Lista de obras -

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

artículo científico publicado en 2015

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

artículo científico publicado en 2010

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia

artículo científico publicado en 2016

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

artículo científico publicado en 2017

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia

artículo científico publicado en 2022

Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

artículo científico publicado en 2014

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

article

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

artículo científico publicado en 2012

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

artículo científico publicado en 2008

Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults

artículo científico publicado en 2019

Common and rare variant analysis in early-onset bipolar disorder vulnerability

artículo científico publicado en 2014

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variation at 10p12.31 near MLLT10 influences meningioma risk

artículo científico publicado en 2011

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

artículo científico publicado en 2009

Effects of BDNF ValMet genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network

artículo científico publicado en 2013

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

artículo científico publicado en 2012

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

artículo científico publicado en 2012

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

article

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

artículo científico publicado en 2012

Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C.

artículo científico publicado en 2013

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant

artículo científico publicado en 2011

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

artículo científico publicado en 2015

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

artículo científico publicado en 2014

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

artículo científico publicado en 2014

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

artículo científico publicado en 2018

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population

artículo científico publicado en 2008

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

artículo científico publicado en 2010

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

artículo científico publicado en 2012

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients

artículo científico publicado en 2010

Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia

artículo científico publicado en 2011

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects

artículo científico publicado en 2014

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

artículo científico publicado en 2014

Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia

artículo científico publicado en 2014

Studies in humans and mice implicate neurocan in the etiology of mania

artículo científico publicado en 2012

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

artículo científico publicado en 2014

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

artículo científico publicado en 2009

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

artículo científico publicado en 2010

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

artículo científico publicado en 2011

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

scientific journal article

ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies

artículo científico publicado en 2013

Lista de obras de

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia

Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

Analysis of shared heritability in common disorders of the brain

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults

Common and rare variant analysis in early-onset bipolar disorder vulnerability

Common genetic variants influence human subcortical brain structures

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Common variation at 10p12.31 near MLLT10 influences meningioma risk

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

Effects of BDNF ValMet genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

Genetic architecture of subcortical brain structures in 38,851 individuals

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Genome-wide association study reveals two new risk loci for bipolar disorder

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C.

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant

Identification of common variants associated with human hippocampal and intracranial volumes

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population

Large recurrent microdeletions associated with schizophrenia

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

New genetic loci link adipose and insulin biology to body fat distribution

Novel genetic loci associated with hippocampal volume

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients

Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia

Studies in humans and mice implicate neurocan in the etiology of mania

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

Susceptibility variants for male-pattern baldness on chromosome 20p11.

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex