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Javier
Costas Costas
Publicacións nas que colabora con Javier Costas Costas (46)
2023
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Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study
Schizophrenia Bulletin, Vol. 49, Núm. 5, pp. 1269-1280
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The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study
Social Psychiatry and Psychiatric Epidemiology, Vol. 58, Núm. 10, pp. 1573-1580
2021
2020
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Interaction between the functional SNP rs2070951 in NR3C2 gene and high levels of plasma corticotropin-releasing hormone associates to postpartum depression
Archives of Women's Mental Health, Vol. 23, Núm. 3, pp. 413-420
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Premorbid Adjustment and IQ in Patients with First-Episode Psychosis: A Multisite Case-Control Study of Their Relationship with Cannabis Use
Schizophrenia Bulletin, Vol. 46, Núm. 3, pp. 517-529
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Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes
Translational Psychiatry, Vol. 10, Núm. 1
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The EUropean Network of National Schizophrenia Networks Studying Gene–Environment Interactions (EU-GEI): Incidence and First-Episode Case–Control Programme
Social Psychiatry and Psychiatric Epidemiology, Vol. 55, Núm. 5, pp. 645-657
2019
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Assessing cross-national invariance of the Community Assessment of Psychic Experiences (CAPE)
Psychological Medicine, Vol. 49, Núm. 15, pp. 2600-2607
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BDNF genetic variants and methylation: effects on cognition in major depressive disorder
Translational Psychiatry, Vol. 9, Núm. 1
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Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene–environment interaction approach
Translational Psychiatry, Vol. 9, Núm. 1
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The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study
The Lancet Psychiatry, Vol. 6, Núm. 5, pp. 427-436
2018
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FKBP5 polymorphisms and hypothalamic-pituitary-adrenal axis negative feedback in major depression and obsessive-compulsive disorder
Journal of Psychiatric Research, Vol. 104, pp. 227-234
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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
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Treated incidence of psychotic disorders in the multinational EU-GEI study
JAMA Psychiatry, Vol. 75, Núm. 1, pp. 36-46
2016
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Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia
Translational Psychiatry, Vol. 6, Núm. 3
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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
2014
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Common variant at 16p11.2 conferring risk of psychosis
Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114