Natália D. Linhares

A human immunodeficiency syndrome caused by mutations in CARMIL2

Tilmann Schober, Thomas Magg, Melanie Laschinger et al. · Nature Communications · 2017 · 123 citations · Full text

Genetic deletion of the alamandine receptor MRGD leads to dilated cardiomyopathy in mice

Aline C. Oliveira, Marcos Barrouin Melo, Daisy Motta‐Santos et al. · American Journal of Physiology-Heart and Circulatory Physiology · 2018 · 71 citations

Molecular Pharmacology, Cardiomyopathy, Heart Failure +14

Familial STAG2 germline mutation defines a new human cohesinopathy

Fernanda Caroline Soardi, Alice Machado-Silva, Natália D. Linhares et al. · npj Genomic Medicine · 2017 · 68 citations · Full text

Nephrotic syndrome and adrenal insufficiency caused by a variant in SGPL1

Natália D. Linhares, Rodrigo Rezende Arantes, Stanley de Almeida Araújo et al. · Clinical Kidney Journal · 2017 · 43 citations · Full text

Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene

Natália D. Linhares, Marta Svartman, Mauro Ivan Salgado et al. · Meta Gene · 2013 · 40 citations · Full text