-
1
-
-
0029980777
-
Number of people with glaucoma worldwide
-
Quigley HA. Number of people with glaucoma worldwide. Br J Ophthalmol. 1996;80:389-393.
-
(1996)
Br J Ophthalmol
, vol.80
, pp. 389-393
-
-
Quigley, H.A.1
-
2
-
-
0032407216
-
The age distribution of primary open angle glaucoma
-
Tuck MW, Crick RP. The age distribution of primary open angle glaucoma. Ophthalmic Epidemiol. 1998;5:173-183.
-
(1998)
Ophthalmic Epidemiol
, vol.5
, pp. 173-183
-
-
Tuck, M.W.1
Crick, R.P.2
-
3
-
-
0036822851
-
Reduction of intraocular pressure and glaucoma progression: Results from the Early Manifest Glaucoma Trial
-
Heijl A, Leske MC, Bengtsson B, Hyman L, Bengtsson B, Hussein M. Reduction of intraocular pressure and glaucoma progression: results from the Early Manifest Glaucoma Trial. Arch Ophthalmol. 2002;120:1268-1279.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 1268-1279
-
-
Heijl, A.1
Leske, M.C.2
Bengtsson, B.3
Hyman, L.4
Bengtsson, B.5
Hussein, M.6
-
4
-
-
0000756925
-
Epidemiology of chronic open angle glaucoma
-
In: Ritch R, Shields M, Krupin T, eds., 2nd ed. St. Louis: Mosby
-
Wilson R, Martone J. Epidemiology of chronic open angle glaucoma. In: Ritch R, Shields M, Krupin T, eds. The Glaucomas. 2nd ed. St. Louis: Mosby; 1996:725-753.
-
(1996)
The Glaucomas
, pp. 725-753
-
-
Wilson, R.1
Martone, J.2
-
5
-
-
0042360494
-
Risk factors associated with the incidence of open-angle glaucoma: The visual impairment project
-
Le A, Mukesh BN, McCarty CA, Taylor HR. Risk factors associated with the incidence of open-angle glaucoma: the visual impairment project. Invest Ophthalmol Vis Sci. 2003;44:3783-3789.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 3783-3789
-
-
Le, A.1
Mukesh, B.N.2
McCarty, C.A.3
Taylor, H.R.4
-
7
-
-
0033808223
-
Investigators. The Advanced Glaucoma Intervention Study (AGIS): 7. The relationship between control of intraocular pressure and visual field deterioration
-
The AGIS Investigators. The Advanced Glaucoma Intervention Study (AGIS): 7. The relationship between control of intraocular pressure and visual field deterioration. Am J Ophthalmol. 2000;130:429-440.
-
(2000)
Am J Ophthalmol
, vol.130
, pp. 429-440
-
-
The, A.G.I.S.1
-
8
-
-
0036269833
-
The Ocular Hypertension Treatment Study: A randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma
-
Kass MA, Heuer DK, Higginbotham EJ, et al. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002;120:701-713.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 701-713
-
-
Kass, M.A.1
Heuer, D.K.2
Higginbotham, E.J.3
-
9
-
-
0038147108
-
The collaborative initial glaucoma treatment study: Baseline visual field and test-retest variability
-
Gillespie BW, Musch DC, Guire KE, et al. The collaborative initial glaucoma treatment study: baseline visual field and test-retest variability. Invest Ophthalmol Vis Sci. 2003;44:2613-2620.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 2613-2620
-
-
Gillespie, B.W.1
Musch, D.C.2
Guire, K.E.3
-
10
-
-
0037251618
-
Factors for glaucoma progression and the effect of treatment: The early manifest glaucoma trial
-
Leske MC, Heijl A, Hussein M, Bengtsson B, Hyman L, Komaroff E. Factors for glaucoma progression and the effect of treatment: the early manifest glaucoma trial. Arch Ophthalmol. 2003;121:48-56.
-
(2003)
Arch Ophthalmol
, vol.121
, pp. 48-56
-
-
Leske, M.C.1
Heijl, A.2
Hussein, M.3
Bengtsson, B.4
Hyman, L.5
Komaroff, E.6
-
11
-
-
0025916983
-
Racial variations in the prevalence of primary open-angle glaucoma. The Baltimore Eye Survey
-
Tielsch JM, Sommer A, Katz J, Royall RM, Quigley HA, Javitt J. Racial variations in the prevalence of primary open-angle glaucoma. The Baltimore Eye Survey. JAMA. 1991;266:369-374.
