-
1
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA. 2012. An integrated map of genetic variation from 1, 092 human genomes. Nature 491(7422):56-65.
-
(2012)
Nature
, vol.491
, Issue.7422
, pp. 56-65
-
-
Abecasis, G.R.1
Auton, A.2
Brooks, L.D.3
DePristo, M.A.4
Durbin, R.M.5
Handsaker, R.E.6
Kang, H.M.7
Marth, G.T.8
McVean, G.A.9
-
2
-
-
84868502906
-
Imputation of exome sequence variants into population-based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project
-
others.
-
Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, Nalls MA, Zhang G, Franceschini N, Fox K, Lange EM and others. 2012. Imputation of exome sequence variants into population-based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. Am J Hum Genet 91(5):794-808.
-
(2012)
Am J Hum Genet
, vol.91
, Issue.5
, pp. 794-808
-
-
Auer, P.L.1
Johnsen, J.M.2
Johnson, A.D.3
Logsdon, B.A.4
Lange, L.A.5
Nalls, M.A.6
Zhang, G.7
Franceschini, N.8
Fox, K.9
Lange, E.M.10
-
3
-
-
79959544027
-
Comparison of methods and sampling designs to test for association between rare variants and quantitative traits
-
Bacanu SA, Nelson MR, Whittaker JC. 2011. Comparison of methods and sampling designs to test for association between rare variants and quantitative traits. Genet Epidemiol 35(4):226-235.
-
(2011)
Genet Epidemiol
, vol.35
, Issue.4
, pp. 226-235
-
-
Bacanu, S.A.1
Nelson, M.R.2
Whittaker, J.C.3
-
4
-
-
84867555327
-
A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders
-
Cheung YH, Wang G, Leal SM, Wang S. 2012. A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders. Genet Epidemiol 36(7):675-685.
-
(2012)
Genet Epidemiol
, vol.36
, Issue.7
, pp. 675-685
-
-
Cheung, Y.H.1
Wang, G.2
Leal, S.M.3
Wang, S.4
-
5
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH. 2004. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305(5685):869-872.
-
(2004)
Science
, vol.305
, Issue.5685
, pp. 869-872
-
-
Cohen, J.C.1
Kiss, R.S.2
Pertsemlidis, A.3
Marcel, Y.L.4
McPherson, R.5
Hobbs, H.H.6
-
7
-
-
58149345887
-
Practical aspects of imputation-driven meta-analysis of genome-wide association studies
-
de Bakker PIW, Ferreira MAR, Jia XM, Neale BM, Raychaudhuri S, Voight BF. 2008. Practical aspects of imputation-driven meta-analysis of genome-wide association studies. Hum Mol Genet 17:R122-R128.
-
(2008)
Hum Mol Genet
, vol.17
-
-
de Bakker, P.I.W.1
Ferreira, M.A.R.2
Jia, X.M.3
Neale, B.M.4
Raychaudhuri, S.5
Voight, B.F.6
-
8
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB. 2010. Rare variants create synthetic genome-wide associations. PLoS Biol 8(1):e1000294.
-
(2010)
PLoS Biol
, vol.8
, Issue.1
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
9
-
-
3242708140
-
Least Angle Regression
-
Efron B, Hastie T, Johnstone I, Tibshirani R. 2004. Least Angle Regression. Ann Stat 32(2):407-409.
-
(2004)
Ann Stat
, vol.32
, Issue.2
, pp. 407-409
-
-
Efron, B.1
Hastie, T.2
Johnstone, I.3
Tibshirani, R.4
-
10
-
-
77952557918
-
Missing heritability and strategies for finding the underlying causes of complex disease
-
Eichler EE, Flint J, Gibson G, Kong A, Leal SM, Moore JH, Nadeau JH. 2010. Missing heritability and strategies for finding the underlying causes of complex disease. Nat Rev Genet 11(6):446-450.
