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 …
Young Lab
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 …
Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia.
PubMed ID: 19112531 Author(s): White T, Lu T, Metlapally R, Katowitz J, Kherani F, Wang TY, Tran-Viet KN, Young TL. Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia. Mol Vis. 2008;14:2458-65. Epub …
Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.
PubMed ID: 17327828 Author(s): Nallasamy S, Paluru PC, Devoto M, Wasserman NF, Zhou J, Young TL. Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota. Mol Vis. 2007 Feb 15;13:229-36. PMID …
Complex trait genetics of refractive error.
PubMed ID: 17210850 Author(s): Young TL, Metlapally R, Shay AE. Complex trait genetics of refractive error. Arch Ophthalmol. 2007 Jan;125(1):38-48. Review. PMID 17210850 Journal: Archives Of Ophthalmology (Chicago, Ill. : 1960), Volume 125, Issue 1, …
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations.
PubMed ID: 17189145 Author(s): Jadico SK, Young DA, Huebner A, Edmond JC, Pollock AN, McDonald-McGinn DM, Li YJ, Zackai EH, Young TL. Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type …
Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations.
PubMed ID: 17070479 Author(s): Jadico SK, Huebner A, McDonald-McGinn DM, Zackai EH, Young TL. Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations. J AAPOS. 2006 Oct;10(5):435-44. PMID 17070479 Journal: Journal Of Aapos …
Small leucine rich repeat proteoglycans (SLRPs) in the human sclera: identification of abundant levels of PRELP.
PubMed ID: 17093390 Author(s): Johnson JM, Young TL, Rada JA. Small leucine rich repeat proteoglycans (SLRPs) in the human sclera: identification of abundant levels of PRELP. Mol Vis. 2006 Sep 13;12:1057-66. PMID 17093390 Journal: Molecular …
Differential gene expression in mouse sclera during ocular development.
PubMed ID: 16638983 Author(s): Zhou J, Rappaport EF, Tobias JW, Young TL. Differential gene expression in mouse sclera during ocular development. Invest Ophthalmol Vis Sci. 2006 May;47(5):1794-802. PMID 16638983 Journal: Investigative Ophthalmology & Visual Science, …