Fundación Pública Galega de Medicina Xenómica
Centro de investigación
Publicacións nas que colabora con Mario Páramo Fernández (7)
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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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
2016
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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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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
2007
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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