-
1
-
-
84899438176
-
Colorectal cancer statistics, 2014
-
Siegel, R., Desantis, C., Jemal, A., Colorectal cancer statistics, 2014. CA Cancer J. Clin. 64 (2014), 104–117.
-
(2014)
CA Cancer J. Clin.
, vol.64
, pp. 104-117
-
-
Siegel, R.1
Desantis, C.2
Jemal, A.3
-
2
-
-
84930028683
-
A model to determine colorectal cancer risk using common genetic susceptibility loci
-
1330–9.e14
-
Hsu, L., Jeon, J., Brenner, H., Gruber, S.B., Schoen, R.E., Berndt, S.I., Chan, A.T., Chang-Claude, J., Du, M., Gong, J., et al. Colorectal Transdisciplinary (CORECT) Study, Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO). A model to determine colorectal cancer risk using common genetic susceptibility loci. Gastroenterology, 148, 2015 1330–9.e14.
-
(2015)
Gastroenterology
, vol.148
-
-
Hsu, L.1
Jeon, J.2
Brenner, H.3
Gruber, S.B.4
Schoen, R.E.5
Berndt, S.I.6
Chan, A.T.7
Chang-Claude, J.8
Du, M.9
Gong, J.10
-
3
-
-
84902993335
-
Estimating the heritability of colorectal cancer
-
Jiao, S., Peters, U., Berndt, S., Brenner, H., Butterbach, K., Caan, B.J., Carlson, C.S., Chan, A.T., Chang-Claude, J., Chanock, S., et al. Estimating the heritability of colorectal cancer. Hum. Mol. Genet. 23 (2014), 3898–3905.
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 3898-3905
-
-
Jiao, S.1
Peters, U.2
Berndt, S.3
Brenner, H.4
Butterbach, K.5
Caan, B.J.6
Carlson, C.S.7
Chan, A.T.8
Chang-Claude, J.9
Chanock, S.10
-
4
-
-
85020095559
-
Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants
-
Markunas, C.A., Johnson, E.O., Hancock, D.B., Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants. Hum. Genet. 136 (2017), 911–919.
-
(2017)
Hum. Genet.
, vol.136
, pp. 911-919
-
-
Markunas, C.A.1
Johnson, E.O.2
Hancock, D.B.3
-
5
-
-
84865822182
-
Systematic localization of common disease-associated variation in regulatory DNA
-
Maurano, M.T., Humbert, R., Rynes, E., Thurman, R.E., Haugen, E., Wang, H., Reynolds, A.P., Sandstrom, R., Qu, H., Brody, J., et al. Systematic localization of common disease-associated variation in regulatory DNA. Science 337 (2012), 1190–1195.
-
(2012)
Science
, vol.337
, pp. 1190-1195
-
-
Maurano, M.T.1
Humbert, R.2
Rynes, E.3
Thurman, R.E.4
Haugen, E.5
Wang, H.6
Reynolds, A.P.7
Sandstrom, R.8
Qu, H.9
Brody, J.10
-
6
-
-
84907533564
-
Functional annotation of putative regulatory elements at cancer susceptibility loci
-
Rosse, S.A., Auer, P.L., Carlson, C.S., Functional annotation of putative regulatory elements at cancer susceptibility loci. Cancer Inform. 13:Suppl 2 (2014), 5–17.
-
(2014)
Cancer Inform.
, vol.13
, pp. 5-17
-
-
Rosse, S.A.1
Auer, P.L.2
Carlson, C.S.3
-
7
-
-
84865777825
-
Linking disease associations with regulatory information in the human genome
-
Schaub, M.A., Boyle, A.P., Kundaje, A., Batzoglou, S., Snyder, M., Linking disease associations with regulatory information in the human genome. Genome Res. 22 (2012), 1748–1759.
-
(2012)
Genome Res.
, vol.22
, pp. 1748-1759
-
-
Schaub, M.A.1
Boyle, A.P.2
Kundaje, A.3
Batzoglou, S.4
Snyder, M.5
-
8
-
-
85046600104
-
De-novo inference of enhancer-gene networks in diverse cellular contexts reveals the long-range regulatory impact of disease-associated variants
-
Wang, J., Greenside, P., Kundaje, A., Kellis, M., De-novo inference of enhancer-gene networks in diverse cellular contexts reveals the long-range regulatory impact of disease-associated variants. Nature 9 (2017), 9–999.
