-
1
-
-
58049217860
-
-
Bethesda, MD: National Human Genome Research Institute. Accessed August 16, 2010, at
-
Hindorff LA, Junkins HA, Hall PN, Mehta JP, Manolio TA. A catalog of published genome-wide association studies. Bethesda, MD: National Human Genome Research Institute. (Accessed August 16, 2010, at http://www.genome.gov/ gwastudies.)
-
A Catalog of Published Genome-wide Association Studies
-
-
Hindorff, L.A.1
Junkins, H.A.2
Hall, P.N.3
Mehta, J.P.4
Manolio, T.A.5
-
2
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein DB. Common genetic variation and human traits. N Engl J Med 2009;360:1696-8.
-
(2009)
N Engl J Med
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
3
-
-
77954407332
-
Genomewide association studies and assessment of the risk of disease
-
Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med 2010;363:166-76.
-
(2010)
N Engl J Med
, vol.363
, pp. 166-176
-
-
Manolio, T.A.1
-
4
-
-
41349103917
-
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout
-
DOI 10.1038/ng.106, PII NG106
-
Vitart V, Rudan I, Hayward C, et al. SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. Nat Genet 2008;40:437-42. (Pubitemid 351450879)
-
(2008)
Nature Genetics
, vol.40
, Issue.4
, pp. 437-442
-
-
Vitart, V.1
Rudan, I.2
Hayward, C.3
Gray, N.K.4
Floyd, J.5
Palmer, C.N.A.6
Knott, S.A.7
Kolcic, I.8
Polasek, O.9
Graessler, J.10
Wilson, J.F.11
Marinaki, A.12
Riches, P.L.13
Shu, X.14
Janicijevic, B.15
Smolej-Narancic, N.16
Gorgoni, B.17
Morgan, J.18
Campbell, S.19
Biloglav, Z.20
Barac-Lauc, L.21
Pericic, M.22
Klaric, I.M.23
Zgaga, L.24
Skaric-Juric, T.25
Wild, S.H.26
Richardson, W.A.27
Hohenstein, P.28
Kimber, C.H.29
Tenesa, A.30
Donnelly, L.A.31
Fairbanks, L.D.32
Aringer, M.33
McKeigue, P.M.34
Ralston, S.H.35
Morris, A.D.36
Rudan, P.37
Hastie, N.D.38
Campbell, H.39
Wright, A.F.40
more..
-
6
-
-
77951477731
-
The role of complement Factor H in age-related macular degeneration: A review
-
Donoso LA, Vrabec T, Kuivaniemi H. The role of complement Factor H in age-related macular degeneration: a review. Surv Ophthalmol 2010;55:227-46.
-
(2010)
Surv Ophthalmol
, vol.55
, pp. 227-246
-
-
Donoso, L.A.1
Vrabec, T.2
Kuivaniemi, H.3
-
7
-
-
77956521660
-
E2-2 protein and Fuchs's corneal dystrophy
-
Baratz KH, Tosakulwong N, Ryu E, et al. E2-2 protein and Fuchs's corneal dystrophy. N Engl J Med 2010;363:1016-24.
-
(2010)
N Engl J Med
, vol.363
, pp. 1016-1024
-
-
Baratz, K.H.1
Tosakulwong, N.2
Ryu, E.3
-
8
-
-
0016201350
-
Fuchs' endothelial dystrophy of the cornea: 29th Sanford Gifford Memorial lecture
-
Hogan MJ, Wood I, Fine M. Fuchs' endothelial dystrophy of the cornea: 29th Sanford Gifford Memorial lecture. Am J Ophthalmol 1974;78:363-83.
-
(1974)
Am J Ophthalmol
, vol.78
, pp. 363-383
-
-
Hogan, M.J.1
Wood, I.2
Fine, M.3
-
11
-
-
34848860827
-
The E-protein Tcf4 interacts with Math1 to regulate differentiation of a specific subset of neuronal progenitors
-
DOI 10.1073/pnas.0707456104
-
Flora A, Garcia JJ, Thaller C, Zoghbi HY. The E-protein Tcf4 interacts with Math1 to regulate differentiation of a specific subset of neuronal progenitors. Proc Natl Acad Sci U S A 2007;104:15382-7. (Pubitemid 47502926)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.39
, pp. 15382-15387
-
-
Flora, A.1
Garcia, J.J.2
Thaller, C.3
Zoghbi, H.Y.4
-
12
-
-
70450198396
-
Epithelial-mesenchymal transitions in development and disease
-
Thiery JP, Acloque H, Huang RY, Nieto MA. Epithelial-mesenchymal transitions in development and disease. Cell 2009;139:871-90.
-
(2009)
Cell
, vol.139
, pp. 871-890
-
-
Thiery, J.P.1
Acloque, H.2
Huang, R.Y.3
Ma, N.4
-
13
-
-
20144388095
-
DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells
-
DOI 10.1038/sj.onc.1208429
-
Eger A, Aigner K, Sonderegger S, et al. DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells. Oncogene 2005;24:2375-85. (Pubitemid 40546696)
-
(2005)
Oncogene
, vol.24
, Issue.14
, pp. 2375-2385
-
-
Eger, A.1
Aigner, K.2
Sonderegger, S.3
Dampier, B.4
Oehler, S.5
Schreiber, M.6
Berx, G.7
Cano, A.8
Beug, H.9
Foisner, R.10
-
14
-
-
35548971958
-
Stem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneas
-
McGowan SL, Edelhauser HF, Pfister RR, Whikehart DR. Stem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneas. Mol Vis 2007;13:1984-2000.
-
(2007)
Mol Vis
, vol.13
, pp. 1984-2000
-
-
McGowan, S.L.1
Edelhauser, H.F.2
Pfister, R.R.3
Whikehart, D.R.4
-
15
-
-
59049098237
-
Stem cells of the adult cornea: From cytometric markers to therapeutic applications
-
Takacs L, Toth E, Berta A, Vereb G. Stem cells of the adult cornea: from cytometric markers to therapeutic applications. Cytometry A 2009;75:54-66.
-
(2009)
Cytometry A
, vol.75
, pp. 54-66
-
-
Takacs, L.1
Toth, E.2
Berta, A.3
Vereb, G.4
-
16
-
-
73149085311
-
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p
-
Riazuddin SA, Zaghloul NA, Al-Saif A, et al. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. Am J Hum Genet 2010;86:45-53.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 45-53
-
-
Riazuddin, S.A.1
Zaghloul, N.A.2
Al-Saif, A.3
-
17
-
-
32244434843
-
Laser in situ keratomileusis in patients with corneal guttata and family history of Fuchs' endothelial dystrophy
-
DOI 10.1016/j.jcrs.2004.05.061, PII S0886335005008035
-
Moshirfar M, Feiz V, Feilmeier MR, Kang PC. Laser in situ keratomileusis in patients with corneal guttata and family history of Fuchs' endothelial dystrophy. J Cataract Refract Surg 2005;31:2281-6. (Pubitemid 43212915)
-
(2005)
Journal of Cataract and Refractive Surgery
, vol.31
, Issue.12
, pp. 2281-2286
-
-
Moshirfar, M.1
Feiz, V.2
Feilmeier, M.R.3
Kang, P.C.4
-
18
-
-
0033887684
-
Vision 2020: The cataract challenge
-
Vision 2020: the cataract challenge. Community Eye Health 2000;13:17-9.
-
(2000)
Community Eye Health
, vol.13
, pp. 17-19
-
-
|