Lista de obras - Sheila J Barton - Dominio Público Uruguay

A double-blind randomised placebo-controlled trial of topical intranasal corticosteroids in 4- to 11-year-old children with persistent bilateral otitis media with effusion in primary care

artículo científico publicado en 2009

A novel common variant in DCST2 is associated with length in early life and height in adulthood

artículo científico publicado en 2014

ANRIL Promoter DNA Methylation: A Perinatal Marker for Later Adiposity

artículo científico publicado en 2017

Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma

artículo científico publicado en 2003

Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma

artículo científico publicado en 2014

Association analysis of brain-derived neurotrophic factor gene polymorphisms in asthmatic families

artículo científico publicado en 2009

Association between perinatal methylation of the neuronal differentiation regulator HES1 and later childhood neurocognitive function and behaviour.

artículo científico publicado en 2015

Association of asthma with a functional promoter polymorphism in the IL16 gene

artículo científico publicado en 2006

Association of tumor necrosis factor-alpha polymorphisms and ozone-induced change in lung function

artículo científico publicado en 2004

Associations between genetic obesity susceptibility and early postnatal fat and lean mass: an individual participant meta-analysis

artículo científico publicado en 2014

Circulating endothelial-coagulative activation markers after smoking cessation: a 12-month observational study

artículo científico publicado en 2010

Copy-number variation genotyping of GSTT1 and GSTM1 gene deletions by real-time PCR.

artículo científico publicado en 2009

Correction of unexpected distributions of P values from analysis of whole genome arrays by rectifying violation of statistical assumptions ⬇️

artículo científico publicado el 11 de marzo de 2013

DNA methylation at birth within the promoter of ANRIL predicts markers of cardiovascular risk at 9 years

artículo científico publicado en 2016

DNA methylation of Th2 lineage determination genes at birth is associated with allergic outcomes in childhood

artículo científico publicado en 2017

DNA methylation signatures in cord blood associated with birthweight are enriched for dmCpGs previously associated with maternal hypertension or pre-eclampsia, smoking and folic acid intake

artículo científico publicado en 2021

Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents

artículo científico publicado en 2015

Differential SLC6A4 methylation: a predictive epigenetic marker of adiposity from birth to adulthood

artículo científico publicado en 2019

Epigenome-wide association study of sarcopenia: findings from the Hertfordshire Sarcopenia Study (HSS)

artículo científico publicado en 2021

FUT2 Genetic Variants and Reported Respiratory and Gastrointestinal Illnesses During Infancy

scholarly article by Sheila J Barton et al published 30 October 2018 in Journal of Infectious Diseases

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

artículo científico publicado en 2019

Genetic association studies of interleukin-13 receptor alpha1 subunit gene polymorphisms in asthma and atopy

artículo científico publicado en 2007

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

artículo científico publicado en 2018

Genome-wide methylation analysis identifies differentially methylated CpG loci associated with severe obesity in childhood

artículo científico publicado en 2015

How to make DNA methylome wide association studies more powerful

artículo científico publicado en 2016

Identification of ATPAF1 as a novel candidate gene for asthma in children

artículo científico publicado en 2011

Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness

artículo científico publicado en 2009

Identification of lipocalin and apolipoprotein A1 as biomarkers of chronic obstructive pulmonary disease

artículo científico publicado en 2010

In Epigenomic Studies, Including Cell-Type Adjustments in Regression Models Can Introduce Multicollinearity, Resulting in Apparent Reversal of Direction of Association

artículo científico publicado en 2019

Influence of Maternal Lifestyle and Diet on Perinatal DNA Methylation Signatures Associated With Childhood Arterial Stiffness at 8 to 9 Years

artículo científico publicado en 2021

Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness

artículo científico publicado en 2016

Lean mass, muscle strength and gene expression in community dwelling older men: findings from the Hertfordshire Sarcopenia Study (HSS).

artículo científico publicado en 2014

Leukotriene B4 receptor locus gene characterisation and association studies in asthma

artículo científico publicado en 2012

Maternal and fetal genetic contribution to gestational weight gain.

artículo científico publicado en 2017

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Maternal dysglycaemia, changes in the infant's epigenome modified with a diet and physical activity intervention in pregnancy: Secondary analysis of a randomised control trial

artículo científico publicado en 2020

Measuring the methylome in clinical samples: improved processing of the Infinium Human Methylation450 BeadChip Array.

artículo científico publicado en 2012

Mitochondrial oxidative capacity and NAD+ biosynthesis are reduced in human sarcopenia across ethnicities

scientific article published on 20 December 2019

Mortality in adult intensive care patients with severe systemic inflammatory response syndromes is strongly associated with the hypo-immune TNF -238A polymorphism

artículo científico publicado en 2009

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

Observer agreement comparing the use of virtual slides with glass slides in the pathology review component of the POSH breast cancer cohort study

artículo científico

PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline

artículo científico publicado en 2009

Perinatal DNA Methylation at CDKN2A Is Associated With Offspring Bone Mass: Findings From the Southampton Women's Survey.

artículo científico publicado en 2017

Placental amino acid transport may be regulated by maternal vitamin D and vitamin D-binding protein: results from the Southampton Women's Survey.

artículo científico publicado en 2015

Polymorphism of the mast cell chymase gene (CMA1) promoter region: lack of association with asthma but association with serum total immunoglobulin E levels in adult atopic dermatitis.

artículo científico publicado en 2004

Polymorphisms in the interleukin-4 and interleukin-4 receptor alpha chain genes confer susceptibility to asthma and atopy in a Caucasian population.

