about
The genetic architecture of type 2 diabetesRare and low-frequency coding variants alter human adult heightGenome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals.Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case-control study.A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.Evaluation of a target region capture sequencing platform using monogenic diabetes as a study-model.A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus.An adult-based insulin resistance genetic risk score associates with insulin resistance, metabolic traits and altered fat distribution in Danish children and adolescents who are overweight or obeseIdentification of novel LEPR mutations in Pakistani families with morbid childhood obesityGenetic Susceptibility for Childhood BMI has no Impact on Weight Loss Following Lifestyle Intervention in Danish ChildrenGenetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based studyPatients with Obesity Caused by Melanocortin-4 Receptor Mutations Can Be Treated with a Glucagon-like Peptide-1 Receptor AgonistIncreased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetesGenetic Determinants of Weight Loss After Bariatric SurgeryAbdominal adiposity and cardiometabolic risk factors in children and adolescents: a Mendelian randomization analysisA trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesityGenetic predisposition to higher body fat yet lower cardiometabolic risk in children and adolescentsSequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variantsAdults with pathogenic MC4R mutations have increased final height and thereby increased bone massScreening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Mette Hollensted
@ast
Mette Hollensted
@en
Mette Hollensted
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Mette Hollensted
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Mette Hollensted
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type
label
Mette Hollensted
@ast
Mette Hollensted
@en
Mette Hollensted
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Mette Hollensted
@nl
Mette Hollensted
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prefLabel
Mette Hollensted
@ast
Mette Hollensted
@en
Mette Hollensted
@es
Mette Hollensted
@nl
Mette Hollensted
@sl
P106
P1153
54970018700
P21
P31
P496
0000-0001-5572-3183