Bruna Lucheze Freire

Multigene Sequencing Analysis of Children Born Small for Gestational Age With Isolated Short Stature

Bruna Lucheze Freire, Thaís Kataoka Homma, Mariana F.A. Funari et al. · The Journal of Clinical Endocrinology & Metabolism · 2019 · 84 citations · Full text

SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling

Yuh‐Charn Lin, Marcello Niceta, Valentina Muto et al. · The American Journal of Human Genetics · 2020 · 64 citations · Full text

Developmental Anomaly, Sclerostin, Developmental Biology +9

Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing

Thaís Kataoka Homma, Bruna Lucheze Freire, Rachel Sayuri Honjo Kawahira et al. · The Journal of Pediatrics · 2019 · 62 citations

Down Syndrome, Developmental Anomaly, Developmental Biology +11

Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause

Thaís Kataoka Homma, Ana Cristina Victorino Krepischi, Tatiane Katsue Furuya et al. · Hormone Research in Paediatrics · 2017 · 40 citations · Full text

Two Patients with Severe Short Stature due to a <b><i>FBN1</i></b> Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia

Christiaan de Bruin, Courtney Finlayson, Mariana F.A. Funari et al. · Hormone Research in Paediatrics · 2016 · 26 citations · Full text