F. Gallastegui

Partial 7q11.23 deletions further implicate <i>GTF2I</i> and <i>GTF2IRD1</i> as the main genes responsible for the Williams–Beuren syndrome neurocognitive profile

Anna Antonell, Miguel Del Campo, Luis F. Magano et al. · Journal of Medical Genetics · 2009 · 160 citations

Life Sciences, Genetics, Molecular Genetics +15

Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

Ivon Cuscó, Aida Medrano, Blanca Gener et al. · Human Molecular Genetics · 2009 · 115 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC

Claudio Toma, Amaia Hervás, Noemí Balmaña et al. · The World Journal of Biological Psychiatry · 2012 · 43 citations · Full text

Life Sciences, Genetics, Neuroscience +14

Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology

D. Pérez-García, Roser Granero, F. Gallastegui et al. · Research in Developmental Disabilities · 2011 · 23 citations

Life Sciences, Genetics, Psychiatry +17

Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis

Olaya Villa, Miguel Del Campo, Marta Salido et al. · American Journal of Medical Genetics Part A · 2007 · 17 citations

Life Sciences, Genetics, Molecular Genetics +17