Bibliografia

  1.  Hewitt, A. W., Bennett, S. L., Richards, J. E., Dimasi, D. P., Booth, A. P., Inglehearn, C., Anwar, R., Yamamoto, T., Fingert, J. H., Heon, E., Craig, J. E., Mackey, D. A.Myocilin gly252-to-arg mutation and glaucoma of intermediate severity in Caucasian individuals.Arch. Ophthal. 125: 98-104, 2007.
  2. Park, B.-C., Tibudan, M., Samaraweera, M., Shen, X., Yue, B. Y. J. T.Interaction between two glaucoma genes, optineurin and myocilin.Genes Cells 12: 969-979, 2007.
  3. Pasutto, F., Mardin, C. Y., Michels-Rautenstrauss, K., Weber, B. H. F., Sticht, H., Chavarria-Soley, G., Rautenstrauss, B., Kruse, F., Reis, A.Profiling of WDR36 missense variants in German patients with glaucoma.Invest. Ophthal. Vis. Sci. 49: 270-274, 2008.
  4. Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, Yang YF, Zenkel M, Schlötzer-Schrehardt U, Mardin CY, Frezzotti P, Edmunds B, Kramer PL, Gramer E, Reis A, Acott TS, Wirtz MK. Variants in ASB10 are associated with open-angle glaucoma. Hum Mol Genet. 15;21(6):1336-49, 2012. Epub 2011 Dec 8.
  5. Azmanov, D. N., Dimitrova, S., Florez, L., Cherninkova, S., Draganov, D., Morar, B., Saat, R., Juan, M., Arostegui, J. I., Ganguly, S., Soodyall, H., Chakrabarti, S., and 10 others.LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.Europ. J. Hum. Genet. 19: 326-333, 2011.
  6. Lemmela, S., Forsman, E., Onkamo, P., Nurmi, H., Laivuori, H., Kivela, T., Puska, P., Heger, M., Eriksson, A., Forsius, H., Jarvela, I.Association of LOXL1 gene with Finnish exfoliation syndrome patients.J. Hum. Genet. 54: 289-297, 2009.
  7. Krumbiegel, M., Pasutto, F., Schlotzer-Schrehardt, U., Uebe, S., Zenkel, M., Mardin, C. Y., Weisschuh, N., Paoli, D., Gramer, E., Becker, C., Ekici, A. B., Weber, B. H. F., Nurnberg, P., Kruse, F. E., Reis, A.Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.Europ. J. Hum. Genet. 19: 186-193, 2011.
  8. Awadalla MS, Burdon KP, Kuot A, Hewitt AW, Craig JE. Matrix metalloproteinase-9 genetic variation and primary angle closure glaucoma in a Caucasian population. Mol Vis 2011; 17: 1420-4 Epub 2011 May 27.
  9. Awadalla MS, Thapa SS, Burdon KP, Hewitt AW, Craig JE. The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population. Mol Vis 2011; 17:2248-54. Epub 2011 Aug 19.
Dezembro 2012