Lista de obras -

A TA-repeat polymorphism in the gene for the estrogen receptor alpha does not correlate with muscle strength or body composition in young adult Swedish women.

artículo científico publicado en 2005

A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling

artículo científico publicado en 2012

A genome-wide approach to identifying novel-imprinted genes.

artículo científico publicado en 2007

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

artículo científico publicado en 2009

A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5.

artículo científico publicado en 2008

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

artículo científico publicado en 2009

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on human blood metabolites

artículo científico publicado en 2014

An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2018

An epigenome-wide association study of total serum immunoglobulin E concentration.

artículo científico publicado en 2015

An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits

artículo científico publicado en 2010

Analysis of the impact of genetic variation on human gene expression

artículo científico publicado en 2010

Assessment of gene-by-sex interaction effect on bone mineral density

artículo científico publicado en 2012

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2019

Capturing functional epigenomes for insight into metabolic diseases

artículo científico publicado en 2020

Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines

artículo científico publicado en 2010

Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants ⬇️

artículo científico publicado en 2015

Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation

artículo científico publicado en 2014

Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro

artículo científico publicado en 2009

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

artículo científico publicado en 2019

Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate Metabolism

scientific article published on 08 August 2019

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

scientific article published on 14 March 2019

Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto-Kakizaki rats improves glucose homeostasis through enhanced FXR signalling

artículo científico publicado en 2020

Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms

artículo científico publicado en 2011

Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population

artículo científico publicado en 2012

Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants

artículo científico publicado en 2015

Erratum: Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

scholarly article published in Nature Genetics

Erratum: Whole-genome sequence-based analysis of thyroid function

artículo científico publicado en 2015

Estimation of physical performance and measurements of habitual physical activity may capture men with high risk to fall--data from the Mr Os Sweden cohort

artículo científico publicado en 2008

Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity

artículo científico publicado en 2014

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

artículo científico publicado en 2017

Gene expression changes with age in skin, adipose tissue, blood and brain

artículo científico publicado en 2013

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

artículo científico publicado en 2013

Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.

artículo científico publicado en 2015

Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women

artículo científico publicado en 2004

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

artículo científico publicado en 2011

Genome-wide mapping identifies beta-1,4-N-acetyl-galactosaminyl-transferase as a novel determinant of sclerostin levels and bone mineral density

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

artículo científico publicado en 2012

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

artículo científico publicado en 2014

Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements

artículo científico publicado en 2013

Global analysis of the impact of environmental perturbation on cis-regulation of gene expression

artículo científico publicado en 2011

Global miRNA expression and correlation with mRNA levels in primary human bone cells

artículo científico publicado en 2015

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

artículo científico publicado en 2009

Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36.

artículo científico publicado en 2016

Human metabolic individuality in biomedical and pharmaceutical research

artículo científico publicado en 2011

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

IL6 and IL1B Polymorphisms are Associated With Fat Mass in Older Men: The MrOS Study Sweden

article

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

artículo científico publicado en 2017

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

artículo científico publicado en 2011

Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies

Impact of common variation in bone-related genes on type 2 diabetes and related traits

artículo científico publicado en 2012

Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids

artículo científico publicado en 2014

Intersection of regulatory pathways controlling hemostasis and hemochorial placentation

artículo científico publicado en 2021

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

artículo científico publicado en 2012

Mapping cis- and trans-regulatory effects across multiple tissues in twins

artículo científico publicado en 2012

Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures

scientific article published on 02 August 2019

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

artículo científico publicado en 2014

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

artículo científico publicado en 2014

Population genomics in a disease targeted primary cell model

artículo científico publicado en 2009

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

artículo científico publicado en 2015

Single-cell analysis of human adipose tissue identifies depot and disease specific cell types

scientific article published on 23 December 2019

Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations

artículo científico publicado en 2009

Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells

artículo científico publicado en 2008

Targeted screening of cis-regulatory variation in human haplotypes

scientific article published on 29 October 2008

The COMT val158met polymorphism is associated with prevalent fractures in Swedish men.

