Lista de obras -

A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

artículo científico publicado en 2016

A neuregulin 1 variant associated with abnormal cortical function and psychotic symptoms

artículo científico publicado en 2006

A validation of the diathesis-stress model for depression in Generation Scotland

article

Altered DNA methylation associated with a translocation linked to major mental illness.

artículo científico publicado en 2018

Alzheimer's disease risk factor complement receptor 1 is associated with depression

artículo científico publicado en 2012

Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1.

artículo científico publicado en 2007

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

article

Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.

artículo científico publicado en 2010

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function

artículo científico publicado en 2016

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

artículo científico publicado en 2015

DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness

artículo científico publicado en 2004

DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder?

artículo científico publicado en 2011

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

artículo científico publicado en 2005

DISC1 genetics, biology and psychiatric illness

artículo científico publicado en 2013

DISC1 in schizophrenia: genetic mouse models and human genomic imaging

artículo científico publicado en 2010

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Developmental expression of orphan G protein-coupled receptor 50 in the mouse brain

artículo científico publicado en 2012

Effects of a Balanced Translocation between Chromosomes 1 and 11 Disrupting the DISC1 Locus on White Matter Integrity

artículo científico publicado en 2015

Effects of gene copy number variants on personality and mood in ageing cohorts

article

Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)

artículo científico publicado en 2015

Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.

artículo científico

Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction

scientific article published on 03 September 2019

GPR50 interacts with neuronal NOGO-A and affects neurite outgrowth

artículo científico publicado en 2009

Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness

artículo científico publicado en 2006

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

artículo científico publicado en 2018

Genetic copy number variation and general cognitive ability

artículo científico publicado en 2012

Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression

artículo científico publicado en 2012

Genome-Wide Meta-Analyses Of Stratified Depression In Generation Scotland And UK Biobank

article

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

artículo científico publicado en 2016

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

artículo científico publicado en 2018

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

article

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

article

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

artículo científico publicado en 2017

Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

artículo científico publicado en 2018

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.

artículo científico publicado en 2018

Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder

article

Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank

artículo científico publicado en 2017

Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort

artículo científico publicado el 2 de agosto de 2016

PKA phosphorylation of NDE1 is DISC1/PDE4 dependent and modulates its interaction with LIS1 and NDEL1

artículo científico publicado en 2011

Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort

artículo científico publicado en 2015

Rediscovering the value of families for psychiatric genetics research

article

Replication of the diathesis-stress model for depression in Generation Scotland

article

Response to Amar J. Klar: The Chromosome 1;11 Translocation Provides the Best Evidence Supporting Genetic Etiology for Schizophrenia and Bipolar Affective Disorders

artículo científico

Response to Amar J. Klar: The chromosome 1;11 translocation provides the best evidence supporting genetic etiology for schizophrenia and bipolar affective disorders.

artículo científico publicado en 2003

Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression

artículo científico publicado en 2016

The DISC1 promoter: characterization and regulation by FOXP2.

artículo científico publicado en 2012

The Stratification Of Major Depressive Disorder Into Genetic Subgroups

scholarly article published 5 May 2017

The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia

artículo científico publicado en 2015

The effects of DISC1 risk variants on brain activation in controls, patients with bipolar disorder and patients with schizophrenia

article

The genetics and biology of DISC1--an emerging role in psychosis and cognition

artículo científico publicado en 2006

White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder

artículo científico publicado en 2012

Lista de obras de

A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

A neuregulin 1 variant associated with abnormal cortical function and psychotic symptoms

A validation of the diathesis-stress model for depression in Generation Scotland

Altered DNA methylation associated with a translocation linked to major mental illness.

Alzheimer's disease risk factor complement receptor 1 is associated with depression

Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1.

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

Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness

DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder?

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

DISC1 genetics, biology and psychiatric illness

DISC1 in schizophrenia: genetic mouse models and human genomic imaging

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Developmental expression of orphan G protein-coupled receptor 50 in the mouse brain

Effects of a Balanced Translocation between Chromosomes 1 and 11 Disrupting the DISC1 Locus on White Matter Integrity

Effects of gene copy number variants on personality and mood in ageing cohorts

Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)

Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.

Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction

GPR50 interacts with neuronal NOGO-A and affects neurite outgrowth

Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

Genetic copy number variation and general cognitive ability

Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression

Genome-Wide Meta-Analyses Of Stratified Depression In Generation Scotland And UK Biobank

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.

Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder

Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank

Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort

PKA phosphorylation of NDE1 is DISC1/PDE4 dependent and modulates its interaction with LIS1 and NDEL1

Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort

Rediscovering the value of families for psychiatric genetics research

Replication of the diathesis-stress model for depression in Generation Scotland

Response to Amar J. Klar: The Chromosome 1;11 Translocation Provides the Best Evidence Supporting Genetic Etiology for Schizophrenia and Bipolar Affective Disorders

Response to Amar J. Klar: The chromosome 1;11 translocation provides the best evidence supporting genetic etiology for schizophrenia and bipolar affective disorders.

Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression

The DISC1 promoter: characterization and regulation by FOXP2.

The Stratification Of Major Depressive Disorder Into Genetic Subgroups

The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia

The effects of DISC1 risk variants on brain activation in controls, patients with bipolar disorder and patients with schizophrenia

The genetics and biology of DISC1--an emerging role in psychosis and cognition

White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder