-
1
-
-
58149156386
-
Cohort studies and the genetics of complex disease
-
Manolio, T. A. (2009) Cohort studies and the genetics of complex disease. Nat. Genet., 41, 5-6.
-
(2009)
Nat. Genet.
, vol.41
, pp. 5-6
-
-
Manolio, T.A.1
-
2
-
-
40949127393
-
How to interpret a genome-wide association study
-
Pearson, T. A. and Manolio, T. A. (2008) How to interpret a genome-wide association study. JAMA, 299, 1335-1344.
-
(2008)
JAMA
, vol.299
, pp. 1335-1344
-
-
Pearson, T.A.1
Manolio, T.A.2
-
3
-
-
84902511942
-
GRASP: Analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database
-
Leslie, R., O'Donnell, C. J. and Johnson, A. D. (2014) GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database. Bioinformatics, 30, i185-i194.
-
(2014)
Bioinformatics
, vol.30
, pp. i185-i194
-
-
Leslie, R.1
O'Donnell, C.J.2
Johnson, A.D.3
-
4
-
-
60549083544
-
An open access database of genome-wide association results
-
Johnson, A. D. and O'Donnell, C. J. (2009) An open access database of genome-wide association results. BMC Med. Genet., 10, 1-17.
-
(2009)
BMC Med. Genet.
, vol.10
, pp. 1-17
-
-
Johnson, A.D.1
O'Donnell, C.J.2
-
5
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S. and Manolio, T. A. (2009) Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. U. S. A., 106, 9362-9367.
-
(2009)
Proc. Natl Acad. Sci. U. S. A.
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
6
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar, P., Henikoff, S. and Ng, P. C. (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat. Protoc., 4, 1073-1081.
-
(2009)
Nat. Protoc.
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
7
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei, I. A., Schmidt, S., Peshkin, L., Ramensky, V. E., Gerasimova, A., Bork, P., Kondrashov, A. S. and Sunyaev, S. R. (2010) A method and server for predicting damaging missense mutations. Nat. Methods, 7, 248-249.
-
(2010)
Nat. Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
8
-
-
84891818318
-
MiRBase: Annotating high confdence microRNAs using deep sequencing data
-
Kozomara, A. and Griffths-Jones, S. (2014) miRBase: annotating high confdence microRNAs using deep sequencing data. Nucleic Acids Res., 42, D68-D73.
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D68-D73
-
-
Kozomara, A.1
Griffths-Jones, S.2
-
9
-
-
84862162057
-
PolymiRTS Database 2.0: Linking polymorphisms in microRNA target sites with human diseases and complex traits
-
Ziebarth, J. D., Bhattacharya, A., Chen, A. and Cui, Y. (2012) PolymiRTS Database 2.0: linking polymorphisms in microRNA target sites with human diseases and complex traits. Nucleic Acids Res., 40, D216-D221.
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. D216-D221
-
-
Ziebarth, J.D.1
Bhattacharya, A.2
Chen, A.3
Cui, Y.4
-
10
-
-
38549087902
-
ORegAnno: An open-access community-driven resource for regulatory annotation
-
Griffth, O. L., Montgomery, S. B., Bernier, B., Chu, B., Kasaian, K., Aerts, S., Mahony, S., Sleumer, M. C., Bilenky, M., Haeussler, M. et al. (2008) ORegAnno: an open-access community-driven resource for regulatory annotation. Nucleic Acids Res., 36, D107-D113.
-
(2008)
Nucleic Acids Res.
, vol.36
, pp. D107-D113
-
-
Griffth, O.L.1
Montgomery, S.B.2
Bernier, B.3
Chu, B.4
Kasaian, K.5
Aerts, S.6
Mahony, S.7
Sleumer, M.C.8
Bilenky, M.9
Haeussler, M.10
-
11
-
-
84891771466
-
The UCSC Genome Browser database: 2014 update
-
Karolchik, D., Barber, G. P., Casper, J., Clawson, H., Cline, M. S., Doekhans, M., Dreszer, T. R., Fujita, P. A., Guruvadoo, L., Haeussler, M. et al. (2014) The UCSC Genome Browser database: 2014 update. Nucleic Acids Res., 42, D764-D770.
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D764-D770
-
-
Karolchik, D.1
Barber, G.P.2
Casper, J.3
Clawson, H.4
Cline, M.S.5
Doekhans, M.6
Dreszer, T.R.7
Fujita, P.A.8
Guruvadoo, L.9
Haeussler, M.10
-
12
-
-
33846112470
-
VISTA Enhancer Browser-A database of tissue-specific human enhancers
-
Visel, A., Minovitsky, S., Dubchak, I. and Pennacchio, L. A. (2007) VISTA Enhancer Browser-a database of tissue-specific human enhancers. Nucleic Acids Res., 35, D88-D92.
