Lista de obras - Scott G Wilson - Dominio Público Uruguay

A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women

article

A comparative study between corresponding structural geometric variables using 2 commonly implemented hip structural analysis algorithms applied to dual-energy X-ray absorptiometry images

artículo científico publicado en 2009

A flexible model for association analysis in sibships with missing genotype data

artículo científico publicado en 2011

A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study

artículo científico publicado en 2010

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

artículo científico publicado en 2013

A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture.

artículo científico publicado en 2011

Adrenalitis and the adrenocortical response of resistant and susceptible mice to acute murine cytomegalovirus infection

artículo científico publicado en 1996

Age-Related Changes in Thyroid Function: A Longitudinal Study of a Community-Based Cohort

article

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

Association between a variation in the phosphodiesterase 4D gene and bone mineral density

artículo científico publicado en 2005

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

artículo científico publicado en 2008

Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2

article

Calcium absorption in postmenopausal osteoporosis: benefit of HRT plus calcitriol, but not HRT alone, in both malabsorbers and normal absorbers

scientific article published on 01 January 2000

Calcium-sensing receptor gene polymorphism A986S does not predict serum calcium level, bone mineral density, calcaneal ultrasound indices, or fracture rate in a large cohort of elderly women.

artículo científico publicado en 2003

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts

scientific article published on 26 March 2020

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

artículo científico publicado en 2009

Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease

artículo científico publicado en 2015

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

Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal

artículo científico publicado en 2013

Copy number variation of the APC gene is associated with regulation of bone mineral density

artículo científico publicado en 2012

DNA methylation and the social gradient of osteoporotic fracture: A conceptual model.

artículo científico

Dysregulated Antibody, Natural Killer Cell and Immune Mediator Profiles in Autoimmune Thyroid Diseases

artículo científico publicado en 2020

Effect of pregnancy and lactation on maternal bone mass and calcium metabolism

artículo científico publicado en 1993

Effects of calcium and vitamin D supplementation on hip bone mineral density and calcium-related analytes in elderly ambulatory Australian women: a five-year randomized controlled trial

artículo científico publicado en 2007

Effects of vitamin D metabolites on intestinal calcium absorption and bone turnover in elderly women

artículo científico publicado en 2002

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

artículo científico publicado en 2011

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With <i>KLF9</i> and <i>DOT1L</i>

artículo científico publicado en 2021

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

artículo científico publicado en 2015

Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts.

artículo científico publicado en 2018

Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia

artículo científico publicado en 2022

Further genetic evidence suggesting a role for the RhoGTPase-RhoGEF pathway in osteoporosis

artículo científico publicado en 2009

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

artículo científico publicado en 2014

Genetic loci linked to pituitary-thyroid axis set points: a genome-wide scan of a large twin cohort

artículo científico publicado en 2008

Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone

artículo científico publicado en 2019

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

artículo científico publicado en 2018

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

artículo científico publicado en 2017

Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer

artículo científico publicado en 2016

Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.

artículo científico publicado en 2010

How many cases of disease in a pedigree imply familial disease?

artículo científico publicado en 2017

Human lactation: forearm trabecular bone loss, increased bone turnover, and renal conservation of calcium and inorganic phosphate with recovery of bone mass following weaning

artículo científico publicado en 1990

Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study

artículo científico publicado en 2008

Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis

artículo científico publicado en 2008

Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease

artículo científico publicado en 2014

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

Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia

artículo científico publicado en 2010

In vitro kinetic properties of the Thr201Met variant of human aromatase gene CYP19A1: functional responses to substrate and product inhibition and enzyme inhibitors.

artículo científico publicado en 2009

Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts

artículo científico publicado en 2014

LRP5 gene polymorphisms predict bone mass and incident fractures in elderly Australian women

article

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

artículo científico publicado en 2018

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.

artículo científico publicado en 2006

Linkage of genes to total lean body mass in normal women

artículo científico publicado en 2007

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

artículo científico publicado en 2009

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

artículo científico publicado en 2007

Metabolomic markers reveal novel pathways of ageing and early development in human populations

scientific article published on 08 July 2013

Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

artículo científico publicado en 2019

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

artículo científico publicado en 2015

No associations between OPG gene polymorphisms or serum levels and measures of osteoporosis in elderly Australian women

article

Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome.

artículo científico publicado en 2006

Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome.

