Anja Lisbeth Frederiksen (Anja L Frederiksen, A L Frederiksen)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 4

Top Topics

Dna Methylation

Depressive Symptoms

Top Venues

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA

American journal of medical genetics. Part A

Calcified tissue international

Clinical genetics

Aalborg Universitet

University of Southern Denmark (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Aalborg Universitet Nov 01 2019

Denmark

Clinical Associate Professor :: Dept of Clinical Medicine

Aalborg Universitetshospital Nov 01 2019

Denmark

Consultant :: Dept of Clinical Genetics

University of Southern Denmark Apr 01 2017 - Oct 31 2019

Denmark

Clinical associate professor :: Dept. of Clinical Research

Odense University Hospital Mar 01 2013 - Oct 31 2019

Denmark

Consultant :: Dept. of Clinical Genetics

Education History

University of Southern Denmark Aug 26 2006

Denmark

PHD

Publications

Simone Rask Nielsen, Stinus Gadegaard Hansen, Claus Bistrup, Klaus Brusgaard, Anja Lisbeth Frederiksen
Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease. Calcified tissue international 111 (6) (2022)
Nicola Hepp, Anja Lisbeth Frederiksen, Morten Duno, Niklas Rye Jørgensen, Jens-Erik Beck Jensen
Biochemical and clinical manifestations in adults with hypophosphatasia: a national cross-sectional study. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 33 (12) (2022)
Anne Benner, Yazeid Alhaidan, Matthew A Lines, Klaus Brusgaard, Diva D De León, Rebecca Sparkes, Anja Lisbeth Frederiksen, Henrik Boye Thybo Christesen
PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only. American journal of medical genetics. Part A 185 (10) (2021)
J H Langdahl, M Larsen, Morten Frost, P H Andersen, K B Yderstraede, J Vissing, M Dunø, M Thomassen, Anja Lisbeth Frederiksen
Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective Cohort. Clinical genetics 93 (4) (2019)