Lista de obras - Anna Murray - Dominio Público Uruguay

A common variant of the interleukin 6 receptor (IL-6r) gene increases IL-6r and IL-6 levels, without other inflammatory effects.

artículo científico publicado en 2007

A common variant of the p16(INK4a) genetic region is associated with physical function in older people

artículo científico publicado en 2007

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine

artículo científico publicado en 2008

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

artículo científico publicado en 2012

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

artículo científico publicado en 2008

A genome-wide association study of depressive symptoms

scientific journal article

A genome-wide association study of early menopause and the combined impact of identified variants

artículo científico publicado en 2013

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

artículo científico publicado en 2011

An investigation of FRAXA intermediate allele phenotype in a longitudinal sample

artículo científico publicado en 2006

Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).

scientific article published on 22 June 2010

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

artículo científico publicado en 2011

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes

scientific article published on December 2007

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

artículo científico publicado en 2010

Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels

article

Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people

artículo científico publicado en 2009

Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study

artículo científico publicado en 2009

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

scientific article published on 19 December 2013

Effects of the diabetes linked TCF7L2 polymorphism in a representative older population

artículo científico publicado en 2006

Expression profiling of type 2 diabetes susceptibility genes in the pancreatic islets, adipose tissue and liver of obese mice

artículo científico publicado en 2013

Filaggrin gene mutations are associated with asthma and eczema in later life

artículo científico publicado en 2008

Genetic determinants of serum testosterone concentrations in men.

artículo científico publicado en 2011

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health

artículo científico publicado en 2016

Genetic insights into biological mechanisms governing human ovarian ageing

artículo científico publicado en 2021

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

artículo científico publicado en 2015

Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?

artículo científico publicado en 2001

Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank

artículo científico publicado en 2016

Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing

artículo científico publicado en 2011

Identifying likely causal connections between gene expression levels using a Mendelian randomization approach

article

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

artículo científico publicado en 2010

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

artículo científico publicado en 2012

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

artículo científico publicado en 2009

Molecular insights into the aetiology of female reproductive ageing.

artículo científico

No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers

artículo científico publicado en 2000

Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers

artículo científico publicado en 2006

Oxidative Metabolism Genes Are Not Responsive to Oxidative Stress in Rodent Beta Cell Lines ⬇️

artículo científico publicado el 20 de febrero de 2012

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Polymorphisms in LMNA and near a SERPINA gene cluster are associated with cognitive function in older people.

artículo científico publicado en 2008

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency

artículo científico publicado en 2013

Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study

artículo científico publicado en 2015

Rare coding variants and X-linked loci associated with age at menarche

artículo científico publicado en 2015

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

artículo científico publicado en 2013

Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

artículo científico publicado en 2017

Reply: Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

Reproductive and menstrual history of females with fragile X expansions

artículo científico publicado en 2000

Response to Prakash et al

scientific article published on 21 December 2018

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

artículo científico publicado en 2016

Stability and haplotype analysis of the FRAXE region

artículo científico publicado en 2000

Structures of CUG Repeats in RNA

artículo científico publicado en 2002

The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people

artículo científico publicado en 2009

The FRAXA and FRAXE allele repeat size of boys from the Avon Longitudinal Study of Parents and Children (ALSPAC)

artículo científico publicado en 2020

The coronary artery disease-associated 9p21 variant and later life 20-year survival to cohort extinction

artículo científico publicado en 2011

The paraoxonase (PON1) Q192R polymorphism is not associated with poor health status or depression in the ELSA or INCHIANTI studies

artículo científico publicado en 2009

The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts

artículo científico publicado en 2013

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively

artículo científico publicado en 2016

What is behind the calcium? The relationship between calcium and necrotic core on virtual histology analyses

artículo científico publicado en 2008

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

artículo científico publicado en 2014

Lista de obras de Anna Murray

A common variant of the interleukin 6 receptor (IL-6r) gene increases IL-6r and IL-6 levels, without other inflammatory effects.

A common variant of the p16(INK4a) genetic region is associated with physical function in older people

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

A genome-wide association study of depressive symptoms

A genome-wide association study of early menopause and the combined impact of identified variants

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

An investigation of FRAXA intermediate allele phenotype in a longitudinal sample

Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels

Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people

Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

Effects of the diabetes linked TCF7L2 polymorphism in a representative older population

Expression profiling of type 2 diabetes susceptibility genes in the pancreatic islets, adipose tissue and liver of obese mice

Filaggrin gene mutations are associated with asthma and eczema in later life

Genetic determinants of serum testosterone concentrations in men.

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health

Genetic insights into biological mechanisms governing human ovarian ageing

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?

Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank

Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing

Identifying likely causal connections between gene expression levels using a Mendelian randomization approach

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

Molecular insights into the aetiology of female reproductive ageing.

No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers

Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers

Oxidative Metabolism Genes Are Not Responsive to Oxidative Stress in Rodent Beta Cell Lines ⬇️

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Polymorphisms in LMNA and near a SERPINA gene cluster are associated with cognitive function in older people.

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency

Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study

Rare coding variants and X-linked loci associated with age at menarche

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

Reply: Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

Reproductive and menstrual history of females with fragile X expansions

Response to Prakash et al

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

Stability and haplotype analysis of the FRAXE region

Structures of CUG Repeats in RNA

The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people

The FRAXA and FRAXE allele repeat size of boys from the Avon Longitudinal Study of Parents and Children (ALSPAC)

The coronary artery disease-associated 9p21 variant and later life 20-year survival to cohort extinction

The paraoxonase (PON1) Q192R polymorphism is not associated with poor health status or depression in the ELSA or INCHIANTI studies

The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts

The transcriptional landscape of age in human peripheral blood

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively

What is behind the calcium? The relationship between calcium and necrotic core on virtual histology analyses

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes