-
1
-
-
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: e1000294. 20126254
-
(2010)
PLoS Biol
, vol.8
, pp. e1000294
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
2
-
-
84898786106
-
Statistical power and significance testing in large-scale genetic studies
-
Sham PC, Purcell SM, (2014) Statistical power and significance testing in large-scale genetic studies. Nat Rev Genet 15: 335–346. 24739678
-
(2014)
Nat Rev Genet
, vol.15
, pp. 335-346
-
-
Sham, P.C.1
Purcell, S.M.2
-
3
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli ET, Goldstein DB, (2010) Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat Rev Genet 11: 415–425. doi: 10.1038/nrg2779 20479773
-
(2010)
Nat Rev Genet
, vol.11
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
4
-
-
84891790401
-
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
-
Welter D, MacArthur J, Morales J, Burdett T, Hall P, et al. (2014) The NHGRI GWAS Catalog, a curated resource of SNP-trait associations. Nucleic Acids Res 42: D1001–D1006. doi: 10.1093/nar/gkt1229 24316577
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D1001-D1006
-
-
Welter, D.1
MacArthur, J.2
Morales, J.3
Burdett, T.4
Hall, P.5
-
5
-
-
84867898425
-
Effect of Genome-Wide Genotyping and Reference Panels on Rare Variants Imputation
-
Zheng H-F, Ladouceur M, Greenwood CMT, Richards JB, (2012) Effect of Genome-Wide Genotyping and Reference Panels on Rare Variants Imputation. Journal of Genetics and Genomics 39: 545–550. 23089364
-
(2012)
Journal of Genetics and Genomics
, vol.39
, pp. 545-550
-
-
Zheng, H.-F.1
Ladouceur, M.2
Greenwood, C.M.T.3
Richards, J.B.4
-
6
-
-
84868502906
-
Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project
-
Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, et al. (2012) Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project. The American Journal of Human Genetics 91: 794–808. doi: 10.1016/j.ajhg.2012.08.031 23103231
-
(2012)
The American Journal of Human Genetics
, vol.91
, pp. 794-808
-
-
Auer, P.L.1
Johnsen, J.M.2
Johnson, A.D.3
Logsdon, B.A.4
Lange, L.A.5
-
7
-
-
84886006191
-
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
-
Duan Q, Liu EY, Auer PL, Zhang G, Lange EM, et al. (2013) Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. Bioinformatics 29: 2744–2749. doi: 10.1093/bioinformatics/btt477 23956302
-
(2013)
Bioinformatics
, vol.29
, pp. 2744-2749
-
-
Duan, Q.1
Liu, E.Y.2
Auer, P.L.3
Zhang, G.4
Lange, E.M.5
-
8
-
-
79953212557
-
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
-
Holm H, Gudbjartsson DF, Sulem P, Masson G, Helgadottir HT, et al. (2011) A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nature Genetics 43: 316–320. doi: 10.1038/ng.781 21378987
-
(2011)
Nature Genetics
, vol.43
, pp. 316-320
-
-
Holm, H.1
Gudbjartsson, D.F.2
Sulem, P.3
Masson, G.4
Helgadottir, H.T.5
-
9
-
-
84865062784
-
A Coalescent Model for Genotype Imputation
-
Jewett EM, Zawistowski M, Rosenberg NA, Zöllner S, (2012) A Coalescent Model for Genotype Imputation. Genetics 191: 1239–1255. 22595242
-
(2012)
Genetics
, vol.191
, pp. 1239-1255
-
-
Jewett, E.M.1
Zawistowski, M.2
Rosenberg, N.A.3
Zöllner, S.4
-
10
-
-
84880483904
-
Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies
-
