-
1
-
-
0027173920
-
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31
-
Sheffield VC, Stone EM, Alward WL, Drack AV, Johnson AT, Streb LM, Nichols BE. 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
Drack, A.V.4
Johnson, A.T.5
Streb, L.M.6
Nichols, B.E.7
-
2
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Identification of a gene that causes primary open angle glaucoma. Science 1997; 275:668-70.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.3
Nguyen, T.D.4
Polansky, J.R.5
Sunden, S.L.6
Nishimura, D.7
Clark, A.F.8
Nystuen, A.9
Nichols, B.E.10
Mackey, D.A.11
Ritch, R.12
Kalenak, J.W.13
Craven, E.R.14
Sheffield, V.C.15
-
3
-
-
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, Brice G, Desai T, Trifan OC, Poinoosawmy D, Crick RP. Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region. Am J Hum Genet 1998; 62:641-52.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 641-652
-
-
Sarfarazi, M.1
Child, A.2
Stoilova, D.3
Brice, G.4
Desai, T.5
Trifan, O.C.6
Poinoosawmy, D.7
Crick, R.P.8
-
4
-
-
18244385269
-
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
-
Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, Heon E, Krupin T, Ritch R, Kreutzer D, Crick RP, Sarfarazi M. Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science 2002; 295:1077-9.
-
(2002)
Science
, vol.295
, pp. 1077-1079
-
-
Rezaie, T.1
Child, A.2
Hitchings, R.3
Brice, G.4
Miller, L.5
Coca-Prados, M.6
Heon, E.7
Krupin, T.8
Ritch, R.9
Kreutzer, D.10
Crick, R.P.11
Sarfarazi, M.12
-
5
-
-
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, Flor JD, Pericak-Vance MA, Rogers K, LaRocque KR, Graham FL, Broomer B, Del Bono E, Haines JL, Hauser M. Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol 2003; 121:1181-3.
-
(2003)
Arch. Ophthalmol.
, vol.121
, pp. 1181-1183
-
-
Wiggs, J.L.1
Auguste, J.2
Allingham, R.R.3
Flor, J.D.4
Pericak-Vance, M.A.5
Rogers, K.6
LaRocque, K.R.7
Graham, F.L.8
Broomer, B.9
Del Bono, E.10
Haines, J.L.11
Hauser, M.12
-
6
-
-
0042362073
-
Different optineurin mutation pattern in primary open-angle glaucoma
-
Leung YF, Fan BJ, Lam DS, Lee WS, Tam PO, Chua JK, Tham CC, Lai JS, Fan DS, Pang CP. Different optineurin mutation pattern in primary open-angle glaucoma. Invest Ophthalmol Vis Sci 2003; 44:3880-4.
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 3880-3884
-
-
Leung, Y.F.1
Fan, B.J.2
Lam, D.S.3
Lee, W.S.4
Tam, P.O.5
Chua, J.K.6
Tham, C.C.7
Lai, J.S.8
Fan, D.S.9
Pang, C.P.10
-
7
-
-
0042566069
-
The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene
-
Tang S, Toda Y, Kashiwagi K, Mabuchi F, Iijima H, Tsukahara S, Yamagata Z. The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene. Hum Genet 2003; 113:276-9.
-
(2003)
Hum. Genet.
, vol.113
, pp. 276-279
-
-
Tang, S.1
Toda, Y.2
Kashiwagi, K.3
Mabuchi, F.4
Iijima, H.5
Tsukahara, S.6
Yamagata, Z.7
-
8
-
-
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; 36:142-50.
-
(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
-
9
-
-
0031036668
-
Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q
-
Wirtz MK, Samples JR, Kramer PL, Rust K, Topinka JR, Yount J, Koler RD, Acott TS. 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
Rust, K.4
Topinka, J.R.5
Yount, J.6
Koler, R.D.7
Acott, T.S.8
-
10
-
-
0031851299
-
A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region
-
Trifan OC, Traboulsi EI, Stoilova D, Alozie I, Nguyen R, Raja S, Sarfarazi M. 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
Alozie, I.4
Nguyen, R.5
Raja, S.6
Sarfarazi, M.7
-
11
-
-
0033000146
-
GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36
-
Wirtz MK, Samples JR, Rust K, Lie J, Nordling L, Schilling K, Acott TS, Kramer PL. GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36. Arch Ophthalmol 1999; 117:237-41.
-
(1999)
Arch. Ophthalmol.
