Lista de obras - Anette P. Gjesing - Dominio Público Uruguay

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

artículo científico publicado en 2017

A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

artículo científico publicado en 2014

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

artículo científico publicado en 2011

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Association of a functional 17beta-estradiol sensitive IL6-174G/C promoter polymorphism with early-onset type 1 diabetes in females

artículo científico publicado en 2003

Association of the beta3-adrenergic receptor Trp64Arg polymorphism with common metabolic traits: studies of 7605 middle-aged white people

artículo científico publicado en 2008

Association studies of novel obesity-related gene variants with quantitative metabolic phenotypes in a population-based sample of 6,039 Danish individuals

artículo científico publicado en 2011

Associations of the Inflammatory Marker YKL-40 with Measures of Obesity and Dyslipidaemia in Individuals at High Risk of Type 2 Diabetes

artículo científico publicado en 2015

Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease ⬇️

artículo científico publicado en 2011

Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes

artículo científico publicado en 2016

Carriers of the TCF7L2 rs7903146 TT genotype have elevated levels of plasma glucose, serum proinsulin and plasma gastric inhibitory polypeptide (GIP) during a meal test

artículo científico publicado en 2010

Correction: Does DNA Methylation of PPARGC1A Influence Insulin Action in First Degree Relatives of Patients with Type 2 Diabetes?

artículo científico publicado en 2013

DNA methylation and gene expression of HIF3A: cross-tissue validation and associations with BMI and insulin resistance

artículo científico publicado en 2016

Does DNA methylation of PPARGC1A influence insulin action in first degree relatives of patients with type 2 diabetes?

artículo científico publicado en 2013

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Evaluation of a target region capture sequencing platform using monogenic diabetes as a study-model

artículo científico publicado en 2014

Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity

artículo científico publicado en 2010

Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traits

artículo científico publicado en 2012

G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans

artículo científico publicado en 2009

Genetic Correlation between Body Fat Percentage and Cardiorespiratory Fitness Suggests Common Genetic Etiology

artículo científico publicado en 2016

Genetic Variations in the Human G Protein-coupled Receptor Class C, Group 6, Member A (GPRC6A) Control Cell Surface Expression and Function

artículo científico publicado en 2016

Genetic and phenotypic correlations between surrogate measures of insulin release obtained from OGTT data

artículo científico publicado en 2015

Genetic evidence of assortative mating in humans

scholarly article

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

artículo científico publicado en 2009

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

artículo científico publicado en 2011

Heterogeneity in glucose response curves during an oral glucose tolerance test and associated cardiometabolic risk

artículo científico publicado en 2016

High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus

artículo científico publicado en 2017

High heritability and genetic correlation of intravenous glucose- and tolbutamide-induced insulin secretion among non-diabetic family members of type 2 diabetic patients

artículo científico publicado en 2014

Homozygous carriers of the TCF7L2 rs7903146 T-allele show altered postprandial response in triglycerides and triglyceride-rich lipoproteins

artículo científico publicado en 2017

Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

artículo científico publicado en 2017

Human pancreatic islet 3D chromatin architecture provides insights into the genetics of type 2 diabetes

article

Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes

scientific article published on 28 June 2019

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

artículo científico publicado en 2015

Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity

scholarly article by Robina Khan Niazi et al published 15 November 2018 in BMC Medical Genetics

Impact of PTBP1 rs11085226 on glucose-stimulated insulin release in adult Danes

artículo científico publicado en 2015

Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes

artículo científico publicado en 2019

Large-scale studies of the HphI insulin gene variable-number-of-tandem-repeats polymorphism in relation to Type 2 diabetes mellitus and insulin release

artículo científico publicado en 2004

Lessons from whole-exome sequencing in MODYX families

scholarly article by Petra Dusatkova et al published June 2014 in Diabetes Research and Clinical Practice

Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes

scientific article published on 08 December 2020

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

Mutation analysis of the preproghrelin gene: no association with obesity and type 2 diabetes

artículo científico publicado en 2005

No consistent effect of ADRB2 haplotypes on obesity, hypertension and quantitative traits of body fatness and blood pressure among 6,514 adult Danes

artículo científico publicado en 2009

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes.

artículo científico publicado en 2012

Renin angiotensinogen system gene polymorphisms and essential hypertension among people of West African descent: a systematic review

artículo científico publicado en 2015

Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report

scientific article published on 05 September 2019

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants

scientific article published on 15 August 2019

Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes

artículo científico publicado en 2011

Studies of associations between the Arg389Gly polymorphism of the beta1-adrenergic receptor gene (ADRB1) and hypertension and obesity in 7677 Danish white subjects.

artículo científico publicado en 2007

Studies of the associations between functional beta2-adrenergic receptor variants and obesity, hypertension and type 2 diabetes in 7,808 white subjects.

