Author details

Full Name

Mette Hollensted

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36400171	14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes.	Diabetes Res Clin Pract	2022
32921795	Obesity treatment effect in Danish children and adolescents carrying Melanocortin-4 Receptor mutations.	International Journal of Obesity	2021
31471646	Adults with pathogenic MC4R mutations have increased final height and thereby increased bone mass.	Journal of Bone and Mineral Metabolism	2020
33045005	Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.	PLoS Genet	2020
31332278	Genetic predisposition to higher body fat yet lower cardiometabolic risk in children and adolescents.	Int J Obes (Lond)	2019
30629617	Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes.	PLoS ONE	2019
31504107	Abdominal adiposity and cardiometabolic risk factors in children and adolescents: a Mendelian randomization analysis.	Am J Clin Nutr	2019
31488071	Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report.	BMC Medical Genetics	2019
31415576	Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants.	PLoS ONE	2019
31001758	Genetic Determinants of Weight Loss After Bariatric Surgery.	Obesity Surgery	2019
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
30514227	Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study.	BMC Medical Genetics	2018
30460774	Genetic Susceptibility for Childhood BMI has no Impact on Weight Loss Following Lifestyle Intervention in Danish Children.		2018
30442103	Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity.	BMC Medical Genetics	2018
29861388	Patients with Obesity Caused by Melanocortin-4 Receptor Mutations Can Be Treated with a Glucagon-like Peptide-1 Receptor Agonist.		2018
29855666	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 obese.	Diabetologia	2018
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28333968	A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.	PLoS ONE	2017
28448500	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
28443625	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Nat Commun	2017
28832619	Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
29264522	High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus.	Journal of the Endocrine Society	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
26558825	Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case-control study.	BMC Medical Genetics	2015
25625282	Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.	PLoS Genet	2015
24476040	Evaluation of a target region capture sequencing platform using monogenic diabetes as a study-model.	BMC Genetics	2014
22325233	The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals.	BMC Medical Genetics	2012