Joshi PK, Prendergast J, Fraser RM, Huffman JE, Vitart V, et al. (2013) Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies. PLoS ONE 8: e68604. doi: 10.1371/journal.pone.0068604 23874685
-
(2013)
PLoS ONE
, vol.8
, pp. e68604
-
-
Joshi, P.K.1
Prendergast, J.2
Fraser, R.M.3
Huffman, J.E.4
Vitart, V.5
-
11
-
-
79956329346
-
Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets
-
Jostins L, Morley KI, Barrett JC, (2011) Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets. European Journal of Human Genetics 19: 662–666. doi: 10.1038/ejhg.2011.10 21364697
-
(2011)
European Journal of Human Genetics
, vol.19
, pp. 662-666
-
-
Jostins, L.1
Morley, K.I.2
Barrett, J.C.3
-
12
-
-
80052877813
-
Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes
-
Li L, Li Y, Browning SR, Browning BL, Slater AJ, et al. (2011) Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes. PLoS ONE 6: e24945. doi: 10.1371/journal.pone.0024945 21949800
-
(2011)
PLoS ONE
, vol.6
, pp. e24945
-
-
Li, L.1
Li, Y.2
Browning, S.R.3
Browning, B.L.4
Slater, A.J.5
-
13
-
-
84859120701
-
Genotype Imputation of MetabochipSNPs Using a Study-Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women’s Health Initiative
-
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, et al. (2012) Genotype Imputation of MetabochipSNPs Using a Study-Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women’s Health Initiative. Genetic Epidemiology 36: 107–117. doi: 10.1002/gepi.21603 22851474
-
(2012)
Genetic Epidemiology
, vol.36
, pp. 107-117
-
-
Liu, E.Y.1
Buyske, S.2
Aragaki, A.K.3
Peters, U.4
Boerwinkle, E.5
-
14
-
-
84869131540
-
Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases
-
Mägi R, Asimit JL, Day-Williams AG, Zeggini E, Morris AP, (2012) Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases. Genetic Epidemiology 36: 785–796. doi: 10.1002/gepi.21675 22951892
-
(2012)
Genetic Epidemiology
, vol.36
, pp. 785-796
-
-
Mägi, R.1
Asimit, J.L.2
Day-Williams, A.G.3
Zeggini, E.4
Morris, A.P.5
-
15
-
-
84855174922
-
Performance of Genotype Imputations Using Data from the 1000 Genomes Project
-
Sung YJ, Wang L, Rankinen T, Bouchard C, Rao DC, (2012) Performance of Genotype Imputations Using Data from the 1000 Genomes Project. Human Heredity 73: 18–25. 22212296
-
(2012)
Human Heredity
, vol.73
, pp. 18-25
-
-
Sung, Y.J.1
Wang, L.2
Rankinen, T.3
Bouchard, C.4
Rao, D.C.5
-
16
-
-
84877816544
-
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant—Phenotype Associations Undetected by HapMap Based Imputation
-
Wood AR, Perry JRB, Tanaka T, Hernandez DG, Zheng H-F, et al. (2013) Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant—Phenotype Associations Undetected by HapMap Based Imputation. PLoS ONE 8: e64343. doi: 10.1371/journal.pone.0064343 23696881
-
(2013)
PLoS ONE
, vol.8
, pp. e64343
-
-
Wood, A.R.1
Perry, J.R.B.2
Tanaka, T.3
Hernandez, D.G.4
Zheng, H.-F.5
-
17
-
-
84865446158
-
Association Between Germline HOXB13 G84E Mutation and Risk of Prostate Cancer
-
Akbari MR, Trachtenberg J, Lee J, Tam S, Bristow R, et al. (2012) Association Between Germline HOXB13 G84E Mutation and Risk of Prostate Cancer. JNCI J Natl Cancer Inst 104: 1260–1262. 22781434
-
(2012)
JNCI J Natl Cancer Inst
, vol.104
, pp. 1260-1262
-
-
Akbari, M.R.1
Trachtenberg, J.2
Lee, J.3
Tam, S.4
Bristow, R.5
-
18
-
-
84864823100
-
Confirmation of the HOXB13 G84E Germline Mutation in Familial Prostate Cancer