artículo científico publicado en 2008

Polymorphism of the follistatin gene in polycystic ovary syndrome

artículo científico publicado en 2007

Polymorphisms in ALOX12, but not ALOX15, Are Significantly Associated With BMD in Postmenopausal Women

artículo científico publicado en 2007

Quantitative linkage analysis for pancreatic B-cell function and insulin resistance in a large twin cohort

artículo científico publicado en 2008

Serum free 1,25-dihydroxyvitamin D and the free 1,25-dihydroxyvitamin D index during a longitudinal study of human pregnancy and lactation

artículo científico publicado en 1990

Serum vitamin D metabolites are not responsible for low turnover osteoporosis in chronic liver disease

artículo científico publicado en 1989

Significant Association between Common Polymorphisms in the Aromatase Gene CYP19A1 and Bone Mineral Density in Postmenopausal Women

article

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

artículo científico publicado en 2009

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

artículo científico publicado en 2012

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

artículo científico publicado en 2017

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 Scott G Wilson

A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women

A comparative study between corresponding structural geometric variables using 2 commonly implemented hip structural analysis algorithms applied to dual-energy X-ray absorptiometry images

A flexible model for association analysis in sibships with missing genotype data

A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture.

Adrenalitis and the adrenocortical response of resistant and susceptible mice to acute murine cytomegalovirus infection

Age-Related Changes in Thyroid Function: A Longitudinal Study of a Community-Based Cohort

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

Association between a variation in the phosphodiesterase 4D gene and bone mineral density

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2

Calcium absorption in postmenopausal osteoporosis: benefit of HRT plus calcitriol, but not HRT alone, in both malabsorbers and normal absorbers

Calcium-sensing receptor gene polymorphism A986S does not predict serum calcium level, bone mineral density, calcaneal ultrasound indices, or fracture rate in a large cohort of elderly women.

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease

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

Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal

Copy number variation of the APC gene is associated with regulation of bone mineral density

DNA methylation and the social gradient of osteoporotic fracture: A conceptual model.

Dysregulated Antibody, Natural Killer Cell and Immune Mediator Profiles in Autoimmune Thyroid Diseases

Effect of pregnancy and lactation on maternal bone mass and calcium metabolism

Effects of calcium and vitamin D supplementation on hip bone mineral density and calcium-related analytes in elderly ambulatory Australian women: a five-year randomized controlled trial

Effects of vitamin D metabolites on intestinal calcium absorption and bone turnover in elderly women

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

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With <i>KLF9</i> and <i>DOT1L</i>

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

Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts.

Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia

Further genetic evidence suggesting a role for the RhoGTPase-RhoGEF pathway in osteoporosis

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

Genetic loci linked to pituitary-thyroid axis set points: a genome-wide scan of a large twin cohort

Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density

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

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

HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer

Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.

How many cases of disease in a pedigree imply familial disease?

Human lactation: forearm trabecular bone loss, increased bone turnover, and renal conservation of calcium and inorganic phosphate with recovery of bone mass following weaning

Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study

Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis

Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease

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

Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia

In vitro kinetic properties of the Thr201Met variant of human aromatase gene CYP19A1: functional responses to substrate and product inhibition and enzyme inhibitors.

Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts

LRP5 gene polymorphisms predict bone mass and incident fractures in elderly Australian women

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.

Linkage of genes to total lean body mass in normal women

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

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

Metabolomic markers reveal novel pathways of ageing and early development in human populations

Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

No associations between OPG gene polymorphisms or serum levels and measures of osteoporosis in elderly Australian women

Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome.

Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome.

Polymorphism of the follistatin gene in polycystic ovary syndrome

Polymorphisms in ALOX12, but not ALOX15, Are Significantly Associated With BMD in Postmenopausal Women

Quantitative linkage analysis for pancreatic B-cell function and insulin resistance in a large twin cohort

Serum free 1,25-dihydroxyvitamin D and the free 1,25-dihydroxyvitamin D index during a longitudinal study of human pregnancy and lactation

Serum vitamin D metabolites are not responsible for low turnover osteoporosis in chronic liver disease

Significant Association between Common Polymorphisms in the Aromatase Gene CYP19A1 and Bone Mineral Density in Postmenopausal Women

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

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

Whole-genome sequence-based analysis of thyroid function.

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