Renan Paulo Martin

Relative frequency of inherited retinal dystrophies in Brazil

Fabiana Louise Motta, Renan Paulo Martin, Rafael Filippelli-Silva et al. · Scientific Reports · 2018 · 63 citations · Full text

IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease

Mara Cananzi, Elizabeth Wohler, Antonio Marzollo et al. · Human Genetics · 2021 · 42 citations · Full text

Inflammation, Ifih1 Loss-of-function Variants, Autoimmune Disease +8

Variant‐level matching for diagnosis and discovery: Challenges and opportunities

Eliete da S. Rodrigues, Sean Griffith, Renan Paulo Martin et al. · Human Mutation · 2022 · 41 citations · Full text

Engineering, Genetics, Databases +18

Angiotensin II Binding to Angiotensin I–Converting Enzyme Triggers Calcium Signaling

Paola Bianchi Guimarães, Érika Costa de Alvarenga, Paula D. Siqueira et al. · Hypertension · 2011 · 34 citations · Full text

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 · 33 citations · Full text