-
1
-
-
79959353702
-
Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans
-
Alsultan, A., Solovieff, N., Aleem, A., Algahtani, F. H., Al-Shehri, A., Osman, M. E., et al. (2011). Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans. Am. J. Hematol. 86, 612-614. doi: 10.1002/ajh.22032
-
(2011)
Am. J. Hematol.
, vol.86
, pp. 612-614
-
-
Alsultan, A.1
Solovieff, N.2
Aleem, A.3
Algahtani, F.H.4
Al-Shehri, A.5
Osman, M.E.6
-
2
-
-
84961360287
-
Bayesian polynomial regression models to fit multiple genetic models for quantitative traits
-
(in press)
-
Bae, H., Perls, T. T., Steinberg, M. H., and Sebastiani, P. (in press). Bayesian polynomial regression models to fit multiple genetic models for quantitative traits. Bayesian Anal. J. doi: 10.1214/13-BA880
-
Bayesian Anal. J.
-
-
Bae, H.1
Perls, T.T.2
Steinberg, M.H.3
Sebastiani, P.4
-
3
-
-
0030211964
-
Bagging predictors
-
Breiman, L. (1996). Bagging predictors. Mach. Learn. 24, 123-140. doi: 10.1007/BF00058655
-
(1996)
Mach. Learn.
, vol.24
, pp. 123-140
-
-
Breiman, L.1
-
4
-
-
84875495451
-
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction
-
Hartley, S. W., Monti, S., Liu, C. T., Steinberg, M. H., and Sebastiani, P. (2012). Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction. Front. Genet. 3:176. doi: 10.3389/fgene.2012.00176
-
(2012)
Front. Genet.
, vol.3
, pp. 176
-
-
Hartley, S.W.1
Monti, S.2
Liu, C.T.3
Steinberg, M.H.4
Sebastiani, P.5
-
5
-
-
84876220173
-
PleioGRiP: genetic risk prediction with pleiotropy
-
Hartley, S. W., and Sebastiani, P. (2013). PleioGRiP: genetic risk prediction with pleiotropy. Bioinformatics 29, 1086-1088. doi: 10.1093/bioinformatics/btt081
-
(2013)
Bioinformatics
, vol.29
, pp. 1086-1088
-
-
Hartley, S.W.1
Sebastiani, P.2
-
6
-
-
80051486102
-
A bayesian method for evaluating and discovering disease loci associations
-
Jiang, X., Barmada, M. M., Cooper, G. F., and Becich, M. J. (2011). A bayesian method for evaluating and discovering disease loci associations. PLoS ONE 6:e22075. doi: 10.1371/journal.pone.0022075
-
(2011)
PLoS ONE
, vol.6
-
-
Jiang, X.1
Barmada, M.M.2
Cooper, G.F.3
Becich, M.J.4
-
7
-
-
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, J., Yan, X., and Zhao, H. (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. doi: 10.1186/1753-6561-5-S9-S37
-
(2011)
BMC Proc
, vol.5
-
-
Kang, J.1
Zheng, W.2
Li, L.3
Lee, J.4
Yan, X.5
Zhao, H.6
-
8
-
-
77956385510
-
Risk prediction using genome-wide association studies
-
Kooperberg, C., Leblanc, M., and Obenchain, V. (2009). Risk prediction using genome-wide association studies. Genet. Epidemiol. 34, 643-652. doi: 10.1002/gepi.20509
-
(2009)
Genet. Epidemiol.
, vol.34
, pp. 643-652
-
-
Kooperberg, C.1
Leblanc, M.2
Obenchain, V.3
-
9
-
-
84906234346
-
Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies
-
Kundu, S., Mihaescu, R., Meijer, C. M., Bakker, R., and Janssens, A. C. (2014). Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies. Front. Genet. 5:179. doi: 10.3389/fgene.2014.00179
-
(2014)
Front. Genet.
