Association study designs for complex diseases

被引:1008
作者
Cardon, LR [1 ]
Bell, JI [1 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Med, Oxford OX3 9DU, England
关键词
D O I
10.1038/35052543
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Assessing the association between DNA variants and disease has been used widely to identify regions of the genome and candidate genes that contribute to disease. However, there are numerous examples of associations that cannot be replicated, which has led to scepticism about the utility of the approach for common conditions. With the discovery of massive numbers of genetic markers and the development of better tools for genotyping, association studies will inevitably proliferate. Now is the time to consider critically the design of such studies, to avoid the mistakes of the past and to maximize their potential to identify new components of disease.
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收藏
页码:91 / 99
页数:9
相关论文
共 95 条
  • [1] Manhattan versus Reykjavik
    Abbott, A
    [J]. NATURE, 2000, 406 (6794) : 340 - 342
  • [2] Extent and distribution of linkage disequilibrium in three genomic regions
    Abecasis, GR
    Noguchi, E
    Heinzmann, A
    Traherne, JA
    Bhattacharyya, S
    Leaves, NI
    Anderson, GG
    Zhang, YM
    Lench, NJ
    Carey, A
    Cardon, LR
    Moffatt, MF
    Cookson, WOC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) : 191 - 197
  • [3] A general test of association for quantitative traits in nuclear families
    Abecasis, GR
    Cardon, LR
    Cookson, WOC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) : 279 - 292
  • [4] Pedigree tests of transmission disequilibrium (Reprinted from European Journal of Human Genetics, Vol 8, pg 545-551,2000)
    Abecasis, Goncalo R.
    Cookson, William O. C.
    Cardon, Lon R.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2017, 25 : S40 - S44
  • [5] Allison DB, 1997, AM J HUM GENET, V60, P676
  • [6] An SNP map of the human genome generated by reduced representation shotgun sequencing
    Altshuler, D
    Pollara, VJ
    Cowles, CR
    Van Etten, WJ
    Baldwin, J
    Linton, L
    Lander, ES
    [J]. NATURE, 2000, 407 (6803) : 513 - 516
  • [7] The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
    Altshuler, D
    Hirschhorn, JN
    Klannemark, M
    Lindgren, CM
    Vohl, MC
    Nemesh, J
    Lane, CR
    Schaffner, SF
    Bolk, S
    Brewer, C
    Tuomi, T
    Gaudet, D
    Hudson, TJ
    Daly, M
    Groop, L
    Lander, ES
    [J]. NATURE GENETICS, 2000, 26 (01) : 76 - 80
  • [8] USE OF POOLED DNA SAMPLES TO DETECT LINKAGE DISEQUILIBRIUM OF POLYMORPHIC RESTRICTION FRAGMENTS AND HUMAN-DISEASE - STUDIES OF THE HLA CLASS-II LOCI
    ARNHEIM, N
    STRANGE, C
    ERLICH, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (20) : 6970 - 6974
  • [9] The power of genomic control
    Bacanu, SA
    Devlin, B
    Roeder, K
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (06) : 1933 - 1944
  • [10] Association mapping of disease loci, by use of a pooled DNA genomic screen
    Barcellos, LF
    Klitz, W
    Field, LL
    Tobias, R
    Bowcock, AM
    Wilson, R
    Nelson, MP
    Nagatomi, J
    Thomson, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (03) : 734 - 747