B. Torrico

发表

Truncating Variant Burden in High Functioning Autism and Pleiotropic Effects of LRP1 Across Psychiatric Phenotypes

Janice M. Fullerton, P. Aloy, J. Fullerton, 2018, bioRxiv.

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

X. Puente, R. Valdés-Mas, M. Bayés, 2014, Molecular Psychiatry.

Analysis of two language-related genes in autism: a case–control association study of FOXP2 and CNTNAP2

M. Bayés, L. Pérez-Jurado, B. Cormand, 2013, Psychiatric genetics.

Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects.

B. Cormand, A. Ormazabal, R. Artuch, 2011, Archives of neurology.

Lack of replication of previous autism spectrum disorder GWAS hits in European populations

B. Franke, E. Bacchelli, A. Battaglia, 2017, Autism research : official journal of the International Society for Autism Research.

Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses

Janice M. Fullerton, B. Franke, C. Freitag, 2020, Journal of clinical medicine.

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

A. Battaglia, C. Freitag, E. Maestrini, 2015, European Journal of Human Genetics.

A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence

Galina A. Erikson, N. Fernàndez-Castillo, B. Cormand, 2016, Scientific Reports.

Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders

N. Fernàndez-Castillo, B. Cormand, A. Reif, 2020, Translational Psychiatry.

Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention

K. Lesch, O. Lao, N. Fernàndez-Castillo, 2021, Genes.

Clinical, Analytical, and Etiologic Aspects

B. Cormand, R. Artuch, B. Pérez-Dueñas, 2011 .

Common and rare variants of microRNA genes in autism spectrum disorders

B. Franke, E. Bacchelli, A. Battaglia, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes

P. Aloy, J. Fullerton, M. Bayés, 2019, Journal of Psychiatry & Neuroscience.

The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction, aggression, and related behavioural traits

R. Corominas, N. Fernàndez-Castillo, B. Cormand, 2023, medRxiv.

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

B. Franke, N. Fernàndez-Castillo, B. Cormand, 2019, bioRxiv.

Common and rare variants of microRNA genes in autism spectrum disorders

B. Franke, E. Bacchelli, A. Battaglia, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits

R. Corominas, N. Fernàndez-Castillo, B. Cormand, 2023, Frontiers in psychiatry.

Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects.

B. Cormand, A. Ormazabal, R. Artuch, 2011, Archives of neurology.