User profiles for Emil V.R. Appel

Vincent Rosenbaum Aaskov

Other name: Emil Vincent Rosenbaum Appel
Novo Nordisk Foundation Center for Basic Metabolic Research
Verified email at zs.com
Cited by 3385

Rare and low-frequency coding variants alter human adult height

…, E Albrecht, KH Allin, M Allison, P Amouyel, EV Appel… - Nature, 2017 - nature.com
Height is a highly heritable, classic polygenic trait with approximately 700 common associated
variants identified through genome-wide association studies so far. Here, we report 83 …

Genome-wide associations for birth weight and correlations with adult disease

…, CEM van Beijsterveldt, G Willemsen, EVR Appel… - Nature, 2016 - nature.com
Birth weight (BW) has been shown to be influenced by both fetal and maternal factors and in
observational studies is reproducibly associated with future risk of adult metabolic diseases …

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

…, H Mbarek, M Müller-Nurasyid, M Standl, EVR Appel… - Nature …, 2019 - nature.com
Birth weight variation is influenced by fetal and maternal genetic and non-genetic factors,
and has been reproducibly associated with future cardio-metabolic health outcomes. In …

The trans-ancestral genomic architecture of glycemic traits

…, Y Wang, P Wu, W Zhang, TS Ahluwalia, EVR Appel… - Nature …, 2021 - nature.com
Glycemic traits are used to diagnose and monitor type 2 diabetes and cardiometabolic health.
To date, most genetic studies of glycemic traits have focused on individuals of European …

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

…, L Pasquali, M Ramos-Rodríguez, EVR Appel… - Nature …, 2019 - nature.com
Genetic studies promise to provide insight into the molecular mechanisms underlying type 2
diabetes (T2D). Variants associated with T2D are often located in tissue-specific enhancer …

[HTML][HTML] Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes

…, C Christensen, I Brandslund, EV Appel… - Nature …, 2018 - nature.com
The reanalysis of existing GWAS data represents a powerful and cost-effective opportunity
to gain insights into the genetics of complex diseases. By reanalyzing publicly available type …

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

…, G Delgado, G Silbernagel, AU Jackson, EV Appel… - Diabetes, 2016 - Am Diabetes Assoc
Genome-wide association studies (GWAS) have found few common variants that influence
fasting measures of insulin sensitivity. We hypothesized that a GWAS of an integrated …

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval

…, G Ahlberg, M Balslev-Harder, EV Appel… - European heart …, 2015 - academic.oup.com
Aims We studied whether variants previously associated with congenital long QT syndrome (cLQTS)
have an effect on the QTc interval in a Danish population sample. Furthermore, we …

[HTML][HTML] Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

…, AE Farmaki, T Bjornland, R Waples, EVR Appel… - Nature …, 2018 - nature.com
The role of rare variants in complex traits remains uncharted. Here, we conduct deep whole
genome sequencing of 1457 individuals from an isolated population, and test for rare variant …

[HTML][HTML] Comparative analyses of QTLs influencing obesity and metabolic phenotypes in pigs and humans

…, T Mark, CB Jørgensen, N Grarup, EVR Appel… - PLoS …, 2015 - journals.plos.org
The pig is a well-known animal model used to investigate genetic and mechanistic aspects of
human disease biology. They are particularly useful in the context of obesity and metabolic …