CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds

Mutations in SOX2 cause anophthalmia

Judy Fantes, Nicola Ragge, Sally Ann Lynch et al. · Nature Genetics · 2003 · 538 citations · Full text

Ocular Disease, Ophthalmology, Genetics +4

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

Margit Burmeister, Jakub Novák, Mei-Ying Liang et al. · Nature Genetics · 1996 · 517 citations

Ocular Disease, Developmental Biology, Retina +7

Developmental expression of a novel murine homeobox gene (Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer

Ivy S.C Liu, Jia-de Chen, Lynda Ploder et al. · Neuron · 1994 · 385 citations

Developmental Biology, Brain Development, Neuroanatomy +10

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

E. Ferda Perçin, Horsford Dj, A.J. Rutherford et al. · Nature Genetics · 2000 · 286 citations

Ocular Disease, Developmental Biology, Retina +8

National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology

Daniel R. Morrison · Journal of Medical Genetics · 2002 · 277 citations · Full text