Joanna Poulton
University of North Carolina at Chapel Hill(US)Nuffield Orthopaedic Centre(GB)University of Oxford(GB)Nuffield Health(GB)Women’s Health Care(US)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Genomics and Rare Diseases, Autophagy in Disease and Therapy
Most-Cited Works
- → Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria(2001)880 cited
- Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.(1991)
- Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.(1996)
- → Noninvasive Imaging beyond the Diffraction Limit of 3D Dynamics in Thickly Fluorescent Specimens(2012)325 cited
- → Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency(2010)249 cited
- → Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number(2004)241 cited
- → Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal Study(2001)232 cited