-
(2010)
Nat Rev Genet
, vol.11
, Issue.6
, pp. 446-450
-
-
Eichler, E.E.1
Flint, J.2
Gibson, G.3
Kong, A.4
Leal, S.M.5
Moore, J.H.6
Nadeau, J.H.7
-
11
-
-
84864923614
-
A permutation procedure to correct for confounders in case-control studies, including tests of rare variation
-
Epstein MP, Duncan R, Jiang Y, Conneely KN, Allen AS, Satten GA. 2012. A permutation procedure to correct for confounders in case-control studies, including tests of rare variation. Am J Hum Genet 91(2):215-223.
-
(2012)
Am J Hum Genet
, vol.91
, Issue.2
, pp. 215-223
-
-
Epstein, M.P.1
Duncan, R.2
Jiang, Y.3
Conneely, K.N.4
Allen, A.S.5
Satten, G.A.6
-
12
-
-
42449133365
-
The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome
-
others.
-
Firmann M, Mayor V, Vidal PM, Bochud M, Pecoud A, Hayoz D, Paccaud F, Preisig M, Song KS, Yuan X and others. 2008. The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome. BMC Cardiovasc Disord 8:6.
-
(2008)
BMC Cardiovasc Disord
, vol.8
, pp. 6
-
-
Firmann, M.1
Mayor, V.2
Vidal, P.M.3
Bochud, M.4
Pecoud, A.5
Hayoz, D.6
Paccaud, F.7
Preisig, M.8
Song, K.S.9
Yuan, X.10
-
13
-
-
77954136357
-
Hints of hidden heritability in GWAS
-
Gibson G. 2010. Hints of hidden heritability in GWAS. Nat Genet 42(7):558-560.
-
(2010)
Nat Genet
, vol.42
, Issue.7
, pp. 558-560
-
-
Gibson, G.1
-
14
-
-
38749145596
-
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms
-
Gorlov IP, Gorlova OY, Sunyaev SR, Spitz MR, Amos CI. 2008. Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms. Am J Hum Genet 82(1):100-112.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 100-112
-
-
Gorlov, I.P.1
Gorlova, O.Y.2
Sunyaev, S.R.3
Spitz, M.R.4
Amos, C.I.5
-
15
-
-
84870705395
-
Population-based resequencing of APOA1 in 10,330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach
-
Haase CL, Frikke-Schmidt R, Nordestgaard BG, Tybjaerg-Hansen A. 2012. Population-based resequencing of APOA1 in 10, 330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach. PLoS Genet 8(11):e1003063.
-
(2012)
PLoS Genet
, vol.8
, Issue.11
-
-
Haase, C.L.1
Frikke-Schmidt, R.2
Nordestgaard, B.G.3
Tybjaerg-Hansen, A.4
-
16
-
-
0034343735
-
Penalized regression with model-based penalties
-
Heckman NE, Ramsay JO. 2000. Penalized regression with model-based penalties. Can J Stat 28(2):241-258.
-
(2000)
Can J Stat
, vol.28
, Issue.2
, pp. 241-258
-
-
Heckman, N.E.1
Ramsay, J.O.2
-
19
-
-
78049484065
-
Penalized regression, standard errors, and Bayesian Lassos
-
Kyung M, Gill J, Ghosh M, Casella G. 2010. Penalized regression, standard errors, and Bayesian Lassos. Bayesian Anal 5(2):369-411.
-
(2010)
Bayesian Anal
, vol.5
, Issue.2
, pp. 369-411
-
-
Kyung, M.1
Gill, J.2
Ghosh, M.3
Casella, G.4
-
20
-
-
84885850443
-
Optimal tests for rare variant effects in sequencing association studies
-
Lee S, Wu MC, Lin X. 2012. Optimal tests for rare variant effects in sequencing association studies. Biostatistics 89:82-93.
-
(2012)
Biostatistics
, vol.89
, pp. 82-93
-
-
Lee, S.1
Wu, M.C.2
Lin, X.3
-
21
-
-
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(3):311-321.
