Mariana Vallim Salles

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

Mubeen Khan, Stéphanie S. Cornelis, Laura Whelan et al. · Genetics in Medicine · 2020 · 142 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Relative frequency of inherited retinal dystrophies in Brazil

Fabiana Louise Motta, Renan Paulo Martin, Rafael Filippelli-Silva et al. · Scientific Reports · 2018 · 67 citations · Full text

Life Sciences, Genetics, Ophthalmology +17

The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes

Fabiana Louise Motta, Mariana Vallim Salles, Kárita Antunes Costa et al. · Scientific Reports · 2017 · 35 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Variants in the <i>ABCA4</i> gene in a Brazilian population with Stargardt disease.

Mariana Vallim Salles, Fabiana Louise Motta, Renan Paulo Martin et al. · PubMed · 2018 · 22 citations

Life Sciences, Genetics, Ophthalmology +17

Gene panel sequencing in Brazilian patients with retinitis pigmentosa

Kárita Antunes Costa, Mariana Vallim Salles, Chris Whitebirch et al. · International Journal of Retina and Vitreous · 2017 · 16 citations · Full text

Life Sciences, Genetics, Ophthalmology +16