artículo científico publicado en 2007

The CTRB1/2 locus affects diabetes susceptibility and treatment via the incretin pathway

artículo científico publicado en 2013

The FOXO3A rs2802292 G-allele associates with improved peripheral and hepatic insulin sensitivity and increased skeletal muscle-FOXO3A mRNA expression in twins

artículo científico publicado en 2010

The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

artículo científico publicado en 2007

The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

The effect of PCSK1 variants on waist, waist-hip ratio and glucose metabolism is modified by sex and glucose tolerance status

artículo científico publicado en 2011

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes

artículo científico publicado en 2015

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

artículo científico publicado en 2016

Variant near ADAMTS9 known to associate with type 2 diabetes is related to insulin resistance in offspring of type 2 diabetes patients--EUGENE2 study

artículo científico publicado en 2009

‘Omics’‐driven discoveries in prevention and treatment of type 2 diabetes ⬇️

artículo científico publicado el 1 de junio de 2012

Lista de obras de Anette P. Gjesing

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Association of a functional 17beta-estradiol sensitive IL6-174G/C promoter polymorphism with early-onset type 1 diabetes in females

Association of the beta3-adrenergic receptor Trp64Arg polymorphism with common metabolic traits: studies of 7605 middle-aged white people

Association studies of novel obesity-related gene variants with quantitative metabolic phenotypes in a population-based sample of 6,039 Danish individuals

Associations of the Inflammatory Marker YKL-40 with Measures of Obesity and Dyslipidaemia in Individuals at High Risk of Type 2 Diabetes

Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease ⬇️

Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes

Carriers of the TCF7L2 rs7903146 TT genotype have elevated levels of plasma glucose, serum proinsulin and plasma gastric inhibitory polypeptide (GIP) during a meal test

Correction: Does DNA Methylation of PPARGC1A Influence Insulin Action in First Degree Relatives of Patients with Type 2 Diabetes?

DNA methylation and gene expression of HIF3A: cross-tissue validation and associations with BMI and insulin resistance

Does DNA methylation of PPARGC1A influence insulin action in first degree relatives of patients with type 2 diabetes?

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Evaluation of a target region capture sequencing platform using monogenic diabetes as a study-model

Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity

Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traits

G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans

Genetic Correlation between Body Fat Percentage and Cardiorespiratory Fitness Suggests Common Genetic Etiology

Genetic Variations in the Human G Protein-coupled Receptor Class C, Group 6, Member A (GPRC6A) Control Cell Surface Expression and Function

Genetic and phenotypic correlations between surrogate measures of insulin release obtained from OGTT data

Genetic evidence of assortative mating in humans

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

Heterogeneity in glucose response curves during an oral glucose tolerance test and associated cardiometabolic risk

High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus

High heritability and genetic correlation of intravenous glucose- and tolbutamide-induced insulin secretion among non-diabetic family members of type 2 diabetic patients

Homozygous carriers of the TCF7L2 rs7903146 T-allele show altered postprandial response in triglycerides and triglyceride-rich lipoproteins

Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

Human pancreatic islet 3D chromatin architecture provides insights into the genetics of type 2 diabetes

Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity

Impact of PTBP1 rs11085226 on glucose-stimulated insulin release in adult Danes

Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes

Large-scale studies of the HphI insulin gene variable-number-of-tandem-repeats polymorphism in relation to Type 2 diabetes mellitus and insulin release

Lessons from whole-exome sequencing in MODYX families

Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Mutation analysis of the preproghrelin gene: no association with obesity and type 2 diabetes

No consistent effect of ADRB2 haplotypes on obesity, hypertension and quantitative traits of body fatness and blood pressure among 6,514 adult Danes

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes.

Renin angiotensinogen system gene polymorphisms and essential hypertension among people of West African descent: a systematic review

Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants

Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes

Studies of associations between the Arg389Gly polymorphism of the beta1-adrenergic receptor gene (ADRB1) and hypertension and obesity in 7677 Danish white subjects.

Studies of the associations between functional beta2-adrenergic receptor variants and obesity, hypertension and type 2 diabetes in 7,808 white subjects.

The CTRB1/2 locus affects diabetes susceptibility and treatment via the incretin pathway

The FOXO3A rs2802292 G-allele associates with improved peripheral and hepatic insulin sensitivity and increased skeletal muscle-FOXO3A mRNA expression in twins

The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

The effect of PCSK1 variants on waist, waist-hip ratio and glucose metabolism is modified by sex and glucose tolerance status

The genetic architecture of type 2 diabetes

The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

Variant near ADAMTS9 known to associate with type 2 diabetes is related to insulin resistance in offspring of type 2 diabetes patients--EUGENE2 study

‘Omics’‐driven discoveries in prevention and treatment of type 2 diabetes ⬇️