-
2
-
-
82455199557
-
Genetic Analysis Workshop 17 mini-exome simulation
-
Almasy L, Dyer TD, Peralta JM, Kent Jr JW, Charlesworth JC, Curran JE, Blangero J. 2011. Genetic Analysis Workshop 17 mini-exome simulation. BMC Proc 5:S2.
-
(2011)
BMC Proc
, vol.5
-
-
Almasy, L.1
Dyer, T.D.2
Peralta, J.M.3
Kent Jr, J.W.4
Charlesworth, J.C.5
Curran, J.E.6
Blangero, J.7
-
3
-
-
1842532350
-
The Bayesian revolution in genetics
-
Beaumont MA, Rannala B. 2004. The Bayesian revolution in genetics. Nat Rev Genet 5:251-261.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 251-261
-
-
Beaumont, M.A.1
Rannala, B.2
-
4
-
-
0001677717
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y. 1995. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Ser B 57:289-300.
-
(1995)
J R Stat Soc Ser B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
5
-
-
78649522135
-
Using biological knowledge to discover higher order interactions in genetic association studies
-
Chen GK, Thomas DC. 2010. Using biological knowledge to discover higher order interactions in genetic association studies. Genet Epidemiol 34:863-878.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 863-878
-
-
Chen, G.K.1
Thomas, D.C.2
-
6
-
-
34547788766
-
Enriching the analysis of genome-wide association studies with hierarchical modeling
-
Chen GK, Witte JS. 2007. Enriching the analysis of genome-wide association studies with hierarchical modeling. Am J Hum Genet 81:397-404.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 397-404
-
-
Chen, G.K.1
Witte, J.S.2
-
7
-
-
82455192533
-
Statistical analysis of rare sequence variants: an overview of collapsing methods
-
this issue.
-
Dering C, Pugh E, Ziegler A. 2011. Statistical analysis of rare sequence variants: an overview of collapsing methods. Genet Epidemiol, this issue.
-
(2011)
Genet Epidemiol
-
-
Dering, C.1
Pugh, E.2
Ziegler, A.3
-
8
-
-
79958077854
-
Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS)
-
Feng T, Elston RC, Zhu X. 2000. Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS). Genet Epidemiol. 35:398-409.
-
(2000)
Genet Epidemiol.
, vol.35
, pp. 398-409
-
-
Feng, T.1
Elston, R.C.2
Zhu, X.3
-
9
-
-
0033926130
-
Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations
-
Goddard KA, Hopkins PJ, Hall JM, Witte JS. 2000. Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations. Am J Hum Genet 66:216-234.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 216-234
-
-
Goddard, K.A.1
Hopkins, P.J.2
Hall, J.M.3
Witte, J.S.4
-
10
-
-
77956890234
-
Monte Carlo sampling methods using Markov chains and their applications
-
Hastings WK. 1970. Monte Carlo sampling methods using Markov chains and their applications. Biometrika 57:97-109.
-
(1970)
Biometrika
, vol.57
, pp. 97-109
-
-
Hastings, W.K.1
-
11
-
-
79959462191
-
Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data
-
Heron EA, O'Dushlaine C, Segurado R, Gallagher L, Gill M. 2007. Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data. Biostatistics 12:445-461.
-
(2007)
Biostatistics
, vol.12
, pp. 445-461
-
-
Heron, E.A.1
O'Dushlaine, C.2
Segurado, R.3
Gallagher, L.4
Gill, M.5
-
12
-
-
0036408751
-
Intrinsic disorder in cell-signaling and cancer-associated proteins
-
Iakoucheva LM, Brown CJ, Lawson JD, Obradovic Z, Dunker AK. 2002. Intrinsic disorder in cell-signaling and cancer-associated proteins. J Mol Biol 323:573-584.
