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359 results

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Page 1
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.
Fingert JH, Robin AL, Stone JL, Roos BR, Davis LK, Scheetz TE, Bennett SR, Wassink TH, Kwon YH, Alward WL, Mullins RF, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: sheffield vc. Hum Mol Genet. 2011 Jun 15;20(12):2482-94. doi: 10.1093/hmg/ddr123. Epub 2011 Mar 29. Hum Mol Genet. 2011. PMID: 21447600 Free PMC article.
Myocilin glaucoma.
Fingert JH, Stone EM, Sheffield VC, Alward WL. Fingert JH, et al. Among authors: sheffield vc. Surv Ophthalmol. 2002 Nov-Dec;47(6):547-61. doi: 10.1016/s0039-6257(02)00353-3. Surv Ophthalmol. 2002. PMID: 12504739 Review.
A case of autism and uniparental disomy of chromosome 1.
Wassink TH, Losh M, Frantz RS, Vieland VJ, Goedken R, Piven J, Sheffield VC. Wassink TH, et al. Among authors: sheffield vc. Hum Genet. 2005 Jul;117(2-3):200-6. doi: 10.1007/s00439-005-1257-4. Epub 2005 May 11. Hum Genet. 2005. PMID: 15887000
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. Among authors: sheffield vc. Ophthalmic Genet. 2006 Jun;27(2):39-41. doi: 10.1080/13816810600677883. Ophthalmic Genet. 2006. PMID: 16754204 No abstract available.
Genome-wide analysis of copy number variants in age-related macular degeneration.
Meyer KJ, Davis LK, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, Scheetz TE, Braun TA, Fingert JH, Alward WL, Kwon YH, Folk JC, Russell SR, Wassink TH, Stone EM, Sheffield VC. Meyer KJ, et al. Among authors: sheffield vc. Hum Genet. 2011 Jan;129(1):91-100. doi: 10.1007/s00439-010-0904-6. Epub 2010 Oct 28. Hum Genet. 2011. PMID: 20981449 Free PMC article.
Copy number variations and primary open-angle glaucoma.
Davis LK, Meyer KJ, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, Scheetz TE, Braun TA, Fingert JH, Alward WL, Kwon YH, Folk JC, Russell SR, Wassink TH, Sheffield VC, Stone EM. Davis LK, et al. Among authors: sheffield vc. Invest Ophthalmol Vis Sci. 2011 Sep 9;52(10):7122-33. doi: 10.1167/iovs.10-5606. Print 2011. Invest Ophthalmol Vis Sci. 2011. PMID: 21310917 Free PMC article.
Linkage of posterior polymorphous corneal dystrophy to 20q11.
Héon E, Mathers WD, Alward WL, Weisenthal RW, Sunden SL, Fishbaugh JA, Taylor CM, Krachmer JH, Sheffield VC, Stone EM. Héon E, et al. Among authors: sheffield vc. Hum Mol Genet. 1995 Mar;4(3):485-8. doi: 10.1093/hmg/4.3.485. Hum Mol Genet. 1995. PMID: 7795607
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.
Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: sheffield vc. Hum Mol Genet. 1999 May;8(5):899-905. doi: 10.1093/hmg/8.5.899. Hum Mol Genet. 1999. PMID: 10196380
359 results