-
1
-
-
34548694283
-
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
-
Thorleifsson G, Magnusson KP, Sulem P, et al. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007;317:1397-1400.
-
(2007)
Science
, vol.317
, pp. 1397-1400
-
-
Thorleifsson, G.1
Magnusson, K.P.2
Sulem, P.3
-
2
-
-
0035232015
-
Lysyl oxidases: A novel multifunctional amine oxidase family
-
Csiszar K. Lysyl oxidases: a novel multifunctional amine oxidase family. Prog Nucleic Acid Res Mol Biol. 2001;70:1-32.
-
(2001)
Prog Nucleic Acid Res Mol Biol
, vol.70
, pp. 1-32
-
-
Csiszar, K.1
-
3
-
-
30044436335
-
The Proregions of lysyl oxidase and lysyl oxidase-like 1 are required for deposition onto elastic fibers
-
Thomassin L, Werneck CC, Broekelmann TJ, et al. The Proregions of lysyl oxidase and lysyl oxidase-like 1 are required for deposition onto elastic fibers. J Biol Chem. 2005;280: 42848-42855.
-
(2005)
J Biol Chem
, vol.280
, pp. 42848-42855
-
-
Thomassin, L.1
Werneck, C.C.2
Broekelmann, T.J.3
-
4
-
-
34548060724
-
Population differences in elastin maturation in optic nerve head tissue and astrocytes
-
Urban Z, Agapova O, Hucthagowder V, et al. Population differences in elastin maturation in optic nerve head tissue and astrocytes. Invest Ophthalmol Vis Sci. 2007;48:3209-3215.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 3209-3215
-
-
Urban, Z.1
Agapova, O.2
Hucthagowder, V.3
-
5
-
-
0026498387
-
Pseudoexfoliative fibrillopathy in visceral organs of a patient with pseudoexfoliation syndrome
-
Streeten BW, Li ZY, Wallace RN, et al. Pseudoexfoliative fibrillopathy in visceral organs of a patient with pseudoexfoliation syndrome. Arch Ophthalmol. 1992;110:1757-1762.
-
(1992)
Arch Ophthalmol
, vol.110
, pp. 1757-1762
-
-
Streeten, B.W.1
Li, Z.Y.2
Wallace, R.N.3
-
6
-
-
36248931611
-
LOXL1 mutations are associated with exfoliation syndrome in patients from Midwestern United States
-
Fingert JH, Alward WLM, Kwon YH, et al. LOXL1 mutations are associated with exfoliation syndrome in patients from Midwestern United States. Am J Ophthalmol. 2007;144: 974-975.
-
(2007)
Am J Ophthalmol
, vol.144
, pp. 974-975
-
-
Fingert, J.H.1
Alward, W.L.M.2
Kwon, Y.H.3
-
7
-
-
38849142513
-
Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma
-
Challa P, Schmidt S, Liu Y, et al. Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma. Mol Vis. 2008;14:146-149.
-
(2008)
Mol Vis
, vol.14
, pp. 146-149
-
-
Challa, P.1
Schmidt, S.2
Liu, Y.3
-
8
-
-
41149152254
-
DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a US clinic-based population with broad ethnic diversity
-
Fan BJ, Pasquale L, Grosskreutz CL, et al. DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a US clinic-based population with broad ethnic diversity. BMC Med Genet. 2008;9:5.
-
(2008)
BMC Med Genet
, vol.9
, pp. 5
-
-
Fan, B.J.1
Pasquale, L.2
Grosskreutz, C.L.3
-
9
-
-
41549097786
-
Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma
-
Aragon-Martin JA, Ritch R, Liebmann J, et al. Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma. Mol Vis. 2008;14:533-541.
-
(2008)
Mol Vis
, vol.14
, pp. 533-541
-
-
Aragon-Martin, J.A.1
Ritch, R.2
Liebmann, J.3
-
10
-
-
45549095460
-
Association of LOXL1 common sequence variations in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma
-
Pasutto F, Krumbiegel M, Mardin CY, et al. Association of LOXL1 common sequence variations in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Invest Ophthalmol Vis Sci. 2008;49:1459-1463.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 1459-1463
-
-
Pasutto, F.1
Krumbiegel, M.2
Mardin, C.Y.3
-
11
-
-
39549105147
-
Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India
-
Ramprasad VL, George R, Soumittra N, et al. Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India. Mol Vis. 2008;14:318-322.
