Genetic Epidemiology 5 - What makes a good genetic association study?

被引:344
作者
Hattersley, AT
McCarthy, MI [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX1 2JD, England
[2] Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter, Devon, England
[3] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0140-6736(05)67531-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic association studies are central to efforts to identify and characterise genomic variants underlying susceptibility to multifactorial disease. However, obtaining robust replication of initial association findings has proved difficult. Much of this inconsistency can be attributed to inadequacies in study design, implementation, and interpretation-inadequately powered sample groups are a major concern. Several additional factors affect the quality of any given association study, with appropriate sample-recruitment strategy, logical variant selection, minimum genotyping error, relevant data analysis, and valid interpretation all essential to generation of robust findings. Replication has a vital role in showing that associations that are identified reflect interesting biological processes rather than methodological quirks. For an unbiased view of the evidence for and against any particular association, study quality, rather than significance value, needs to play the dominant part.
引用
收藏
页码:1315 / 1323
页数:9
相关论文
共 88 条
  • [41] The impact of genotyping error on haplotype reconstruction and frequency estimation
    Kirk, KM
    Cardon, LR
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (10) : 616 - 622
  • [42] Complement factor H polymorphism in age-related macular degeneration
    Klein, RJ
    Zeiss, C
    Chew, EY
    Tsai, JY
    Sackler, RS
    Haynes, C
    Henning, AK
    SanGiovanni, JP
    Mane, SM
    Mayne, ST
    Bracken, MB
    Ferris, FL
    Ott, J
    Barnstable, C
    Hoh, J
    [J]. SCIENCE, 2005, 308 (5720) : 385 - 389
  • [43] Impact of genotyping errors on type I error rate of the haplotype-sharing transmission/disequilibrium test (HS-TDT)
    Knapp, M
    Becker, T
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) : 589 - 591
  • [44] In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading
    Knight, JC
    Keating, BJ
    Rockett, KA
    Kwiatkowski, DR
    [J]. NATURE GENETICS, 2003, 33 (04) : 469 - 475
  • [45] Multiple comparisons in studies of gene x gene and gene x environment interaction
    Kraft, P
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) : 582 - 584
  • [46] GENETIC DISSECTION OF COMPLEX TRAITS - GUIDELINES FOR INTERPRETING AND REPORTING LINKAGE RESULTS
    LANDER, E
    KRUGLYAK, L
    [J]. NATURE GENETICS, 1995, 11 (03) : 241 - 247
  • [47] Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations
    Little, J
    Bradley, L
    Bray, MS
    Clyne, M
    Dorman, J
    Ellsworth, DL
    Hanson, J
    Khoury, M
    Lau, J
    O'Brien, TR
    Rothman, N
    Stroup, D
    Taioli, E
    Thomas, D
    Vainio, H
    Wacholder, S
    Weinberg, C
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2002, 156 (04) : 300 - 310
  • [48] Allelic variation in gene expression is common in the human genome
    Lo, HS
    Wang, ZN
    Hu, Y
    Yang, HH
    Gere, S
    Buetow, KH
    Lee, MP
    [J]. GENOME RESEARCH, 2003, 13 (08) : 1855 - 1862
  • [49] Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
    Lohmueller, KE
    Pearce, CL
    Pike, M
    Lander, ES
    Hirschhorn, JN
    [J]. NATURE GENETICS, 2003, 33 (02) : 177 - 182
  • [50] rVista for comparative sequence-based discovery of functional transcription factor binding sites
    Loots, GG
    Ovcharenko, I
    Pachter, L
    Dubchak, I
    Rubin, EM
    [J]. GENOME RESEARCH, 2002, 12 (05) : 832 - 839