-
(1991)
JAMA
, vol.266
, pp. 369-374
-
-
Tielsch, J.M.1
Sommer, A.2
Katz, J.3
Royall, R.M.4
Quigley, H.A.5
Javitt, J.6
-
12
-
-
37349078627
-
Risk factors for incident open-angle glaucoma: The Barbados Eye Studies
-
Leske MC, Wu SY, Hennis A, Honkanen R, Nemesure B. Risk factors for incident open-angle glaucoma: the Barbados Eye Studies. Ophthalmology. 2008;115:85-93.
-
(2008)
Ophthalmology
, vol.115
, pp. 85-93
-
-
Leske, M.C.1
Wu, S.Y.2
Hennis, A.3
Honkanen, R.4
Nemesure, B.5
-
13
-
-
0019123337
-
Biostatistical analysis of the collaborative glaucoma study. I. Summary report of the risk factors for glaucomatous visual-field defects
-
Armaly MF, Krueger DE, Maunder L, et al. Biostatistical analysis of the collaborative glaucoma study. I. Summary report of the risk factors for glaucomatous visual-field defects. Arch Ophthalmol. 1980;98:2163-2171.
-
(1980)
Arch Ophthalmol
, vol.98
, pp. 2163-2171
-
-
Armaly, M.F.1
Krueger, D.E.2
Maunder, L.3
-
14
-
-
0018416804
-
Multivariate analysis of the risk of glaucomatous visual field loss
-
Hart WM, Jr, Yablonski M, Kass MA, Becker B. Multivariate analysis of the risk of glaucomatous visual field loss. Arch Ophthalmol. 1979;97:1455-1458.
-
(1979)
Arch Ophthalmol
, vol.97
, pp. 1455-1458
-
-
Hart Jr., W.M.1
Yablonski, M.2
Kass, M.A.3
Becker, B.4
-
15
-
-
0018833092
-
Prognostic significance of optic disk cupping in ocular hypertensive patients
-
Yablonski ME, Zimmerman TJ, Kass MA, Becker B. Prognostic significance of optic disk cupping in ocular hypertensive patients. Am J Ophthalmol. 1980;89:585-592.
-
(1980)
Am J Ophthalmol
, vol.89
, pp. 585-592
-
-
Yablonski, M.E.1
Zimmerman, T.J.2
Kass, M.A.3
Becker, B.4
-
16
-
-
0032407480
-
Genetic risk of primary open-angle glaucoma. Population-based familial aggregation study
-
Wolfs RC, Klaver CC, Ramrattan RS, van Duijn CM, Hofman A, de Jong PT. Genetic risk of primary open-angle glaucoma. Population-based familial aggregation study. Arch Ophthalmol. 1998;116:1640-1645.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 1640-1645
-
-
Wolfs, R.C.1
Klaver, C.C.2
Ramrattan, R.S.3
van Duijn, C.M.4
Hofman, A.5
de Jong, P.T.6
-
17
-
-
0033278168
-
Chronic open-angle glaucoma and associated ophthalmic findings in monozygotic twins and their spouses in Iceland
-
Gottfredsdottir MS, Sverrisson T, Musch DC, Stefansson E. Chronic open-angle glaucoma and associated ophthalmic findings in monozygotic twins and their spouses in Iceland. J Glaucoma. 1999;8:134-139.
-
(1999)
J Glaucoma
, vol.8
, pp. 134-139
-
-
Gottfredsdottir, M.S.1
Sverrisson, T.2
Musch, D.C.3
Stefansson, E.4
-
18
-
-
0023544319
-
Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study
-
Teikari JM. Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study. Acta Ophthalmol (Copenh). 1987;65:715-720.
-
(1987)
Acta Ophthalmol (Copenh)
, vol.65
, pp. 715-720
-
-
Teikari, J.M.1
-
19
-
-
20144382615
-
Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1
-
Monemi S, Spaeth G, DaSilva A, et al. Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet. 2005;14:725-733.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 725-733
-
-
Monemi, S.1
Spaeth, G.2
Dasilva, A.3
-
20
-
-
0031970713
-
Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region
-
Sarfarazi M, Child A, Stoilova D, et al. Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region. Am J Hum Genet. 1998;62:641-652.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 641-652
-
-
Sarfarazi, M.1
Child, A.2
Stoilova, D.3
-
21
-
-
0027173920
-
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31
-
Sheffield VC, Stone EM, Alward WL, et al. Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31. Nat Genet. 1993;4:47-50.
