-
1
-
-
42349112088
-
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges
-
DOI 10.1038/nrg2344, PII NRG2344
-
McCarthy,M.I., Abecasis,G.R., Cardon,L.R., Goldstein,D.B., Little,J., Ioannidis,J.P. and Hirschhorn,J.N. (2008) Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat. Rev. Genet., 9, 356-369. (Pubitemid 351556063)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.A.6
Hirschhorn, J.N.7
-
2
-
-
62549085618
-
Human genetic variation and its contribution to complex traits
-
Frazer,K.A., Murray,S.S., Schork,N.J. and Topol,E.J. (2009) Human genetic variation and its contribution to complex traits. Nat. Rev. Genet., 10, 241-251.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 241-251
-
-
Frazer, K.A.1
Murray, S.S.2
Schork, N.J.3
Topol, E.J.4
-
3
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Consortium,W.T.C.C.
-
Consortium,W.T.C.C. (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 447, 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
4
-
-
34748848639
-
The NCBI dbGaP database of genotypes and phenotypes
-
DOI 10.1038/ng1007-1181, PII NG10071181
-
Mailman,M.D., Feolo,M., Jin,Y., Kimura,M., Tryka,K., Bagoutdinov,R., Hao,L., Kiang,A., Paschall,J., Phan,L. et al. (2007) The NCBI dbGaP database of genotypes and phenotypes. Nat. Genet., 39, 1181-1186. (Pubitemid 47482671)
-
(2007)
Nature Genetics
, vol.39
, Issue.10
, pp. 1181-1186
-
-
Mailman, M.D.1
Feolo, M.2
Jin, Y.3
Kimura, M.4
Tryka, K.5
Bagoutdinov, R.6
Hao, L.7
Kiang, A.8
Paschall, J.9
Phan, L.10
Popova, N.11
Pretel, S.12
Ziyabari, L.13
Lee, M.14
Shao, Y.15
Wang, Z.Y.16
Sirotkin, K.17
Ward, M.18
Kholodov, M.19
Zbicz, K.20
Beck, J.21
Kimelman, M.22
Shevelev, S.23
Preuss, D.24
Yaschenko, E.25
Graeff, A.26
Ostell, J.27
Sherry, S.T.28
more..
-
5
-
-
58149186476
-
HGVbaseG2P: A central genetic association database
-
Thorisson,G.A., Lancaster,O., Free,R.C., Hastings,R.K., Sarmah,P., Dash,D., Brahmachari,S.K. and Brookes,A.J. (2009) HGVbaseG2P: a central genetic association database. Nucleic Acids Res., 37, D797-D802.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Thorisson, G.A.1
Lancaster, O.2
Free, R.C.3
Hastings, R.K.4
Sarmah, P.5
Dash, D.6
Brahmachari, S.K.7
Brookes, A.J.8
-
6
-
-
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. USA, 106, 9362-9367.
-
(2009)
Proc. Natl Acad. Sci. USA
, 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
-
7
-
-
80053050838
-
GWAS Integrator: A bioinformatics tool to explore human genetic associations reported in published genome-wide association studies
-
Yu,W., Yesupriya,A., Wulf,A., Hindorff,L.A., Dowling,N., Khoury,M.J. and Gwinn,M. (2011) GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies. Eur. J. Hum. Genet., 19, 1095-1099.
-
(2011)
Eur. J. Hum. Genet.
, vol.19
, pp. 1095-1099
-
-
Yu, W.1
Yesupriya, A.2
Wulf, A.3
Hindorff, L.A.4
Dowling, N.5
Khoury, M.J.6
Gwinn, M.7
-
8
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer,K.A., Ballinger,D.G., Cox,D.R., Hinds,D.A., Stuve,L.L., Gibbs,R.A., Belmont,J.W., Boudreau,A., Hardenbol,P., Leal,S.M. et al. (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
-
9
-
-
43749105558
-
Linkage disequilibrium-understanding the evolutionary past and mapping the medical future
-
Slatkin,M. (2008) Linkage disequilibrium-understanding the evolutionary past and mapping the medical future. Nat. Rev. Genet., 9, 477-485.
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 477-485
-
-
Slatkin, M.1
-
10
-
-
55449120805
-
Genetic mapping in human disease
-
Altshuler,D., Daly,M.J. and Lander,E.S. (2008) Genetic mapping in human disease. Science, 322, 881-888.
-
(2008)
Science
, vol.322
, pp. 881-888
-
-
Altshuler, D.1
Daly, M.J.2
Lander, E.S.3
-
11
-
-
79959524146
-
A haplotype map of the human genome
-
Consortium,T.I.H.
-
Consortium,T.I.H. (2005) A haplotype map of the human genome. Nature, 437, 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
12
-
-
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, 6.
-
(2009)
BMC Med. Genet.
, vol.10
, pp. 6
-
-
Johnson, A.D.1
O'Donnell, C.J.2
-
13
-
-
0033678320
-
The D' measure of overall gametic disequilibrium between pairs of multiallelic loci
-
Zapata,C. (2000) The D' measure of overall gametic disequilibrium between pairs of multiallelic loci. Evolution, 54, 1809-1812.
