Fingert JH - Search Results

1

TBK1 and flanking genes in human retina.

Fingert JH, Darbro BW, Qian Q, Van Rheeden R, Miller K, Riker M, Solivan-Timpe F, Roos BR, Robin AL, Mullins RF. Fingert JH, et al. Ophthalmic Genet. 2014 Mar;35(1):35-40. doi: 10.3109/13816810.2013.768674. Epub 2013 Feb 20. Ophthalmic Genet. 2014. PMID: 23421332 Free PMC article.

2

The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from Iowa.

Fingert JH, Kwon YH, Moore PA, Johnston RM, Kim KY, Sheffield VC, Alward WL, Stone EM. Fingert JH, et al. Ophthalmic Genet. 2006 Jun;27(2):39-41. doi: 10.1080/13816810600677883. Ophthalmic Genet. 2006. PMID: 16754204 No abstract available.

3

Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His.

Grassi MA, Fingert JH, Scheetz TE, Roos BR, Ritch R, West SK, Kawase K, Shire AM, Mullins RF, Stone EM. Grassi MA, et al. Among authors: fingert jh. Hum Mutat. 2006 Sep;27(9):921-5. doi: 10.1002/humu.20359. Hum Mutat. 2006. PMID: 16865697

4

Mitochondrial variant G4132A is associated with familial non-arteritic anterior ischemic optic neuropathy in one large pedigree.

Fingert JH, Grassi MA, Janutka JC, East JS, Howard JG, Sheffield VC, Jacobson DM, Hayreh SS, Stone EM. Fingert JH, et al. Ophthalmic Genet. 2007 Mar;28(1):1-7. doi: 10.1080/13816810701199399. Ophthalmic Genet. 2007. PMID: 17454741

5

Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.

Shankar SP, Fingert JH, Carelli V, Valentino ML, King TM, Daiger SP, Salomao SR, Berezovsky A, Belfort R Jr, Braun TA, Sheffield VC, Sadun AA, Stone EM. Shankar SP, et al. Among authors: fingert jh. Ophthalmic Genet. 2008 Mar;29(1):17-24. doi: 10.1080/13816810701867607. Ophthalmic Genet. 2008. PMID: 18363168

6

Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family.

Shah SS, Al-Rajhi A, Brandt JD, Mannis MJ, Roos B, Sheffield VC, Syed NA, Stone EM, Fingert JH. Shah SS, et al. Among authors: fingert jh. Ophthalmic Genet. 2008 Mar;29(1):41-5. doi: 10.1080/13816810701850033. Ophthalmic Genet. 2008. PMID: 18363173

7

Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmus.

Fingert JH, Roos B, Eyestone ME, Pham JD, Mellot ML, Stone E. Fingert JH, et al. Ophthalmic Genet. 2010 Jun;31(2):77-80. doi: 10.3109/13816810903584989. Ophthalmic Genet. 2010. PMID: 20450309

8

Complement component C5a activates ICAM-1 expression on human choroidal endothelial cells.

Skeie JM, Fingert JH, Russell SR, Stone EM, Mullins RF. Skeie JM, et al. Among authors: fingert jh. Invest Ophthalmol Vis Sci. 2010 Oct;51(10):5336-42. doi: 10.1167/iovs.10-5322. Epub 2010 May 19. Invest Ophthalmol Vis Sci. 2010. PMID: 20484595 Free PMC article.

9

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy.

Rosenberg T, Roos B, Johnsen T, Bech N, Scheetz TE, Larsen M, Stone EM, Fingert JH. Rosenberg T, et al. Among authors: fingert jh. Mol Vis. 2010 Dec 9;16:2659-68. Mol Vis. 2010. PMID: 21179233 Free PMC article.

10

Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort.

Kuehn MH, Wang K, Roos B, Stone EM, Kwon YH, Alward WL, Mullins RF, Fingert JH. Kuehn MH, et al. Among authors: fingert jh. Mol Vis. 2011 Feb 8;17:430-5. Mol Vis. 2011. PMID: 21321670 Free PMC article.

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