-
(1993)
Nat Genet
, vol.4
, pp. 47-50
-
-
Sheffield, V.C.1
Stone, E.M.2
Alward, W.L.3
-
22
-
-
0030586892
-
Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region
-
Stoilova D, Child A, Trifan OC, Crick RP, Coakes RL, Sarfarazi M. Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region. Genomics. 1996;36:142-150.
-
(1996)
Genomics
, vol.36
, pp. 142-150
-
-
Stoilova, D.1
Child, A.2
Trifan, O.C.3
Crick, R.P.4
Coakes, R.L.5
Sarfarazi, M.6
-
23
-
-
0031851299
-
A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region
-
Trifan OC, Traboulsi EI, Stoilova D, et al. A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region. Am J Ophthalmol. 1998;126:17-28.
-
(1998)
Am J Ophthalmol
, vol.126
, pp. 17-28
-
-
Trifan, O.C.1
Traboulsi, E.I.2
Stoilova, D.3
-
24
-
-
0031036668
-
Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q
-
Wirtz MK, Samples JR, Kramer PL, et al. Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q. Am J Hum Genet. 1997;60:296-304.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 296-304
-
-
Wirtz, M.K.1
Samples, J.R.2
Kramer, P.L.3
-
25
-
-
0033000146
-
GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36
-
Wirtz MK, Samples JR, Rust K, et al. GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36. Arch Ophthalmol. 1999;117:237-241.
-
(1999)
Arch Ophthalmol
, vol.117
, pp. 237-241
-
-
Wirtz, M.K.1
Samples, J.R.2
Rust, K.3
-
26
-
-
26944474438
-
Evidence for a novel glaucoma locus at chromosome 3p21-22
-
Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Evidence for a novel glaucoma locus at chromosome 3p21-22. Hum Genet. 2005;117:249-257.
-
(2005)
Hum Genet
, vol.117
, pp. 249-257
-
-
Baird, P.N.1
Foote, S.J.2
MacKey, D.A.3
Craig, J.4
Speed, T.P.5
Bureau, A.6
-
27
-
-
32844462772
-
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q
-
Pang CP, Fan BJ, Canlas O, et al. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q. Mol Vis. 2006;12:85-92.
-
(2006)
Mol Vis
, vol.12
, pp. 85-92
-
-
Pang, C.P.1
Fan, B.J.2
Canlas, O.3
-
28
-
-
34047220974
-
A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q
-
Wang DY, Fan BJ, Chua JK, et al. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q. Invest Ophthalmol Vis Sci. 2006;47:5315-5321.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 5315-5321
-
-
Wang, D.Y.1
Fan, B.J.2
Chua, J.K.3
-
29
-
-
2442656776
-
A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12
-
Wiggs JL, Lynch S, Ynagi G, et al. A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12. Am J Hum Genet. 2004;74:1314-1320.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1314-1320
-
-
Wiggs, J.L.1
Lynch, S.2
Ynagi, G.3
-
30
-
-
0142195787
-
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
-
Alward WL, Kwon YH, Kawase K, et al. Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma. Am J Ophthalmol. 2003;136:904-910.
-
(2003)
Am J Ophthalmol
, vol.136
, pp. 904-910
-
-
Alward, W.L.1
Kwon, Y.H.2
Kawase, K.3
-
31
-
-
0043063895
-
Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma
-
Wiggs JL, Auguste J, Allingham RR, et al. Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol. 2003;121:1181-1183.
-
(2003)
Arch Ophthalmol
, vol.121
, pp. 1181-1183
-
-
Wiggs, J.L.1
Auguste, J.2
Allingham, R.R.3
-
32
-
-
33947238222
-
No association between variations in the WDR36 gene and primary open-angle glaucoma
-
Fingert JH, Alward WL, Kwon YH, et al. No association between variations in the WDR36 gene and primary open-angle glaucoma. Arch Ophthalmol. 2007;125:434-436.
