Intet billede af Mette Christoffersen
20102025

Publikationer pr. år

Personlig profil

Expertise

Genetic epidemiology; next generation sequencing, aging, familial hypercholesterolemia; amyloidosis; cardiovascular disease

Primære forskningsområder

Visible aging signs - such as hair graying, facial wrinkles and baldness - as risk markers for age-related disease and poor health.

Identification of novel heritable factors for familial hypercholesterolemia in the general population.

Transthyretin amyloidosis in the general population.

Aktuel forskning

I am currently involved in two primary research projects:

1. To examine the spectrum of genetic variants in the TTR gene (encoding transthyretin) in the Danish general population - and to determine the correation with plasma transthyretin levels, amyloidosis and amyloidosis related phenotypes.

2. A study on the molecular origin of disturbed lipid metabolism (i.e. LDL and triglyceride metabolism) in order to identify novel targets for pharmaceutical intervention and hereby improving treatment of cardiovascular disease. Our role in this project is to validate whether potential pharmaceutical targets indeed affect intermediate lipid phenotypes and risk of cardiovascular disease in the general population. This is done with the use of Next Generation Sequencing in the very large and well-defined population-based studies - the Copenhagen City Heart Study and the Copenhagen General Population Study - as well as large case-control studies in patients with coronary artery disease.

Mulige interessekonflikter

None

Fingeraftryk

Dyk ned i forskningsemnerne, hvor Mette Christoffersen er aktive. Disse emneetiketter kommer fra denne persons arbejder. Sammen danner de et unikt fingerprint.
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