Lista de obras - Kathryn L Evans - Dominio Público Uruguay

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

artículo científico publicado en 2001

A Contiguous Clone Map over 3 Mb on the Long Arm of Chromosome 11 across a Balanced Translocation Associated with Schizophrenia

artículo científico publicado en 1995

A case-control association study and family-based expression analysis of the bipolar disorder candidate gene PI4K2B

artículo científico publicado en 2009

A meta-analysis of genome-wide association studies of epigenetic age acceleration

artículo científico publicado en 2019

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

artículo científico publicado en 2006

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

An epigenetic predictor of death captures multi-modal measures of brain health

scientific article published on 03 December 2019

An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort

article

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

artículo científico publicado en 2007

Assessment of dried blood spots for DNA methylation profiling

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

article

Association analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophrenia

article

Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population

artículo científico publicado en 2006

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

scientific article published on 09 October 2020

Bayesian reassessment of the epigenetic architecture of complex traits

artículo científico publicado en 2020

Birth weight associations with DNA methylation differences in an adult population

artículo científico publicado en 2020

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

artículo científico publicado en 2020

Cohort Profile: Stratifying Resilience and Depression Longitudinally (STRADL): a questionnaire follow-up of Generation Scotland: Scottish Family Health Study (GS:SFHS).

artículo científico publicado en 2017

Cohort profile for the STratifying Resilience and Depression Longitudinally (STRADL) study: A depression-focused investigation of Generation Scotland, using detailed clinical, cognitive, and neuroimaging assessments

artículo científico publicado en 2019

Computational comparison of human genomic sequence assemblies for a region of chromosome 4.

artículo científico publicado en 2002

Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p

scientific article published on 30 March 2010

DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan

artículo científico publicado en 2014

DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness

artículo científico publicado en 2018

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

article published in 2018

DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder

artículo científico publicado en 2016

DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses

artículo científico publicado en 2022

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

Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).

artículo científico publicado en 1993

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.

artículo científico publicado en 1995

Epigenetic prediction of complex traits and death

article by Daniel L McCartney et al published 27 September 2018 in Genome Biology

Epigenetic prediction of major depressive disorder

artículo científico publicado en 2020

Epigenetic signatures of starting and stopping smoking

artículo científico publicado en 2018

Epigenome-wide association study of alcohol consumption in N = 8161 individuals and relevance to alcohol use disorder pathophysiology: identification of the cystine/glutamate transporter SLC7A11 as a top target

artículo científico publicado en 2021

Expression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia

artículo científico publicado en 2014

GWAS on family history of Alzheimer's disease.

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.

artículo científico publicado en 2003

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

artículo científico publicado en 2017

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

artículo científico publicado en 2021

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

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

Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I

article

Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD

artículo científico publicado en 2019

Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip

artículo científico publicado en 2016

Impact of a microRNA MIR137 susceptibility variant on brain function in people at high genetic risk of schizophrenia or bipolar disorder

artículo científico publicado en 2012

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

scientific article published on 23 August 2019

In silico identification of transcripts and SNPs from a region of 4p linked with bipolar affective disorder

scientific article published on 01 August 2000

Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease

artículo científico publicado en 2018

Juvenile stress produces long-lasting changes in hippocampal DISC1, GSK3ß and NRG1 expression.

artículo científico publicado en 2014

Markers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorder

artículo científico publicado en 2001

Methylome-wide association study of antidepressant use in Generation Scotland and the Netherlands Twin Register implicates the innate immune system

artículo científico publicado en 2021

Methylome-wide association study of early life stressors and adult mental health

artículo científico publicado en 2022

Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

artículo científico publicado en 2000

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders

artículo científico publicado en 2016

Preliminary investigation of miRNA expression in individuals at high familial risk of bipolar disorder.

artículo científico publicado en 2015

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

artículo científico publicado en 2017

Regional localisation of 19 brain expressed sequence tags to human chromosome 11 using PCR amplification of somatic cell hybrid DNAs

artículo científico publicado en 1995

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

artículo científico publicado en 2002

SUSPECTS: enabling fast and effective prioritization of positional candidates

artículo científico publicado en 2006

Speeding disease gene discovery by sequence based candidate prioritization

artículo científico publicado en 2005

SuRFing the genomics wave: an R package for prioritising SNPs by functionality

artículo científico publicado en 2014

The DISC1 promoter: characterization and regulation by FOXP2.

artículo científico publicado en 2012

The DNA sequence of the human X chromosome

artículo científico publicado en 2005

The PDE4B gene confers sex-specific protection against schizophrenia

artículo científico publicado en 2007

The effects of a neuregulin 1 variant on white matter density and integrity

artículo científico publicado en 2007

Lista de obras de Kathryn L Evans

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

A Contiguous Clone Map over 3 Mb on the Long Arm of Chromosome 11 across a Balanced Translocation Associated with Schizophrenia

A case-control association study and family-based expression analysis of the bipolar disorder candidate gene PI4K2B

A meta-analysis of genome-wide association studies of epigenetic age acceleration

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

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

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

An epigenetic predictor of death captures multi-modal measures of brain health

An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort

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

Assessment of dried blood spots for DNA methylation profiling

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

Association analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophrenia

Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

Bayesian reassessment of the epigenetic architecture of complex traits

Birth weight associations with DNA methylation differences in an adult population

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

Cohort Profile: Stratifying Resilience and Depression Longitudinally (STRADL): a questionnaire follow-up of Generation Scotland: Scottish Family Health Study (GS:SFHS).

Cohort profile for the STratifying Resilience and Depression Longitudinally (STRADL) study: A depression-focused investigation of Generation Scotland, using detailed clinical, cognitive, and neuroimaging assessments

Computational comparison of human genomic sequence assemblies for a region of chromosome 4.

Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p

DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan

DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder

DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses

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

Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.

Epigenetic prediction of complex traits and death

Epigenetic prediction of major depressive disorder

Epigenetic signatures of starting and stopping smoking

Epigenome-wide association study of alcohol consumption in N = 8161 individuals and relevance to alcohol use disorder pathophysiology: identification of the cystine/glutamate transporter SLC7A11 as a top target

Expression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia

GWAS on family history of Alzheimer's disease.

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

Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.

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

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

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

Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I

Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD

Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip

Impact of a microRNA MIR137 susceptibility variant on brain function in people at high genetic risk of schizophrenia or bipolar disorder

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

In silico identification of transcripts and SNPs from a region of 4p linked with bipolar affective disorder

Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease

Juvenile stress produces long-lasting changes in hippocampal DISC1, GSK3ß and NRG1 expression.

Markers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorder

Methylome-wide association study of antidepressant use in Generation Scotland and the Netherlands Twin Register implicates the innate immune system

Methylome-wide association study of early life stressors and adult mental health

Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders

Preliminary investigation of miRNA expression in individuals at high familial risk of bipolar disorder.

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

Regional localisation of 19 brain expressed sequence tags to human chromosome 11 using PCR amplification of somatic cell hybrid DNAs

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

SUSPECTS: enabling fast and effective prioritization of positional candidates

Speeding disease gene discovery by sequence based candidate prioritization

SuRFing the genomics wave: an R package for prioritising SNPs by functionality

The DISC1 promoter: characterization and regulation by FOXP2.

The DNA sequence of the human X chromosome

The PDE4B gene confers sex-specific protection against schizophrenia

The effects of a neuregulin 1 variant on white matter density and integrity