Indexed keywords
ARTICLE;
GENETIC ASSOCIATION;
GENETIC SCREENING;
GENETIC VARIABILITY;
HETEROZYGOTE;
HUMAN;
PHENOTYPE;
PRIORITY JOURNAL;
SIMULATION;
CASE CONTROL STUDY;
COMPUTER SIMULATION;
EQUIPMENT;
GENE;
GENETICS;
PROBABILITY;
REGULATORY SEQUENCE;
SAMPLE SIZE;
CASE-CONTROL STUDIES;
COMPUTER SIMULATION;
EFFECT MODIFIERS (EPIDEMIOLOGY);
GENES;
HUMANS;
PROBABILITY;
REGULATORY SEQUENCES, NUCLEIC ACID;
SAMPLE SIZE;
1
84972545970
A survey of exact inference for contingency tables
Agresti A (1992) A survey of exact inference for contingency tables. Stat Sci 7:131-153
(1992)
Stat Sci
, vol.7
, pp. 131-153
Agresti, A.1
2
44349132708
Common and rare variants in multifactorial susceptibility to common diseases
Bodmer W, Bonilla C (2008) Common and rare variants in multifactorial susceptibility to common diseases. Nat Genet 40:695-701
(2008)
Nat Genet
, vol.40
, pp. 695-701
Bodmer, W.1
Bonilla, C.2
3
84950619301
Counting the number of rxc contingency tables with fixed margins
Gail M, Mantel N (1977) Counting the number of rxc contingency tables with fixed margins. J Am Statist Assoc 72:859-862
(1977)
J Am Statist Assoc
, vol.72
, pp. 859-862
Gail, M.1
Mantel, N.2
4
0036184745
Generating samples under a Wright-Fisher neutral model of genetic variation
Hudson RR (2002) Generating samples under a Wright-Fisher neutral model of genetic variation. Bioinformatics 18:337-338
(2002)
Bioinformatics
, vol.18
, pp. 337-338
Hudson, R.R.1
5
50949095168
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
Li B, Leal SM (2008) Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet 83:311-321
(2008)
Am J Hum Genet
, vol.83
, pp. 311-321
Li, B.1
Leal, S.M.2
6
67149117126
Discovery of rare variants via sequencing: Implications for the design of complex trait association studies
Li B, Leal SM (2009) Discovery of rare variants via sequencing: implications for the design of complex trait association studies. PLoS Genet 5:e1000481
(2009)
PLoS Genet
, vol.5
Li, B.1
Leal, S.M.2
7
43049146524
A HapMap harvest of insights into the genetics of common disease
Manolio TA, Brooks LD, Collins FS (2008) A HapMap harvest of insights into the genetics of common disease. J Clin Invest 118:1590-1605
(2008)
J Clin Invest
, vol.118
, pp. 1590-1605
Manolio, T.A.1
Brooks, L.D.2
Collins, F.S.3
8
0036799545
The allelic architecture of human disease genes: Common disease-common variant or not?
Pritchard JK, Cox NJ (2002) The allelic architecture of human disease genes: common disease-common variant or not? Hum Mol Genet 11:2417-2423
(2002)
Hum Mol Genet
, vol.11
, pp. 2417-2423
Pritchard, J.K.1
Cox, N.J.2
9
0035451780
On the allelic spectrum of human disease
Reich D, Lander E (2001) On the allelic spectrum of human disease. Trends Genet 17:502-510
(2001)
Trends Genet
, vol.17
, pp. 502-510
Reich, D.1
Lander, E.2
10
0002310686
Enumeration of R9C tables with repeated row totals
Saunders I (1984) Enumeration of R9C tables with repeated row totals. Appl Stat 33:340-352
(1984)
Appl Stat
, vol.33
, pp. 340-352
Saunders, I.1
11
0000198347
Small sample performance of some estimators of the truncated binomial distribution
Thomas DG, Gart JJ (1971) Small sample performance of some estimators of the truncated binomial distribution. J Am Stat Assoc 66:169-177
(1971)
J Am Stat Assoc
, vol.66
, pp. 169-177
Thomas, D.G.1
Gart, J.J.2