[1] BOTSTEIN D,WHITE R L,SKOLNICK M,et al.Construction of a genetic linkage map in man using restriction fragment length polymorphisms[J].Am J Hum Genet,1980,32(3):314-331.
[2] CARLSON C S,EBERLE M A,RIEDER M J,et al.Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans[J].Nat genet,2003,33(4):518-521.
[3] CARLSON C S,EBERLE M A,RIEDER M J,et al.Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium[J].Am J Hum Genet,2004,74(1):106-120.
[4] PATIL N,BERNO A J,HINDS D A,et al.Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21[J].Science,2001,294(5547):1719-1723.
[5] HALLDORSSON B V,BAFNA V,LIPPERT R,et al.Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies[J].Genome Res,2004,14(8):1633-1640.
[6] WASSENAAR C A,DONG Q,WEI Q,et al.Relationship between CYP2A6 and CHRNA5-CHRNA3-CHRNB4 variation and smoking behaviors and lung cancer risk[J].J Natl Cancer Inst,2011,103(17):1342-1346.
[7] SCHONFELD S J,NETA G,STURGIS E M,et al.Common genetic variants in sex hormone pathway genes and papillary thyroid cancer risk[J].Thyroid,2012,22(2):151-156.
[8] WANG M,YUAN L,WU D,et al.A novel XPF-357A>C polymorphism predicts risk and recurrence of bladder cancer[J].Oncogene,2010,29(13):1920-1928.
[9] ZHANG Y,LIU B,JIN M,et al.Genetic polymorphisms of transforming growth factor-beta1 and its receptors and colorectal cancer susceptibility:a population-based case-control study in China[J].Cancer Lett,2009,275(1):102-108.
[10] JIANG L,ZHOU P,SUN A,et al.Functional variant(-1304T>G) in the MKK4 promoter is associated with decreased risk of acute myeloid leukemia in a southern Chinese population[J].Cancer Sci,2011,102(8):1462-1468.
[11] WANG M,QIN C,ZHU J,et al.Genetic variants of XRCC1,APE1,and ADPRT genes and risk of bladder cancer[J].DNA Cell Biol,2010,29(6):303-311.
[12] ZHANG Z,QIU L,WANG M,et al.The FAS ligand promoter polymorphism,rs763110(-844C>T),contributes to cancer susceptibility:evidence from 19 case-control studies[J].Eur J Hum Genet,2009,17(10):1294-1303.
[13] PEARCE C L,DOHERTY J A,VAN D J,et al.Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk[J].Hum Mol Genet,2011,20(11):2263-2272.
[14] YAO S,ZIRPOLI G,BOVBJERG D H,et al.Variants in the vitamin D pathway,serum levels of vitamin D,and estrogen receptor negative breast cancer among African-American women:a case-control study[J].Breast Cancer Res,2012,14(2):1-13.
[15] SUN X,NAMKUNG J,ZHU X,et al.Capability of common SNPs to tag rare variants[J].BMC Proc,2011,5(9):1-5.
[16] AMOS C I,WU X,BRODERICK P,et al.Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1[J].Nat Genet,2008,40(5):616-622.
[17] ROUKOS D H.Personal genomics and genome-wide association studies:novel discoveries but limitations for practical personalized medicine[J].Ann Surg Oncol,2009,16(3):772-773.
[18] BRODERICK P,CARVAJAL L,PITTMAN A M,et al.A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk[J].Nat Genet,2007,39(11):1315-1317.
[19] CUI R,KAMATANI Y,TAKAHASHI A,et al.Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk[J].Gastroenterology,2009,137(5):1768-1775.
[20] WANG L D,ZHOU F Y,LI X M,et al.Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54[J].Nat Genet,2010,42(9):759-763.
[21] WU C,HU Z,HE Z,et al.Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations[J].Nat Genet,2011,43(7):679-684.
[22] National Human Genome Research Institute.- 12-21].http://www.genome.gov/26525384.
[23] FAYE L L,BULL S B.Two-stage study designs combining genome-wide association studies,tag single-nucleotide polymorphisms,and exome sequencing:accuracy of genetic effect estimates[J].BMC Proc,2011,5(9):1-9.
[24] CHRISTENSEN K,MURRAY J C.What genome-wide association studies can do for medicine[J].New Engl J Med,2007,356(11):1094-1097.
[25] COETZEE S G,RHIE S K,BERMAN B P,et al.FunciSNP:an R/bioconductor tool integrating functional non-coding data sets with genetic association studies to identify candidate regulatory SNPs[J].Nucleic Acids Res,2012:1-9.
[26] ROUKOS D H.Genome-wide association studies:how predictable is a person's cancer risk？[J].Expert Rev Anticanc,2009,9(4):389-392. |