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 434-436
-
-
Fingert, J.H.1
Alward, W.L.2
Kwon, Y.H.3
-
33
-
-
0030778592
-
Mutations in the TIGR gene in familial primary open-angle glaucoma in Japan
-
Suzuki Y, Shirato S, Taniguchi F, Ohara K, Nishimaki K, Ohta S. Mutations in the TIGR gene in familial primary open-angle glaucoma in Japan. Am J Hum Genet. 1997;61:1202-1204.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1202-1204
-
-
Suzuki, Y.1
Shirato, S.2
Taniguchi, F.3
Ohara, K.4
Nishimaki, K.5
Ohta, S.6
-
34
-
-
17944385621
-
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)
-
Alward WL, Fingert JH, Coote MA, et al. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A). N Engl J Med. 1998;338:1022-1027.
-
(1998)
N Engl J Med
, vol.338
, pp. 1022-1027
-
-
Alward, W.L.1
Fingert, J.H.2
Coote, M.A.3
-
35
-
-
0036733041
-
Variations in the myocilin gene in patients with open-angle glaucoma
-
Alward WL, Kwon YH, Khanna CL, et al. Variations in the myocilin gene in patients with open-angle glaucoma. Arch Ophthalmol. 2002;120:1189-1197.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 1189-1197
-
-
Alward, W.L.1
Kwon, Y.H.2
Khanna, C.L.3
-
36
-
-
0344889215
-
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
-
Fingert JH, Heon E, Liebmann JM, et al. Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet. 1999;8:899-905.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 899-905
-
-
Fingert, J.H.1
Heon, E.2
Liebmann, J.M.3
-
37
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone EM, Fingert JH, Alward WL, et al. Identification of a gene that causes primary open angle glaucoma. Science. 1997;275:668-670.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.3
-
39
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn JN, Daly MJ. Genome-wide association studies for common diseases and complex traits. Nat Rev Genet. 2005;6:95-108.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
40
-
-
17244379811
-
Complement factor H polymorphism and age-related macular degeneration
-
Edwards AO, Ritter R, III, Abel KJ, Manning A, Panhuysen C, Farrer LA. Complement factor H polymorphism and age-related macular degeneration. Science. 2005;308:421-424.
-
(2005)
Science
, vol.308
, pp. 421-424
-
-
Edwards, A.O.1
Ritter III, R.2
Abel, K.J.3
Manning, A.4
Panhuysen, C.5
Farrer, L.A.6
-
41
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein RJ, Zeiss C, Chew EY, et al. Complement factor H polymorphism in age-related macular degeneration. Science. 2005;308:385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
-
42
-
-
11144294168
-
Anterior segment development relevant to glaucoma
-
Gould DB, Smith RS, John SW. Anterior segment development relevant to glaucoma. Int J Dev Biol. 2004;48:1015-1029.
-
(2004)
Int J Dev Biol
, vol.48
, pp. 1015-1029
-
-
Gould, D.B.1
Smith, R.S.2
John, S.W.3
-
43
-
-
0036157114
-
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene
-
Vincent AL, Billingsley G, Buys Y, et al. Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Am J Hum Genet. 2002;70:448-460.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 448-460
-
-
Vincent, A.L.1
Billingsley, G.2
Buys, Y.3
-
44
-
-
33645860816
-
Primary role of CYP1B1 in Indian juvenile-onset POAG patients
-
Acharya M, Mookherjee S, Bhattacharjee A, et al. Primary role of CYP1B1 in Indian juvenile-onset POAG patients. Mol Vis. 2006;12:399-404.
-
(2006)
Mol Vis
, vol.12
, pp. 399-404
-
-
Acharya, M.1
Mookherjee, S.2
Bhattacharjee, A.3
-
45
-
-
44149120064
-
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
-
Bhattacharjee A, Banerjee D, Mookherjee S, et al. Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis. 2008;14:841-850.
-
(2008)
Mol Vis
, vol.14
, pp. 841-850
-
-
Bhattacharjee, A.1
Banerjee, D.2
Mookherjee, S.3
-
46
-
-
27944470375
-
Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma
-
Melki R, Lefort N, Brezin AP, Garchon HJ. Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma. Mol Vis. 2005;11:1012-1017.
