SNL-Lennart Levi Laboratory
SNL Laboratory
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublications in collaboration with researchers from Complexo Hospitalario Universitario de Santiago (24)
2024
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Biocompatibility Testing of UV-Curable Polydimethylsiloxane for Human Umbilical Vein Endothelial Cell Culture on-a-Chip
ACS Omega, Vol. 9, Núm. 28, pp. 30281-30293
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Community Activities in Primary Care: A Literature Review
Journal of Primary Care and Community Health, Vol. 15
2021
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Attitudes and intentions toward COVID-19 vaccination among Spanish adults: A descriptive cross-sectional study
Vaccines, Vol. 9, Núm. 10
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Soluble angiotensin-converting enzyme levels in heart failure or acute coronary syndrome: revisiting its modulation and prognosis value
Journal of Molecular Medicine, Vol. 99, Núm. 12, pp. 1741-1753
2020
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Diagnostic accuracy of IL1β in saliva: The development of predictive models for estimating the probability of the occurrence of periodontitis in non-smokers and smokers
Journal of Clinical Periodontology, Vol. 47, Núm. 6, pp. 702-714
2019
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Inflammatory effects of in vivo glycated albumin from cardiovascular patients
Biomedicine and Pharmacotherapy, Vol. 113
2018
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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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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
2014
2013
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Deterioro cognitivo y funcionalidad en la esquizofrenia
Revista gallega de psiquiatría y neurociencias, Núm. 12, pp. 45-51
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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
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Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia
Biological Psychiatry, Vol. 71, Núm. 2, pp. 169-177
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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
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Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: New data and meta-analysis
Journal of Psychiatric Research, Vol. 45, Núm. 1, pp. 7-14
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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