-
Breyer JP, Avritt TG, McReynolds KM, Dupont WD, Smith JR, (2012) Confirmation of the HOXB13 G84E Germline Mutation in Familial Prostate Cancer. Cancer Epidemiol Biomarkers Prev 21: 1348–1353. 22714738
-
(2012)
Cancer Epidemiol Biomarkers Prev
, vol.21
, pp. 1348-1353
-
-
Breyer, J.P.1
Avritt, T.G.2
McReynolds, K.M.3
Dupont, W.D.4
Smith, J.R.5
-
19
-
-
84877248238
-
The G84E mutation of HOXB13 is associated with increased risk for prostate cancer: results from the REDUCE trial
-
Chen Z, Greenwood C, Isaacs WB, Foulkes WD, Sun J, et al. (2013) The G84E mutation of HOXB13 is associated with increased risk for prostate cancer: results from the REDUCE trial. Carcinogenesis 34: 1260–1264. doi: 10.1093/carcin/bgt055 23393222
-
(2013)
Carcinogenesis
, vol.34
, pp. 1260-1264
-
-
Chen, Z.1
Greenwood, C.2
Isaacs, W.B.3
Foulkes, W.D.4
Sun, J.5
-
20
-
-
84856176782
-
Germline mutations in HOXB13 and prostate-cancer risk
-
Ewing CM, Ray AM, Lange EM, Zuhlke KA, Robbins CM, et al. (2012) Germline mutations in HOXB13 and prostate-cancer risk. New England Journal of Medicine 366: 141–149. 22236224
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 141-149
-
-
Ewing, C.M.1
Ray, A.M.2
Lange, E.M.3
Zuhlke, K.A.4
Robbins, C.M.5
-
21
-
-
84870531459
-
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer
-
Gudmundsson J, Sulem P, Gudbjartsson DF, Masson G, Agnarsson BA, et al. (2012) A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. Nature Genetics 44: 1326–9. doi: 10.1038/ng.2437 23104005
-
(2012)
Nature Genetics
, vol.44
, pp. 1326-1329
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
Masson, G.4
Agnarsson, B.A.5
-
22
-
-
84899068774
-
G84E mutation in HOXB13 is firmly associated with prostate cancer risk: a meta-analysis
-
Huang H, Cai B, (2014) G84E mutation in HOXB13 is firmly associated with prostate cancer risk: a meta-analysis. Tumor Biol 35: 1177–1182. doi: 10.1007/s13277-013-1157-5 24026887
-
(2014)
Tumor Biol
, vol.35
, pp. 1177-1182
-
-
Huang, H.1
Cai, B.2
-
23
-
-
84872308743
-
-
International Consortium for Prostate Cancer Genetics, Xu J, Lange EM, Lu L, Zheng SL, et al. (2012) HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics.
-
(2012)
-
-
-
24
-
-
84888839080
-
A Population-based Assessment of Germline HOXB13 G84E Mutation and Prostate Cancer Risk
-
Karlsson R, Aly M, Clements M, Zheng L, Adolfsson J, et al. (2014) A Population-based Assessment of Germline HOXB13 G84E Mutation and Prostate Cancer Risk. European Urology 65: 169–176. 22841674
-
(2014)
European Urology
, vol.65
, pp. 169-176
-
-
Karlsson, R.1
Aly, M.2
Clements, M.3
Zheng, L.4
Adolfsson, J.5
-
25
-
-
84875229518
-
The G84E mutation in the HOXB13 gene is associated with an increased risk of prostate cancer in Poland
-
Kluźniak W, Wokołorczyk D, Kashyap A, Jakubowska A, Gronwald J, et al. (2013) The G84E mutation in the HOXB13 gene is associated with an increased risk of prostate cancer in Poland. The Prostate 73: 542–548. doi: 10.1002/pros.22594 23334858
-
(2013)
The Prostate
, vol.73
, pp. 542-548
-
-
Kluźniak, W.1
Wokołorczyk, D.2
Kashyap, A.3
Jakubowska, A.4
Gronwald, J.5
-
26
-
-
84876581228
-
HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk
-