-
(2017)
Nature
, vol.9
, pp. 9-999
-
-
Wang, J.1
Greenside, P.2
Kundaje, A.3
Kellis, M.4
-
9
-
-
84864953892
-
Optimal tests for rare variant effects in sequencing association studies
-
Lee, S., Wu, M.C., Lin, X., Optimal tests for rare variant effects in sequencing association studies. Biostatistics 13 (2012), 762–775.
-
(2012)
Biostatistics
, vol.13
, pp. 762-775
-
-
Lee, S.1
Wu, M.C.2
Lin, X.3
-
10
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
Li, B., Leal, S.M., Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am. J. Hum. Genet. 83 (2008), 311–321.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
11
-
-
84876410197
-
A unified mixed-effects model for rare-variant association in sequencing studies
-
Sun, J., Zheng, Y., Hsu, L., A unified mixed-effects model for rare-variant association in sequencing studies. Genet. Epidemiol. 37 (2013), 334–344.
-
(2013)
Genet. Epidemiol.
, vol.37
, pp. 334-344
-
-
Sun, J.1
Zheng, Y.2
Hsu, L.3
-
12
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu, M.C., Lee, S., Cai, T., Li, Y., Boehnke, M., Lin, X., Rare-variant association testing for sequencing data with the sequence kernel association test. Am. J. Hum. Genet. 89 (2011), 82–93.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
13
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen, B.E., Browning, S.R., A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet., 5, 2009, e1000384.
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000384
-
-
Madsen, B.E.1
Browning, S.R.2
-
14
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin, D.-Y., Tang, Z.-Z., A general framework for detecting disease associations with rare variants in sequencing studies. Am. J. Hum. Genet. 89 (2011), 354–367.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 354-367
-
-
Lin, D.-Y.1
Tang, Z.-Z.2
-
15
-
-
84895858942
-
A general framework for estimating the relative pathogenicity of human genetic variants
-
Kircher, M., Witten, D.M., Jain, P., O'Roak, B.J., Cooper, G.M., Shendure, J., A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 46 (2014), 310–315.
-
(2014)
Nat. Genet.
, vol.46
, pp. 310-315
-
-
Kircher, M.1
Witten, D.M.2
Jain, P.3
O'Roak, B.J.4
Cooper, G.M.5
Shendure, J.6
-
16
-
-
84897459814
-
An atlas of active enhancers across human cell types and tissues
-
Andersson, R., Gebhard, C., Miguel-Escalada, I., Hoof, I., Bornholdt, J., Boyd, M., Chen, Y., Zhao, X., Schmidl, C., Suzuki, T., et al. An atlas of active enhancers across human cell types and tissues. Nature 507 (2014), 455–461.
-
(2014)
Nature
, vol.507
, pp. 455-461
-
-
Andersson, R.1
Gebhard, C.2
Miguel-Escalada, I.3
Hoof, I.4
Bornholdt, J.5
Boyd, M.6
Chen, Y.7
Zhao, X.8
Schmidl, C.9
Suzuki, T.10
-
17
-
-
84891685308
-
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
-
Battle, A., Mostafavi, S., Zhu, X., Potash, J.B., Weissman, M.M., McCormick, C., Haudenschild, C.D., Beckman, K.B., Shi, J., Mei, R., et al. Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals. Genome Res. 24 (2014), 14–24.
-
(2014)
Genome Res.
, vol.24
, pp. 14-24
-
-
Battle, A.1
Mostafavi, S.2
Zhu, X.3
Potash, J.B.4
Weissman, M.M.5
McCormick, C.6
Haudenschild, C.D.7
Beckman, K.B.8
Shi, J.9
Mei, R.10
-
18
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. Nature 489 (2012), 57–74.
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
-
19
-
-
84929001104
-
Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans
-
GTEx Consortium. Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 348 (2015), 648–660.
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
-
20
-
-
84939209563
-
Gateways to the FANTOM5 promoter level mammalian expression atlas
-
Lizio, M., Harshbarger, J., Shimoji, H., Severin, J., Kasukawa, T., Sahin, S., Abugessaisa, I., Fukuda, S., Hori, F., Ishikawa-Kato, S., et al., FANTOM consortium. Gateways to the FANTOM5 promoter level mammalian expression atlas. Genome Biol., 16, 2015, 22.
