-
4
-
-
1942451910
-
Genetic factors of age-related macular degeneration
-
Tuo J, Bojanowski CM, Chan CC. Genetic factors of age-related macular degeneration. Prog Retin Eye Res 2004;23: 229-49.
-
(2004)
Prog Retin Eye Res
, vol.23
, pp. 229-249
-
-
Tuo, J.1
Bojanowski, C.M.2
Chan, C.C.3
-
6
-
-
3242703945
-
Age-related maculopathy: A genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions
-
Weeks DE, Conley YP, Tsai HJ, Mah TS, Schmidt S, Postel EA, et al. Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions. Am J Hum Genet 2004;75: 174-89.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 174-189
-
-
Weeks, D.E.1
Conley, Y.P.2
Tsai, H.J.3
Mah, T.S.4
Schmidt, S.5
Postel, E.A.6
-
7
-
-
0032438352
-
Genetic risk of age-related maculopathy. Population-based familial aggregation study
-
Klaver CCW, Wolfs RCW, Assink JJM, van Duijn CM, Hofman A, de Jong PTV. Genetic risk of age-related maculopathy. Population-based familial aggregation study. Arch Ophthalmol 1998;116:1646-51.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 1646-1651
-
-
Klaver, C.C.W.1
Wolfs, R.C.W.2
Assink, J.J.M.3
Van Duijn, C.M.4
Hofman, A.5
De Jong, P.T.V.6
-
9
-
-
0028244159
-
Heredity and age-related macular degeneration. Observations in monozygotic twins
-
Klein ML, Mauldin WM, Stoumbos VD. Heredity and age-related macular degeneration. Observations in monozygotic twins. Arch Ophthalmol 1994;112:932-7.
-
(1994)
Arch Ophthalmol
, vol.112
, pp. 932-937
-
-
Klein, M.L.1
Mauldin, W.M.2
Stoumbos, V.D.3
-
10
-
-
0028875171
-
A twin study of age-related macular degeneration
-
Meyers SM, Greene T, Gutman FA. A twin study of age-related macular degeneration. Am J Ophthalmol 1995;120: 757-66.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 757-766
-
-
Meyers, S.M.1
Greene, T.2
Gutman, F.A.3
-
11
-
-
0042786559
-
Genetics of macular dystrophies and implications for age-related macular degeneration
-
Klaver CCW, Allikmets R. Genetics of macular dystrophies and implications for age-related macular degeneration. Dev Ophthalmol 2003;37:155-69.
-
(2003)
Dev Ophthalmol
, vol.37
, pp. 155-169
-
-
Klaver, C.C.W.1
Allikmets, R.2
-
12
-
-
0035475141
-
Molecular genetics of age-related macular degeneration
-
Stone EM, Sheffield VC, Hageman GS. Molecular genetics of age-related macular degeneration. Hum Mol Genet 2001;10: 2285-92.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2285-2292
-
-
Stone, E.M.1
Sheffield, V.C.2
Hageman, G.S.3
-
13
-
-
12144288320
-
Age-related macular degeneration: A high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease
-
Abecasis GR, Yashar BM, Zhao Y, Ghiasvand NM, Zareparsi S, Branham KE, et al. Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease. Am J Hum Genet 2004;74:482-94.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 482-494
-
-
Abecasis, G.R.1
Yashar, B.M.2
Zhao, Y.3
Ghiasvand, N.M.4
Zareparsi, S.5
Branham, K.E.6
-
14
-
-
10744233559
-
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: A genetic model for age-related macular degeneration
-
Hayward C, Shu X, Cideciyan AV, Lennon A, Barran P, Zareparsi S, et al. Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration. Hum Mol Genet 2003;12:2657-67.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2657-2667
-
-
Hayward, C.1
Shu, X.2
Cideciyan, A.V.3
Lennon, A.4
Barran, P.5
Zareparsi, S.6
-
15
-
-
0348013124
-
Analysis of the ARMD1 locus: Evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large family
-
Schultz DW, Klein ML, Humpert AJ, Luzier CW, Persun V, Schain M, et al. Analysis of the ARMD1 locus: evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large family. Hum Mol Genet 2003;12:3315-23.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3315-3323
-
-
Schultz, D.W.1
Klein, M.L.2
Humpert, A.J.3
Luzier, C.W.4
Persun, V.5
Schain, M.6
-
16
-
-
0034533059
-
Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration
-
Kimura K, Isashiki Y, Sonoda S, Kakiuchi-Matsumoto T, Ohba N. Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration. Am J Ophthalmol 2000;130:769-73.
-
(2000)
Am J Ophthalmol
, vol.130
, pp. 769-773
-
-
Kimura, K.1
Isashiki, Y.2
Sonoda, S.3
Kakiuchi-Matsumoto, T.4
Ohba, N.5
-
17
-
-
0032231956
-
Genetic association of apolipoprotein e with age-related macular degeneration
-
Klaver CC, Kliffen M, van Duijn CM, Hofman A, Cruts M, Grobbee DE, et al. Genetic association of apolipoprotein E with age-related macular degeneration. Am J Hum Genet 1998;63:200-6.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 200-206
-
-
Klaver, C.C.1
Kliffen, M.2
Van Duijn, C.M.3
Hofman, A.4
Cruts, M.5
Grobbee, D.E.6
-
18
-
-
0032014838
-
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration
-
Souied EH, Benlian P, Amouyel P, Feingold J, Lagarde JP, Munnich A, et al. The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration. Am J Ophthalmol 1998;125:353-9.