Laitinen VH, Wahlfors T, Saaristo L, Rantapero T, Pelttari LM, et al. (2013) HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk. Cancer Epidemiol Biomarkers Prev 22: 452–460. doi: 10.1158/1055-9965.EPI-12-1000-T 23292082
-
(2013)
Cancer Epidemiol Biomarkers Prev
, vol.22
, pp. 452-460
-
-
Laitinen, V.H.1
Wahlfors, T.2
Saaristo, L.3
Rantapero, T.4
Pelttari, L.M.5
-
27
-
-
84874042482
-
Population-Based Estimate of Prostate Cancer Risk for Carriers of the HOXB13 Missense Mutation G84E
-
MacInnis RJ, Severi G, Baglietto L, Dowty JG, Jenkins MA, et al. (2013) Population-Based Estimate of Prostate Cancer Risk for Carriers of the HOXB13 Missense Mutation G84E. PLoS ONE 8: e54727. doi: 10.1371/journal.pone.0054727 23457453
-
(2013)
PLoS ONE
, vol.8
, pp. e54727
-
-
MacInnis, R.J.1
Severi, G.2
Baglietto, L.3
Dowty, J.G.4
Jenkins, M.A.5
-
28
-
-
84878859598
-
Germline Homeobox B13 (HOXB13) G84E Mutation and Prostate Cancer Risk in European Descendants: A Meta-analysis of 24 213 Cases and 73 631 Controls
-
Shang Z, Zhu S, Zhang H, Li L, Niu Y, (2013) Germline Homeobox B13 (HOXB13) G84E Mutation and Prostate Cancer Risk in European Descendants: A Meta-analysis of 24 213 Cases and 73 631 Controls. European Urology 64: 173–176. doi: 10.1016/j.eururo.2013.03.007 23518396
-
(2013)
European Urology
, vol.64
, pp. 173-176
-
-
Shang, Z.1
Zhu, S.2
Zhang, H.3
Li, L.4
Niu, Y.5
-
29
-
-
84875790154
-
HOXB13 mutations in a population-based, case-control study of prostate cancer
-
Stott-Miller M, Karyadi DM, Smith T, Kwon EM, Kolb S, et al. (2013) HOXB13 mutations in a population-based, case-control study of prostate cancer. The Prostate 73: 634–641. doi: 10.1002/pros.22604 23129385
-
(2013)
The Prostate
, vol.73
, pp. 634-641
-
-
Stott-Miller, M.1
Karyadi, D.M.2
Smith, T.3
Kwon, E.M.4
Kolb, S.5
-
30
-
-
84876547982
-
HOXB13 Mutation and Prostate Cancer: Studies of Siblings and Aggressive Disease
-
Witte JS, Mefford J, Plummer SJ, Liu J, Cheng I, et al. (2013) HOXB13 Mutation and Prostate Cancer: Studies of Siblings and Aggressive Disease. Cancer Epidemiol Biomarkers Prev 22: 675–680. doi: 10.1158/1055-9965.EPI-12-1154 23396964
-
(2013)
Cancer Epidemiol Biomarkers Prev
, vol.22
, pp. 675-680
-
-
Witte, J.S.1
Mefford, J.2
Plummer, S.J.3
Liu, J.4
Cheng, I.5
-
31
-
-
36749045193
-
HOXB13 promotes ovarian cancer progression
-
Miao J, Wang Z, Provencher H, Muir B, Dahiya S, et al. (2007) HOXB13 promotes ovarian cancer progression. PNAS 104: 17093–17098. 17942676
-
(2007)
PNAS
, vol.104
, pp. 17093-17098
-
-
Miao, J.1
Wang, Z.2
Provencher, H.3
Muir, B.4
Dahiya, S.5
-
32
-
-
84877965505
-
Deregulation of HOX B13 expression in urinary bladder cancer progression
-
Marra L, Cantile M, Scognamiglio G, Perdonà S, La Mantia E, et al. (2013) Deregulation of HOX B13 expression in urinary bladder cancer progression. Curr Med Chem 20: 833–839. 23276138
-
(2013)
Curr Med Chem
, vol.20
, pp. 833-839
-
-
Marra, L.1
Cantile, M.2
Scognamiglio, G.3
Perdonà, S.4
La Mantia, E.5
-
33
-
-
84924375314
-
PP076: HOX B13 and HOX C13 expression in oral squamous cell carcinoma: A tissue microarray based immunohistochemical study
-
Sabatino R, Cantile M, Aquino G, Scognamiglio G, Madonna C, et al. (2013) PP076: HOX B13 and HOX C13 expression in oral squamous cell carcinoma: A tissue microarray based immunohistochemical study. Oral Oncology 49, Supplement 1: S120.