-
(2015)
Genome Biol.
, vol.16
, pp. 22
-
-
Lizio, M.1
Harshbarger, J.2
Shimoji, H.3
Severin, J.4
Kasukawa, T.5
Sahin, S.6
Abugessaisa, I.7
Fukuda, S.8
Hori, F.9
Ishikawa-Kato, S.10
-
21
-
-
78651338017
-
ENCODE whole-genome data in the UCSC genome browser (2011 update)
-
Raney, B.J., Cline, M.S., Rosenbloom, K.R., Dreszer, T.R., Learned, K., Barber, G.P., Meyer, L.R., Sloan, C.A., Malladi, V.S., Roskin, K.M., et al. ENCODE whole-genome data in the UCSC genome browser (2011 update). Nucleic Acids Res. 39 (2011), D871–D875.
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. D871-D875
-
-
Raney, B.J.1
Cline, M.S.2
Rosenbloom, K.R.3
Dreszer, T.R.4
Learned, K.5
Barber, G.P.6
Meyer, L.R.7
Sloan, C.A.8
Malladi, V.S.9
Roskin, K.M.10
-
22
-
-
84923362619
-
Integrative analysis of 111 reference human epigenomes
-
Kundaje, A., Meuleman, W., Ernst, J., Bilenky, M., Yen, A., Heravi-Moussavi, A., Kheradpour, P., Zhang, Z., Wang, J., Ziller, M.J., et al., Roadmap Epigenomics Consortium. Integrative analysis of 111 reference human epigenomes. Nature 518 (2015), 317–330.
-
(2015)
Nature
, vol.518
, pp. 317-330
-
-
Kundaje, A.1
Meuleman, W.2
Ernst, J.3
Bilenky, M.4
Yen, A.5
Heravi-Moussavi, A.6
Kheradpour, P.7
Zhang, Z.8
Wang, J.9
Ziller, M.J.10
-
23
-
-
84901686870
-
An atlas of genetic influences on human blood metabolites
-
Shin, S.-Y., Fauman, E.B., Petersen, A.-K., Krumsiek, J., Santos, R., Huang, J., Arnold, M., Erte, I., Forgetta, V., Yang, T.-P., et al., Multiple Tissue Human Expression Resource (MuTHER) Consortium. An atlas of genetic influences on human blood metabolites. Nat. Genet. 46 (2014), 543–550.
-
(2014)
Nat. Genet.
, vol.46
, pp. 543-550
-
-
Shin, S.-Y.1
Fauman, E.B.2
Petersen, A.-K.3
Krumsiek, J.4
Santos, R.5
Huang, J.6
Arnold, M.7
Erte, I.8
Forgetta, V.9
Yang, T.-P.10
-
24
-
-
85039994149
-
Impact of regulatory variation across human ipscs and differentiated cells
-
Banovich, N., Li, Y., Raj, A., Ward, M., Greenside, P., Calderon, D., Tung, P.-Y., Burnett, J., Myrthil, M., Thomas, S., et al. Impact of regulatory variation across human ipscs and differentiated cells. Genome Res. 28 (2018), 122–131.
-
(2018)
Genome Res.
, vol.28
, pp. 122-131
-
-
Banovich, N.1
Li, Y.2
Raj, A.3
Ward, M.4
Greenside, P.5
Calderon, D.6
Tung, P.-Y.7
Burnett, J.8
Myrthil, M.9
Thomas, S.10
-
25
-
-
85000443086
-
Partitioning heritability by functional annotation using genome-wide association summary statistics
-
Finucane, H.K., Bulik-Sullivan, B., Gusev, A., Trynka, G., Reshef, Y., Loh, P.R., Anttila, V., Xu, H., Zang, C., Farh, K., et al. ReproGen Consortium Schizophrenia Working Group of the Psychiatric Genomics Consortium, RACI Consortium. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat. Genet. 47 (2015), 1228–1235.
-
(2015)
Nat. Genet.
