PubMed ID: 24168726 Author(s): Guggenheim JA, McMahon G, Northstone K, Mandel Y, Kaiserman I, Stone RA, Lin X, Saw SM, Forward H, Mackey DA, Yazar S, Young TL, Williams C. Birth order and myopia. Ophthalmic …
Young Lab
Whole genome expression profiling of normal human fetal and adult ocular tissues.
PubMed ID: 24016867 Author(s): Young TL, Hawthorne F, Feng S, Luo X, St Germain E, Wang M, Metlapally R. Whole genome expression profiling of normal human fetal and adult ocular tissues. Exp Eye Res. 2013 …
Genetic contributions to myopic refractive error: Insights from human studies and supporting evidence from animal models.
PubMed ID: 23379998 Author(s): Hawthorne FA, Young TL. Genetic contributions to myopic refractive error: Insights from human studies and supporting evidence from animal models. Exp Eye Res. 2013 Sep;114:141-9. doi: 10.1016/j.exer.2012.12.015. Epub 2013 Feb 1. …
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
PubMed ID: 24144296 Author(s): Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, …
Myopia-related fundus changes in Singapore adults with high myopia.
PubMed ID: 23499368 Author(s): Chang L, Pan CW, Ohno-Matsui K, Lin X, Cheung GC, Gazzard G, Koh V, Hamzah H, Tai ES, Lim SC, Mitchell P, Young TL, Aung T, Wong TY, Saw SM. Myopia-related …
Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.
PubMed ID: 23643385 Author(s): Tran-Viet KN, Powell C, Barathi VA, Klemm T, Maurer-Stroh S, Limviphuvadh V, Soler V, Ho C, Yanovitch T, Schneider G, Li YJ, Nading E, Metlapally R, Saw SM, Goh L, Rozen …
Copy number variation at chromosome 5q21.2 is associated with intraocular pressure.
PubMed ID: 23599335 Author(s): Nag A, Venturini C, Hysi PG, Arno M, Aldecoa-Otalora Astarloa E, Macgregor S, Hewitt AW, Young TL, Mitchell P, Viswanathan AC, Mackey DA, Hammond CJ. Copy number variation at chromosome 5q21.2 …
Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis.
PubMed ID: 23349227 Author(s): Soler VJ, Tran-Viet KN, Galiacy SD, Limviphuvadh V, Klemm TP, St Germain E, Fournié PR, Guillaud C, Maurer-Stroh S, Hawthorne F, Suarez C, Kantelip B, Afshari NA, Creveaux I, Luo X, …
Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.
PubMed ID: 23422819 Author(s): Hawthorne F, Feng S, Metlapally R, Li YJ, Tran-Viet KN, Guggenheim JA, Malecaze F, Calvas P, Rosenberg T, Mackey DA, Venturini C, Hysi PG, Hammond CJ, Young TL. Association mapping of …