Cláudia Irene Emílio de Castro

Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems

Carla S. D’Angelo, José Albino da Paz, Chong Ae Kim et al. · European Journal of Medical Genetics · 2006 · 122 citations

Psychiatry, Genetic Disorder, Medicine +7

A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity

Monica Castro Varela, Alex Y. Simoes-Sato, Chong Ae Kim et al. · European Journal of Medical Genetics · 2006 · 85 citations

New Case, Genetic Disorder, Genetics +10

Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity

Carla S. D’Angelo, Monica Castro Varela, Cláudia Irene Emílio de Castro et al. · Molecular Cytogenetics · 2018 · 48 citations · Full text

Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia

Carla S. D’Angelo, Ilana Kohl, Monica Castro Varela et al. · American Journal of Medical Genetics Part A · 2009 · 40 citations

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants

Carla S. D’Angelo, Ilana Kohl, Monica Castro Varela et al. · American Journal of Medical Genetics Part A · 2013 · 29 citations