Lista de obras -

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4.

artículo científico publicado en 2013

Ageing-friendly cities for assessing older adults' decline: IoT-based system for continuous monitoring of frailty risks using smart city infrastructure

scientific article published on 21 June 2019

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.

artículo científico publicado en 2015

Clinical guideline for the treatment of dual pathology in the adult population

artículo científico publicado en 2016

Clinical picture of a patient with a novel PSEN1 mutation (L424V).

artículo científico publicado en 2008

Cognitive behavioral intervention via a smartphone app for non-professional caregivers with depressive symptoms: study protocol for a randomized controlled trial

artículo científico publicado en 2018

Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility

artículo científico publicado en 2015

Emotion regulation strategies in trauma-related disorders: pathways linking neurobiology and clinical manifestations.

artículo científico publicado en 2016

Excitatory and inhibitory conversive experiences: neurobiological features involving positive and negative conversion symptoms

artículo científico

Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths

scientific article published on 18 July 2019

Identification of genes carrying rare variants of moderate to large effect in schizophrenia: A replication study.

artículo científico publicado en 2017

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.

artículo científico publicado en 2017

Interaction between COMT haplotypes and cannabis in schizophrenia: A case-only study in two samples from Spain

article

No evidence that major mtDNA European haplogroups confer risk to schizophrenia

article

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.

artículo científico publicado en 2015

Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.

artículo científico publicado en 2013

S187. SEARCHING FOR BRAIN CO-EXPRESSION MODULES THAT CONTRIBUTE DISPROPORTIONATELY TO THE COMMON POLYGENIC RISK FOR SCHIZOPHRENIA.

artículo científico publicado en 2018

Suicide mortality trends in Galicia, Spain and their relationship with economic indicators

artículo científico publicado en 2015

Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.

artículo científico publicado en 2016

The role of emotion dysregulation in Conversion Disorder

artículo científico publicado en 2018

[A preliminary study of low dosage zuclopenthixol depot in Alzheimer's disease]

scientific article published on 01 March 1996

[Clinical features of familial Creutzfeldt-Jakob disease and the E200K mutation in Spain]

scientific article published on 01 February 2007

[Late-onset bipolar disorder following right thalamic injury]

scientific article published on 01 July 2009

Lista de obras de

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4.

Ageing-friendly cities for assessing older adults' decline: IoT-based system for continuous monitoring of frailty risks using smart city infrastructure

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.

Clinical guideline for the treatment of dual pathology in the adult population

Clinical picture of a patient with a novel PSEN1 mutation (L424V).

Cognitive behavioral intervention via a smartphone app for non-professional caregivers with depressive symptoms: study protocol for a randomized controlled trial

Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility

Emotion regulation strategies in trauma-related disorders: pathways linking neurobiology and clinical manifestations.

Excitatory and inhibitory conversive experiences: neurobiological features involving positive and negative conversion symptoms

Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths

Identification of genes carrying rare variants of moderate to large effect in schizophrenia: A replication study.

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.

Interaction between COMT haplotypes and cannabis in schizophrenia: A case-only study in two samples from Spain

No evidence that major mtDNA European haplogroups confer risk to schizophrenia

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.

Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.

S187. SEARCHING FOR BRAIN CO-EXPRESSION MODULES THAT CONTRIBUTE DISPROPORTIONATELY TO THE COMMON POLYGENIC RISK FOR SCHIZOPHRENIA.

Suicide mortality trends in Galicia, Spain and their relationship with economic indicators

Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.

The role of emotion dysregulation in Conversion Disorder

[A preliminary study of low dosage zuclopenthixol depot in Alzheimer's disease]

[Clinical features of familial Creutzfeldt-Jakob disease and the E200K mutation in Spain]

[Late-onset bipolar disorder following right thalamic injury]