, vol.47
, pp. 1228-1235
-
-
Finucane, H.K.1
Bulik-Sullivan, B.2
Gusev, A.3
Trynka, G.4
Reshef, Y.5
Loh, P.R.6
Anttila, V.7
Xu, H.8
Zang, C.9
Farh, K.10
-
26
-
-
84908324508
-
Integrating functional data to prioritize causal variants in statistical fine-mapping studies
-
Kichaev, G., Yang, W.Y., Lindstrom, S., Hormozdiari, F., Eskin, E., Price, A.L., Kraft, P., Pasaniuc, B., Integrating functional data to prioritize causal variants in statistical fine-mapping studies. PLoS Genet., 10, 2014, e1004722.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004722
-
-
Kichaev, G.1
Yang, W.Y.2
Lindstrom, S.3
Hormozdiari, F.4
Eskin, E.5
Price, A.L.6
Kraft, P.7
Pasaniuc, B.8
-
27
-
-
85033379332
-
Association analysis identifies 65 new breast cancer risk loci
-
Michailidou, K., Lindström, S., Dennis, J., Beesley, J., Hui, S., Kar, S., Lemaçon, A., Soucy, P., Glubb, D., Rostamianfar, A., et al. NBCS Collaborators ABCTB Investigators, ConFab/AOCS Investigators. Association analysis identifies 65 new breast cancer risk loci. Nature 551 (2017), 92–94.
-
(2017)
Nature
, vol.551
, pp. 92-94
-
-
Michailidou, K.1
Lindström, S.2
Dennis, J.3
Beesley, J.4
Hui, S.5
Kar, S.6
Lemaçon, A.7
Soucy, P.8
Glubb, D.9
Rostamianfar, A.10
-
28
-
-
84897855294
-
Obesity-associated variants within FTO form long-range functional connections with IRX3
-
Smemo, S., Tena, J.J., Kim, K.H., Gamazon, E.R., Sakabe, N.J., Gómez-Marín, C., Aneas, I., Credidio, F.L., Sobreira, D.R., Wasserman, N.F., et al. Obesity-associated variants within FTO form long-range functional connections with IRX3. Nature 507 (2014), 371–375.
-
(2014)
Nature
, vol.507
, pp. 371-375
-
-
Smemo, S.1
Tena, J.J.2
Kim, K.H.3
Gamazon, E.R.4
Sakabe, N.J.5
Gómez-Marín, C.6
Aneas, I.7
Credidio, F.L.8
Sobreira, D.R.9
Wasserman, N.F.10
-
29
-
-
85034777436
-
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data
-
Bien, S.A., Auer, P.L., Harrison, T.A., Qu, C., Connolly, C.M., Greenside, P.G., Chen, S., Berndt, S.I., Bézieau, S., Kang, H.M., et al., GECCO and CCFR. Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data. PLoS ONE, 12, 2017, e0186518.
-
(2017)
PLoS ONE
, vol.12
, pp. e0186518
-
-
Bien, S.A.1
Auer, P.L.2
Harrison, T.A.3
Qu, C.4
Connolly, C.M.5
Greenside, P.G.6
Chen, S.7
Berndt, S.I.8
Bézieau, S.9
Kang, H.M.10
-
30
-
-
84912117315
-
GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation
-
Chung, D., Yang, C., Li, C., Gelernter, J., Zhao, H., GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation. PLoS Genet., 10, 2014, e1004787.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004787
-
-
Chung, D.1
Yang, C.2
Li, C.3
Gelernter, J.4
Zhao, H.5
-
31
-
-
84940780615
-
A gene-based association method for mapping traits using reference transcriptome data
-
Gamazon, E.R., Wheeler, H.E., Shah, K.P., Mozaffari, S.V., Aquino-Michaels, K., Carroll, R.J., Eyler, A.E., Denny, J.C., Nicolae, D.L., Cox, N.J., Im, H.K., GTEx Consortium. A gene-based association method for mapping traits using reference transcriptome data. Nat. Genet. 47 (2015), 1091–1098.
-
(2015)
Nat. Genet.
, vol.47
, pp. 1091-1098
-
-
Gamazon, E.R.1
Wheeler, H.E.2
Shah, K.P.3
Mozaffari, S.V.4
Aquino-Michaels, K.5
Carroll, R.J.6
Eyler, A.E.7
Denny, J.C.8
Nicolae, D.L.9
Cox, N.J.10
Im, H.K.11
-
32
-
-
84959547986
-
Integrative approaches for large-scale transcriptome-wide association studies
-
Gusev, A., Ko, A., Shi, H., Bhatia, G., Chung, W., Penninx, B.W.J.H., Jansen, R., de Geus, E.J.C., Boomsma, D.I., Wright, F.A., et al. Integrative approaches for large-scale transcriptome-wide association studies. Nat. Genet. 48 (2016), 245–252.
