| The large-conductance Ca2+-activated K+ channel is essential for innate immunity J Ahluwalia, A Tinker, LH Clapp, MR Duchen, AY Abramov, S Pope, ... Nature 427 (6977), 853-858, 2004 | 266 | 2004 |
| Consequences of long-term oral administration of the mitochondria-targeted antioxidant MitoQ to wild-type mice S Rodriguez-Cuenca, HM Cochemé, A Logan, I Abakumova, TA Prime, ... Free Radical Biology and Medicine 48 (1), 161-172, 2010 | 240 | 2010 |
| Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease L Dunn, GFG Allen, A Mamais, H Ling, A Li, KE Duberley, IP Hargreaves, ... Neurobiology of aging 35 (5), 1111-1115, 2014 | 218 | 2014 |
| Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia E Meyer, KJ Carss, J Rankin, JME Nichols, D Grozeva, AP Joseph, ... Nature genetics 49 (2), 223-237, 2017 | 214 | 2017 |
| Loss of PLA2G6 leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction KJ Kinghorn, JI Castillo-Quan, F Bartolome, PR Angelova, L Li, S Pope, ... Brain 138 (7), 1801-1816, 2015 | 182 | 2015 |
| Oxidative stress and mitochondrial dysfunction in neurodegeneration; cardiolipin a critical target? S Pope, JM Land, SJR Heales Biochimica et Biophysica Acta (BBA)-Bioenergetics 1777 (7-8), 794-799, 2008 | 181 | 2008 |
| Missense dopamine transporter mutations associate with adult parkinsonism and ADHD FH Hansen, T Skjørringe, S Yasmeen, NV Arends, MA Sahai, K Erreger, ... The Journal of clinical investigation 124 (7), 3107-3120, 2014 | 155 | 2014 |
| Mutations in PROSC disrupt cellular pyridoxal phosphate homeostasis and cause vitamin-B6-dependent epilepsy N Darin, E Reid, L Prunetti, L Samuelsson, RA Husain, M Wilson, ... The American Journal of Human Genetics 99 (6), 1325-1337, 2016 | 147 | 2016 |
| Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies T Opladen, E López-Laso, E Cortès-Saladelafont, TS Pearson, HS Sivri, ... Orphanet journal of rare diseases 15, 1-30, 2020 | 110 | 2020 |
| Synthesis and analysis of conjugates of the major vitamin E metabolite, α-CEHC SAS Pope, GE Burtin, PT Clayton, DJ Madge, DPR Muller Free Radical Biology and Medicine 33 (6), 807-817, 2002 | 99 | 2002 |
| Multicentre prospective cohort study of body mass index and postoperative complications following gastrointestinal surgery TM Drake, D Nepogodiev, SJ Chapman, JC Glasbey, C Khatri, CY Kong, ... British Journal of Surgery 103 (9), 1157-1172, 2016 | 84 | 2016 |
| Clinical, pathological and functional characterization of riboflavin-responsive neuropathy A Manole, Z Jaunmuktane, I Hargreaves, MHR Ludtmann, V Salpietro, ... Brain 140 (11), 2820-2837, 2017 | 80 | 2017 |
| Cerebral folate deficiency: analytical tests and differential diagnosis S Pope, R Artuch, S Heales, S Rahman Journal of Inherited Metabolic Disease 42 (4), 655-672, 2019 | 77 | 2019 |
| Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons L Parviainen, S Dihanich, GW Anderson, AM Wong, HR Brooks, R Abeti, ... Acta neuropathologica communications 5, 1-21, 2017 | 73 | 2017 |
| PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ... Annals of Neurology 86 (2), 225-240, 2019 | 69 | 2019 |
| A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compounds SAS Pope, PT Clayton, DPR Muller Archives of biochemistry and biophysics 381 (1), 8-15, 2000 | 62 | 2000 |
| Body mass index and complications following major gastrointestinal surgery: a prospective, international cohort study and meta‐analysis EuroSurg Collaborative, R Blanco‐Colino, S Lee, SK Kamarajah, P Vasko, ... Colorectal Disease 20 (8), O215-O225, 2018 | 58 | 2018 |
| Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: a potential treatment target? GA Horvath, M Demos, C Shyr, A Matthews, L Zhang, S Race, ... Molecular genetics and metabolism 117 (1), 42-48, 2016 | 48 | 2016 |
| A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy CL Alston, M Morak, C Reid, IP Hargreaves, SAS Pope, JM Land, ... Neuromuscular disorders 20 (2), 131-135, 2010 | 47 | 2010 |
| Astrocytes protect against copper-catalysed loss of extracellular glutathione SAS Pope, R Milton, SJR Heales Neurochemical research 33, 1410-1418, 2008 | 47 | 2008 |
