The International HapMap Project
暂无分享,去创建一个
[1] R. Lewontin. The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. , 1964, Genetics.
[2] T. Ohta,et al. Linkage disequilibrium due to random genetic drift , 1969 .
[3] J. Crow,et al. The direction of linkage disequilibrium. , 1974, Genetics.
[4] J. Karam,et al. A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus , 1984, Diabetes.
[5] K. Buetow,et al. Nonuniform recombination within the human beta-globin gene cluster. , 1984, American journal of human genetics.
[6] Nonuniform recombination within the human beta-globin gene cluster: A reply to B. S. Weir and W. G. Hill. , 1986, American journal of human genetics.
[7] D. Mccormick. Sequence the Human Genome , 1986, Bio/Technology.
[8] W. G. Hill,et al. Nonuniform recombination within the human beta-globin gene cluster. , 1986, American journal of human genetics.
[9] R. Hudson,et al. Estimating the recombination parameter of a finite population model without selection. , 1987, Genetical research.
[10] L. Tsui,et al. Identification of the cystic fibrosis gene: genetic analysis. , 1989, Science.
[11] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.
[12] R E LaPorte,et al. Worldwide differences in the incidence of type I diabetes are associated with amino acid variation at position 57 of the HLA-DQ beta chain. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[13] H. Cann,et al. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. , 1990, Genomics.
[14] Wen-Hsiung Li,et al. Low nucleotide diversity in man. , 1991, Genetics.
[15] Eric Lander,et al. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland , 1992, Nature Genetics.
[16] S. Kahler,et al. The Genetic Basis of Common Diseases , 1993 .
[17] R. Cann. The history and geography of human genes , 1995, The Journal of Asian Studies.
[18] Paolo Menozzi,et al. The History and Geography of Human Genes. Princeton, NJ (Princeton University Press) 1994. , 1994 .
[19] S. Wilton,et al. Apolipoprotein E and Alzheimer's disease , 1995 .
[20] D. F. Roberts,et al. The History and Geography of Human Genes , 1996 .
[21] J. Todd,et al. The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry. , 1996, Human molecular genetics.
[22] S. Tishkoff,et al. Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins , 1996, Science.
[23] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[24] G Barbujani,et al. An apportionment of human DNA diversity. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[25] B. Dahlbäck,et al. Resistance to Activated Protein C Caused by the Factor V R506Q Mutation ls a Common Risk Factor for Venous Thrombosis , 1997, Thrombosis and Haemostasis.
[26] J. Kere,et al. Microsatellite diversity and the demographic history of modern humans. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[27] Francis S. Collins,et al. Variations on a Theme: Cataloging Human DNA Sequence Variation , 1997, Science.
[28] B. Dahlbck. Resistance to activated protein C caused by the R506Q mutation in the gene for factor V is a common risk factor for venous thrombosis. , 1997, Journal of internal medicine. Supplement.
[29] Johan Auwerx,et al. A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity , 1998, Nature Genetics.
[30] C. Nusbaum,et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. , 1998, Science.
[31] B. Dastugue,et al. [Apolipoprotein E and Alzheimer's disease]. , 1998, Annales de biologie clinique.
[32] M. Cargill. Characterization of single-nucleotide polymorphisms in coding regions of human genes , 1999, Nature Genetics.
[33] N. Shen,et al. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis , 1999, Nature Genetics.
[34] A. Chakravarti. Population genetics—making sense out of sequence , 1999, Nature Genetics.
[35] E. Lander,et al. Characterization of single-nucleotide polymorphisms in coding regions of human genes , 1999 .
[36] N. Risch. Searching for genetic determinants in the new millennium , 2000, Nature.
[37] E S Lander,et al. The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. , 2000, Nature genetics.
[38] Eric S. Lander,et al. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes , 2000, Nature Genetics.
[39] M. W. Foster,et al. Genetic research and culturally specific risks: one size does not fit all. , 2000, Trends in genetics : TIG.
[40] Pui-Yan Kwok,et al. Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28 , 2000, Nature Genetics.