-
(2016)
Nat. Genet.
, vol.48
, pp. 245-252
-
-
Gusev, A.1
Ko, A.2
Shi, H.3
Bhatia, G.4
Chung, W.5
Penninx, B.W.J.H.6
Jansen, R.7
de Geus, E.J.C.8
Boomsma, D.I.9
Wright, F.A.10
-
33
-
-
84873288058
-
Integrative eQTL-based analyses reveal the biology of breast cancer risk loci
-
Li, Q., Seo, J.-H., Stranger, B., McKenna, A., Pe'er, I., Laframboise, T., Brown, M., Tyekucheva, S., Freedman, M.L., Integrative eQTL-based analyses reveal the biology of breast cancer risk loci. Cell 152 (2013), 633–641.
-
(2013)
Cell
, vol.152
, pp. 633-641
-
-
Li, Q.1
Seo, J.-H.2
Stranger, B.3
McKenna, A.4
Pe'er, I.5
Laframboise, T.6
Brown, M.7
Tyekucheva, S.8
Freedman, M.L.9
-
34
-
-
84976485236
-
EPS: an empirical Bayes approach to integrating pleiotropy and tissue-specific information for prioritizing risk genes
-
Liu, J., Wan, X., Ma, S., Yang, C., EPS: an empirical Bayes approach to integrating pleiotropy and tissue-specific information for prioritizing risk genes. Bioinformatics 32 (2016), 1856–1864.
-
(2016)
Bioinformatics
, vol.32
, pp. 1856-1864
-
-
Liu, J.1
Wan, X.2
Ma, S.3
Yang, C.4
-
35
-
-
77951439152
-
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS
-
Nicolae, D.L., Gamazon, E., Zhang, W., Duan, S., Dolan, M.E., Cox, N.J., Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. PLoS Genet., 6, 2010, e1000888.
-
(2010)
PLoS Genet.
, vol.6
, pp. e1000888
-
-
Nicolae, D.L.1
Gamazon, E.2
Zhang, W.3
Duan, S.4
Dolan, M.E.5
Cox, N.J.6
-
36
-
-
84876847154
-
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
-
Schork, A.J., Thompson, W.K., Pham, P., Torkamani, A., Roddey, J.C., Sullivan, P.F., Kelsoe, J.R., O'Donovan, M.C., Furberg, H., Schork, N.J., et al. Tobacco and Genetics Consortium Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genet., 9, 2013, e1003449.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003449
-
-
Schork, A.J.1
Thompson, W.K.2
Pham, P.3
Torkamani, A.4
Roddey, J.C.5
Sullivan, P.F.6
Kelsoe, J.R.7
O'Donovan, M.C.8
Furberg, H.9
Schork, N.J.10
-
37
-
-
84904959814
-
Covariate-modulated local false discovery rate for genome-wide association studies
-
Zablocki, R.W., Schork, A.J., Levine, R.A., Andreassen, O.A., Dale, A.M., Thompson, W.K., Covariate-modulated local false discovery rate for genome-wide association studies. Bioinformatics 30 (2014), 2098–2104.
-
(2014)
Bioinformatics
, vol.30
, pp. 2098-2104
-
-
Zablocki, R.W.1
Schork, A.J.2
Levine, R.A.3
Andreassen, O.A.4
Dale, A.M.5
Thompson, W.K.6
-
38
-
-
84958257565
-
Predicting effects of noncoding variants with deep learning-based sequence model
-
Zhou, J., Troyanskaya, O.G., Predicting effects of noncoding variants with deep learning-based sequence model. Nat. Methods 12 (2015), 931–934.
-
(2015)
Nat. Methods
, vol.12
, pp. 931-934
-
-
Zhou, J.1
Troyanskaya, O.G.2
-
39
-
-
84891697734
-
Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits
-
Corradin, O., Saiakhova, A., Akhtar-Zaidi, B., Myeroff, L., Willis, J., Cowper-Sal lari, R., Lupien, M., Markowitz, S., Scacheri, P.C., Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits. Genome Res. 24 (2014), 1–13.
