A Genome-Wide Association Study of Optic Disc Parameters

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

(2009) Manir Ali et al.   AMERICAN JOURNAL OF HUMAN GENETICS

GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data

(2009) Karol Estrada et al.   BIOINFORMATICS

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

(2009) Mehrnaz Narooie-Nejad et al.   HUMAN MOLECULAR GENETICS

Primary Open-Angle Glaucoma

(2009) Young H. Kwon et al.   NEW ENGLAND JOURNAL OF MEDICINE

Zeb1 links epithelial-mesenchymal transition and cellular senescence

(2008) Y. Liu et al.   DEVELOPMENT

SIX1mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR

(2008) Amit Kochhar et al.   HUMAN MUTATION

A Comprehensive Negative Regulatory Program Controlled by Brn3b to Ensure Ganglion Cell Specification from Multipotential Retinal Precursors

(2008) F. Qiu et al.   JOURNAL OF NEUROSCIENCE

Optic disc size in a population-based study in central India: the Central India Eye and Medical Study (CIEMS)

(2007) Vinay Nangia et al.   ACTA OPHTHALMOLOGICA