| Utility of quantitative T-cell responses versus unstimulated interferon-γ for the diagnosis of pleural tuberculosis K Dheda, RN van Zyl-Smit, LA Sechi, M Badri, R Meldau, S Meldau, ... European Respiratory Journal 34 (5), 1118-1126, 2009 | 111 | 2009 |
| Quantitative lung T cell responses aid the rapid diagnosis of pulmonary tuberculosis K Dheda, RN van Zyl-Smit, R Meldau, S Meldau, G Symons, H Khalfey, ... Thorax 64 (10), 847-853, 2009 | 76 | 2009 |
| Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans G van der Watt, EP Owen, P Berman, S Meldau, N Watermeyer, SE Olpin, ... Molecular genetics and metabolism 101 (2-3), 178-182, 2010 | 59 | 2010 |
| MT-ND5 mutation exhibits highly variable neurological manifestations at low mutant load YS Ng, NZ Lax, P Maddison, CL Alston, EL Blakely, PD Hepplewhite, ... EBioMedicine 30, 86-93, 2018 | 56 | 2018 |
| Understanding the implications of mitochondrial DNA variation in the health of black southern African populations: The 2014 Workshop F Van der Westhuizen, PZ Sinxadi, C Dandara, I Smuts, G Riordan, ... Wiley, 2015 | 19 | 2015 |
| Identification of a single MPV17 nonsense‐associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy S Meldau, RJ De Lacy, GTM Riordan, EA Goddard, K Pillay, KJ Fieggen, ... Clinical genetics 93 (5), 1093-1096, 2018 | 15 | 2018 |
| Haplogroup context is less important in the penetrance of mitochondrial DNA complex I mutations compared to mt-tRNA mutations H O’Keefe, RA Queen, S Meldau, P Lord, JL Elson Journal of Molecular Evolution 86, 395-403, 2018 | 11 | 2018 |
| Increased blood-derived mitochondrial DNA copy number in African ancestry individuals with Parkinson's disease AC Müller-Nedebock, S Meldau, C Lombard, S Abrahams, ... Parkinsonism & Related Disorders 101, 1-5, 2022 | 8 | 2022 |
| Could we offer mitochondrial donation or similar assisted reproductive technology to South African patients with mitochondrial DNA disease? S Meldau, G Riordan, F Van der Westhuizen, JL Elson, I Smuts, ... South African Medical Journal 106 (3), 234-236, 2016 | 7 | 2016 |
| Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B L Roberts, S Julius, S Dawlat, S Yildiz, G Rebello, S Meldau, K Pillay, ... Human Mutation 41 (11), 1871-1876, 2020 | 6 | 2020 |
| Mitochondrial molecular genetic results in a South African cohort: Divergent mitochondrial and nuclear DNA findings S Meldau, EP Owen, K Khan, GT Riordan Journal of Clinical Pathology 75 (1), 34-38, 2022 | 5 | 2022 |
| Pitfalls of relying on genetic testing only to diagnose inherited metabolic disorders in non-western populations-5 cases of pyruvate dehydrogenase deficiency from South Africa S Meldau, C Fratter, LN Bhengu, K Sergeant, K Khan, GT Riordan, ... Molecular Genetics and Metabolism Reports 24, 100629, 2020 | 5 | 2020 |
| Liddle’s syndrome in an African male due to a novel frameshift mutation in the beta-subunit of the epithelial sodium channel gene R Freercks, S Meldau, E Jones, J Ensor, C Weimers-Willard, B Rayner Cardiovascular journal of Africa 28 (5), e4-e6, 2017 | 4 | 2017 |
| Teenaged siblings with progressive neurocognitive disease D Haarburger, R Renison, S Meldau, R Eastman, G van der Watt Clinical Chemistry 59 (8), 1160-1164, 2013 | 4 | 2013 |
| A case for genomic medicine in South African paediatric patients with neuromuscular disease SV Raga, JM Wilmshurst, I Smuts, S Meldau, S Bardien, M Schoonen, ... Frontiers in Pediatrics 10, 1033299, 2022 | 2 | 2022 |
| Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study M Bisschoff, I Smuts, M Dercksen, M Schoonen, BC Vorster, ... Orphanet Journal of Rare Diseases 19 (1), 15, 2024 | 1 | 2024 |
| A novel mitochondrial DNA variant in MT-ND6: m. 14430A> C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiency S Meldau, S Ackermann, G Riordan, GF van der Watt, C Spencer, S Raga, ... Molecular Genetics and Metabolism Reports 39, 101078, 2024 | | 2024 |
| Validation of PHASE for deriving N-acetyltransferase 2 haplotypes in the Western Cape mixed ancestry population C Swart, S Meldau, CM Centner, AD Marais, F Omar African Journal of Laboratory Medicine 9 (1), 1-7, 2020 | | 2020 |
| HIGH DISEASE PREVALENCE AND SINGLE MUTATION FREQUENCY FOR GLUTARYL-COA DEHYDROGENASE DEFICIENCY IN BLACK SOUTH AFRICANS GF Van der Watt, EP Owen, P Berman, N Watermeyer, SE Olpin, ... JOURNAL OF INHERITED METABOLIC DISEASE 33, S38-S38, 2010 | | 2010 |
| CORRESPONDING AUTHOR: Surita Meldau S Meldau, R De Lacy, G Riordan, E Goddard, K Pillay, K Fieggen, ... | | |
George Frederick Van Der WattEmail confirmado em uct.ac.za