-
(2000)
Evolution
, vol.54
, pp. 1809-1812
-
-
Zapata, C.1
-
14
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
DOI 10.1038/35075590
-
Reich,D.E., Cargill,M., Bolk,S., Ireland,J., Sabeti,P.C., Richter,D.J., Lavery,T., Kouyoumjian,R., Farhadian,S.F., Ward,R. et al. (2001) Linkage disequilibrium in the human genome. Nature, 411, 199-204. (Pubitemid 32455179)
-
(2001)
Nature
, vol.411
, Issue.6834
, pp. 199-204
-
-
Reich, D.E.1
Cargili, M.2
Boik, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
15
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry,S.T., Ward,M.H., Kholodov,M., Baker,J., Phan,L., Smigielski,E.M. and Sirotkin,K. (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res., 29, 308-311. (Pubitemid 32054478)
-
(2001)
Nucleic Acids Research
, vol.29
, Issue.1
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.-H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
Sirotkin, K.7
-
16
-
-
75549089335
-
Ensembl's 10th year
-
Flicek,P., Aken,B.L., Ballester,B., Beal,K., Bragin,E., Brent,S., Chen,Y., Clapham,P., Coates,G., Fairley,S. et al. (2010) Ensembl's 10th year. Nucleic Acids Res., 38, D557-D562.
-
(2010)
Nucleic Acids Res.
, vol.38
-
-
Flicek, P.1
Aken, B.L.2
Ballester, B.3
Beal, K.4
Bragin, E.5
Brent, S.6
Chen, Y.7
Clapham, P.8
Coates, G.9
Fairley, S.10
-
17
-
-
61549115034
-
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease
-
Wang,K., Zhang,H., Kugathasan,S., Annese,V., Bradfield,J.P., Russell,R.K., Sleiman,P.M., Imielinski,M., Glessner,J., Hou,C. et al. (2009) Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease. Am. J. Hum. Genet., 84, 399-405.
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 399-405
-
-
Wang, K.1
Zhang, H.2
Kugathasan, S.3
Annese, V.4
Bradfield, J.P.5
Russell, R.K.6
Sleiman, P.M.7
Imielinski, M.8
Glessner, J.9
Hou, C.10
-
18
-
-
78549251736
-
Analysing biological pathways in genome-wide association studies
-
Wang,K., Li,M. and Hakonarson,H. (2010) Analysing biological pathways in genome-wide association studies. Nat. Rev. Genet., 11, 843-854.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 843-854
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
19
-
-
79959898376
-
Prioritizing candidate disease genes by network-based boosting of genome-wide association data
-
Lee,I., Blom,U.M., Wang,P.I., Shim,J.E. and Marcotte,E.M. (2011) Prioritizing candidate disease genes by network-based boosting of genome-wide association data. Genome Res., 21, 1109-1121.
-
(2011)
Genome Res.
, vol.21
, pp. 1109-1121
-
-
Lee, I.1
Blom, U.M.2
Wang, P.I.3
Shim, J.E.4
Marcotte, E.M.5
-
20
-
-
67649584052
-
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder
-
Holmans,P., Green,E.K., Pahwa,J.S., Ferreira,M.A., Purcell,S.M., Sklar,P., Owen,M.J., O'Donovan,M.C. and Craddock,N. (2009) Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. Am. J. Hum. Genet., 85, 13-24.
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 13-24
-
-
Holmans, P.1
Green, E.K.2
Pahwa, J.S.3
Ferreira, M.A.4
Purcell, S.M.5
Sklar, P.6
Owen, M.J.7
O'Donovan, M.C.8
Craddock, N.9
-
21
-
-
56649097558
-
GSEA-SNP: Applying gene set enrichment analysis to SNP data from genome-wide association studies
-
DOI 10.1093/bioinformatics/btn516
-
Holden,M., Deng,S., Wojnowski,L. and Kulle,B. (2008) GSEA-SNP: applying gene set enrichment analysis to SNP data from genome-wide association studies. Bioinformatics, 24, 2784-2785. (Pubitemid 352722627)
-
(2008)
Bioinformatics
, vol.24
, Issue.23
, pp. 2784-2785
-
-
Holden, M.1
Deng, S.2
Wojnowski, L.3
Kulle, B.4
-
22
-
-
65549084289
-
Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
-
Baranzini,S.E., Galwey,N.W., Wang,J., Khankhanian,P., Lindberg,R., Pelletier,D., Wu,W., Uitdehaag,B.M., Kappos,L., Polman,C.H. et al. (2009) Pathway and network-based analysis of genome-wide association studies in multiple sclerosis. Hum. Mol. Genet., 18, 2078-2090.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2078-2090
-
-
Baranzini, S.E.1
Galwey, N.W.2
Wang, J.3
Khankhanian, P.4
Lindberg, R.5
Pelletier, D.6
Wu, W.7
Uitdehaag, B.M.8
Kappos, L.9
Polman, C.H.10
-
23
-
-
67149113481
-
Reflect: Augmented browsing for the life scientist
-
Pafilis,E., O'Donoghue,S.I., Jensen,L.J., Horn,H., Kuhn,M., Brown,N.P. and Schneider,R. (2009) Reflect: augmented browsing for the life scientist. Nat. Biotechnol., 27, 508-510.
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 508-510
-
-
Pafilis, E.1
O'Donoghue, S.I.2
Jensen, L.J.3
Horn, H.4
Kuhn, M.5
Brown, N.P.6
Schneider, R.7
|