Renata Moldenhauer Minillo

Molecular analysis of the CTSK gene in a cohort of 33 Brazilian families with pycnodysostosis from a cluster in a Brazilian Northeast region

Thaís Fenz Araujo, Erlane Marques Ribeiro, Anderson Pontes Arruda et al. · European journal of medical research · 2016 · 23 citations · Full text

Novel Deletion of <b><i>SERPINF1</i></b> Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families

Renata Moldenhauer Minillo, Nara Sobreira, Maria de Fátima de Faria Soares et al. · Molecular Syndromology · 2014 · 22 citations · Full text

Novel Deletion, Oi Type Vi, Genetics +18

The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients

Jarbas Maciel de Oliveira, Nuria Bengala Zurro, Antônio Victor Campos Coelho et al. · European Journal of Human Genetics · 2022 · 17 citations · Full text

Epidemiology, Cancer Risk, Genetic Disorder +7

Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes

Caio Robledo D’ Angioli Costa Quaio, Antônio Victor Campos Coelho, Livia Maria Silva Moura et al. · Frontiers in Genetics · 2022 · 10 citations · Full text