-
(2005)
Mol Vis
, vol.11
, pp. 1012-1017
-
-
Melki, R.1
Lefort, N.2
Brezin, A.P.3
Garchon, H.J.4
-
47
-
-
0037092596
-
Anterior segment dysgenesis and the developmental glaucomas are complex traits
-
Gould DB, John SW. Anterior segment dysgenesis and the developmental glaucomas are complex traits. Hum Mol Genet. 2002;11:1185-1193.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1185-1193
-
-
Gould, D.B.1
John, S.W.2
-
48
-
-
0002681486
-
Classification of glaucomas
-
In: Ritch R, Shields M, Krupin T, eds., 2nd ed. St. Louis: Mosby
-
Shields M, Ritch R, Krupin T. Classification of glaucomas. In: Ritch R, Shields M, Krupin T, eds. The Glaucomas. 2nd ed. St. Louis: Mosby; 1996:717-725.
-
(1996)
The Glaucomas
, pp. 717-725
-
-
Shields, M.1
Ritch, R.2
Krupin, T.3
-
49
-
-
33846907614
-
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations
-
Strungaru MH, Dinu I, Walter MA. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations. Invest Ophthalmol Vis Sci. 2007;48:228-237.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 228-237
-
-
Strungaru, M.H.1
Dinu, I.2
Walter, M.A.3
-
50
-
-
33646104926
-
A review of anterior segment dysgeneses
-
Idrees F, Vaideanu D, Fraser SG, Sowden JC, Khaw PT. A review of anterior segment dysgeneses. Surv Ophthalmol. 2006;51:213-231.
-
(2006)
Surv Ophthalmol
, vol.51
, pp. 213-231
-
-
Idrees, F.1
Vaideanu, D.2
Fraser, S.G.3
Sowden, J.C.4
Khaw, P.T.5
-
51
-
-
0034090670
-
LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye
-
Pressman CL, Chen H, Johnson RL. LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye. Genesis. 2000;26:15-25.
-
(2000)
Genesis
, vol.26
, pp. 15-25
-
-
Pressman, C.L.1
Chen, H.2
Johnson, R.L.3
-
52
-
-
33845271685
-
Nail-patella syndrome and its association with glaucoma: A review of eight families
-
Mimiwati Z, Mackey DA, Craig JE, et al. Nail-patella syndrome and its association with glaucoma: a review of eight families. Br J Ophthalmol. 2006;90:1505-1509.
-
(2006)
Br J Ophthalmol
, vol.90
, pp. 1505-1509
-
-
Mimiwati, Z.1
MacKey, D.A.2
Craig, J.E.3
-
54
-
-
23644447910
-
Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy
-
Bongers EM, Huysmans FT, Levtchenko E, et al. Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy. Eur J Hum Genet. 2005;13:935-946.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 935-946
-
-
Bongers, E.M.1
Huysmans, F.T.2
Levtchenko, E.3
-
55
-
-
0030825171
-
Cosegregation of open-angle glaucoma and the nail-patella syndrome
-
Lichter PR, Richards JE, Downs CA, Stringham HM, Boehnke M, Farley FA. Cosegregation of open-angle glaucoma and the nail-patella syndrome. Am J Ophthalmol. 1997;124:506-515.
-
(1997)
Am J Ophthalmol
, vol.124
, pp. 506-515
-
-
Lichter, P.R.1
Richards, J.E.2
Downs, C.A.3
Stringham, H.M.4
Boehnke, M.5
Farley, F.A.6
-
56
-
-
0037338559
-
Nail patella syndrome: A review of the phenotype aided by developmental biology
-
Sweeney E, Fryer A, Mountford R, Green A, McIntosh I. Nail patella syndrome: a review of the phenotype aided by developmental biology. J Med Genet. 2003;40:153-162.