artículo científico publicado en 2003

Relation of FTO gene variants to fetal growth trajectories: Findings from the Southampton Women's survey

artículo científico publicado en 2015

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.

artículo científico publicado en 2017

Review of factors that influence the abundance of ions produced in a tandem mass spectrometer and statistical methods for discovering these factors

artículo científico publicado en 2009

The cysteinyl-leukotriene type 1 receptor polymorphism 927T/C is associated with atopy severity but not with asthma.

artículo científico publicado en 2006

The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes

artículo científico publicado en 2014

The role of LTA4H and ALOX5AP polymorphism in asthma and allergy susceptibility.

artículo científico publicado en 2008

Topical intranasal corticosteroids in 4-11 year old children with persistent bilateral otitis media with effusion in primary care: double blind randomised placebo controlled trial

artículo científico publicado en 2009

Using statistical models to identify factors that have a role in defining the abundance of ions produced by tandem MS.

artículo científico publicado en 2007

Lista de obras de Sheila J Barton

A double-blind randomised placebo-controlled trial of topical intranasal corticosteroids in 4- to 11-year-old children with persistent bilateral otitis media with effusion in primary care

A novel common variant in DCST2 is associated with length in early life and height in adulthood

ANRIL Promoter DNA Methylation: A Perinatal Marker for Later Adiposity

Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma

Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma

Association analysis of brain-derived neurotrophic factor gene polymorphisms in asthmatic families

Association between perinatal methylation of the neuronal differentiation regulator HES1 and later childhood neurocognitive function and behaviour.

Association of asthma with a functional promoter polymorphism in the IL16 gene

Association of tumor necrosis factor-alpha polymorphisms and ozone-induced change in lung function

Associations between genetic obesity susceptibility and early postnatal fat and lean mass: an individual participant meta-analysis

Circulating endothelial-coagulative activation markers after smoking cessation: a 12-month observational study

Copy-number variation genotyping of GSTT1 and GSTM1 gene deletions by real-time PCR.

Correction of unexpected distributions of P values from analysis of whole genome arrays by rectifying violation of statistical assumptions ⬇️

DNA methylation at birth within the promoter of ANRIL predicts markers of cardiovascular risk at 9 years

DNA methylation of Th2 lineage determination genes at birth is associated with allergic outcomes in childhood

DNA methylation signatures in cord blood associated with birthweight are enriched for dmCpGs previously associated with maternal hypertension or pre-eclampsia, smoking and folic acid intake

Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents

Differential SLC6A4 methylation: a predictive epigenetic marker of adiposity from birth to adulthood

Epigenome-wide association study of sarcopenia: findings from the Hertfordshire Sarcopenia Study (HSS)

FUT2 Genetic Variants and Reported Respiratory and Gastrointestinal Illnesses During Infancy

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

Genetic association studies of interleukin-13 receptor alpha1 subunit gene polymorphisms in asthma and atopy

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Genome-wide methylation analysis identifies differentially methylated CpG loci associated with severe obesity in childhood

How to make DNA methylome wide association studies more powerful

Identification of ATPAF1 as a novel candidate gene for asthma in children

Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness

Identification of lipocalin and apolipoprotein A1 as biomarkers of chronic obstructive pulmonary disease

In Epigenomic Studies, Including Cell-Type Adjustments in Regression Models Can Introduce Multicollinearity, Resulting in Apparent Reversal of Direction of Association

Influence of Maternal Lifestyle and Diet on Perinatal DNA Methylation Signatures Associated With Childhood Arterial Stiffness at 8 to 9 Years

Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness

Lean mass, muscle strength and gene expression in community dwelling older men: findings from the Hertfordshire Sarcopenia Study (HSS).

Leukotriene B4 receptor locus gene characterisation and association studies in asthma

Maternal and fetal genetic contribution to gestational weight gain.

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal dysglycaemia, changes in the infant's epigenome modified with a diet and physical activity intervention in pregnancy: Secondary analysis of a randomised control trial

Measuring the methylome in clinical samples: improved processing of the Infinium Human Methylation450 BeadChip Array.

Mitochondrial oxidative capacity and NAD+ biosynthesis are reduced in human sarcopenia across ethnicities

Mortality in adult intensive care patients with severe systemic inflammatory response syndromes is strongly associated with the hypo-immune TNF -238A polymorphism

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

Observer agreement comparing the use of virtual slides with glass slides in the pathology review component of the POSH breast cancer cohort study

PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline

Perinatal DNA Methylation at CDKN2A Is Associated With Offspring Bone Mass: Findings From the Southampton Women's Survey.

Placental amino acid transport may be regulated by maternal vitamin D and vitamin D-binding protein: results from the Southampton Women's Survey.

Polymorphism of the mast cell chymase gene (CMA1) promoter region: lack of association with asthma but association with serum total immunoglobulin E levels in adult atopic dermatitis.

Polymorphisms in the interleukin-4 and interleukin-4 receptor alpha chain genes confer susceptibility to asthma and atopy in a Caucasian population.

Relation of FTO gene variants to fetal growth trajectories: Findings from the Southampton Women's survey

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.

Review of factors that influence the abundance of ions produced in a tandem mass spectrometer and statistical methods for discovering these factors

The cysteinyl-leukotriene type 1 receptor polymorphism 927T/C is associated with atopy severity but not with asthma.

The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes

The role of LTA4H and ALOX5AP polymorphism in asthma and allergy susceptibility.

Topical intranasal corticosteroids in 4-11 year old children with persistent bilateral otitis media with effusion in primary care: double blind randomised placebo controlled trial

Using statistical models to identify factors that have a role in defining the abundance of ions produced by tandem MS.