Detalhe da pesquisa
1.
Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status.
Mol Vis
; 23: 548-560, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28848318
2.
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet
; 8(4): e1002654, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22570617
3.
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.
Hum Mol Genet
; 20(23): 4707-13, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21873608
4.
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma.
Mol Vis
; 14: 2484-91, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19112534
5.
Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States.
J Glaucoma
; 15(5): 358-63, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16988596
6.
DNA sequence variants in the tyrosinase-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma.
Mol Vis
; 8: 127-9, 2002 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-12011806
7.
The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables.
J Glaucoma
; 22(7): 517-25, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22828004
8.
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.
Am J Ophthalmol
; 155(2): 342-353.e5, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23111177
9.
Lack of association of polymorphisms in elastin with pseudoexfoliation syndrome and glaucoma.
J Glaucoma
; 19(7): 432-6, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20051886