Mario
Páramo Fernández
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublicacións en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (31)
2023
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Efficacy of a Cognitive Behavioral Intervention for the Prevention of Depression in Nonprofessional Caregivers Administered through a Smartphone App: A Randomized Controlled Trial
Journal of Clinical Medicine, Vol. 12, Núm. 18
2022
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A polygenic approach to the association between smoking and schizophrenia
Addiction Biology, Vol. 27, Núm. 1
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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
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Determination of antidepressants and benzodiazepines in paired hair and nail samples
Forensic Science International, Vol. 326
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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
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Predictors of persistence in patients with schizophrenia treated with aripiprazole once-monthly long-acting injection in the Spanish clinical practice: a retrospective, observational study
European psychiatry : the journal of the Association of European Psychiatrists, Vol. 64, Núm. 1, pp. e40
2020
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Determination of antipsychotic drugs in nails and hair by liquid chromatography tandem mass spectrometry and evaluation of their incorporation into keratinized matrices
Journal of Pharmaceutical and Biomedical Analysis, Vol. 189
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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
2019
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Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths
Forensic Science International: Genetics, Vol. 42, pp. 203-212
2018
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Genome wide analysis of rare copy number variations in alcohol abuse or dependence
Journal of Psychiatric Research, Vol. 103, pp. 212-218
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Identification of genes carrying rare variants of moderate to large effect in schizophrenia: A replication study
Schizophrenia Research
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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
2017
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An LC-MS/MS methodological approach to the analysis of hair for amphetamine-type-stimulant (ATS) drugs, including selected synthetic cathinones and piperazines
Drug Testing and Analysis, Vol. 9, Núm. 1, pp. 96-105
2016
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Emotion regulation strategies in trauma-related disorders: Pathways linking neurobiology and clinical manifestations
Reviews in the Neurosciences, Vol. 27, Núm. 4, pp. 385-395
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Excitatory and inhibitory conversive experiences: Neurobiological features involving positive and negative conversion symptoms
Reviews in the Neurosciences, Vol. 27, Núm. 1, pp. 101-110
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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
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An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders
Clinica Chimica Acta, Vol. 445, pp. 34-40
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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
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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