Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.
暂无分享,去创建一个
Johan T den Dunnen | Simon Heath | Fernando Rivadeneira | Albert Hofman | Johannes R Vingerling | Manfred Kayser | Cornelia M van Duijn | A Cecile J W Janssens | Oscar Lao | Fan Liu | Yurii S Aulchenko | A. Hofman | A. Uitterlinden | W. V. van IJcken | S. Heath | F. Rivadeneira | A. Janssens | D. Zélénika | C. V. van Duijn | P. D. de Jong | J. D. den Dunnen | B. Oostra | J. Vingerling | Y. Aulchenko | O. Lao | K. van Duijn | Mark Vermeulen | M. Kayser | C. Klaver | D. Despriet | A. Janssens | F. Liu | Ben A Oostra | Andre G Uitterlinden | Diana Zelenika | P. Arp | M. Jhamai | Paulus T V M de Jong | Kate van Duijn | Pascal Arp | Wilfred F J van Ijcken | Mark Vermeulen | Mila M Jhamai | Dominiek D G Despriet | Caroline C W Klaver | Fan Liu | W. V. van Ijcken | A. Uitterlinden | A. Hofman | B. Oostra | C. V. van Duijn | Kate van Duijn | Mila Jhamai
[1] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[2] Matthew Thomas,et al. Multilocus OCA2 genotypes specify human iris colors , 2007, Human Genetics.
[3] J. Gulcher,et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes , 2007, Nature Genetics.
[4] Yurii S. Aulchenko,et al. BIOINFORMATICS APPLICATIONS NOTE doi:10.1093/bioinformatics/btm108 Genetics and population analysis GenABEL: an R library for genome-wide association analysis , 2022 .
[5] Wei Chen,et al. A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. , 2007, American journal of human genetics.
[6] D. Reich,et al. Population Structure and Eigenanalysis , 2006, PLoS genetics.
[7] Chiara Sabatti,et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies , 2006, Nature Genetics.
[8] P. Frost. European hair and eye color: A case of frequency-dependent sexual selection? , 2006 .
[9] Dorret I. Boomsma,et al. Replicated Linkage for Eye Color on 15q Using Comparative Ratings of Sibling Pairs , 2006, Behavior genetics.
[10] Tadeusz Sarna,et al. Melanin in human irides of different color and age of donors. , 2005, Pigment cell research.
[11] F. Clerget-Darpoux,et al. Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma , 2005, European Journal of Human Genetics.
[12] C. V. van Duijn,et al. The Effect of Genetic Drift in a Young Genetically Isolated Population , 2005 .
[13] Cornelia M van Duijn,et al. The effect of genetic drift in a young genetically isolated population. , 2005, Annals of human genetics.
[14] Richard Hodgson,et al. Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation , 2005, Human mutation.
[15] R. Sturm,et al. Eye colour: portals into pigmentation genes and ancestry. , 2004, Trends in genetics : TIG.
[16] L. Cardon,et al. Linkage disequilibrium in young genetically isolated Dutch population , 2004, European Journal of Human Genetics.
[17] Sarah E Medland,et al. A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q. , 2004, Twin research : the official journal of the International Society for Twin Studies.
[18] Wei Chen,et al. Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. , 2003, Human molecular genetics.
[19] A. Hofman,et al. Determinants of disease and disability in the elderly: The Rotterdam elderly study , 1991, European Journal of Epidemiology.
[20] Matthew Thomas,et al. Sequences associated with human iris pigmentation. , 2003, Genetics.
[21] E. Eichler,et al. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons. , 2003, American journal of human genetics.
[22] B. Oostra,et al. A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly. , 2003, Human molecular genetics.
[23] A. Halpern,et al. P gene as an inherited biomarker of human eye color. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[24] D. Galas,et al. A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population. , 2002, American journal of medical genetics.
[25] S. Gabriel,et al. The Structure of Haplotype Blocks in the Human Genome , 2002, Science.
[26] Robin Holmes,et al. A polymorphism in the agouti signaling protein gene is associated with human pigmentation. , 2002, American journal of human genetics.
[27] D. Schaid,et al. Score tests for association between traits and haplotypes when linkage phase is ambiguous. , 2002, American journal of human genetics.
[28] M. Brilliant. The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH. , 2001, Pigment cell research.
[29] R. Schultz,et al. Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human. , 2000, Genome research.
[30] K. Roeder,et al. Genomic Control for Association Studies , 1999, Biometrics.
[31] L. Stubbs,et al. The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. , 1999, Human molecular genetics.
[32] L. Almasy,et al. Multipoint quantitative-trait linkage analysis in general pedigrees. , 1998, American journal of human genetics.
[33] K. Cruickshanks,et al. Eye color changes past early childhood. The Louisville Twin Study. , 1997, Archives of ophthalmology.
[34] I H Wallow,et al. The color of the human eye: a review of morphologic correlates and of some conditions that affect iridial pigmentation. , 1997, Survey of ophthalmology.
[35] I H Wallow,et al. Melanocytes and iris color. Electron microscopic findings. , 1996, Archives of ophthalmology.
[36] R. Spritz,et al. Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2). , 1995, American journal of human genetics.
[37] R. Cann. The history and geography of human genes , 1995, The Journal of Asian Studies.
[38] Paolo Menozzi,et al. The History and Geography of Human Genes. Princeton, NJ (Princeton University Press) 1994. , 1994 .
[39] J. White,et al. Hypopigmentation in Angelman syndrome. , 1993, American journal of medical genetics.
[40] R. Spritz,et al. A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism , 1993, Nature.
[41] M. Farrall,et al. The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12. , 1992, American journal of human genetics.
[42] M. Butler. Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome. , 1989, American journal of human genetics.
[43] Shirley A. Miller,et al. A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.
[44] J. White,et al. Hypopigmentation in the Prader-Willi syndrome. , 1987, American journal of human genetics.
[45] J. Hanley,et al. The meaning and use of the area under a receiver operating characteristic (ROC) curve. , 1982, Radiology.
[46] R. Sokal,et al. Spatial autocorrelation in biology: 1. Methodology , 1978 .
[47] R. Beals,et al. An Introduction To Anthropology , 1977 .