken,et al. A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. , 1999, American journal of human genetics.
[43] Manuel A. R. Ferreira,et al. Genetics and population analysis A multivariate test of association , 2009 .
[44] R. Havlik,et al. Heritability of clinical chemistries in an older twin cohort: The NHLBI Twin Study , 1987, Genetic epidemiology.
[45] R. Collins,et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease , 2008, Nature Genetics.
[46] N. Martin,et al. Heritabilities of apolipoprotein and lipid levels in three countries. , 2002, Twin research : the official journal of the International Society for Twin Studies.
[47] D. Strachan,et al. LDL-cholesterol concentrations: a genome-wide association study , 2008, The Lancet.
[48] Tom R. Gaunt,et al. Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. , 2009, American journal of human genetics.
[49] N. Milman,et al. Relationship between serum ferritin and risk factors for ischaemic heart disease in 2235 Danes aged 30–60 years , 1999, Journal of internal medicine.
[50] Tanya M. Teslovich,et al. Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids , 2010, Nature.
[51] R. Elston,et al. A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotype. , 1990, American journal of human genetics.
[52] N. Wray,et al. Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo , 2008, Molecular Psychiatry.
[53] M. Rieder,et al. Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. , 2008, American journal of human genetics.
[54] Sarah E. Medland,et al. A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications , 2011, Biological Psychiatry.
[55] D. Jacobs,et al. Serum gamma-glutamyltransferase predicts non-fatal myocardial infarction and fatal coronary heart disease among 28,838 middle-aged men and women. , 2006, European heart journal.
[56] Luigi Ferrucci,et al. Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. , 2008, American journal of human genetics.
[57] Berrit C Stroehla,et al. Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review. , 2002, American journal of epidemiology.
[58] G. Geffen,et al. Genetics of Cognition: Outline of a Collaborative Twin Study , 2001, Twin Research.
[59] N. Martin,et al. Plasma lipids in twins. Environmental and genetic influences. , 1983, Atherosclerosis.
[60] Shahrul Mt-Isa,et al. Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. , 2009, JAMA.
[61] H. Deng,et al. Bivariate association analyses for the mixture of continuous and binary traits with the use of extended generalized estimating equations , 2009, Genetic epidemiology.
[62] Joseph H Abramson,et al. Butyrylcholinesterase activity, cardiovascular risk factors, and mortality in middle-aged and elderly men and women in Jerusalem. , 2006, Clinical chemistry.
[63] Andre Franke,et al. Current software for genotype imputation , 2009, Human Genomics.