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Nature Cell Biology|April 21, 2018
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryosVasileios I Floros, Angela Pyle, Sabine Dietmann, et al.American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 2011
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3Rita Horvath, Birgit Czermin, Sweena Gulati, et al.Neurology|March 3, 2017
Genetic heterogeneity of motor neuropathiesBoglarka Bansagi, Helen Griffin, Roger G Whittaker, et al.Human Molecular Genetics|January 13, 2022
Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial diseaseFlorian A Rosenberger, Jia Xin Tang, Kate Sergeant, et al.EMBO Molecular Medicine|February 29, 2020
Metabolic effects of bezafibrate in mitochondrial diseaseHannah Steele, Aurora Gomez-Duran, Angela Pyle, et al.Plos Genetics|April 1, 2022
Heteroplasmic mitochondrial DNA variants in cardiovascular diseasesClaudia Calabrese, Angela Pyle, Helen Griffin, et al.Plos One|December 29, 2012
Non-random mtDNA segregation patterns indicate a metastable heteroplasmic segregation unit in m.3243A>G cybrid cellsAnton K Raap, Roshan S Jahangir Tafrechi, Frans M van de Rijke, et al.Plos Genetics|June 6, 2014
Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNAJohn W Yarham, Tek N Lamichhane, Angela Pyle, et al.American Journal of Medical Genetics. Part A|October 14, 2024
Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic ExpansionHebatallah M Hassaan, Angela Pyle, Nihal Almenabawy, et al.Pageof 10