-
(2003)
J Med Genet
, vol.40
, pp. 153-162
-
-
Sweeney, E.1
Fryer, A.2
Mountford, R.3
Green, A.4
McIntosh, I.5
-
57
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, et al. The structure of haplotype blocks in the human genome. Science. 2002;296:2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
-
58
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21:263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
59
-
-
0037101844
-
Specific haplotypes of the P-selectin gene are associated with myocardial infarction
-
Tregouet DA, Barbaux S, Escolano S, et al. Specific haplotypes of the P-selectin gene are associated with myocardial infarction. Hum Mol Genet. 2002;11:2015-2023.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2015-2023
-
-
Tregouet, D.A.1
Barbaux, S.2
Escolano, S.3
-
60
-
-
0038485740
-
Novel anterior segment phenotypes resulting from forkhead gene alterations: Evidence for cross-species conservation of function
-
Lehmann OJ, Tuft S, Brice G, et al. Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function. Invest Ophthalmol Vis Sci. 2003;44:2627-2633.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 2627-2633
-
-
Lehmann, O.J.1
Tuft, S.2
Brice, G.3
-
61
-
-
0037406767
-
Corneal abnormalities in Pax6+/- small eye mice mimic human aniridia-related keratopathy
-
Ramaesh T, Collinson JM, Ramaesh K, Kaufman MH, West JD, Dhillon B. Corneal abnormalities in Pax6+/- small eye mice mimic human aniridia-related keratopathy. Invest Ophthalmol Vis Sci. 2003;44:1871-1878.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 1871-1878
-
-
Ramaesh, T.1
Collinson, J.M.2
Ramaesh, K.3
Kaufman, M.H.4
West, J.D.5
Dhillon, B.6
-
62
-
-
1242316165
-
Markedly increased central corneal thickness: An unrecognized finding in congenital aniridia
-
Brandt JD, Casuso LA, Budenz DL. Markedly increased central corneal thickness: an unrecognized finding in congenital aniridia. Am J Ophthalmol. 2004;137:348-350.
-
(2004)
Am J Ophthalmol
, vol.137
, pp. 348-350
-
-
Brandt, J.D.1
Casuso, L.A.2
Budenz, D.L.3
-
63
-
-
34247141933
-
Reduced human and murine corneal thickness in an Axenfeld-Rieger syndrome subtype
-
Asai-Coakwell M, Backhouse C, Casey RJ, Gage PJ, Lehmann OJ. Reduced human and murine corneal thickness in an Axenfeld-Rieger syndrome subtype. Invest Ophthalmol Vis Sci. 2006;47:4905-4909.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 4905-4909
-
-
Asai-Coakwell, M.1
Backhouse, C.2
Casey, R.J.3
Gage, P.J.4
Lehmann, O.J.5
-
64
-
-
0036272299
-
The Ocular Hypertension Treatment Study: Baseline factors that predict the onset of primary open-angle glaucoma
-
Gordon MO, Beiser JA, Brandt JD, et al. The Ocular Hypertension Treatment Study: baseline factors that predict the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002;120:714-720.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 714-720
-
-
Gordon, M.O.1
Beiser, J.A.2
Brandt, J.D.3
-
65
-
-
0027269723
-
The effect of corneal thickness on applanation tonometry
-
Whitacre MM, Stein RA, Hassanein K. The effect of corneal thickness on applanation tonometry. Am J Ophthalmol. 1993;115:592-596.
-
(1993)
Am J Ophthalmol
, vol.115
, pp. 592-596
-
-
Whitacre, M.M.1
Stein, R.A.2
Hassanein, K.3
-
66
-
-
0035163029
-
Correlation between central corneal thickness, applanation tonometry, and direct intracameral IOP readings
-
Feltgen N, Leifert D, Funk J. Correlation between central corneal thickness, applanation tonometry, and direct intracameral IOP readings. Br J Ophthalmol. 2001;85:85-87.
-
(2001)
Br J Ophthalmol
, vol.85
, pp. 85-87
-
-
Feltgen, N.1
Leifert, D.2
Funk, J.3
-
67
-
-
0036235038
-
Effect of corneal thickness on intraocular pressure measurements with the pneumotonometer, Goldmann applanation tonometer, and Tono-Pen
-
Bhan A, Browning AC, Shah S, Hamilton R, Dave D, Dua HS. Effect of corneal thickness on intraocular pressure measurements with the pneumotonometer, Goldmann applanation tonometer, and Tono-Pen. Invest Ophthalmol Vis Sci. 2002;43:1389-1392.
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 1389-1392
-
-
Bhan, A.1
Browning, A.C.2
Shah, S.3
Hamilton, R.4
Dave, D.5
Dua, H.S.6
-
69
-
-
0031848594
-
Applanation tonometry and correction according to corneal thickness
-
Stodtmeister R. Applanation tonometry and correction according to corneal thickness. Acta Ophthalmol Scand. 1998;76:319-324.