-
(2008)
Mol Vis
, vol.14
, pp. 318-322
-
-
Ramprasad, V.L.1
George, R.2
Soumittra, N.3
-
12
-
-
39049133729
-
Lysyl Oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population
-
Hayashi H, Gotoh N, Ueda Y, et al. Lysyl Oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population. Am J Ophthalmol. 2008;145:582-585.
-
(2008)
Am J Ophthalmol
, vol.145
, pp. 582-585
-
-
Hayashi, H.1
Gotoh, N.2
Ueda, Y.3
-
13
-
-
39749149076
-
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people
-
Hewitt AW, Sharma S, Burdon KP, et al. Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people. Hum Mol Genet. 2007;17:710-716.
-
(2007)
Hum Mol Genet
, vol.17
, pp. 710-716
-
-
Hewitt, A.W.1
Sharma, S.2
Burdon, K.P.3
-
14
-
-
43949113250
-
Lysyl oxidaselike protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population
-
Mossbock G, Renner W, Faschinger C, et al. Lysyl oxidaselike protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population. Mol Vis. 2008; 14:857-861.
-
(2008)
Mol Vis
, vol.14
, pp. 857-861
-
-
Mossbock, G.1
Renner, W.2
Faschinger, C.3
-
15
-
-
53149112354
-
Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese
-
Ozaki M, Lee KY, Vithana EN, et al. Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese. Invest Ophthalmol Vis Sci. 2008;49:3976-3980.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 3976-3980
-
-
Ozaki, M.1
Lee, K.Y.2
Vithana, E.N.3
-
17
-
-
47249148389
-
The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas
-
Chakrabarti S, Rao KN, Kaur I, et al. The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas. Invest Ophthalmol Vis Sci. 2008;49:2343-2347.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 2343-2347
-
-
Chakrabarti, S.1
Rao, K.N.2
Kaur, I.3
-
18
-
-
48949109588
-
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations
-
Liu Y, Schmidt S, Qin X, et al. Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations. Invest Ophthalmol Vis Sci. 2008;49: 3465-3468.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 3465-3468
-
-
Liu, Y.1
Schmidt, S.2
Qin, X.3
-
19
-
-
48949116403
-
Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma
-
Rao KN, Ritch R, Dorairaj SK, et al. Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma. Mol Vis. 2008;14:1254-1262.
-
(2008)
Mol Vis
, vol.14
, pp. 1254-1262
-
-
Rao, K.N.1
Ritch, R.2
Dorairaj, S.K.3
-
20
-
-
34548292504
-
PLINK: A toolset for whole-genome association and population-based linkage analysis
-
Purcell S, Neale B, Todd-Brown K, et al. PLINK: a toolset for whole-genome association and population-based linkage analysis. Am J Hum Genet. 2007;81:559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
21
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, et al. 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
-
22
-
-
12244264435
-
Genetic Power Calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics. 2003;19:149-150.
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
23
-
-
34848910727
-
Open-angle glaucoma-an epidemiologic overview
-
Leske MC. Open-angle glaucoma-an epidemiologic overview. Ophthalmic Epidemiol. 2007;14:166-172.
-
(2007)
Ophthalmic Epidemiol
, vol.14
, pp. 166-172
-
-
Leske, M.C.1
-
24
-
-
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
-
25
-
-
0033805401
-
Combined exfoliation and pigment dispersion: Paradigm of an overlap syndrome
-
Ritch R, Mudumbai R, Liebmann JM. Combined exfoliation and pigment dispersion: paradigm of an overlap syndrome. Ophthalmology. 2000;107:1004-1008.
-
(2000)
Ophthalmology
, vol.107
, pp. 1004-1008
-
-
Ritch, R.1
Mudumbai, R.2
Liebmann, J.M.3
-
26
-
-
0031849842
-
Familienanamnese Glaukom und Risikofaktoren bei Pigmentglaukom.
-
Gramer E, Thiele H, Ritch R. Familienanamnese Glaukom und Risikofaktoren bei Pigmentglaukom. Klin Monatsbl Augenheilkd. 1998;212:454-464.
-
(1998)
Klin Monatsbl Augenheilkd
, vol.212
, pp. 454-464
-
-
Gramer, E.1
Thiele, H.2
Ritch, R.3
-
27
-
-
0030985537
-
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36
-
Andersen JS, Pralea AM, DelBono EA, et al. A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36. Arch Ophthalmol. 1997;115:384-388.
-
(1997)
Arch Ophthalmol
, vol.115
, pp. 384-388
-
-
Andersen, J.S.1
Pralea, A.M.2
DelBono, E.A.3
|