-
(2013)
Oral Oncology
, vol.49
, pp. S120
-
-
Sabatino, R.1
Cantile, M.2
Aquino, G.3
Scognamiglio, G.4
Madonna, C.5
-
34
-
-
78650921551
-
Predictive relevance of HOXB13 protein expression for tamoxifen benefit in breast cancer
-
Jerevall P-L, Jansson A, Fornander T, Skoog L, Nordenskjöld B, et al. (2010) Predictive relevance of HOXB13 protein expression for tamoxifen benefit in breast cancer. Breast Cancer Res 12: R53. doi: 10.1186/bcr2612 20649975
-
(2010)
Breast Cancer Res
, vol.12
, pp. R53
-
-
Jerevall, P.-L.1
Jansson, A.2
Fornander, T.3
Skoog, L.4
Nordenskjöld, B.5
-
35
-
-
84878936080
-
Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer
-
Akbari MR, Anderson LN, Buchanan DD, Clendenning M, Jenkins MA, et al. (2013) Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer. Cancer Epidemiology 37: 424–427. doi: 10.1016/j.canep.2013.03.003 23541221
-
(2013)
Cancer Epidemiology
, vol.37
, pp. 424-427
-
-
Akbari, M.R.1
Anderson, L.N.2
Buchanan, D.D.3
Clendenning, M.4
Jenkins, M.A.5
-
36
-
-
84864511887
-
Association of a HOXB13 Variant with Breast Cancer
-
Alanee S, Couch F, Offit K, (2012) Association of a HOXB13 Variant with Breast Cancer. New England Journal of Medicine 367: 480–481. doi: 10.1056/NEJMc1205138 22853031
-
(2012)
New England Journal of Medicine
, vol.367
, pp. 480-481
-
-
Alanee, S.1
Couch, F.2
Offit, K.3
-
37
-
-
84901741339
-
Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer
-
Saunders EJ, Dadaev T, Leongamornlert DA, Jugurnauth-Little S, Tymrakiewicz M, et al. (2014) Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer. PLoS Genet 10: e1004129. doi: 10.1371/journal.pgen.1004129 24550738
-
(2014)
PLoS Genet
, vol.10
, pp. e1004129
-
-
Saunders, E.J.1
Dadaev, T.2
Leongamornlert, D.A.3
Jugurnauth-Little, S.4
Tymrakiewicz, M.5
-
38
-
-
34548292504
-
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, et al. (2007) PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses. The American Journal of Human Genetics 81: 559–575. 17701901
-
(2007)
The American Journal of Human Genetics
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
-
39
-
-
33748776023
-
California Men’s Health Study (CMHS): a multiethnic cohort in a managed care setting
-
Enger SM, Van Den Eeden SK, Sternfeld B, Loo RK, Quesenberry CP, et al. (2006) California Men’s Health Study (CMHS): a multiethnic cohort in a managed care setting. BMC Public Health 6: 172. 16813653
-
(2006)
BMC Public Health
, vol.6
, pp. 172
-
-
Enger, S.M.1
Van Den Eeden, S.K.2
Sternfeld, B.3
Loo, R.K.4
Quesenberry, C.P.5
-
41
-
-
39749181521
-
Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation
-
Li JZ, Absher DM, Tang H, Southwick AM, Casto AM, et al. (2008) Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation. Science 319: 1100–1104. doi: 10.1126/science.1153717 18292342
-
(2008)
Science
, vol.319
, pp. 1100-1104
-
-
Li, J.Z.1
Absher, D.M.2
Tang, H.3
Southwick, A.M.4
Casto, A.M.5
-
42
-
-
79960700796
-
Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array
-
Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, et al. (2011) Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array. Genomics 98: 79–89. doi: 10.1016/j.ygeno.2011.04.005 21565264
-
(2011)
Genomics
, vol.98
, pp. 79-89
-
-
Hoffmann, T.J.1
Kvale, M.N.2
Hesselson, S.E.3
Zhan, Y.4
Aquino, C.5
-
43
-
-
10844266655
-
HOXB13 Induces Growth Suppression of Prostate Cancer Cells as a Repressor of Hormone-Activated Androgen Receptor Signaling
-
Jung C, Kim R-S, Zhang H-J, Lee S-J, Jeng M-H, (2004) HOXB13 Induces Growth Suppression of Prostate Cancer Cells as a Repressor of Hormone-Activated Androgen Receptor Signaling. Cancer Res 64: 9185–9192. 15604291
-
(2004)
Cancer Res
, vol.64
, pp. 9185-9192
-
-
Jung, C.1
Kim, R.-S.2
Zhang, H.-J.3
Lee, S.-J.4
Jeng, M.-H.5
-
44
-
-
70449123571
-
