Genetics of Craniosynostosis: Genes, Syndromes, Mutations and Genotype-Phenotype CorrelationsMaria Rita Passos‐Bueno, Erika Yeh, Roberto D. Fanganiello et al.|Frontiers of oral physiology/Frontiers of oral biology|2008Cited by 161
Apert p.Ser252Trp Mutation in FGFR2 Alters Osteogenic Potential and Gene Expression of Cranial Periosteal CellsRoberto D. Fanganiello, Maria Rita Passos‐Bueno, Eduardo M. Reis et al.|Molecular Medicine|2007Cited by 39
Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert SyndromeErika Yeh, Maria Rita Passos‐Bueno, G.H. Holmes et al.|PLoS ONE|2013Cited by 20
FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in FibroblastsErika Yeh, Maria Rita Passos‐Bueno, Nivaldo Alonso et al.|Stem Cell Reviews and Reports|2011Cited by 16
Cell Type-Dependent Nonspecific Fibroblast Growth Factor Signaling in Apert SyndromeErika Yeh, Maria Rita Passos‐Bueno, Rodrigo Atique et al.|Stem Cells and Development|2016Cited by 5