-
(2002)
J Mol Biol
, vol.323
, pp. 573-584
-
-
Iakoucheva, L.M.1
Brown, C.J.2
Lawson, J.D.3
Obradovic, Z.4
Dunker, A.K.5
-
13
-
-
65249164859
-
Validating, augmenting, and refining genome-wide association signals
-
Ioannidis JP, Thomas G, Daly MJ. 2009. Validating, augmenting, and refining genome-wide association signals. Nat Rev Genet 10:318-329.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 318-329
-
-
Ioannidis, J.P.1
Thomas, G.2
Daly, M.J.3
-
14
-
-
82455183179
-
Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated data
-
Kang J, Zheng W, Li L, Lee JS, Yan X, Zhao HY. 2011. Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated data. BMC Proc 5:S37.
-
(2011)
BMC Proc
, vol.5
-
-
Kang, J.1
Zheng, W.2
Li, L.3
Lee, J.S.4
Yan, X.5
Zhao, H.Y.6
-
15
-
-
38049023107
-
Hierarchical Bayes prioritization of marker associations from a genome-wide association scan for further investigation
-
Lewinger JP, Conti DV, Baurley JW, Triche TJ, Thomas DC. 2007. Hierarchical Bayes prioritization of marker associations from a genome-wide association scan for further investigation. Genet Epidemiol 31:871-882.
-
(2007)
Genet Epidemiol
, vol.31
, pp. 871-882
-
-
Lewinger, J.P.1
Conti, D.V.2
Baurley, J.W.3
Triche, T.J.4
Thomas, D.C.5
-
16
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
Li BS, 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.S.1
Leal, S.M.2
-
17
-
-
82455200164
-
Using the posterior distribution of deviance to measure evidence of association for rare susceptibility variants
-
Lorenzo Bermejo J, Beckmann L, Chang-Claude J, Fischer C. 2011. Using the posterior distribution of deviance to measure evidence of association for rare susceptibility variants. BMC Proc 5:S38.
-
(2011)
BMC Proc
, vol.5
-
-
Lorenzo Bermejo, J.1
Beckmann, L.2
Chang-Claude, J.3
Fischer, C.4
-
18
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen B, Browning S. 2009. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet 5:e1000384.
-
(2009)
PLoS Genet
, vol.5
-
-
Madsen, B.1
Browning, S.2
-
19
-
-
5744249209
-
Equations of state calculations by fast computing machines
-
Metropolis N, Rosenbluth AW, Rosenbluth MN, Teller AH, Teller E. 1953. Equations of state calculations by fast computing machines. J Chem Phys 21:1087-1092.
-
(1953)
J Chem Phys
, vol.21
, pp. 1087-1092
-
-
Metropolis, N.1
Rosenbluth, A.W.2
Rosenbluth, M.N.3
Teller, A.H.4
Teller, E.5
-
20
-
-
78449274394
-
Interrogating local population structure for fine mapping in genome-wide association studies
-
Qin H, Morris N, Kang SJ, Li M, Tayo B, Lyon H, Hirschhorn J, Cooper RS, Zhu X. 2011. Interrogating local population structure for fine mapping in genome-wide association studies. Bioinformatics 26:2961-2968.
-
(2011)
Bioinformatics
, vol.26
, pp. 2961-2968
-
-
Qin, H.1
Morris, N.2
Kang, S.J.3
Li, M.4
Tayo, B.5
Lyon, H.6
Hirschhorn, J.7
Cooper, R.S.8
Zhu, X.9
-
21
-
-
0034973984
-
High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence
-
Rannala B, Reeve JP. 2001. High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence. Am J Hum Genet 69:159-178.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 159-178
-
-
Rannala, B.1
Reeve, J.P.2
-
22
-
-
82455183181
-
Rare variant density across the genome and across populations
-
Raska P, Zhu X. 2011. Rare variant density across the genome and across populations. BMC Proc 5:S39.