artículo científico publicado en 2007

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

artículo científico publicado en 2011

The impact of estradiol on bone mineral density is modulated by the specific estrogen receptor-alpha cofactor retinoblastoma-interacting zinc finger protein-1 insertion/deletion polymorphism

artículo científico publicado en 2007

The positive effect of dietary vitamin D intake on bone mineral density in men is modulated by the polyadenosine repeat polymorphism of the vitamin D receptor

artículo científico publicado en 2006

The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue

artículo científico publicado en 2013

Tissue effect on genetic control of transcript isoform variation

artículo científico publicado en 2009

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

artículo científico publicado en 2009

Type I collagen alpha1 Sp1 polymorphism and the risk of cruciate ligament ruptures or shoulder dislocations

artículo científico publicado en 2008

UCP1 expression-associated gene signatures of human epicardial adipose tissue

scientific article published on 18 April 2019

Vitamin D Receptor 3′ Haplotypes Are Unequally Expressed in Primary Human Bone Cells and Associated With Increased Fracture Risk: The MrOS Study in Sweden and Hong Kong

scholarly article by Elin Grundberg et al published 19 March 2007 in Journal of Bone and Mineral Research

Whole-genome sequence-based analysis of thyroid function.

artículo científico publicado en 2015

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

artículo científico publicado en 2015

Lista de obras de

A TA-repeat polymorphism in the gene for the estrogen receptor alpha does not correlate with muscle strength or body composition in young adult Swedish women.

A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling

A genome-wide approach to identifying novel-imprinted genes.

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5.

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on human blood metabolites

An atlas of genetic influences on osteoporosis in humans and mice

An epigenome-wide association study of total serum immunoglobulin E concentration.

An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits

Analysis of the impact of genetic variation on human gene expression

Assessment of gene-by-sex interaction effect on bone mineral density

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

Capturing functional epigenomes for insight into metabolic diseases

Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines

Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants ⬇️

Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation

Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate Metabolism

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto-Kakizaki rats improves glucose homeostasis through enhanced FXR signalling

Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms

Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population

Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants

Erratum: Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

Erratum: Whole-genome sequence-based analysis of thyroid function

Estimation of physical performance and measurements of habitual physical activity may capture men with high risk to fall--data from the Mr Os Sweden cohort

Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Gene expression changes with age in skin, adipose tissue, blood and brain

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.

Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

Genome-wide mapping identifies beta-1,4-N-acetyl-galactosaminyl-transferase as a novel determinant of sclerostin levels and bone mineral density

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

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

Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements

Global analysis of the impact of environmental perturbation on cis-regulation of gene expression

Global miRNA expression and correlation with mRNA levels in primary human bone cells

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36.

Human metabolic individuality in biomedical and pharmaceutical research

Hundreds of variants clustered in genomic loci and biological pathways affect human height

IL6 and IL1B Polymorphisms are Associated With Fat Mass in Older Men: The MrOS Study Sweden

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies

Impact of common variation in bone-related genes on type 2 diabetes and related traits

Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids

Intersection of regulatory pathways controlling hemostasis and hemochorial placentation

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

Mapping cis- and trans-regulatory effects across multiple tissues in twins

Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

Population genomics in a disease targeted primary cell model

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

Single-cell analysis of human adipose tissue identifies depot and disease specific cell types

Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations

Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells

Targeted screening of cis-regulatory variation in human haplotypes

The COMT val158met polymorphism is associated with prevalent fractures in Swedish men.

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

The impact of estradiol on bone mineral density is modulated by the specific estrogen receptor-alpha cofactor retinoblastoma-interacting zinc finger protein-1 insertion/deletion polymorphism

The positive effect of dietary vitamin D intake on bone mineral density in men is modulated by the polyadenosine repeat polymorphism of the vitamin D receptor

The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue

Tissue effect on genetic control of transcript isoform variation

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

Type I collagen alpha1 Sp1 polymorphism and the risk of cruciate ligament ruptures or shoulder dislocations

UCP1 expression-associated gene signatures of human epicardial adipose tissue

Vitamin D Receptor 3′ Haplotypes Are Unequally Expressed in Primary Human Bone Cells and Associated With Increased Fracture Risk: The MrOS Study in Sweden and Hong Kong

Whole-genome sequence-based analysis of thyroid function.

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture