Lista de obras - Elvira Bramon - Dominio Público Uruguay

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

artículo científico publicado en 2013

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

artículo científico publicado en 2010

A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains

artículo científico

Abnormal P300 in people with high risk of developing psychosis.

artículo científico publicado en 2008

Abnormal frontoparietal synaptic gain mediating the P300 in patients with psychotic disorder and their unaffected relatives.

artículo científico publicado en 2017

Acute effects of cannabinoids on addiction endophenotypes are moderated by genes encoding the CB1 receptor and FAAH enzyme

scientific article published on 23 April 2019

Alterations in white matter evident before the onset of psychosis.

artículo científico publicado en 2012

Altered brain function directly related to structural abnormalities in people at ultra high risk of psychosis: longitudinal VBM-fMRI study

artículo científico publicado en 2010

Altered effect of dopamine transporter 3'UTR VNTR genotype on prefrontal and striatal function in schizophrenia.

artículo científico publicado en 2009

Analysis of multiple phenotypes in genome-wide genetic mapping studies

artículo científico publicado en 2013

Are auditory P300 and duration MMN heritable and putative endophenotypes of psychotic bipolar disorder? A Maudsley Bipolar Twin and Family Study

artículo científico publicado en 2009

Association between BDNF val66 met genotype and episodic memory

artículo científico publicado en 2005

Association between hippocampal volume and P300 event related potential in psychosis: support for the Kraepelinian divide

artículo científico publicado en 2011

Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating

artículo científico publicado en 2012

Association of Genetic Risks for Schizophrenia and Bipolar DisorderWith Specific and Generic Brain Structural Endophenotypes

scientific article published on 01 October 2004

Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains.

artículo científico publicado en 2017

Auditory P300 in patients with bipolar disorder and their unaffected relatives

artículo científico publicado en 2008

COMT (Val(158/108)Met) genotype moderates the impact of antipsychotic medication on verbal IQ in twins with schizophrenia

artículo científico publicado en 2011

COMT gene polymorphism and corpus callosum morphometry in preterm born adults

artículo científico publicado en 2010

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

artículo científico publicado en 2010

Cerebral metabolism in major depressive disorder: a voxel-based meta-analysis of positron emission tomography studies.

artículo científico publicado en 2014

Cognitive performance in presumed obligate carriers for psychosis

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

artículo científico publicado en 2012

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

artículo científico publicado en 2010

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

artículo científico publicado en 2009

Dermatoglyphics and Schizophrenia: a meta-analysis and investigation of the impact of obstetric complications upon a-b ridge count.

artículo científico publicado en 2005

Differential effects of DAAO on regional activation and functional connectivity in schizophrenia, bipolar disorder and controls.

artículo científico publicado en 2011

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

artículo científico publicado en 2010

Distribution of symptom dimensions across Kraepelinian divisions.

artículo científico publicado en 2006

Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis?

artículo científico publicado en 2010

Economic impact of early intervention in people at high risk of psychosis.

artículo científico publicado en 2009

Effect of D-amino acid oxidase activator (DAOA; G72) on brain function during verbal fluency

artículo científico publicado en 2011

Effect of DISC1 on the P300 waveform in psychosis

artículo científico publicado en 2011

Elevated striatal dopamine function linked to prodromal signs of schizophrenia

artículo científico publicado en 2009

Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives

scientific article published on 01 December 2019

Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene

artículo científico publicado en 2006

Epistasis between the DAT 3' UTR VNTR and the COMT Val158Met SNP on cortical function in healthy subjects and patients with schizophrenia

scholarly article

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women

artículo científico publicado en 2016

Evidence of association of KIBRA genotype with episodic memory in families of psychotic patients and controls.

artículo científico publicado en 2010

Exaggerated neural response to emotional faces in patients with bipolar disorder and their first-degree relatives

artículo científico publicado en 2010

Executive functioning in familial bipolar I disorder patients and their unaffected relatives

artículo científico publicado en 2011

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

Failure to deactivate medial prefrontal cortex in people at high risk for psychosis.

artículo científico publicado en 2015

Familial liability to schizophrenia and premorbid adjustment.

artículo científico publicado en 2007

Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: a combined twin and family study.

artículo científico publicado en 2008

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

scientific journal article

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

artículo científico publicado en 2020

Genetic modelling of childhood social development and personality in twins and siblings with schizophrenia.

artículo científico publicado en 2009

Genetic overlap between P300, P50, and duration mismatch negativity

artículo científico publicado en 2006

Genetic overlap between bipolar illness and event-related potentials.

artículo científico publicado en 2007

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genetic vulnerability to psychosis and cortical function: epistatic effects between DAAO and G72.

artículo científico publicado en 2012

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

artículo científico publicado en 2009

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Gray matter alterations related to P300 abnormalities in subjects at high risk for psychosis: longitudinal MRI-EEG study.

artículo científico publicado en 2010

Heritability and reliability of P300, P50 and duration mismatch negativity.

artículo científico publicado en 2006

Impaired prefrontal synaptic gain in people with psychosis and their relatives during the mismatch negativity.

artículo científico publicado en 2015

Increased inferior frontal activation during word generation: a marker of genetic risk for schizophrenia but not bipolar disorder?

artículo científico publicado en 2009

Insight in individuals with an At Risk Mental State.

artículo científico publicado en 2007

Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder

scientific article published on 07 October 2020

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

artículo científico publicado en 2011

Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function.

artículo científico publicado en 2012

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study.

artículo científico publicado en 2005

Is there an association between the COMT gene and P300 endophenotypes?

artículo científico publicado en 2006

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Long-term maternal recall of obstetric complications in schizophrenia research

artículo científico publicado en 2011

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Memory functioning in familial bipolar I disorder patients and their relatives.

artículo científico publicado en 2009

Meta-analysis of the P300 and P50 waveforms in schizophrenia

article

Neural correlates of executive function and working memory in the 'at-risk mental state'.

artículo científico publicado en 2009

Neural correlates of movement generation in the 'at-risk mental state'.

artículo científico publicado en 2010

Neural correlates of visuospatial working memory in the 'at-risk mental state'.

artículo científico publicado en 2010

Neuregulin-1 and the P300 waveform--a preliminary association study using a psychosis endophenotype.

artículo científico publicado en 2008

Neurodevelopmental impairment, dopamine sensitisation, and social adversity in schizophrenia

artículo científico publicado en 2002

Neuropsychological and neuroimaging underpinnings of schizoaffective disorder: a systematic review.

artículo científico publicado en 2016

No association of Disrupted-in-Schizophrenia-1 variation with prefrontal function in patients with schizophrenia and bipolar disorder.

artículo científico publicado en 2010

Obstetric complications in patients with schizophrenia and their unaffected siblings

scientific article published on 01 January 2005

Outreach and support in south London (OASIS): implementation of a clinical service for prodromal psychosis and the at risk mental state

artículo científico publicado en 2005

P300 waveform and dopamine transporter availability: a controlled EEG and SPECT study in medication-naive patients with schizophrenia and a meta-analysis

artículo científico publicado en 2013

P50 auditory evoked potential suppression in bipolar disorder patients with psychotic features and their unaffected relatives

artículo científico publicado en 2006

Patterns of deficits in brain function in bipolar disorder and schizophrenia: a cluster analytic study

artículo científico publicado en 2012

Prefrontal function at presentation directly related to clinical outcome in people at ultrahigh risk of psychosis.

artículo científico publicado en 2009

Reduced mismatch negativity predates the onset of psychosis

artículo científico publicado en 2011

Regional brain morphometry in patients with schizophrenia or bipolar disorder and their unaffected relatives

artículo científico publicado en 2006

Resting EEG in psychosis and at-risk populations--a possible endophenotype?

artículo científico publicado en 2014

Risk variant of oligodendrocyte lineage transcription factor 2 is associated with reduced white matter integrity

artículo científico publicado en 2012

Schizophrenia polygenic risk score influence on white matter microstructure

artículo científico publicado en 2019

Selective attention deficits reflect increased genetic vulnerability to schizophrenia

article published in 2008

Sensory gating deficits in the attenuated psychosis syndrome

artículo científico publicado en 2014

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Spatial working memory ability in individuals at ultra high risk for psychosis

artículo científico publicado en 2013

Spatial working memory in individuals at high risk for psychosis: longitudinal fMRI study

artículo científico publicado en 2010

Striatal dopamine transporter availability in drug-naive patients with schizophrenia: a case-control SPECT study with [(99m)Tc]-TRODAT-1 and a meta-analysis

artículo científico publicado en 2011

Stroop-test interference in bipolar disorder

Substantial shared genetic influences on schizophrenia and event-related potentials.

artículo científico publicado en 2007

Superior temporal lobe dysfunction and frontotemporal dysconnectivity in subjects at risk of psychosis and in first-episode psychosis

artículo científico publicado en 2009

Sustained attention in bipolar I disorder patients with familial psychosis and their first-degree relatives.

artículo científico publicado en 2012

Thalamic neurochemical abnormalities in individuals with prodromal symptoms of schizophrenia - relationship to auditory event-related potentials

artículo científico publicado en 2010

The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder

artículo científico publicado en 2019

The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project

artículo científico publicado en 2017

The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives

artículo científico publicado en 2012

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

artículo científico publicado en 2017

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

artículo científico publicado en 2014

The early auditory gamma-band response is heritable and a putative endophenotype of schizophrenia.

artículo científico publicado en 2009

The effect of COMT, BDNF, 5-HTT, NRG1 and DTNBP1 genes on hippocampal and lateral ventricular volume in psychosis.

artículo científico publicado en 2009

The effect of CYP2D6 variation on antipsychotic-induced hyperprolactinaemia: a systematic review and meta-analysis

artículo científico publicado en 2020

The genetic and environmental influences of event-related gamma oscillations on bipolar disorder

artículo científico publicado en 2011

The impact of CACNA1C allelic variation on effective connectivity during emotional processing in bipolar disorder

artículo científico publicado en 2013

The impact of CACNA1C gene, and its epistasis with ZNF804A, on white matter microstructure in health, schizophrenia and bipolar disorder1.

