Nanna Cornelius
Copenhagen, Denmark
Last Updated: 09/26/2026
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Found 10 publications
Comparative Assessment of Diagnostic Homologous Recombination Deficiency-Associated Mutational Signatures in Ovarian Cancer.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: March 16, 2021
Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters.
Journal: Mitochondrion
Published: October 06, 2016
Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development.
Journal: Molecular cytogenetics
Published: November 06, 2015
Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited Disorders.
Journal: JIMD reports
Published: June 16, 2015
Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolism.
Journal: Journal of inherited metabolic disease
Published: February 18, 2015
A mosaic small supernumerary marker chromosome 17 in a patient with Tourette syndrome, ADHD and intellectual disability: A case story and review of the literature.
Journal: Psychiatry research
Published: January 09, 2015
Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblasts.
Journal: Human molecular genetics
Published: April 05, 2014
Genetic and cellular modifiers of oxidative stress: what can we learn from fatty acid oxidation defects?
Journal: Molecular genetics and metabolism
Published: August 30, 2013
Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.
Journal: Human molecular genetics
Published: June 04, 2013
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency.
Journal: Human molecular genetics
Published: May 22, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026