The Homeodomain Protein HOXB13 Regulates the Cellular Response to Androgens
-
Norris JD, Chang C-Y, Wittmann BM, Kunder RS, Cui H, et al. (2009) The Homeodomain Protein HOXB13 Regulates the Cellular Response to Androgens. Molecular Cell 36: 405–416. doi: 10.1016/j.molcel.2009.10.020 19917249
-
(2009)
Molecular Cell
, vol.36
, pp. 405-416
-
-
Norris, J.D.1
Chang, C.-Y.2
Wittmann, B.M.3
Kunder, R.S.4
Cui, H.5
-
45
-
-
67651222400
-
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
-
Howie BN, Donnelly P, Marchini J, (2009) A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies. PLoS Genet 5: e1000529. doi: 10.1371/journal.pgen.1000529 19543373
-
(2009)
PLoS Genet
, vol.5
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
46
-
-
69749099417
-
Fast model-based estimation of ancestry in unrelated individuals
-
Alexander DH, Novembre J, Lange K, (2009) Fast model-based estimation of ancestry in unrelated individuals. Genome Res 19: 1655–1664. doi: 10.1101/gr.094052.109 19648217
-
(2009)
Genome Res
, vol.19
, pp. 1655-1664
-
-
Alexander, D.H.1
Novembre, J.2
Lange, K.3
-
47
-
-
81955167912
-
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm
-
Hoffmann TJ, Zhan Y, Kvale MN, Hesselson SE, Gollub J, et al. (2011) Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. Genomics 98: 422–430. doi: 10.1016/j.ygeno.2011.08.007 21903159
-
(2011)
Genomics
, vol.98
, pp. 422-430
-
-
Hoffmann, T.J.1
Zhan, Y.2
Kvale, M.N.3
Hesselson, S.E.4
Gollub, J.5
-
48
-
-
84856478855
-
A linear complexity phasing method for thousands of genomes
-
Delaneau O, Marchini J, Zagury J-F, (2012) A linear complexity phasing method for thousands of genomes. Nature Methods 9: 179–181. doi: 10.1038/nmeth.1785 22138821
-
(2012)
Nature Methods
, vol.9
, pp. 179-181
-
-
Delaneau, O.1
Marchini, J.2
Zagury, J.-F.3
-
49
-
-
84863845193
-
Genotype Imputation with Thousands of Genomes
-
Howie B, Marchini J, Stephens M, (2011) Genotype Imputation with Thousands of Genomes. G3 1: 457–470. 22384356
-
(2011)
G3
, vol.1
, pp. 457-470
-
-
Howie, B.1
Marchini, J.2
Stephens, M.3
-
50
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR, (2012) Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nature Genetics 44: 955–959. doi: 10.1038/ng.2354 22820512
-
(2012)
Nature Genetics
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
51
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B, (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11: 499–511. 20517342
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
52
-
-
84924427804
-
-
R Core Team (2012) R: A language and environment for statistical computing. Available: http://www.R-project.org.
-
-
-
-
54
-
-
62649089065
-
Genotype-Imputation Accuracy across Worldwide Human Populations
-
Huang L, Li Y, Singleton AB, Hardy JA, Abecasis G, et al. (2009) Genotype-Imputation Accuracy across Worldwide Human Populations. The American Journal of Human Genetics 84: 235–250. doi: 10.1016/j.ajhg.2009.01.013 19215730
-
(2009)
The American Journal of Human Genetics
, vol.84
, pp. 235-250
-
-
Huang, L.1
Li, Y.2
Singleton, A.B.3
Hardy, J.A.4
Abecasis, G.5
-
55
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nature Genetics 38: 904–909. 16862161
-
(2006)
Nature Genetics
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
-
56
-
-
84860771128
-
A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits
-
Bhattacharjee S, Rajaraman P, Jacobs KB, Wheeler WA, Melin BS, et al. (2012) A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits. The American Journal of Human Genetics 90: 821–835. doi: 10.1016/j.ajhg.2012.03.015 22560090
-
(2012)
The American Journal of Human Genetics
, vol.90
, pp. 821-835
-
-
Bhattacharjee, S.1
Rajaraman, P.2
Jacobs, K.B.3
Wheeler, W.A.4
Melin, B.S.5
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