Carla S. D’Angelo

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

Two New Cases of 1p21.3 Deletions and an Unbalanced Translocation t(8;12) among Individuals with Syndromic Obesity

Carla S. D’Angelo, Mauren F. Moller dos Santos, Luis Garcia Alonso et al. · Molecular Syndromology · 2015 · 57 citations · Full text

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

High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation

Fernanda Sarquis Jehee, Ana Cristina Victorino Krepischi, Kátia M. Rocha et al. · Journal of Medical Genetics · 2008 · 41 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +13

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