artículo científico publicado en 2016

The impact of psychosis genome-wide associated ZNF804A variation on verbal fluency connectivity

artículo científico publicado en 2017

The interplay between genetics, cognition and schizophrenia

artículo científico publicado en 2019

The relationship between eye movement and brain structural abnormalities in patients with schizophrenia and their unaffected relatives

artículo científico publicado en 2005

Transcriptome-wide association study reveals two genes that influence mismatch negativity

artículo científico publicado en 2021

What causes the onset of psychosis?

artículo científico publicado en 2005

White matter alterations related to P300 abnormalities in individuals at high risk for psychosis: an MRI-EEG study

artículo científico publicado en 2011

White matter microstructural abnormalities in families multiply affected with bipolar I disorder: a diffusion tensor tractography study

artículo científico publicado en 2013

White matter microstructural impairments and genetic liability to familial bipolar I disorder

artículo científico publicado en 2009

Lista de obras de Elvira Bramon

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains

Abnormal P300 in people with high risk of developing psychosis.

Abnormal frontoparietal synaptic gain mediating the P300 in patients with psychotic disorder and their unaffected relatives.

Acute effects of cannabinoids on addiction endophenotypes are moderated by genes encoding the CB1 receptor and FAAH enzyme

Alterations in white matter evident before the onset of psychosis.

Altered brain function directly related to structural abnormalities in people at ultra high risk of psychosis: longitudinal VBM-fMRI study

Altered effect of dopamine transporter 3'UTR VNTR genotype on prefrontal and striatal function in schizophrenia.

Analysis of multiple phenotypes in genome-wide genetic mapping studies

Are auditory P300 and duration MMN heritable and putative endophenotypes of psychotic bipolar disorder? A Maudsley Bipolar Twin and Family Study

Association between BDNF val66 met genotype and episodic memory

Association between hippocampal volume and P300 event related potential in psychosis: support for the Kraepelinian divide

Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating

Association of Genetic Risks for Schizophrenia and Bipolar DisorderWith Specific and Generic Brain Structural Endophenotypes

Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains.

Auditory P300 in patients with bipolar disorder and their unaffected relatives

COMT (Val(158/108)Met) genotype moderates the impact of antipsychotic medication on verbal IQ in twins with schizophrenia

COMT gene polymorphism and corpus callosum morphometry in preterm born adults

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

Cerebral metabolism in major depressive disorder: a voxel-based meta-analysis of positron emission tomography studies.

Cognitive performance in presumed obligate carriers for psychosis

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Common variants conferring risk of schizophrenia

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Dermatoglyphics and Schizophrenia: a meta-analysis and investigation of the impact of obstetric complications upon a-b ridge count.

Differential effects of DAAO on regional activation and functional connectivity in schizophrenia, bipolar disorder and controls.

Disruption of the neurexin 1 gene is associated with schizophrenia

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

Distribution of symptom dimensions across Kraepelinian divisions.

Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis?

Economic impact of early intervention in people at high risk of psychosis.

Effect of D-amino acid oxidase activator (DAOA; G72) on brain function during verbal fluency

Effect of DISC1 on the P300 waveform in psychosis

Elevated striatal dopamine function linked to prodromal signs of schizophrenia

Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives

Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene

Epistasis between the DAT 3' UTR VNTR and the COMT Val158Met SNP on cortical function in healthy subjects and patients with schizophrenia

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women

Evidence of association of KIBRA genotype with episodic memory in families of psychotic patients and controls.

Exaggerated neural response to emotional faces in patients with bipolar disorder and their first-degree relatives

Executive functioning in familial bipolar I disorder patients and their unaffected relatives

Expanding the range of ZNF804A variants conferring risk of psychosis

Failure to deactivate medial prefrontal cortex in people at high risk for psychosis.

Familial liability to schizophrenia and premorbid adjustment.

Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: a combined twin and family study.

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

Genetic modelling of childhood social development and personality in twins and siblings with schizophrenia.

Genetic overlap between P300, P50, and duration mismatch negativity

Genetic overlap between bipolar illness and event-related potentials.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Genetic vulnerability to psychosis and cortical function: epistatic effects between DAAO and G72.

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

Gray matter alterations related to P300 abnormalities in subjects at high risk for psychosis: longitudinal MRI-EEG study.

Heritability and reliability of P300, P50 and duration mismatch negativity.

Impaired prefrontal synaptic gain in people with psychosis and their relatives during the mismatch negativity.

Increased inferior frontal activation during word generation: a marker of genetic risk for schizophrenia but not bipolar disorder?

Insight in individuals with an At Risk Mental State.

Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function.

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study.

Is there an association between the COMT gene and P300 endophenotypes?

Large recurrent microdeletions associated with schizophrenia

Long-term maternal recall of obstetric complications in schizophrenia research

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Memory functioning in familial bipolar I disorder patients and their relatives.

Meta-analysis of the P300 and P50 waveforms in schizophrenia

Neural correlates of executive function and working memory in the 'at-risk mental state'.

Neural correlates of movement generation in the 'at-risk mental state'.