Variants associated with common disease are not unusually differentiated in frequency across populations.
暂无分享,去创建一个
[1] Geoffrey B. Nilsen,et al. Whole-Genome Patterns of Common DNA Variation in Three Human Populations , 2005, Science.
[2] Michael Bamshad,et al. Deconstructing the relationship between genetics and race , 2004, Nature Reviews Genetics.
[3] Steven J. Schrodi,et al. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. , 2004, American journal of human genetics.
[4] T. Ottenhoff,et al. Is there a future for TNF promoter polymorphisms? , 2004, Genes and Immunity.
[5] N. Saitou,et al. Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. , 2004, American journal of human genetics.
[6] M. Daly,et al. Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region. , 2004, Diabetes.
[7] W. Koh,et al. Interaction between cyclooxygenase-2 gene polymorphism and dietary n-6 polyunsaturated fatty acids on colon cancer risk: The Singapore Chinese Health Study , 2004, British Journal of Cancer.
[8] S. Gabriel,et al. Assessing the impact of population stratification on genetic association studies , 2004, Nature Genetics.
[9] J. Gulcher,et al. The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke , 2004, Nature Genetics.
[10] Matthew W. Hahn,et al. Positive Selection on a Human-Specific Transcription Factor Binding Site Regulating IL4 Expression , 2003, Current Biology.
[11] C. Wan,et al. Association study between late-onset Alzheimer's disease and the transferrin gene polymorphisms in Chinese , 2003, Neuroscience Letters.
[12] T. Kurz,et al. Association study of the IL13 variant Arg110Gln in atopic diseases and juvenile idiopathic arthritis. , 2003, The Journal of allergy and clinical immunology.
[13] R. Nitsch,et al. Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2 , 2003, Neurogenetics.
[14] K. Stefánsson,et al. Prion susceptibility and protective alleles exhibit marked geographic differences , 2003, Human mutation.
[15] C. Iwai,et al. Arg389Gly polymorphism of the human beta1-adrenergic receptor in patients with nonfatal acute myocardial infarction. , 2003, American heart journal.
[16] N. Risch,et al. The importance of race and ethnic background in biomedical research and clinical practice. , 2003, The New England journal of medicine.
[17] R. Cooper,et al. Race and genomics. , 2003, The New England journal of medicine.
[18] J. Ilonen,et al. Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis. , 2003, Human immunology.
[19] B. Müller-Myhsok,et al. Genomewide linkage analysis identifies polymorphism in the human interferon-gamma receptor affecting Helicobacter pylori infection. , 2003, American journal of human genetics.
[20] E. Lander,et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease , 2003, Nature Genetics.
[21] M. Feldman,et al. Genetic Structure of Human Populations , 2002, Science.
[22] S. Chanock,et al. Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. , 2002, Blood.
[23] M. Shriver,et al. Interrogating a high-density SNP map for signatures of natural selection. , 2002, Genome research.
[24] Hiroshi Sato,et al. Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction , 2002, Nature Genetics.
[25] R. Noelle,et al. Combined effects of calcineurin inhibitors or sirolimus with anti-CD40L mAb on alloengraftment under nonmyeloablative conditions. , 2002, Blood.
[26] J. Ray,et al. Common C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene and the Risk of Venous Thromboembolism: Meta-Analysis of 31 Studies , 2002, Pathophysiology of Haemostasis and Thrombosis.
[27] Hua Tang,et al. Categorization of humans in biomedical research: genes, race and disease , 2002, Genome Biology.
[28] M. Rämet,et al. Surfactant Protein D Gene Polymorphism Associated with Severe Respiratory Syncytial Virus Infection , 2002, Pediatric Research.
[29] K. Allebrandt,et al. Variability of the paraoxonase gene (PON1) in Euro- and Afro-Brazilians. , 2002, Toxicology and applied pharmacology.
[30] J. Hirschhorn,et al. A comprehensive review of genetic association studies , 2002, Genetics in Medicine.
[31] Yusuke Nakamura,et al. Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy. , 2002, American journal of human genetics.
[32] L. Jorde,et al. Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations. , 2002, American journal of human genetics.
[33] M Freedman,et al. Single Nucleotide Polymorphisms in Multiple Novel Thrombospondin Genes May Be Associated With Familial Premature Myocardial Infarction , 2001, Circulation.
[34] D. Osei-Hyiaman,et al. Association of a novel point mutation (C159G) of the CTLA4 gene with type 1 diabetes in West Africans but not in Chinese. , 2001, Diabetes.