[41] M. W. Foster,et al. Involving Study Populations in the Review of Genetic Research , 2000, Journal of Law, Medicine & Ethics.
[42] K. Dawson. The decay of linkage disequilibrium under random union of gametes: how to calculate Bennett's principal components. , 2000, Theoretical population biology.
[43] E. Juengst. Commentary: What “Community Review” Can and Cannot Do , 2000, Journal of Law, Medicine & Ethics.
[44] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[45] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[46] M. Daly,et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.
[47] S. P. Fodor,et al. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.
[48] Jonathan C. Cohen,et al. An Apolipoprotein Influencing Triglycerides in Humans and Mice Revealed by Comparative Sequencing , 2001, Science.
[49] A. Jeffreys,et al. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex , 2001, Nature Genetics.
[50] Mourad Sahbatou,et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease , 2001, Nature.
[51] M. Daly,et al. High-resolution haplotype structure in the human genome , 2001, Nature Genetics.
[52] Judy H. Cho,et al. [Letters to Nature] , 1975, Nature.
[53] Frank Dudbridge,et al. Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.
[54] L R Cardon,et al. Extent and distribution of linkage disequilibrium in three genomic regions. , 2001, American journal of human genetics.
[55] Pardis C Sabeti,et al. Linkage disequilibrium in the human genome , 2001, Nature.
[56] J. Mullikin,et al. SSAHA: a fast search method for large DNA databases. , 2001, Genome research.
[57] D. Nickerson,et al. Variation is the spice of life , 2001, Nature Genetics.
[58] P. Marshall,et al. Ethical Challenges in Community‐Based Research , 2001, The American journal of the medical sciences.
[59] P. Donnelly,et al. Estimating recombination rates from population genetic data. , 2001, Genetics.
[60] Sinead B. O'Leary,et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease , 2001, Nature Genetics.
[61] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[62] S. Gabriel,et al. The Structure of Haplotype Blocks in the Human Genome , 2002, Science.
[63] M. Feldman,et al. Genetic Structure of Human Populations , 2002, Science.
[64] N. E. Morton,et al. The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[65] Steuart Rorke,et al. Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness , 2002, Nature.
[66] M. W. Foster,et al. Race, ethnicity, and genomics: social classifications as proxies of biological heterogeneity. , 2002, Genome research.
[67] Ellen Wright Clayton,et al. The Complex Relationship of Genetics, Groups, and Health: What it Means for Public Health , 2002, The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics.
[68] Hiroshi Sato,et al. Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction , 2002, Nature Genetics.
[69] Lon R. Cardon,et al. A first-generation linkage disequilibrium map of human chromosome 22 , 2002, Nature.
[70] H. Stefánsson,et al. Neuregulin 1 and susceptibility to schizophrenia. , 2002, American journal of human genetics.
[71] P. Fearnhead,et al. A coalescent-based method for detecting and estimating recombination from gene sequences. , 2002, Genetics.
[72] Richard A. King,et al. The genetic basis of common diseases. , 2002 .
[73] G. McVean,et al. Estimating recombination rates from population-genetic data , 2003, Nature Reviews Genetics.
[74] Mark Gurney,et al. The gene encoding phosphodiesterase 4D confers risk of ischemic stroke , 2003, Nature Genetics.
[75] S. Gabriel,et al. Quality and completeness of SNP databases , 2003, Nature Genetics.
[76] D. Botstein,et al. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease , 2003, Nature Genetics.
[77] Y. Ohnishi,et al. Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction , 2003, Nature Genetics.
[78] Deborah A. Nickerson,et al. Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans , 2003, Nature Genetics.
[79] Svante Pääbo,et al. The mosaic that is our genome , 2003, Nature.
[80] Nicholas W Wood,et al. Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. , 2003, Trends in genetics : TIG.
[81] W. G. Hill,et al. Linkage disequilibrium in finite populations , 1968, Theoretical and Applied Genetics.
[82] Howard C. Berg,et al. Genetic analysis , 1957, Nature Biotechnology.