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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: wassink th. 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.
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: wassink th. 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: wassink th. 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.
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. 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
Pax6 3' deletion results in aniridia, autism and mental retardation.
Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, Wassink TH. Davis LK, et al. Among authors: wassink th. Hum Genet. 2008 May;123(4):371-8. doi: 10.1007/s00439-008-0484-x. Epub 2008 Mar 6. Hum Genet. 2008. PMID: 18322702 Free PMC article. Review.
Evaluation of FOXP2 as an autism susceptibility gene.
Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, Sheffield VC. Wassink TH, et al. Am J Med Genet. 2002 Jul 8;114(5):566-9. doi: 10.1002/ajmg.10415. Am J Med Genet. 2002. PMID: 12116195
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC. Wassink TH, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44. doi: 10.1002/ajmg.b.30180. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15892143 Free article.
89 results