, vol.5
, pp. 179
-
-
Kundu, S.1
Mihaescu, R.2
Meijer, C.M.3
Bakker, R.4
Janssens, A.C.5
-
10
-
-
79955643147
-
Beyond missing heritability: prediction of complex traits
-
Makowsky, R., Pajewski, N. M., Klimentidis, Y. C., Vazquez, A. I., Duarte, C. W., Allison, D. B., et al. (2011). Beyond missing heritability: prediction of complex traits. PLoS Genet. 7:e1002051. doi: 10.1371/journal.pgen.1002051
-
(2011)
PLoS Genet
, vol.7
-
-
Makowsky, R.1
Pajewski, N.M.2
Klimentidis, Y.C.3
Vazquez, A.I.4
Duarte, C.W.5
Allison, D.B.6
-
11
-
-
56749101779
-
Genotype score in addition to common risk factors for prediction of type 2 diabetes
-
Meigs, J. B., Shrader, P., Sullivan, L. M., McAteer, J. B., Fox, C. S., Dupuis, J., et al. (2008). Genotype score in addition to common risk factors for prediction of type 2 diabetes. N. Engl. J. Med. 359, 2208-2219. doi: 10.1056/NEJMoa0804742
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 2208-2219
-
-
Meigs, J.B.1
Shrader, P.2
Sullivan, L.M.3
McAteer, J.B.4
Fox, C.S.5
Dupuis, J.6
-
12
-
-
18844431843
-
Ensemble methods and partial least squares regression
-
Mevik, B.-H., Segtnan, V. H., and Næs, T. (2004). Ensemble methods and partial least squares regression. J. Chemom. 18, 498-507. doi: 10.1002/cem.895
-
(2004)
J. Chemom.
, vol.18
, pp. 498-507
-
-
Mevik, B.-H.1
Segtnan, V.H.2
Næs, T.3
-
13
-
-
84903649037
-
Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models
-
Milton, J. N., Gordeuk, V. R., Taylor, J. G. T., Gladwin, M. T., Steinberg, M. H., and Sebastiani, P. (2014). Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models. Circ. Cardiovasc. Genet. 7, 110-115. doi: 10.1161/CIRCGENETICS.113.000387
-
(2014)
Circ. Cardiovasc. Genet.
, vol.7
, pp. 110-115
-
-
Milton, J.N.1
Gordeuk, V.R.2
Taylor, J.G.T.3
Gladwin, M.T.4
Steinberg, M.H.5
Sebastiani, P.6
-
14
-
-
33745599582
-
A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility
-
Moore, J. H., Gilbert, J. C., Tsai, C. T., Chiang, F. T., Holden, T., Barney, N., et al. (2006). A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility. J. Theor. Biol. 241, 252-261. doi: 10.1016/j.jtbi.2005.11.036
-
(2006)
J. Theor. Biol.
, vol.241
, pp. 252-261
-
-
Moore, J.H.1
Gilbert, J.C.2
Tsai, C.T.3
Chiang, F.T.4
Holden, T.5
Barney, N.6
-
15
-
-
77149120471
-
Association between a literature-based genetic risk score and cardiovascular events in women
-
Paynter, N. P., Chasman, D. I., Pare, G., Buring, J. E., Cook, N. R., Miletich, J. P., et al. (2010). Association between a literature-based genetic risk score and cardiovascular events in women. JAMA 303, 631-637. doi: 10.1001/jama.2010.119
-
(2010)
JAMA
, vol.303
, pp. 631-637
-
-
Paynter, N.P.1
Chasman, D.I.2
Pare, G.3
Buring, J.E.4
Cook, N.R.5
Miletich, J.P.6
-
16
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell, S. M., Wray, N. R., Stone, J. L., Visscher, P. M., O'donovan, M. C., Sullivan, P. F., et al. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460, 748-752. doi: 10.1038/nature08185
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'donovan, M.C.5
Sullivan, P.F.6
-
17
-
-
25144441907
-
Mining genetic epidemiology data with Bayesian networks I: Bayesian networks and example application (plasma apoE levels)
-
Rodin, A. S., and Boerwinkle, E. (2005). Mining genetic epidemiology data with Bayesian networks I: Bayesian networks and example application (plasma apoE levels). Bioinformatics 21, 3273-3278. doi: 10.1093/bioinformatics/bti505
-
(2005)
Bioinformatics
, vol.21
, pp. 3273-3278
-
-
Rodin, A.S.1
Boerwinkle, E.2
-
18
-
-
84906222536
-
Genetic-based prediction of disease traits: prediction is very difficult, especially about the future(dagger)
-
Schrodi, S. J., Mukherjee, S., Shan, Y., Tromp, G., Sninsky, J. J., Callear, A. P., et al. (2014). Genetic-based prediction of disease traits: prediction is very difficult, especially about the future(dagger). Front. Genet. 5:162. doi: 10.3389/fgene.2014.00162
-
(2014)
Front. Genet.