-
(2008)
Am J Hum Genet
, vol.83
, Issue.3
, pp. 311-321
-
-
Li, B.S.1
Leal, S.M.2
-
22
-
-
66449114324
-
SNP detection for massively parallel whole-genome resequencing
-
Li RQ, Li YR, Fang XD, Yang HM, Wang J, Kristiansen K. 2009a. SNP detection for massively parallel whole-genome resequencing. Genome Res 19(6):1124-1132.
-
(2009)
Genome Res
, vol.19
, Issue.6
, pp. 1124-1132
-
-
Li, R.Q.1
Li, Y.R.2
Fang, X.D.3
Yang, H.M.4
Wang, J.5
Kristiansen, K.6
-
24
-
-
78249272314
-
To identify associations with rare variants, just WHaIT: weighted haplotype and imputation-based tests
-
Li Y, Byrnes AE, Li M. 2010a. To identify associations with rare variants, just WHaIT: weighted haplotype and imputation-based tests. Am J Hum Genet 87(5):728-735.
-
(2010)
Am J Hum Genet
, vol.87
, Issue.5
, pp. 728-735
-
-
Li, Y.1
Byrnes, A.E.2
Li, M.3
-
25
-
-
78649508578
-
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR. 2010b. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34(8):816-834.
-
(2010)
Genet Epidemiol
, vol.34
, Issue.8
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
Scheet, P.4
Abecasis, G.R.5
-
26
-
-
15944388957
-
An efficient Monte Carlo approach to assessing statistical significance in genomic studies
-
Lin DY. 2005. An efficient Monte Carlo approach to assessing statistical significance in genomic studies. Bioinformatics 21(6):781-787.
-
(2005)
Bioinformatics
, vol.21
, Issue.6
, pp. 781-787
-
-
Lin, D.Y.1
-
27
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin DY, Tang ZZ. 2011. A general framework for detecting disease associations with rare variants in sequencing studies. Am J Hum Genet 89:354-367.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 354-367
-
-
Lin, D.Y.1
Tang, Z.Z.2
-
28
-
-
84859120701
-
Genotype imputation of metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the women's health initiative
-
others.
-
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, Carlson C, Carty C, Crawford DC, Haessler J, Hindorff LA and others. 2012. Genotype imputation of metabochip SNPs using a study-specific reference panel of ~4, 000 haplotypes in African Americans from the women's health initiative. Genet Epidemiol 36(2):107-117.
-
(2012)
Genet Epidemiol
, vol.36
, Issue.2
, pp. 107-117
-
-
Liu, E.Y.1
Buyske, S.2
Aragaki, A.K.3
Peters, U.4
Boerwinkle, E.5
Carlson, C.6
Carty, C.7
Crawford, D.C.8
Haessler, J.9
Hindorff, L.A.10
-
29
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen BE, Browning SR. 2009. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet 5(2):e1000384.
-
(2009)
PLoS Genet
, vol.5
, Issue.2
-
-
Madsen, B.E.1
Browning, S.R.2
-
30
-
-
55549147191
-
Personal genomes: the case of the missing heritability
-
Maher B. 2008. Personal genomes: the case of the missing heritability. Nature 456(7218):18-21.
-
(2008)
Nature
, vol.456
, Issue.7218
, pp. 18-21
-
-
Maher, B.1
-
31
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A. 2009. Finding the missing heritability of complex diseases. Nature 461(7265):747-753.
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
McCarthy, M.I.7
Ramos, E.M.8
Cardon, L.R.9
Chakravarti, A.10
-
32
-
-
84871078801
-
Testing genetic association with rare variants in admixed populations
-
Mao X, Li Y, Liu Y, Lange L, Li M. 2013. Testing genetic association with rare variants in admixed populations. Genet Epidemiol 37(1):38-47.
-
(2013)
Genet Epidemiol
, vol.37
, Issue.1
, pp. 38-47
-
-
Mao, X.1
Li, Y.2
Liu, Y.3
Lange, L.4
Li, M.5
-
33
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B. 2010. Genotype imputation for genome-wide association studies. Nat Rev Genet 11(7):499-511.
-
(2010)
Nat Rev Genet
, vol.11
, Issue.7
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
34
-
-
33846014328
-
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST)
-
Morgenthaler S, Thilly WG. 2007. A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). Mutat Res 615(1-2):28-56.