-
(2014)
Genome Res.
, vol.24
, pp. 1-13
-
-
Corradin, O.1
Saiakhova, A.2
Akhtar-Zaidi, B.3
Myeroff, L.4
Willis, J.5
Cowper-Sal lari, R.6
Lupien, M.7
Markowitz, S.8
Scacheri, P.C.9
-
40
-
-
84991598798
-
Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen-receptor-positive breast cancer through fgf10 and mrps30 regulation
-
Ghoussaini, M., French, J.D., Michailidou, K., Nord, S., Beesley, J., Canisus, S., Hillman, K.M., Kaufmann, S., Sivakumaran, H., Moradi Marjaneh, M., et al. kConFab/AOCS Investigators, NBCS Collaborators. Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen-receptor-positive breast cancer through fgf10 and mrps30 regulation. Am. J. Hum. Genet. 99 (2016), 903–911.
-
(2016)
Am. J. Hum. Genet.
, vol.99
, pp. 903-911
-
-
Ghoussaini, M.1
French, J.D.2
Michailidou, K.3
Nord, S.4
Beesley, J.5
Canisus, S.6
Hillman, K.M.7
Kaufmann, S.8
Sivakumaran, H.9
Moradi Marjaneh, M.10
-
41
-
-
84924365586
-
The genetic and mechanistic basis for variation in gene regulation
-
Pai, A.A., Pritchard, J.K., Gilad, Y., The genetic and mechanistic basis for variation in gene regulation. PLoS Genet., 11, 2015, e1004857.
-
(2015)
PLoS Genet.
, vol.11
, pp. e1004857
-
-
Pai, A.A.1
Pritchard, J.K.2
Gilad, Y.3
-
42
-
-
85044824194
-
Identification of 55,000 replicated dna methylation qtl
-
McRae, A., Marioni, R.E., Shah, S., Yang, J., Powell, J.E., Harris, S.E., Gibson, J., Henders, A.K., Bowdler, L., Painter, J.N., et al. Identification of 55,000 replicated dna methylation qtl. bioRxiv, 2017, 10.1101/166710.
-
(2017)
bioRxiv
-
-
McRae, A.1
Marioni, R.E.2
Shah, S.3
Yang, J.4
Powell, J.E.5
Harris, S.E.6
Gibson, J.7
Henders, A.K.8
Bowdler, L.9
Painter, J.N.10
-
43
-
-
0003790433
-
Quadpack: A Subroutine Package for Automatic Integration
-
Springer-Verlag Berlin Heidelberg
-
Piessens, R., deDoncker Kapenga, E., Uberhuber, C., Kahaner, D., Quadpack: A Subroutine Package for Automatic Integration. 1983, Springer-Verlag Berlin Heidelberg.
-
(1983)
-
-
Piessens, R.1
deDoncker Kapenga, E.2
Uberhuber, C.3
Kahaner, D.4
-
44
-
-
0001008882
-
Algorithm as 155: The distribution of a linear combination of chi-square random variables
-
Davies, R.B., Algorithm as 155: The distribution of a linear combination of chi-square random variables. J. Royal Stat. Soc. C 29 (1980), 323–333.
-
(1980)
J. Royal Stat. Soc. C
, vol.29
, pp. 323-333
-
-
Davies, R.B.1
-
45
-
-
58549103276
-
A new chi-square approximation to the distribution of non-negative definite quadratic forms in non-central normal variables
-
Liu, H., Tang, Y., Zhang, H.H., A new chi-square approximation to the distribution of non-negative definite quadratic forms in non-central normal variables. Comput. Stat. Data Anal. 53 (2009), 853–856.
-
(2009)
Comput. Stat. Data Anal.
, vol.53
, pp. 853-856
-
-
Liu, H.1
Tang, Y.2
Zhang, H.H.3
-
46
-
-
0344168195
-
Saddlepoint aapproximation for distribution of quadratic forms in normal variables
-
Kuonen, D., Saddlepoint aapproximation for distribution of quadratic forms in normal variables. Biometrika 86 (1999), 929–935.