, vol.117
, pp. 237-241
-
-
Wirtz, M.K.1
Samples, J.R.2
Rust, K.3
Lie, J.4
Nordling, L.5
Schilling, K.6
Acott, T.S.7
Kramer, P.L.8
-
12
-
-
0034639929
-
Genome-wide scan for adult onset primary open angle glaucoma
-
Wiggs JL, Allingham RR, Hossain A, Kern J, Auguste J, DelBono EA, Broomer B, Graham FL, Hauser M, Pericak-Vance M, Haines JL. Genome-wide scan for adult onset primary open angle glaucoma. Hum Mol Genet 2000; 9:1109-17.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1109-1117
-
-
Wiggs, J.L.1
Allingham, R.R.2
Hossain, A.3
Kern, J.4
Auguste, J.5
DelBono, E.A.6
Broomer, B.7
Graham, F.L.8
Hauser, M.9
Pericak-Vance, M.10
Haines, J.L.11
-
13
-
-
0038620208
-
A genome-wide scan for primary open-angle glaucoma (POAG): The Barbados Family Study of Open-Angle Glaucoma
-
Barbados Family Study Group
-
Nemesure B, Jiao X, He Q, Leske MC, Wu SY, Hennis A, Mendell N, Redman J, Garchon HJ, Agarwala R, Schaffer AA, Hejtmancik F, Barbados Family Study Group. A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma. Hum Genet 2003; 112:600-9.
-
(2003)
Hum. Genet.
, vol.112
, pp. 600-609
-
-
Nemesure, B.1
Jiao, X.2
He, Q.3
Leske, M.C.4
Wu, S.Y.5
Hennis, A.6
Mendell, N.7
Redman, J.8
Garchon, H.J.9
Agarwala, R.10
Schaffer, A.A.11
Hejtmancik, F.12
-
14
-
-
0028636499
-
Intraocular pressure and prevalence of glaucoma in elderly people in Finland: A population-based study
-
Hirvela H, Tuulonen A, Laatikainen L. Intraocular pressure and prevalence of glaucoma in elderly people in Finland: a population-based study. Int Ophthalmol 1994-95; 18:299-307.
-
(1994)
Int. Ophthalmol.
, vol.18
, pp. 299-307
-
-
Hirvela, H.1
Tuulonen, A.2
Laatikainen, L.3
-
15
-
-
0025807959
-
The middle-Norway eye-screening study. II. Prevalence of simple and capsular glaucoma
-
Ringvold A, Blika S, Elsas T, Guldahl J, Brevik T, Hesstvedt P, Hoff K, Hoisen H, Kjorsvik S, Rossvold I. The middle-Norway eye-screening study. II. Prevalence of simple and capsular glaucoma. Acta Ophthalmol (Copenh) 1991; 69:273-80.
-
(1991)
Acta Ophthalmol. (Copenh)
, vol.69
, pp. 273-280
-
-
Ringvold, A.1
Blika, S.2
Elsas, T.3
Guldahl, J.4
Brevik, T.5
Hesstvedt, P.6
Hoff, K.7
Hoisen, H.8
Kjorsvik, S.9
Rossvold, I.10
-
16
-
-
0037733995
-
The role of TIGR and OPTN in Finnish glaucoma families: A clinical and molecular genetic study
-
Forsman E, Lemmela S, Varilo T, Kristo P, Forsius H, Sankila EM, Jarvela I. The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study. Mol Vis 2003; 9:217-22 http://www.molvis.org/molvis/v9/a32/).
-
(2003)
Mol. Vis.
, vol.9
, pp. 217-222
-
-
Forsman, E.1
Lemmela, S.2
Varilo, T.3
Kristo, P.4
Forsius, H.5
Sankila, E.M.6
Jarvela, I.7
-
17
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63:259-66.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
18
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984; 36:460-5.
-
(1984)
Am. J. Hum. Genet.
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
19
-
-
0022646961
-
Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis
-
Lathrop GM, Lalouel JM, White RL. Construction of human linkage maps: likelihood calculations for multilocus linkage analysis. Genet Epidemiol 1986; 3:39-52.
-
(1986)
Genet. Epidemiol.
, vol.3
, pp. 39-52
-
-
Lathrop, G.M.1
Lalouel, J.M.2
White, R.L.3
-
20
-
-
0028968329
-
A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci
-
Terwilliger JD. A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am J Hum Genet 1995; 56:777-87.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 777-787
-
-
Terwilliger, J.D.1
-
21
-
-
0003408936
-
-
3rd ed. Baltimore: The Johns Hopkins University Press
-
Ott J. Analysis of Human Genetic Linkage. 3rd ed. Baltimore: The Johns Hopkins University Press; 1999.
-
(1999)
Analysis of Human Genetic Linkage
-
-
Ott, J.1
-
22
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 1996; 58:1323-37.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
24
-
-
0032869123
-
Molecular genetics of the Finnish disease heritage
-
Peltonen L, Jalanko A, Varilo T. Molecular genetics of the Finnish disease heritage. Hum Mol Genet 1999; 8:1913-23.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1913-1923
-
-
Peltonen, L.1
Jalanko, A.2
Varilo, T.3
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