-
(2011)
BMC Proc
, vol.5
-
-
Raska, P.1
Zhu, X.2
-
23
-
-
3442879338
-
Assessing the function of genetic variants in candidate gene association studies
-
Rebbeck TR, Spitz M, Wu X. 2004. Assessing the function of genetic variants in candidate gene association studies. Nat Rev Genet 5:589-594.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 589-594
-
-
Rebbeck, T.R.1
Spitz, M.2
Wu, X.3
-
24
-
-
0024313579
-
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism
-
Tajima F. 1989. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585-595.
-
(1989)
Genetics
, vol.123
, pp. 585-595
-
-
Tajima, F.1
-
25
-
-
82455214951
-
Prioritizing single-nucleotide variations that potentially regulate alternative splicing
-
Teng M, Wang Y, Wang G, Jung J, Edenberg HJ, Sanford JR, Liu Y. 2011. Prioritizing single-nucleotide variations that potentially regulate alternative splicing. BMC Proc 5:S40.
-
(2011)
BMC Proc
, vol.5
-
-
Teng, M.1
Wang, Y.2
Wang, G.3
Jung, J.4
Edenberg, H.J.5
Sanford, J.R.6
Liu, Y.7
-
26
-
-
82455194299
-
Comparison of SNP-based and gene-based association studies in detecting rare variants using unrelated individuals
-
Tong L, Tayo B, Yang J, Cooper RS. 2011. Comparison of SNP-based and gene-based association studies in detecting rare variants using unrelated individuals. BMC Proc 5:S41.
-
(2011)
BMC Proc
, vol.5
-
-
Tong, L.1
Tayo, B.2
Yang, J.3
Cooper, R.S.4
-
28
-
-
79951997040
-
Adjustment for local ancestry in genetic association analysis of admixed populations
-
Wang X, Zhu X, Qin H, Cooper RS, Ewens WJ, Li C, Li M. 2011 Adjustment for local ancestry in genetic association analysis of admixed populations. Bioinformatics 27:670-677.
-
(2011)
Bioinformatics
, vol.27
, pp. 670-677
-
-
Wang, X.1
Zhu, X.2
Qin, H.3
Cooper, R.S.4
Ewens, W.J.5
Li, C.6
Li, M.7
-
29
-
-
82455214950
-
Collapsing ROC approach for risk prediction research on both common and rare variants
-
Wei C, Lu Q. 2011. Collapsing ROC approach for risk prediction research on both common and rare variants. BMC Proc 5:S42.
-
(2011)
BMC Proc
, vol.5
-
-
Wei, C.1
Lu, Q.2
-
30
-
-
77953121307
-
Powerful SNP-set analysis for case-control genome-wide association studies
-
Wu MC, Kraft P, Epstein MP, Taylor DM, Chanock SJ, Hunter DJ, Lin X. 2010. Powerful SNP-set analysis for case-control genome-wide association studies. Am J Hum Genet 86:929-942.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 929-942
-
-
Wu, M.C.1
Kraft, P.2
Epstein, M.P.3
Taylor, D.M.4
Chanock, S.J.5
Hunter, D.J.6
Lin, X.7
-
31
-
-
82455170532
-
Region-based and pathway-based QTL mapping using a P-value combination method
-
Yang HC, Chen CW. 2011. Region-based and pathway-based QTL mapping using a P-value combination method. BMC Proc 5:S43.
-
(2011)
BMC Proc
, vol.5
-
-
Yang, H.C.1
Chen, C.W.2
-
32
-
-
79960749427
-
A nonparametric method for building predictive genetic tests on high-dimensional data
-
Ye C, Cui Y, Wei C, Elston RC, Zhu J, Lu Q. 2011. A nonparametric method for building predictive genetic tests on high-dimensional data. Hum Hered 71:161-170.
-
(2011)
Hum Hered
, vol.71
, pp. 161-170
-
-
Ye, C.1
Cui, Y.2
Wei, C.3
Elston, R.C.4
Zhu, J.5
Lu, Q.6
|