, vol.5
, pp. 162
-
-
Schrodi, S.J.1
Mukherjee, S.2
Shan, Y.3
Tromp, G.4
Sninsky, J.J.5
Callear, A.P.6
-
19
-
-
16844366938
-
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
-
Sebastiani, P., Ramoni, M. F., Nolan, V., Baldwin, C. T., and Steinberg, M. H. (2005). Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat. Genet. 37, 435-440. doi: 10.1038/ng1533
-
(2005)
Nat. Genet.
, vol.37
, pp. 435-440
-
-
Sebastiani, P.1
Ramoni, M.F.2
Nolan, V.3
Baldwin, C.T.4
Steinberg, M.H.5
-
20
-
-
84855955362
-
Genetic signatures of exceptional longevity in humans
-
Sebastiani, P., Solovieff, N., Dewan, A. T., Walsh, K. M., Puca, A., Hartley, S. W., et al. (2012a). Genetic signatures of exceptional longevity in humans. PLoS ONE 7:e29848. doi: 10.1371/journal.pone.0029848
-
(2012)
PLoS ONE
, vol.7
-
-
Sebastiani, P.1
Solovieff, N.2
Dewan, A.T.3
Walsh, K.M.4
Puca, A.5
Hartley, S.W.6
-
21
-
-
84866447463
-
Naive Bayesian classifier and genetic risk score for genetic risk prediction of a categorical trait: not so different after all!
-
Sebastiani, P., Solovieff, N., and Sun, J. X. (2012b). Naive Bayesian classifier and genetic risk score for genetic risk prediction of a categorical trait: not so different after all! Front. Genet. 3:26. doi: 10.3389/fgene.2012.00026
-
(2012)
Front Genet
, vol.3
, pp. 26
-
-
Sebastiani, P.1
Solovieff, N.2
Sun, J.X.3
-
22
-
-
73449129712
-
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes
-
Wei, Z., Wang, K., Qu, H. Q., Zhang, H., Bradfield, J., Kim, C., et al. (2009). From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes. PLoS Genet. 5:e1000678. doi: 10.1371/journal.pgen.1000678
-
(2009)
PLoS Genet
, vol.5
-
-
Wei, Z.1
Wang, K.2
Qu, H.Q.3
Zhang, H.4
Bradfield, J.5
Kim, C.6
-
23
-
-
82455170504
-
Disease risk prediction with rare and common variants
-
Wu, C., Walsh, K., Dewan, A., Hoh, J., and Wang, Z. (2011). Disease risk prediction with rare and common variants. BMC Proc. 5:S61. doi: 10.1186/1753-6561-5-S9-S61
-
(2011)
BMC Proc
, vol.5
-
-
Wu, C.1
Walsh, K.2
Dewan, A.3
Hoh, J.4
Wang, Z.5
-
24
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
Yang, J., Manolio, T. A., Pasquale, L. R., Boerwinkle, E., Caporaso, N., Cunningham, J. M., et al. (2010). Genome partitioning of genetic variation for complex traits using common SNPs. Nat. Genet. 43, 519-525. doi: 10.1038/ng.823
-
(2010)
Nat. Genet.
, vol.43
, pp. 519-525
-
-
Yang, J.1
Manolio, T.A.2
Pasquale, L.R.3
Boerwinkle, E.4
Caporaso, N.5
Cunningham, J.M.6
-
25
-
-
79952593025
-
Quantitative trait prediction based on genetic marker-array data, a simulation study
-
Yip, W. K., and Lange, C. (2011). Quantitative trait prediction based on genetic marker-array data, a simulation study. Bioinformatics 27, 745-748. doi: 10.1093/bioinformatics/btr024
-
(2011)
Bioinformatics
, vol.27
, pp. 745-748
-
-
Yip, W.K.1
Lange, C.2
|