PubMed ID: 19471602 Author(s): Yanovitch T, Li YJ, Metlapally R, Abbott D, Viet KN, Young TL. Hepatocyte growth factor and myopia: genetic association analyses in a Caucasian population. Mol Vis. 2009 May 20;15:1028-35. PMID 19471602 …
Young Lab
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.
PubMed ID: 19098318 Author(s): Metlapally R, Michaelides M, Bulusu A, Li YJ, Schwartz M, Rosenberg T, Hunt DM, Moore AT, Züchner S, Rickman CB, Young TL. Evaluation of the X-linked high-grade myopia locus (MYP1) with …
Myocilin polymorphisms and high myopia in subjects of European origin.
PubMed ID: 19180258 Author(s): Zayats T, Yanovitch T, Creer RC, McMahon G, Li YJ, Young TL, Guggenheim JA. Myocilin polymorphisms and high myopia in subjects of European origin. Mol Vis. 2009;15:213-22. Epub 2009 Jan 26. …
The effects of fetal surgery on retinopathy of prematurity development.
PubMed ID: 23861606 Author(s): Nallasamy S, Davidson SL, Howell LJ, Hedrick H, Flake AW, Crombleholme TM, Adzick NS, Young TL. The effects of fetal surgery on retinopathy of prematurity development. Ophthalmol Eye Dis. 2009 Oct …
Molecular genetics of human myopia: an update.
PubMed ID: 19104467 Author(s): Young TL. Molecular genetics of human myopia: an update. Optom Vis Sci. 2009 Jan;86(1):E8-E22. doi: 10.1097/OPX.0b013e3181940655. PMID 19104467 Journal: Optometry And Vision Science : Official Publication Of The American Academy Of …
Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters.
PubMed ID: 18831064 Author(s): Schneider A, Bardakjian TM, Zhou J, Hughes N, Keep R, Dorsainville D, Kherani F, Katowitz J, Schimmenti LA, Hummel M, Fitzpatrick DR, Young TL. Familial recurrence of SOX2 anophthalmia syndrome: phenotypically …
Comment on ‘A PAX6 gene polymorphism is associated with genetic predisposition to extreme myopia’.
PubMed ID: 18219338 Author(s): Zayats T, Guggenheim JA, Hammond CJ, Young TL. Comment on ‘A PAX6 gene polymorphism is associated with genetic predisposition to extreme myopia’. Eye (Lond). 2008 Apr;22(4):598-9; author reply 599. doi: 10.1038/sj.eye.6703096. …
Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia.
PubMed ID: 18385794 Author(s): Zhou J, Kherani F, Bardakjian TM, Katowitz J, Hughes N, Schimmenti LA, Schneider A, Young TL. Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients …
Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia.
PubMed ID: 18334955 Author(s): Metlapally R, Li YJ, Tran-Viet KN, Bulusu A, White TR, Ellis J, Kao D, Young TL. Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and …