Marina Garcia Garrido

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Susanne Kohl, Ditta Zobor, Wei‐Chieh Chiang et al. · Nature Genetics · 2015 · 216 citations

Life Sciences, Genetics, Neuroscience +14

Gene therapy restores vision and delays degeneration in the CNGB1-/- mouse model of retinitis pigmentosa

Susanne Koch, Vithiyanjali Sothilingam, Marina Garcia Garrido et al. · Human Molecular Genetics · 2012 · 102 citations · Full text

Medicine, Genetics, Ophthalmology +17

Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene

C. Henrique Alves, Alicia Sanz Sanz, Bo-Kyung Park et al. · Human Molecular Genetics · 2012 · 85 citations · Full text

Medicine, Genetics, Ophthalmology +17

Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis

Lucie P. Pellissier, C. Henrique Alves, Peter M. J. Quinn et al. · PLoS Genetics · 2013 · 73 citations · Full text

Life Sciences, Developmental Biology, Genetics +17

Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2

Dagmar Knoflach, Vasily Kerov, Simone B. Sartori et al. · Channels · 2013 · 68 citations · Full text

Life Sciences, Genetics, Neuroscience +15