Bàrbara Torrico

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

Claudio Toma, Bàrbara Torrico, Amaia Hervás et al. · Molecular Psychiatry · 2013 · 124 citations · Full text

Heterozygous Truncating Mutations, Mendelian Disorder, Syndromic Autism +11

Cerebral Folate Deficiency Syndromes in Childhood

Belén Pérez‐Dueñas, Aída Ormazábal, Claudio Toma et al. · Archives of Neurology · 2011 · 67 citations

Analysis of two language-related genes in autism

Claudio Toma, Amaia Hervás, Bàrbara Torrico et al. · Psychiatric Genetics · 2012 · 58 citations · Full text

Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

Bàrbara Torrico, Noèlia Fernàndez‐Castillo, Amaia Hervás et al. · European Journal of Human Genetics · 2015 · 42 citations · Full text

Neurodevelopmental Disorders, Rare Variants, Syndromic Autism +9

Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures

Nina Roth Mota, Geert Poelmans, Marieke Klein et al. · Neuropsychopharmacology · 2020 · 39 citations · Full text