-
(2007)
Mutat Res
, vol.615
, Issue.1-2
, pp. 28-56
-
-
Morgenthaler, S.1
Thilly, W.G.2
-
35
-
-
79953752624
-
Testing for an unusual distribution of rare variants
-
Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ. 2011. Testing for an unusual distribution of rare variants. PLoS Genet 7(3):e1001322.
-
(2011)
PLoS Genet
, vol.7
, Issue.3
-
-
Neale, B.M.1
Rivas, M.A.2
Voight, B.F.3
Altshuler, D.4
Devlin, B.5
Orho-Melander, M.6
Kathiresan, S.7
Purcell, S.M.8
Roeder, K.9
Daly, M.J.10
-
36
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S, Walker N, Riches D, Egholm M, Todd JA. 2009. Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 324(5925):387-389.
-
(2009)
Science
, vol.324
, Issue.5925
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
37
-
-
84863541347
-
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
-
Nelson MR, Wegmann D, Ehm MG, Kessner D, St Jean P, Verzilli C, Shen J, Tang Z, Bacanu SA, Fraser D. 2012. An abundance of rare functional variants in 202 drug target genes sequenced in 14, 002 people. Science 337(6090):100-114.
-
(2012)
Science
, vol.337
, Issue.6090
, pp. 100-114
-
-
Nelson, M.R.1
Wegmann, D.2
Ehm, M.G.3
Kessner, D.4
St Jean, P.5
Verzilli, C.6
Shen, J.7
Tang, Z.8
Bacanu, S.A.9
Fraser, D.10
-
38
-
-
77953121877
-
Pooled association tests for rare variants in exon-resequencing studies
-
Price AL, Kryukov GV, de Bakker PI, Purcell SM, Staples J, Wei LJ, Sunyaev SR. 2010. Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet 86(6):832-838.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.6
, pp. 832-838
-
-
Price, A.L.1
Kryukov, G.V.2
de Bakker, P.I.3
Purcell, S.M.4
Staples, J.5
Wei, L.J.6
Sunyaev, S.R.7
-
39
-
-
79960943621
-
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
-
others.
-
Sanna S, Li B, Mulas A, Sidore C, Kang HM, Jackson AU, Piras MG, Usala G, Maninchedda G, Sassu A and others. 2011. Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability. PLoS Genet 7(7):e1002198.
-
(2011)
PLoS Genet
, vol.7
, Issue.7
-
-
Sanna, S.1
Li, B.2
Mulas, A.3
Sidore, C.4
Kang, H.M.5
Jackson, A.U.6
Piras, M.G.7
Usala, G.8
Maninchedda, G.9
Sassu, A.10
-
40
-
-
27544497650
-
Calibrating a coalescent simulation of human genome sequence variation
-
Schaffner SF, Foo C, Gabriel S, Reich D, Daly MJ, Altshuler D. 2005. Calibrating a coalescent simulation of human genome sequence variation. Genome Res 15(11):1576-1583.
-
(2005)
Genome Res
, vol.15
, Issue.11
, pp. 1576-1583
-
-
Schaffner, S.F.1
Foo, C.2
Gabriel, S.3
Reich, D.4
Daly, M.J.5
Altshuler, D.6
-
41
-
-
85194972808
-
Regression shrinkage and selection via the LASSO
-
Tibshirani R. 1996. Regression shrinkage and selection via the LASSO. J Ro Stat Soc Ser B 58:267-288.
-
(1996)
J Ro Stat Soc Ser B
, vol.58
, pp. 267-288
-
-
Tibshirani, R.1
-
42
-
-
84868680733
-
An optimum projection and noise reduction approach for detecting rare and common variants associated with complex diseases
-
Turkmen A, Lin S. 2012. An optimum projection and noise reduction approach for detecting rare and common variants associated with complex diseases. Hum Hered 74(1):51-60.