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. D88-D92
-
-
Visel, A.1
Minovitsky, S.2
Dubchak, I.3
Pennacchio, L.A.4
-
13
-
-
84891783174
-
Activities at the Universal Protein Resource (UniProt)
-
UniProt Consortium. (2014) Activities at the Universal Protein Resource (UniProt). Nucleic Acids Res., 42, D191-D198.
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D191-D198
-
-
UniProt Consortium1
-
14
-
-
80053443801
-
Temporal trends in results availability form genome-wide association studies
-
Johnson, A. D., Leslie, R. and O'Donnell, CJ. (2011) Temporal trends in results availability form genome-wide association studies. PLoS Genet., 7, e1002269.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1002269
-
-
Johnson, A.D.1
Leslie, R.2
O'Donnell, C.J.3
-
15
-
-
84921725723
-
Data use under the NIH GWAS Data Sharing Policy and future directions
-
Paltoo, D. N., Rodriguez, L. L., Feolo, M., Gillanders, E., Ramos, E. M., Rutter, J. L., Sherry, S., Wang, V. O., Bailey, A., Baker, R. et al. (2014) Data use under the NIH GWAS Data Sharing Policy and future directions. Nat. Genet., 46, 934-938.
-
(2014)
Nat. Genet.
, vol.46
, pp. 934-938
-
-
Paltoo, D.N.1
Rodriguez, L.L.2
Feolo, M.3
Gillanders, E.4
Ramos, E.M.5
Rutter, J.L.6
Sherry, S.7
Wang, V.O.8
Bailey, A.9
Baker, R.10
-
16
-
-
84902901169
-
Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs
-
Zhang, X., Gierman, H. J., Levy, D., Plump, A., Dobrin, R., Goring, H. H., Curran, J. E., Johnson, M. P., Blangero, J., Kim, S. K. et al. (2014) Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs. BMC Genomics, 15, 532.
-
(2014)
BMC Genomics
, vol.15
, pp. 532
-
-
Zhang, X.1
Gierman, H.J.2
Levy, D.3
Plump, A.4
Dobrin, R.5
Goring, H.H.6
Curran, J.E.7
Johnson, M.P.8
Blangero, J.9
Kim, S.K.10
-
17
-
-
81355142141
-
Non-coding RNAs in human disease
-
Esteller, M. (2011) Non-coding RNAs in human disease. Nat. Rev. Genet., 12, 861-874.
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 861-874
-
-
Esteller, M.1
-
18
-
-
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. (2012) Systematic localization of common disease-associated variation in regulatory DNA. Science, 337, 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
-
19
-
-
7444260846
-
The ENCODE (ENCyclopedia of DNA Elements) Project
-
Encode Project Consortium. (2004) The ENCODE (ENCyclopedia Of DNA Elements) Project. Science, 306, 636-640.
-
(2004)
Science
, vol.306
, pp. 636-640
-
-
Encode Project Consortium1
-
20
-
-
34250305146
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
-
Encode Project Consortium. (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature, 447, 799-816.
-
(2007)
Nature
, vol.447
, pp. 799-816
-
-
Encode Project Consortium1
-
21
-
-
84899633396
-
Defining functional DNA elements in the human genome
-
Kellis, M., Wold, B., Snyder, M. P., Bernstein, B. E., Kundaje, A., Marinov, G. K., Ward, L. D., Birney, E., Crawford, G. E., Dekker, J. et al. (2014) Defining functional DNA elements in the human genome. Proc. Natl Acad. Sci. U. S. A., 111, 6131-6138.
-
(2014)
Proc. Natl Acad. Sci. U. S. A.
, vol.111
, pp. 6131-6138
-
-
Kellis, M.1
Wold, B.2
Snyder, M.P.3
Bernstein, B.E.4
Kundaje, A.5
Marinov, G.K.6
Ward, L.D.7
Birney, E.8
Crawford, G.E.9
Dekker, J.10
-
22
-
-
80051499915
-
Rare variant association testing for sequencing data using the sequence kernel association test (SKAT)
-
Wu, M. C., Lee, S., Cai, T., Li, Y., Boehnke, M. and Lin, X. (2011) Rare variant association testing for sequencing data using the sequence kernel association test (SKAT). Am. J. Hum. Genet., 89, 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
|