List of works - Thomas V. Fernandez

Apolipoprotein E alleles in childhood-onset schizophrenia

scientific article published on 01 April 1999

Childhood-onset schizophrenia: progressive brain changes during adolescence

scientific article

Data blitz debuts at the AACAP annual meeting

scientific article

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

scientific article published in June 2008

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

scientific article

Elevated functional connectivity along a corticostriatal loop and the mechanism of auditory/verbal hallucinations in patients with schizophrenia

scientific article

Gene variants associated with antisocial behaviour: a latent variable approach.

scientific article published on 03 July 2013

Genetic susceptibility and neurotransmitters in Tourette syndrome

scientific article

Genome-wide association study of Tourette's syndrome

scientific article

L-histidine decarboxylase and Tourette's syndrome

scientific article

Lessons from childhood-onset schizophrenia

scientific article published on 01 March 2000

Leveraging aggression risk gene expression in the developing and adult human brain to guide future precision interventions

scientific article published on 12 October 2020

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.

scientific article published in November 2008

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

scientific article (publication date: June 2011)

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

scientific article published in October 2013

Premorbid speech and language impairments in childhood-onset schizophrenia: association with risk factors

scientific article

Progressive cortical change during adolescence in childhood-onset schizophrenia. A longitudinal magnetic resonance imaging study

scientific article

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

scientific article published on 14 December 2011

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

scientific article

Transcranial magnetic stimulation of Wernicke's and Right homologous sites to curtail "voices": a randomized trial

scientific article

List of works by Thomas V. Fernandez

Apolipoprotein E alleles in childhood-onset schizophrenia

Childhood-onset schizophrenia: progressive brain changes during adolescence

Data blitz debuts at the AACAP annual meeting

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

Elevated functional connectivity along a corticostriatal loop and the mechanism of auditory/verbal hallucinations in patients with schizophrenia

Gene variants associated with antisocial behaviour: a latent variable approach.

Genetic susceptibility and neurotransmitters in Tourette syndrome

Genome-wide association study of Tourette's syndrome

L-histidine decarboxylase and Tourette's syndrome

Lessons from childhood-onset schizophrenia

Leveraging aggression risk gene expression in the developing and adult human brain to guide future precision interventions

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Premorbid speech and language impairments in childhood-onset schizophrenia: association with risk factors

Progressive cortical change during adolescence in childhood-onset schizophrenia. A longitudinal magnetic resonance imaging study

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

Transcranial magnetic stimulation of Wernicke's and Right homologous sites to curtail "voices": a randomized trial