| Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease L Craven, HA Tuppen, GD Greggains, SJ Harbottle, JL Murphy, LM Cree, ... Nature 465 (7294), 82-85, 2010 | 569 | 2010 |
| Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions T Taivassalo, JL Gardner, RW Taylor, AM Schaefer, J Newman, ... Brain 129 (12), 3391-3401, 2006 | 220 | 2006 |
| Resistance training in patients with single, large-scale deletions of mitochondrial DNA JL Murphy, EL Blakely, AM Schaefer, L He, P Wyrick, RG Haller, ... Brain 131 (11), 2832-2840, 2008 | 184 | 2008 |
| Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance G Pfeffer, GS Gorman, H Griffin, M Kurzawa-Akanbi, EL Blakely, I Wilson, ... Brain 137 (5), 1323-1336, 2014 | 171 | 2014 |
| Transmission of mitochondrial DNA disorders: possibilities for the future DT Brown, M Herbert, VK Lamb, PF Chinnery, RW Taylor, RN Lightowlers, ... The Lancet 368 (9529), 87-89, 2006 | 121 | 2006 |
| Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle JP Grady, JL Murphy, EL Blakely, RG Haller, RW Taylor, DM Turnbull, ... PLoS One 9 (12), e114462, 2014 | 66 | 2014 |
| Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathy JL Murphy, TE Ratnaike, E Shang, G Falkous, EL Blakely, CL Alston, ... Neuromuscular Disorders 22 (8), 690-698, 2012 | 55 | 2012 |
| Research into policy: a brief history of mitochondrial donation L Craven, M Herbert, A Murdoch, J Murphy, JL Davies, DM Turnbull Stem Cells (Dayton, Ohio) 34 (2), 265, 2016 | 42 | 2016 |
| Mitochondrial DNA deletions in muscle satellite cells: implications for therapies S Spendiff, M Reza, JL Murphy, G Gorman, EL Blakely, RW Taylor, ... Human molecular genetics 22 (23), 4739-4747, 2013 | 39 | 2013 |
| Detection of cytochrome c oxidase activity and mitochondrial proteins in single cells DJ Mahad, I Ziabreva, G Campbell, F Laulund, JL Murphy, AK Reeve, ... Journal of neuroscience methods 184 (2), 310-319, 2009 | 39 | 2009 |
| Experimental strategies towards treating mitochondrial DNA disorders JL Gardner, L Craven, DM Turnbull, RW Taylor Bioscience reports 27 (1-3), 139-150, 2007 | 36 | 2007 |
| Scientific and ethical issues in mitochondrial donation L Craven, J Murphy, DM Turnbull, RW Taylor, GS Gorman, R McFarland The new bioethics 24 (1), 57-73, 2018 | 32 | 2018 |
| Mitochondrial donation—hope for families with mitochondrial DNA disease L Craven, JL Murphy, DM Turnbull Emerging topics in life sciences 4 (2), 151-154, 2020 | 10 | 2020 |
| CO 2 DNM2 mutations cause multiple mtDNA deletions in muscle: A novel disorder of mtDNA maintenance KJ Krishnan, G Nelson, NB Romero, T Ratnaike, EL Blakely, ... Neuromuscular Disorders 22 (9), 839, 2012 | 1 | 2012 |
| A JOU G Pfeffer, GS Gorman, H Griffin, M Kurzawa-Akanbi, EL Blakely, I Wilson, ... | | 2014 |
| P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance GS Gorman, G Pfeffer, H Griffin, M Kurzawa-Akanbi, EL Blakely, I Wilson, ... Neuromuscular Disorders 24, S15, 2014 | | 2014 |
| P28 Investigating mitochondrial dysfunction in the myofibrillar and other protein aggregate myopathies A Vincent, JL Murphy, R Barresi, RW Taylor, DM Turnbull Neuromuscular Disorders 24, S14, 2014 | | 2014 |
| HMG Advance Access published July 11, 2013 S Spendiff, M Reza, JL Murphy, G Gorman, EL Blakely, RW Taylor, ... | | 2013 |
| P62 Long term endurance training and deconditioning in patients with mitochondrial myopathy JL Murphy, TE Ratnaike, E Shang, G Falkous, EL Blakely, CL Alston, ... Neuromuscular Disorders, S24, 2012 | | 2012 |
| Long term endurance training and deconditioning in patients with mitochondrial myopathy JL Murphy, TE Ratnaike, E Shang, G Falkous, EL Blakely, CL Alston, ... United Kingdom Neuromuscular Translational Research Conference, 2012 | | 2012 |