-
(1998)
Acta Ophthalmol Scand
, vol.76
, pp. 319-324
-
-
Stodtmeister, R.1
-
70
-
-
1842504236
-
Corneal thickness in glaucoma screening, diagnosis, and management
-
Brandt JD. Corneal thickness in glaucoma screening, diagnosis, and management. Curr Opin Ophthalmol. 2004;15:85-89.
-
(2004)
Curr Opin Ophthalmol
, vol.15
, pp. 85-89
-
-
Brandt, J.D.1
-
71
-
-
35448974197
-
Association between primary open-angle glaucoma and WDR36 DNA sequence variants in Japanese
-
Miyazawa A, Fuse N, Mengkegale M, et al. Association between primary open-angle glaucoma and WDR36 DNA sequence variants in Japanese. Mol Vis. 2007;13:1912-1919.
-
(2007)
Mol Vis
, vol.13
, pp. 1912-1919
-
-
Miyazawa, A.1
Fuse, N.2
Mengkegale, M.3
-
72
-
-
54449100316
-
Intraocular pressure, central corneal thickness, and prevalence of open-angle glaucoma: The Los Angeles Latino Eye Study
-
July 29, Epub ahead of print
-
Francis BA, Varma R, Chopra V, Lai MY, Shtir C, Azen SP. Intraocular pressure, central corneal thickness, and prevalence of open-angle glaucoma: The Los Angeles Latino Eye Study. Am J Ophthalmol. July 29 2008.[Epub ahead of print]
-
(2008)
Am J Ophthalmol
-
-
Francis, B.A.1
Varma, R.2
Chopra, V.3
Lai, M.Y.4
Shtir, C.5
Azen, S.P.6
-
73
-
-
3843076445
-
The human LMX1B gene: Transcription unit, promoter, and pathogenic mutations
-
Dunston JA, Hamlington JD, Zaveri J, et al. The human LMX1B gene: transcription unit, promoter, and pathogenic mutations. Genomics. 2004;84:565-576.
-
(2004)
Genomics
, vol.84
, pp. 565-576
-
-
Dunston, J.A.1
Hamlington, J.D.2
Zaveri, J.3
-
74
-
-
0036272052
-
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions
-
Lehmann OJ, Ebenezer ND, Ekong R, et al. Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions. Invest Ophthalmol Vis Sci. 2002;43:1843-1849.
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 1843-1849
-
-
Lehmann, O.J.1
Ebenezer, N.D.2
Ekong, R.3
-
75
-
-
43449103925
-
PAX6 dosage effects on corneal development, growth, and wound healing
-
Dora N, Ou J, Kucerova R, Parisi I, West JD, Collinson JM. PAX6 dosage effects on corneal development, growth, and wound healing. Dev Dyn. 2008;237:1295-1306.
-
(2008)
Dev Dyn
, vol.237
, pp. 1295-1306
-
-
Dora, N.1
Ou, J.2
Kucerova, R.3
Parisi, I.4
West, J.D.5
Collinson, J.M.6
-
76
-
-
0034284545
-
Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders
-
Kozlowski K, Walter MA. Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders. Hum Mol Genet. 2000;9:2131-2139.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2131-2139
-
-
Kozlowski, K.1
Walter, M.A.2
-
77
-
-
34447336145
-
Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis
-
Gould DB, Marchant JK, Savinova OV, Smith RS, John SW. Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis. Hum Mol Genet. 2007;16:798-807.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 798-807
-
-
Gould, D.B.1
Marchant, J.K.2
Savinova, O.V.3
Smith, R.S.4
John, S.W.5
-
78
-
-
0036117988
-
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes
-
Rohr C, Prestel J, Heidet L, et al. The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes. J Clin Invest. 2002;109:1073-1082.
-
(2002)
J Clin Invest
, vol.109
, pp. 1073-1082
-
-
Rohr, C.1
Prestel, J.2
Heidet, L.3
-
79
-
-
0035134740
-
Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome
-
Morello R, Zhou G, Dreyer SD, et al. Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome. Nat Genet. 2001;27:205-208.
-
(2001)
Nat Genet
, vol.27
, pp. 205-208
-
-
Morello, R.1
Zhou, G.2
Dreyer, S.D.3
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