Julie L. Murphy

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease

Lyndsey Craven, Helen Tuppen, Gareth D. Greggains et al. · Nature · 2010 · 476 citations · Full text

Mitochondrial Function, Genetics, Human Embryos +8

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance

Gerald Pfeffer, Gráinne S. Gorman, Helen Griffin et al. · Brain · 2014 · 174 citations · Full text

Mitochondrial Dna Maintenance, Ocular Disease, Mendelian Disorder +13

Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle

John P. Grady, Julie L. Murphy, Emma L. Blakely et al. · PLoS ONE · 2014 · 69 citations · Full text

Muscle Function, Genetics, Dna Analysis +19

Cytochrome c oxidase-intermediate fibres: Importance in understanding the pathogenesis and treatment of mitochondrial myopathy

Julie L. Murphy, Thiloka Ratnaike, Ersong Shang et al. · Neuromuscular Disorders · 2012 · 49 citations · Full text

Mitochondrial DNA deletions in muscle satellite cells: implications for therapies

Sally Spendiff, Mojgan Reza, Julie L. Murphy et al. · Human Molecular Genetics · 2013 · 36 citations · Full text

Mitochondrial Myopathy, Mtdna Mutation, Mitochondrial Function +13