Genome-wide scan for adult onset primary open angle glaucoma

Human Molecular Genetics

Volumn 9, Issue 7, 2000, Pages 1109-1117

  Wiggs, J L ^c   Allingham, R R ^a   Hossain, A ^b   Kern, J ^c   Auguste, J ^c   DelBono, E A ^c   Broomer, B ^a   Graham, F Lennon ^a   Hauser, M ^a   Pericak Vance, M ^a   Haines, J L ^b  

^a DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME 14; CHROMOSOME 17; CHROMOSOME 17P; CHROMOSOME 17Q; CHROMOSOME 19; CHROMOSOME 2; CHROMOSOME 6; CHROMOSOME 9; GENE LOCATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; OPEN ANGLE GLAUCOMA; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

EID: 0034639929     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.7.1109     Document Type: Article

References (25)

1. Quigley, H.A. (1993) Open-angle glaucoma. N. Engl. J. Med., 328, 1097-1106.
2. Klein, B.E., Klein, R., Sponsel, W.E., Franke, T., Cantor, L.B., Martone, J. and Menage, M.J. (1992) Prevalence of glaucoma. The Beaver Dam Eye Study. Ophthalmology, 99, 1499-1504.
3. Tielsch, J.M., Sommer, A., Katz, J., Royall, R.M., Quigley, H.A. and Javitt, J. (1991) Racial variation in the prevalence of primary open-angle glaucoma. The Baltimore Eye Survey. JAMA, 266, 369-374.
4. Charliat, G., Jolly, D. and Blanchard, F. (1994) Genetic risk factor in primary open-angle glaucoma: a case-control study. Ophthalmic Epidemiol., 3, 131-138.
5. Perkins, E.S. (1974) Family studies in glaucoma. Br. J. Ophthalmol., 58, 529-535.
6. Shin, D.H., Becker, B. and Kolker, A.E. (1977) Family history in primary open-angle glaucoma. Arch. Ophthalmol., 95, 598-600.
7. Wilson, M.R., Hertzmark, E., Walker, A.M., Childs-Shaw, K. and Epstein, D.L. (1987) A case-control study of risk factors in open angle glaucoma. Arch. Ophthalmol., 105, 1066-1071.
8. Teikari, J.M. (1987) Genetic factors in open-angle (simple and capsular) glaucoma: a population-based twin study. Acta Ophthalmol. (Copenh.), 65, 715-720.
9. Goldschmidt, E. (1973) The heredity of glaucoma. Acta Ophthalmol. (Copenh.), 120, 27-31.
10. Stoilova, D., Child, A., Trifan, O.C., Crick, R.P., Coakes, R.L. and Sarfarazi, M. (1996) Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region. Genomics, 36, 142-150.
11. Wirtz, M.K., Samples, J.R., Kramer, P.L., Rust, K., Topinka, J.R., Yount, J., Koler, R.D. and Acott, T.S. (1997) Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q. Am. J. Hum. Genet., 60, 296-304.
12. Trifan, O.C., Traboulsi, E.I., Stoilova, D., Alozie, I., Nguyen, I., Rasa, S. and Sarfarazi, M. (1998) The third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region. Am. J. Ophthalmol., 126, 17-28.
13. Sarfarazi, M., Child, A., Stoilova, D., Brice, G., Desai, T., Trifan, O.C., Poinoosawmy, D. and Crick, R.P. (1998) Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region. Am. J. Hum. Genet., 62, 641-652.
14. Wirtz, M.K., Samples, J.R., Rust, K., Lie, J., Nordling, L., Schilling, K., Acott, T.S. and Kramer, P.L. (1999) GLC1F. a new primary open-angle glaucoma locus, maps to 7q35-q36. Arch. Ophthalmol., 117, 237-241.
15. Stone, E.M., Fingert, J.H., Alward, W.L.M., Nguyen, T.D., Polansky, J.R., Sunden, S.L.F., Nishimura, D., Clark, A.F., Nystuen, A., Nichols, B.E. et al. (1997) Identification of a gene that causes primary open angle glaucoma. Science, 275, 668-670.
16. Wiggs, J.L., Allingham, R.R., Vollrath, D., Jones, K., DeLaPaz, M., Kern, J., Patterson, K., DelBono, E.A., Pericak-Vance, M.A. and Haines, J.L. (1998) Prevalence of mutations in T1GR/Myocilin in patients with adult and juvenile primary open angle glaucoma. Am. J. Hum. Genet., 63, 1549-1552.
17. Alward, W.L.M., Fingert, J.H., Coote, M.A., Johnson, A.T., Lerner, S.F., Junqua, D., Durcan, F.J., McCartney, P.J., Mackey, D.A., Sheffield, V.C. and Stone, E.M. (1998) Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A). N. Engl. J. Med., 338, 1022-1027.
18. Suzuki, Y., Shirato, S., Taniguchi, F., Ohara, K., Nishimaki, K. and Ohta, S. (1997) Mutations in the TIGR gene in familial primary open-angle glaucoma in Japan. Am. J. Hum. Genet., 61, 1202-1204.
19. Adam, M.F., Belmouden, A., Binisti, P., Brézin, A.P., Valtot, F., Béchetoille, A., Dascotte, J.-C., Copin, B., Gomez, L., Chaventre, A. et al. (1997) Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma. Hum. Mol. Genet., 6, 2091-2097.
20. Polansky, J.R., Fauss, D.J., Chen, P., Chen, H., Lutjen-Drecoll, E., Johnson, D., Kurtz, R.M., Ma, Z.D., Bloom, E. and Nguyen, T.D. (1997) Cellular pharamacology and molecular biology of the trabecular meshwork inducible glucocorticoid response gene product. Ophthalmologica, 211, 126-139.
21. Ortego, J., Escribano, J. and Coca-Prados, M. (1997) Cloning and characterization of subtracted cDNAs from a human ciliary body library encoding TIGR, a protein involved in juvenile open angle glaucoma with homology to myosin and olfactomedin. FEBS Lett., 413, 349-353.
22. O'Connell, J.R. and Weeks, D.E. (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance. Nature Genet., 11, 402-408.
23. Kruglyak, L., Daly, M.J., Reeve-Daly, M.P. and Lander, E.S. (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am. J. Hum. Genet., 58, 1347-1363.
24. Hinds, D. and Risch, N. (1996) The ASPEX package: affected sibpair mapping. ftp://lahmed.stanford.edu/pub/aspex.
25. Vance, J.M., Slotterbeck, B., Yamaoka, L., Haynes, C., Roses, A.D. and Pericak-Vance, M.A. (1996) A fluorescent genotyping system for multiple users, flexibility and high output. Am. J. Hum. Genet., 59, A239.