-
(2012)
Hum Hered
, vol.74
, Issue.1
, pp. 51-60
-
-
Turkmen, A.1
Lin, S.2
-
43
-
-
80051636106
-
Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression
-
Tzeng JY, Zhang D, Pongpanich M, Smith C, McCarthy MI, Sale MM, Worrall BB, Hsu FC, Thomas DC, Sullivan PF. 2011. Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression. Am J Hum Genet 89(2):277-288.
-
(2011)
Am J Hum Genet
, vol.89
, Issue.2
, pp. 277-288
-
-
Tzeng, J.Y.1
Zhang, D.2
Pongpanich, M.3
Smith, C.4
McCarthy, M.I.5
Sale, M.M.6
Worrall, B.B.7
Hsu, F.C.8
Thomas, D.C.9
Sullivan, P.F.10
-
44
-
-
77956534324
-
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Harkonarson H. 2010. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nuc Acids Res 38(16):e164.
-
(2010)
Nuc Acids Res
, vol.38
, Issue.16
-
-
Wang, K.1
Li, M.2
Harkonarson, H.3
-
45
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X. 2011. Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 89(1):82-93.
-
(2011)
Am J Hum Genet
, vol.89
, Issue.1
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
46
-
-
84863879353
-
Coordinate descent algorithms for lasso penalized regression
-
Wu TT, Lange K. 2008. Coordinate descent algorithms for lasso penalized regression. Ann Appl Stat 2(1):224-244.
-
(2008)
Ann Appl Stat
, vol.2
, Issue.1
, pp. 224-244
-
-
Wu, T.T.1
Lange, K.2
-
47
-
-
65149104817
-
SCAD-penalized regression in high-dimensional partially linear models
-
Xie HL, Huang J. 2009. SCAD-penalized regression in high-dimensional partially linear models. Ann Stat 37(2):673-696.
-
(2009)
Ann Stat
, vol.37
, Issue.2
, pp. 673-696
-
-
Xie, H.L.1
Huang, J.2
-
48
-
-
84864686318
-
Multiple regression methods show great potential for rare variant association tests
-
Xu C, Ladouceur M, Dastani Z, Richards JB, Ciampi A, Greenwood CM. 2012. Multiple regression methods show great potential for rare variant association tests. PLoS One 7(8):e41694.
-
(2012)
PLoS One
, vol.7
, Issue.8
-
-
Xu, C.1
Ladouceur, M.2
Dastani, Z.3
Richards, J.B.4
Ciampi, A.5
Greenwood, C.M.6
-
49
-
-
84855295482
-
Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects
-
Yi N, Liu N, Zhi D, Li J. 2011. Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects. PLoS Genet 7(12):e1002382.
-
(2011)
PLoS Genet
, vol.7
, Issue.12
-
-
Yi, N.1
Liu, N.2
Zhi, D.3
Li, J.4
-
50
-
-
78249243049
-
Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes
-
Zawistowski M, Gopalakrishnan S, Ding J, Li Y, Grimm S, Zollner S. 2010. Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes. Am J Hum Genet 87(5):604-617.
-
(2010)
Am J Hum Genet
, vol.87
, Issue.5
, pp. 604-617
-
-
Zawistowski, M.1
Gopalakrishnan, S.2
Ding, J.3
Li, Y.4
Grimm, S.5
Zollner, S.6
-
51
-
-
77957233032
-
Association screening of common and rare genetic variants by penalized regression
-
Zhou H, Sehl ME, Sinsheimer JS, Lange K. 2010. Association screening of common and rare genetic variants by penalized regression. Bioinformatics 26(19):2375-2382.
-
(2010)
Bioinformatics
, vol.26
, Issue.19
, pp. 2375-2382
-
-
Zhou, H.1
Sehl, M.E.2
Sinsheimer, J.S.3
Lange, K.4
-
52
-
-
16244401458
-
Regularization and variable selection via the elastic net
-
Zou H, Hastie T. 2005. Regularization and variable selection via the elastic net. J R Stat Soc Ser B 67:301-320.
-
(2005)
J R Stat Soc Ser B
, vol.67
, pp. 301-320
-
-
Zou, H.1
Hastie, T.2
|