Publicacións nas que colabora con Mario Páramo Fernández (18)

2021

  1. 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

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 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

  3. The role of emotion dysregulation in Conversion Disorder

    Actas Espanolas de Psiquiatria, Vol. 46, Núm. 3, pp. 92-103

2016

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

    Reviews in the Neurosciences, Vol. 27, Núm. 4, pp. 385-395

  2. Excitatory and inhibitory conversive experiences: Neurobiological features involving positive and negative conversion symptoms

    Reviews in the Neurosciences, Vol. 27, Núm. 1, pp. 101-110

  3. 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

2010

  1. Testing the antagonistic pleiotropy model of schizophrenia susceptibility by analysis of DAOA, PPP1R1B, and APOL1 genes

    Psychiatry Research, Vol. 179, Núm. 2, pp. 126-129

2007

  1. Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population

    Schizophrenia Research, Vol. 90, Núm. 1-3, pp. 123-129