Fiona M. Robertson
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion.
Journal: American journal of medical genetics. Part A
Published: May 20, 2024
Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis.
Journal: Nature cancer
Published: February 05, 2022
Feasibility and impact of haplogroup matching for mitochondrial replacement treatment.
Journal: EMBO reports
Published: December 17, 2021
The Isolation and Deep Sequencing of Mitochondrial DNA.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: June 03, 2021
Age-associated mitochondrial DNA mutations cause metabolic remodelling that contributes to accelerated intestinal tumorigenesis.
Journal: Nature cancer
Published: October 19, 2020
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 18, 2020
Mitochondrial DNA Damage and Brain Aging in Human Immunodeficiency Virus.
Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Published: December 16, 2019
Recent advances in understanding the molecular genetic basis of mitochondrial disease.
Journal: Journal of inherited metabolic disease
Published: January 21, 2019
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.
Journal: EMBO molecular medicine
Published: September 12, 2018
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Last Updated: 09/26/2026