Víctor Pérez Sola

Dr. Víctor Pérez Sola


Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 1994 in Archives of General Psychiatry
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Journal Article
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FAFrancesc Artigas
Francesc Artigas
VSVíctor Pérez Sola
Víctor Pérez Sola
EAEnrique Alvarez
Enrique Alvarez
From JAMA Psychiatry — Pindolol Induces a Rapid Improvement of Depressed Patients Treated With Serotonin Reuptake Inhibitors

13 January 2010 in Neuropsychopharmacology
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Journal Article
Open access
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VSVirginia Soria
Virginia Soria
EMErika Martínez-Amorós
Erika Martínez-Amorós
GEGeòrgia Escaramís
Geòrgia Escaramís
JVJoaquín Valero
Joaquín Valero
RPRosario Pérez-Egea
Rosario Pérez-Egea
MUMIKEL URRETAVIZCAYA
MIKEL URRETAVIZCAYA
Disruptions in circadian rhythms have been described in mood disorders (MD), but the involvement of genetic variation in genes pertaining to the molecular circadian machinery in the susceptibility to MD has not been conclusively determined. We examined 209 single-nucleotide polymorphisms (SNPs) covering 19 circadian genes (ADCYAP1, ARNTL, ARNTL2, BHLHB2, BHLHB3, CLOCK, CRY1, CRY2, CSNK1E, DBP, NPAS2, NR1D1, PER1, PER2, PER3, RORA, TIMELESS, VIP, and VIPR2) in a sample of 534 MD patients (335 with unipolar major mood depression (MDD) and 199 with bipolar disorder (BD)) and 440 community-based screened controls. Nominally, statistically significant associations were found in 15 circadian genes. The gene-wide test, corrected for the number of SNPs analyzed in each gene, identified significant associations in CRY1 (rs2287161), NPAS2 (rs11123857), and VIPR2 (rs885861) genes with the combined MD sample. In the MDD subsample, the same SNPs in CRY1 and NPAS2 of the combined sample remained associated, whereas in the BD subsample CLOCK (rs10462028) and VIP (rs17083008) were specifically associated. The association with an SNP located 3′ near CRY1 gene in MDD remained statistically significant after permutation correction at experiment level (p=0.007). Significant additive effects were found between the SNPs that were statistically significant at the gene-wide level. We also found evidence of associations between two-marker haplotypes in CRY1 and NPAS2 genes and MD. Our data support the contribution of the circadian system to the genetic susceptibility to MD and suggest that different circadian genes may have specific effects on MD polarity.

1 May 1997 in The Lancet
Verified
Journal Article
Closed access
VSVíctor Pérez Sola
Víctor Pérez Sola
IGInmaculada Gilaberte
Inmaculada Gilaberte
DFDouglas Faries
Douglas Faries
EAEnrique Alvarez
Enrique Alvarez
FAFrancesc Artigas
Francesc Artigas

1 May 2009 in Behaviour Research and Therapy
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Journal Article
Closed access
JSJoaquim Soler
Joaquim Soler
JPJuan Carlos Pascual
Juan Carlos Pascual
TTThaïs Tiana
Thaïs Tiana
ACAnabel Cebrià
Anabel Cebrià
JBJudith Barrachina
Judith Barrachina
VSVíctor Pérez Sola
Víctor Pérez Sola

18 July 2011 in International Journal of Neuropsychopharmacology
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Journal Article
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EAEnrique Alvarez
Enrique Alvarez
VSVíctor Pérez Sola
Víctor Pérez Sola
MDMarianne Dragheim
Marianne Dragheim
HLHenrik Loft
Henrik Loft
FAFrancesc Artigas
Francesc Artigas
The efficacy, safety, and tolerability of Lu AA21004 vs. placebo using venlafaxine XR as active reference in patients with DSM-IV-TR major depressive

22 July 2011 in International Journal of Neuropsychopharmacology
Verified
Journal Article
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DPDolors Puigdemont
Dolors Puigdemont
RPRosario Pérez-Egea
Rosario Pérez-Egea
MPMaria J. Portella
Maria J. Portella
JMJoan Molet
Joan Molet
JDJavier de Diego-Adeliño
Javier de Diego-Adeliño
VSVíctor Pérez Sola
Víctor Pérez Sola
Deep brain stimulation (DBS) is currently tested as an experimental therapy for patients with treatment-resistant depression (TRD). Here we report on