Kátia M. Rocha

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies

Rocío Acuña‐Hidalgo, Pelagia Derizioti, Marloes Steehouwer et al. · PLoS Genetics · 2017 · 68 citations · Full text

Setbp1 Stability, Mixed-phenotype Acute Leukemia, Genetics +16

Genetic contribution for non‐syndromic cleft lip with or without cleft palate (NS CL/P) in different regions of Brazil and implications for association studies

Luciano Abreu Brito, Lucas Alvizi Cruz, Kátia M. Rocha et al. · American Journal of Medical Genetics Part A · 2011 · 53 citations

Schinzel–Giedion syndrome in two Brazilian patients: Report of a novel mutation in <i>SETBP1</i> and literature review of the clinical features

Ellaine Dóris Fernandes Carvalho, Rachel Sayuri Honjo, Monize Lazar Magalhães et al. · American Journal of Medical Genetics Part A · 2015 · 51 citations

IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population

Luciano Abreu Brito, Camila Fernandes Silva Bassi, Cibele Masotti et al. · American Journal of Medical Genetics Part A · 2012 · 48 citations

Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil

Luciano Abreu Brito, Lívia Máris Ribeiro Paranaiba, Camila Fernandes Silva Bassi et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2012 · 47 citations