Lista de obras - Javier Costas - Dominio Público Uruguay

A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia

artículo científico publicado en 2008

A genomic approach to alcoholism

artículo científico publicado en 2015

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4.

artículo científico publicado en 2013

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.

artículo científico publicado en 2015

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

article by Noa Carrera et al published January 2012 in Biological Psychiatry

Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women

artículo científico publicado en 2010

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

artículo científico publicado en 2019

Clock gene polygenic risk score and seasonality in major depressive disorder and bipolar disorder

artículo científico publicado en 2020

Comment on “Current understanding of ZIP and ZnT zinc transporters in human health and diseases”

article

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Coping strategies and postpartum depressive symptoms: A structural equation modelling approach

artículo científico publicado en 2015

Coping strategies for postpartum depression: a multi-centric study of 1626 women.

artículo científico publicado en 2015

Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility

artículo científico publicado en 2015

Discoidin domain receptor 1 gene variants are associated with decreased white matter fractional anisotropy and decreased processing speed in schizophrenia

article

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach

article

Enrichment of rare genetic variants in astrocyte gene enriched co-expression modules altered in postmortem brain samples of schizophrenia

article

Evidence of association of the DISC1 interactome gene set with schizophrenia from GWAS

artículo científico publicado en 2019

Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae

artículo científico publicado en 2011

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

artículo científico publicado en 2016

FKBP5 polymorphisms and hypothalamic-pituitary-adrenal axis negative feedback in major depression and obsessive-compulsive disorder

scientific article published on 09 August 2018

Factor Structure of the Spanish Version of the Edinburgh Postnatal Depression Scale

article

GDF: Dealing with High-throughput Genotyping Multiplatform Data for Medical and Population Genetic Applications

article published in 2012

Generalized lattice graphs for 2D-visualization of biological information

artículo científico publicado en 2009

Genetic epistasis in female suicide attempters.

artículo científico publicado en 2012

Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis.

artículo científico publicado en 2008

Genome sequence of Aedes aegypti, a major arbovirus vector

artículo científico publicado en 2007

Genome wide analysis of rare copy number variations in alcohol abuse or dependence

Grandmaternal Diethylstilbesterol and Attention-Deficit/Hyperactivity Disorder in Children

scientific article published on 01 December 2018

Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis

artículo científico publicado en 2010

Identification of genes carrying rare variants of moderate to large effect in schizophrenia: A replication study.

artículo científico publicado en 2017

Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment

artículo científico publicado en 2009

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.

artículo científico publicado en 2017

Identification of relevant hub genes for early intervention at gene coexpression modules with altered predicted expression in schizophrenia

artículo científico publicado en 2019

Interaction between COMT haplotypes and cannabis in schizophrenia: A case-only study in two samples from Spain

article

Interaction between the functional SNP rs2070951 in NR3C2 gene and high levels of plasma corticotropin-releasing hormone associates to postpartum depression

artículo científico publicado en 2019

Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia

artículo científico publicado en 2014

Mood changes after delivery: role of the serotonin transporter gene

artículo científico publicado en 2008

No evidence that major mtDNA European haplogroups confer risk to schizophrenia

article

Nucleotide variation in central nervous system genes among male suicide attempters

artículo científico publicado en 2010

Potential involvement of serotonin receptor genes with age of onset and gender in schizophrenia: A preliminary study in a Spanish sample

article

Relationships between substance abuse/dependence and psychiatric disorders based on polygenic scores

scientific article published on 19 July 2018

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

artículo científico publicado en 2014

Research letter: is neuroticism a risk factor for postpartum depression?

artículo científico publicado en 2012

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.

artículo científico publicado en 2015

Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.

artículo científico publicado en 2013

Sequencing of Culex quinquefasciatus establishes a platform for mosquito comparative genomics

artículo científico publicado en 2010

Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.

artículo científico publicado en 2016

The discoidin domain receptor 1 gene has a functional A2RE sequence

artículo científico publicado en 2011

The highly pleiotropic gene SLC39A8 as an opportunity to gain insight into the molecular pathogenesis of schizophrenia

artículo científico publicado en 2017

The role of SHANK2 rare variants in schizophrenia susceptibility

artículo científico publicado en 2015

The role of personality dimensions, depressive symptoms and other psychosocial variables in predicting postpartum suicidal ideation: a cohort study

artículo científico publicado en 2019

Lista de obras de Javier Costas

A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia

A genomic approach to alcoholism

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4.

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

Clock gene polygenic risk score and seasonality in major depressive disorder and bipolar disorder

Comment on “Current understanding of ZIP and ZnT zinc transporters in human health and diseases”

Common variant at 16p11.2 conferring risk of psychosis.

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Common variants conferring risk of schizophrenia

Coping strategies and postpartum depressive symptoms: A structural equation modelling approach

Coping strategies for postpartum depression: a multi-centric study of 1626 women.

Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility

Discoidin domain receptor 1 gene variants are associated with decreased white matter fractional anisotropy and decreased processing speed in schizophrenia

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach

Enrichment of rare genetic variants in astrocyte gene enriched co-expression modules altered in postmortem brain samples of schizophrenia

Evidence of association of the DISC1 interactome gene set with schizophrenia from GWAS

Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

FKBP5 polymorphisms and hypothalamic-pituitary-adrenal axis negative feedback in major depression and obsessive-compulsive disorder

Factor Structure of the Spanish Version of the Edinburgh Postnatal Depression Scale

GDF: Dealing with High-throughput Genotyping Multiplatform Data for Medical and Population Genetic Applications

Generalized lattice graphs for 2D-visualization of biological information

Genetic epistasis in female suicide attempters.

Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis.

Genome sequence of Aedes aegypti, a major arbovirus vector

Genome wide analysis of rare copy number variations in alcohol abuse or dependence

Grandmaternal Diethylstilbesterol and Attention-Deficit/Hyperactivity Disorder in Children

Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis

Identification of genes carrying rare variants of moderate to large effect in schizophrenia: A replication study.

Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.

Identification of relevant hub genes for early intervention at gene coexpression modules with altered predicted expression in schizophrenia

Interaction between COMT haplotypes and cannabis in schizophrenia: A case-only study in two samples from Spain

Interaction between the functional SNP rs2070951 in NR3C2 gene and high levels of plasma corticotropin-releasing hormone associates to postpartum depression

Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia

Mood changes after delivery: role of the serotonin transporter gene

No evidence that major mtDNA European haplogroups confer risk to schizophrenia

Nucleotide variation in central nervous system genes among male suicide attempters

Potential involvement of serotonin receptor genes with age of onset and gender in schizophrenia: A preliminary study in a Spanish sample

Relationships between substance abuse/dependence and psychiatric disorders based on polygenic scores

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

Research letter: is neuroticism a risk factor for postpartum depression?

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.

Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.

Sequencing of Culex quinquefasciatus establishes a platform for mosquito comparative genomics

Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.

The discoidin domain receptor 1 gene has a functional A2RE sequence

The highly pleiotropic gene SLC39A8 as an opportunity to gain insight into the molecular pathogenesis of schizophrenia

The role of SHANK2 rare variants in schizophrenia susceptibility

The role of personality dimensions, depressive symptoms and other psychosocial variables in predicting postpartum suicidal ideation: a cohort study