-
(1999)
Biometrika
, vol.86
, pp. 929-935
-
-
Kuonen, D.1
-
47
-
-
85046591792
-
FastSKAT: Sequence kernel association tests for very large sets of markers
-
Lumley, T., Brody, J.A., Peloso, G., Morrison, A., Rice, K., FastSKAT: Sequence kernel association tests for very large sets of markers. bioRxiv 085639, 2018 https://doi.org/10.1101/085639.
-
(2018)
bioRxiv 085639
-
-
Lumley, T.1
Brody, J.A.2
Peloso, G.3
Morrison, A.4
Rice, K.5
-
48
-
-
84864923614
-
A permutation procedure to correct for confounders in case-control studies, including tests of rare variation
-
Epstein, M.P., Duncan, R., Jiang, Y., Conneely, K.N., Allen, A.S., Satten, G.A., A permutation procedure to correct for confounders in case-control studies, including tests of rare variation. Am. J. Hum. Genet. 91 (2012), 215–223.
-
(2012)
Am. J. Hum. Genet.
, vol.91
, 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
-
49
-
-
84860841594
-
Epigenomic enhancer profiling defines a signature of colon cancer
-
Akhtar-Zaidi, B., Cowper-Sal-lari, R., Corradin, O., Saiakhova, A., Bartels, C.F., Balasubramanian, D., Myeroff, L., Lutterbaugh, J., Jarrar, A., Kalady, M.F., et al. Epigenomic enhancer profiling defines a signature of colon cancer. Science 336 (2012), 736–739.
-
(2012)
Science
, vol.336
, pp. 736-739
-
-
Akhtar-Zaidi, B.1
Cowper-Sal-lari, R.2
Corradin, O.3
Saiakhova, A.4
Bartels, C.F.5
Balasubramanian, D.6
Myeroff, L.7
Lutterbaugh, J.8
Jarrar, A.9
Kalady, M.F.10
-
50
-
-
84961751151
-
Parallel shRNA and CRISPR-Cas9 screens enable antiviral drug target identification
-
Deans, R.M., Morgens, D.W., Ökesli, A., Pillay, S., Horlbeck, M.A., Kampmann, M., Gilbert, L.A., Li, A., Mateo, R., Smith, M., et al. Parallel shRNA and CRISPR-Cas9 screens enable antiviral drug target identification. Nat. Chem. Biol. 12 (2016), 361–366.
-
(2016)
Nat. Chem. Biol.
, vol.12
, pp. 361-366
-
-
Deans, R.M.1
Morgens, D.W.2
Ökesli, A.3
Pillay, S.4
Horlbeck, M.A.5
Kampmann, M.6
Gilbert, L.A.7
Li, A.8
Mateo, R.9
Smith, M.10
-
51
-
-
84908352138
-
Genome-scale crispr-mediated control of gene repression and activation
-
Gilbert, L.A., Horlbeck, M.A., Adamson, B., Villalta, J.E., Chen, Y., Whitehead, E.H., Guimaraes, C., Panning, B., Ploegh, H.L., Bassik, M.C., et al. Genome-scale crispr-mediated control of gene repression and activation. Cell 159 (2014), 647–661.
-
(2014)
Cell
, vol.159
, pp. 647-661
-
-
Gilbert, L.A.1
Horlbeck, M.A.2
Adamson, B.3
Villalta, J.E.4
Chen, Y.5
Whitehead, E.H.6
Guimaraes, C.7
Panning, B.8
Ploegh, H.L.9
Bassik, M.C.10
-
52
-
-
84937856311
-
Next-generation libraries for robust RNA interference-based genome-wide screens
-
Kampmann, M., Horlbeck, M.A., Chen, Y., Tsai, J.C., Bassik, M.C., Gilbert, L.A., Villalta, J.E., Kwon, S.C., Chang, H., Kim, V.N., Weissman, J.S., Next-generation libraries for robust RNA interference-based genome-wide screens. Proc. Natl. Acad. Sci. USA 112 (2015), E3384–E3391.
-
(2015)
Proc. Natl. Acad. Sci. USA
, vol.112
, pp. E3384-E3391
-
-
Kampmann, M.1
Horlbeck, M.A.2
Chen, Y.3
Tsai, J.C.4
Bassik, M.C.5
Gilbert, L.A.6
Villalta, J.E.7
Kwon, S.C.8
Chang, H.9
Kim, V.N.10
Weissman, J.S.11
|