[35] D. Kwiatkowski,et al. Unusual haplotypic structure of IL8, a susceptibility locus for a common respiratory virus. , 2001, American journal of human genetics.
[36] M. Xiong,et al. A polymorphism in the promoter region of catalase is associated with blood pressure levels , 2001, Human Genetics.
[37] Y. Ohnishi,et al. Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease. , 2001, American journal of human genetics.
[38] D. Kwiatkowski,et al. Association of respiratory syncytial virus bronchiolitis with the interleukin 8 gene region in UK families , 2000, Thorax.
[39] Eric S. Lander,et al. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes , 2000, Nature Genetics.
[40] V. Chinchilli,et al. Polymorphisms of human SP‐A, SP‐B, and SP‐D genes: association of SP‐B Thr131Ile with ARDS , 2000, Clinical genetics.
[41] A. Carter,et al. α-Fibrinogen Thr312Ala polymorphism and venous thromboembolism , 2000 .
[42] M. Carrington,et al. Interleukin-1 polymorphisms associated with increased risk of gastric cancer , 2000, Nature.
[43] L. Murray,et al. Association of interleukin‐1 gene polymorphisms with Alzheimer's disease , 2000, Annals of neurology.
[44] atthew,et al. THE ASSOCIATION OF ATOPY WITH A GAIN-OF-FUNCTION MUTATION IN THE a SUBUNIT OF THE INTERLEUKIN-4 RECEPTOR , 2000 .
[45] E. Groot,et al. An IL-13 promoter polymorphism associated with increased risk of allergic asthma , 1999, Genes and Immunity.
[46] P. Grant,et al. Prevalence of Three Common Polymorphisms in the A-subunit Gene of Factor XIII in Patients with Coronary Artery Disease , 1999, Thrombosis and Haemostasis.
[47] B. Lämmle,et al. Association of two silent polymorphisms of platelet glycoprotein la/lla receptor with risk of myocardial infarction: a case-control study , 1999, The Lancet.
[48] J. Corral,et al. Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease. , 1998, Blood.
[49] J S Yudkin,et al. The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis. , 1998, The Journal of clinical investigation.
[50] D. Arveiler,et al. The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction. , 1998, Human molecular genetics.
[51] H Yasue,et al. Association of the missense Glu298Asp variant of the endothelial nitric oxide synthase gene with myocardial infarction. , 1998, Journal of the American College of Cardiology.
[52] J. Clegg,et al. Worldwide distribution of a common methylenetetrahydrofolate reductase mutation. , 1998, American journal of human genetics.
[53] Shibasaki,et al. Association of asthma and the interleukin‐4 promoter gene in Japanese , 1998, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.
[54] D. Sanghera,et al. DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease. , 1998, American journal of human genetics.
[55] T. Chatila,et al. The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor. , 1997, The New England journal of medicine.
[56] J J Goedert,et al. Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC), ALIVE Study. , 1997, Science.
[57] R. Snow,et al. A high frequency African coding polymorphism in the N-terminal domain of ICAM-1 predisposing to cerebral malaria in Kenya. , 1997, Human molecular genetics.
[58] Jennifer J. Pointon,et al. Global prevalence of putative haemochromatosis mutations. , 1997, Journal of medical genetics.
[59] B. Weir. Genetic Data Analysis II. , 1997 .
[60] Bengt Zöller,et al. A Common Thrombomodulin Amino Acid Dimorphism Is Associated with Myocardial Infarction , 1997, Thrombosis and Haemostasis.
[61] M. C. Ellis,et al. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis , 1996, Nature Genetics.
[62] C. Rotimi,et al. Polymorphisms of renin-angiotensin genes among Nigerians, Jamaicans, and African Americans. , 1996, Hypertension.
[63] N. Dzimiri,et al. World distribution of factor V Leiden , 1996, The Lancet.
[64] J. Macher,et al. BalI and MspI polymorphisms of the dopamine D3 receptor gene in African Blacks and Caucasians. , 1996, Human heredity.
[65] A. Marian,et al. A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease. , 1995, The Journal of clinical investigation.
[66] Ian Jackson,et al. Variants of the melanocyte–stimulating hormone receptor gene are associated with red hair and fair skin in humans , 1995, Nature Genetics.
[67] G. Baumann,et al. E-selectin polymorphism and atherosclerosis: an association study. , 1994, Human molecular genetics.
[68] K K Kidd,et al. Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[69] B. Weir,et al. ESTIMATING F‐STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE , 1984, Evolution; international journal of organic evolution.
[70] R. Lewontin. The Apportionment of Human Diversity , 1972 .