Storry JR, Olsson ML: The ABO group system revisited: review and update. Immunohematology. 2009, 25: 48-59.
CAS
PubMed
Google Scholar
Yamamoto F, McNeill PD, Hakomori S: Genomic organization of human histo-blood group ABO genes. Glycobiology. 1995, 5: 51-58. 10.1093/glycob/5.1.51.
Article
CAS
PubMed
Google Scholar
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, et al: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011, 43: 333-338. 10.1038/ng.784.
Article
PubMed Central
CAS
PubMed
Google Scholar
Qi L, Cornelis MC, Kraft P, Jensen M, van Dam RM, Sun Q, Girman CJ, Laurie CC, Mirel DB, Hunter DJ, et al: Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes. Hum Mol Genet. 2010, 19: 1856-1862. 10.1093/hmg/ddq057.
Article
PubMed Central
CAS
PubMed
Google Scholar
Paterson AD, Lopes-Virella MF, Waggott D, Boright AP, Hosseini SM, Carter RE, Shen E, Mirea L, Bharaj B, Sun L, et al: Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Arterioscler Thromb Vasc Biol. 2009, 29: 1958-1967. 10.1161/ATVBAHA.109.192971.
Article
PubMed Central
CAS
PubMed
Google Scholar
Barbalic M, Dupuis J, Dehghan A, Bis JC, Hoogeveen RC, Schnabel RB, Nambi V, Bretler M, Smith NL, Peters A, et al: Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum Mol Genet. 2010, 19: 1863-1872. 10.1093/hmg/ddq061.
Article
PubMed Central
CAS
PubMed
Google Scholar
Ganesh SK, Zakai NA, van Rooij FJ, Soranzo N, Smith AV, Nalls MA, Chen MH, Kottgen A, Glazer NL, Dehghan A, et al: Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat Genet. 2009, 41: 1191-1198. 10.1038/ng.466.
Article
PubMed Central
CAS
PubMed
Google Scholar
Kamatani Y, Matsuda K, Okada Y, Kubo M, Hosono N, Daigo Y, Nakamura Y, Kamatani N: Genome-wide association study of hematological and biochemical traits in a Japanese Population. Nat Genet. 2010, 42: 210-215. 10.1038/ng.531.
Article
CAS
PubMed
Google Scholar
Lo KS, Wilson JG, Lange LA, Folsom AR, Galarneau G, Ganesh SK, Grant SF, Keating BJ, McCarroll SA, Mohler ER, et al: Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Hum Genet. 2011, 129: 307-317. 10.1007/s00439-010-0925-1.
Article
PubMed Central
PubMed
Google Scholar
Yip SP: Sequence variation at the human ABO locus. Ann Hum Genet. 2002, 66: 1-27. 10.1017/S0003480001008995.
Article
CAS
PubMed
Google Scholar
Cho YS, Go MJ, Kim YJ, Heo JY, Oh JH, Ban HJ, Yoon D, Lee MH, Kim DJ, Park M, et al: A large-scale genome-wide association study of Asian population uncover genetic factors influencing eight quantitative traits. Nat Genet. 2009, 41: 527-534. 10.1038/ng.357.
Article
CAS
PubMed
Google Scholar
Kim YJ, Go MJ, Hu C, Hong CB, Kim YK, Lee JY, Hwang JY, Oh JH, Kim DJ, Kim S, et al: Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. Nat Genet. 2011, 43: 990-995. 10.1038/ng.939.
Article
CAS
PubMed
Google Scholar
Itsara A, Cooper GM, Baker C, Girirajan S, Li J, Absher D, Krauss RM, Myers RM, Ridker PM, Chasman DI, et al: Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet. 2009, 84: 148-161. 10.1016/j.ajhg.2008.12.014.
Article
PubMed Central
CAS
PubMed
Google Scholar
Jakobsson M, Scholz SW, Scheet P, Gibbs JR, VanLiere JM, Fung HC, Szpiech ZA, Degnan JH, Wang K, Guerreiro R, et al: Genotype, haplotype and copy-number variation in worldwide human populations. Nature. 2008, 451: 998-1003. 10.1038/nature06742.
Article
CAS
PubMed
Google Scholar
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, et al: Origins and functional impact of copy number variation in the human genome. Nature. 2010, 464: 704-712. 10.1038/nature08516.
Article
PubMed Central
CAS
PubMed
Google Scholar
McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, Wysoker A, Shapero MH, de Bakker PI, Maller JB, Kirby A, et al: Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet. 2008, 40: 1166-1174. 10.1038/ng.238.
Article
CAS
PubMed
Google Scholar
Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O’Hara R, Casalunovo T, Conlin LK, D’Arcy M, et al: High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Res. 2009, 19: 1682-1690. 10.1101/gr.083501.108.
Article
PubMed Central
CAS
PubMed
Google Scholar
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M: PennCNV: an integrated hidden Markov model designed for high resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res. 2007, 17: 1665-1674. 10.1101/gr.6861907.
Article
PubMed Central
CAS
PubMed
Google Scholar
Hong KW, Lim JE, Kim YJ, Cho NH, Shin C, Oh B: KARE Genomewide Association Study of Blood Pressure Using Imputed SNPs. Genomics & Informatics. 2010, 8: 103-107. 10.5808/GI.2010.8.3.103.
Article
Google Scholar
Wright S: The genetical structure of populations. Nature. 1950, 15: 323-354.
Google Scholar
Barrett JC, Fry B, Maller J, Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005, 28: 1323-1328.
Google Scholar
Pique-Regi R, Monso-Varona J, Ortega A, Seeger RC, Triche TJ, Asgharzadeh S: Sparse representation and Bayesian detection of genome copy number alterations from microarray data. Bioinformatics. 2008, 24: 309-318. 10.1093/bioinformatics/btm601.
Article
PubMed Central
CAS
PubMed
Google Scholar
Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Wellcome Trust Case Control Consortium, et al: Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature. 2010, 464: 713-720. 10.1038/nature08979.
Article
CAS
PubMed
Google Scholar
Purcell S, Neale B, Todd-Brown K, Tomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, et al: PLINK: a tool set for whole-genome association and population based linkage analyses. Am J Hum Genet. 2007, 81: 559-575. 10.1086/519795.
Article
PubMed Central
CAS
PubMed
Google Scholar