Publicaciones en las que colabora con Mario Páramo Fernández (21)

2024

  1. Brief psychological intervention for suicide prevention based on problem-solving applied in different formats to people over 50 years old: protocol for a randomized controlled trial

    BMC Psychiatry, Vol. 24, Núm. 1

2022

  1. A polygenic approach to the association between smoking and schizophrenia

    Addiction Biology, Vol. 27, Núm. 1

  2. Association between psychiatric hospitalizations of patients with schizophrenia and polygenic risk scores based on genes with altered expression by antipsychotics

    Acta Psychiatrica Scandinavica, Vol. 146, Núm. 2, pp. 139-150

2021

  1. Epidemiological characteristics and hospitalization trajectories prior to suicide in Galicia between 2013 and 2016

    Revista de Psiquiatria y Salud Mental

  2. Genetic predisposition to alcohol dependence: The combined role of polygenic risk to general psychopathology and to high alcohol consumption

    Drug and Alcohol Dependence, Vol. 221

2020

  1. Identification of relevant hub genes for early intervention at gene coexpression modules with altered predicted expression in schizophrenia

    Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 98

2018

  1. Genome wide analysis of rare copy number variations in alcohol abuse or dependence

    Journal of Psychiatric Research, Vol. 103, pp. 212-218

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

    Schizophrenia Research

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

    European Archives of Psychiatry and Clinical Neuroscience, Vol. 268, Núm. 6, pp. 585-592

2016

  1. Guía de práctica clínica para el tratamiento de la patología dual en población adulta

    Adicciones: Revista de socidrogalcohol, Vol. 28, Núm. 1, pp. 3-5

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

    Schizophrenia Research, Vol. 174, Núm. 1-3, pp. 10-16

2015

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

    Clinica Chimica Acta, Vol. 445, pp. 34-40

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

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 168, Núm. 7, pp. 528-535

  3. 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

    Journal of Psychiatric Research, Vol. 66-67, pp. 38-44

2014

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

    Psychiatry Research

2013

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

    Annals of Human Genetics, Vol. 77, Núm. 6, pp. 504-512

2012

  1. Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

    Biological Psychiatry, Vol. 71, Núm. 2, pp. 169-177

  2. No evidence that major mtDNA European haplogroups confer risk to schizophrenia

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 159 B, Núm. 4, pp. 414-421

2011

  1. Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: New data and meta-analysis

    Journal of Psychiatric Research, Vol. 45, Núm. 1, pp. 7-14

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

    Schizophrenia Research, Vol. 127, Núm. 1-3, pp. 22-27