-
(1998)
Am J Ophthalmol
, vol.125
, pp. 353-359
-
-
Souied, E.H.1
Benlian, P.2
Amouyel, P.3
Feingold, J.4
Lagarde, J.P.5
Munnich, A.6
-
19
-
-
0036158627
-
CST3 genotype associated with exudative age related macular degeneration
-
Zurdel J, Finckh U, Menzer G, Nitsch RM, Richard G. CST3 genotype associated with exudative age related macular degeneration. Br J Ophthalmol 2002;86:214-9.
-
(2002)
Br J Ophthalmol
, vol.86
, pp. 214-219
-
-
Zurdel, J.1
Finckh, U.2
Menzer, G.3
Nitsch, R.M.4
Richard, G.5
-
20
-
-
0031037951
-
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
-
Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet 1997;15:236-46.
-
(1997)
Nat Genet
, vol.15
, pp. 236-246
-
-
Allikmets, R.1
Singh, N.2
Sun, H.3
Shroyer, N.F.4
Hutchinson, A.5
Chidambaram, A.6
-
22
-
-
0033794871
-
Simple and complex ABCR: Genetic predisposition to retinal disease
-
Allikmets R. Simple and complex ABCR: genetic predisposition to retinal disease. Am J Hum Genet 2000;67:793-9.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 793-799
-
-
Allikmets, R.1
-
23
-
-
0035032384
-
An analysis of allelic variation of phenotype in Stargardt macular dystrophy: Fundus flavimaculata
-
Webster AR, Héon E, Lotery AJ, Vandenburgh K, Casavant TL, Oh KT, et al. An analysis of allelic variation of phenotype in Stargardt macular dystrophy: fundus flavimaculata. Invest Ophthalmol Vis Sci 2001;42:1179-89.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 1179-1189
-
-
Webster, A.R.1
Héon, E.2
Lotery, A.J.3
Vandenburgh, K.4
Casavant, T.L.5
Oh, K.T.6
-
24
-
-
0034758592
-
Null missense ABCR (ABCA4) mutations in a family with Stargardt disease and retinitis pigmentosa
-
Shroyer NF, Lewis RA, Yatsenko AN, Lupski JR. Null missense ABCR (ABCA4) mutations in a family with Stargardt disease and retinitis pigmentosa. Invest Ophthalmol Vis Sci 2001;42:2757-61.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 2757-2761
-
-
Shroyer, N.F.1
Lewis, R.A.2
Yatsenko, A.N.3
Lupski, J.R.4
-
25
-
-
0035168415
-
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
-
Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, et al. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Nat Genet 2001; 27:89-93.
-
(2001)
Nat Genet
, vol.27
, pp. 89-93
-
-
Zhang, K.1
Kniazeva, M.2
Han, M.3
Li, W.4
Yu, Z.5
Yang, Z.6
-
26
-
-
17344364275
-
Identification of the gene responsible for Best macular dystrophy
-
Petrukhin K, Koisti MJ, Bakall B, Li W, Xie G, Marknell T, et al. Identification of the gene responsible for Best macular dystrophy. Nat Genet 1998;19:241-7.
-
(1998)
Nat Genet
, vol.19
, pp. 241-247
-
-
Petrukhin, K.1
Koisti, M.J.2
Bakall, B.3
Li, W.4
Xie, G.5
Marknell, T.6
-
27
-
-
0342804259
-
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
-
Kramer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, et al. Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. Eur J Hum Genet 2000;8: 286-92.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 286-292
-
-
Kramer, F.1
White, K.2
Pauleikhoff, D.3
Gehrig, A.4
Passmore, L.5
Rivera, A.6
-
28
-
-
0028097367
-
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy
-
Weber BH, Vogt G, Pruett RC, Stohr H, Felbor U. Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy. Nat Genet 1994;8: 352-6.
-
(1994)
Nat Genet
, vol.8
, pp. 352-356
-
-
Weber, B.H.1
Vogt, G.2
Pruett, R.C.3
Stohr, H.4
Felbor, U.5
-
29
-
-
0030901104
-
Inhibition of angiogenesis by tissue inhibitor of metalloproteinase-3
-
Anand-Apte B, Pepper MS, Voest E, Montesano R, Olsen B, Murphy G, et al. Inhibition of angiogenesis by tissue inhibitor of metalloproteinase-3. Invest Ophthalmol Vis Sci 1997; 38:817-23.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 817-823
-
-
Anand-Apte, B.1
Pepper, M.S.2
Voest, E.3
Montesano, R.4
Olsen, B.5
Murphy, G.6
-
30
-
-
3242685047
-
Age-related macular degeneration and the extracellular matrix
-
Johnson LV, Anderson DH. Age-related macular degeneration and the extracellular matrix. N Engl J Med 2004;351: 320-2.
-
(2004)
N Engl J Med
, vol.351
, pp. 320-322
-
-
Johnson, L.V.1
Anderson, D.H.2
-
31
-
-
0033027071
-
A single EFEMP1 mutation associated with both malattia leventinese and Doyne honeycomb retinal dystrophy
-
Stone EM, Lotery AJ, Munier FL, Héon E, Piguet B, Guymer RH, et al. A single EFEMP1 mutation associated with both malattia leventinese and Doyne honeycomb retinal dystrophy. Nat Genet 1999;22:199-202.
-
(1999)
Nat Genet
, vol.22
, pp. 199-202
-
-
Stone, E.M.1
Lotery, A.J.2
Munier, F.L.3
Héon, E.4
Piguet, B.5
Guymer, R.H.6
-
32
-
-
0034994792
-
Dominant radial drusen and Arg345Trp EFEMP1 mutation
-
Matsumoto M, Traboulsi EI. Dominant radial drusen and Arg345Trp EFEMP1 mutation. Am J Ophthalmol 2001;131: 810-2.
-
(2001)
Am J Ophthalmol
, vol.131
, pp. 810-812
-
-
Matsumoto, M.1
Traboulsi, E.I.2
|