| A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis D Thyagarajan, S Shanske, M Vazquez‐Memije, D Devivo, S Dimauro Annals of neurology 38 (3), 468-472, 1995 | 248 | 1995 |
| A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy D Thyagarajan, S Bressman, C Bruno, S Przedborski, S Shanske, T Lynch, ... Annals of neurology 48 (5), 730-736, 2000 | 222 | 2000 |
| Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease DM Kirby, A Boneh, CW Chow, A Ohtake, MT Ryan, D Thyagarajan, ... Annals of Neurology: Official Journal of the American Neurological …, 2003 | 136 | 2003 |
| The fate of human sperm-derived mtDNA in somatic cells G Manfredi, D Thyagarajan, LC Papadopoulou, F Pallotti, EA Schon The American Journal of Human Genetics 61 (4), 953-960, 1997 | 135 | 1997 |
| Magnetic resonance imaging in brachial plexopathy of cancer D Thyagarajan, T Cascino, G Harms Neurology 45 (3), 421-427, 1995 | 125 | 1995 |
| Normal variants of human mitochondrial DNA and translation products: the building of a reference data base S Marzuki, AS Noer, P Lertrit, D Thyagarajan, R Kapsa, P Utthanaphol, ... Human genetics 88, 139-145, 1991 | 110 | 1991 |
| Voice changes in Parkinson’s disease: What are they telling us? A Ma, KK Lau, D Thyagarajan Journal of Clinical Neuroscience 72, 1-7, 2020 | 106 | 2020 |
| A tRNA (Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome. AS Noer, H Sudoyo, P Lertrit, D Thyagarajan, P Utthanaphol, R Kapsa, ... American journal of human genetics 49 (4), 715, 1991 | 101 | 1991 |
| Rapid‐onset dystonia‐parkinsonism in a second family A Brashear, D DeLeon, SB Bressman, D Thyagarajan, MR Farlow, ... Neurology 48 (4), 1066-1069, 1997 | 94 | 1997 |
| Multiple symmetrical lipomatosis—a mitochondrial disorder of brown fat C Plummer, PJ Spring, R Marotta, J Chin, G Taylor, D Sharpe, ... Mitochondrion 13 (4), 269-276, 2013 | 93 | 2013 |
| A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I. P Lertrit, AS Noer, MJ Jean-Francois, R Kapsa, X Dennett, D Thyagarajan, ... American journal of human genetics 51 (3), 457, 1992 | 92 | 1992 |
| Dopamine restores cognitive motivation in Parkinson’s disease S McGuigan, SH Zhou, MB Brosnan, D Thyagarajan, MA Bellgrove, ... Brain 142 (3), 719-732, 2019 | 87 | 2019 |
| Platelet α-and γ-synucleins in Parkinson's disease and normal control subjects QX Li, BCV Campbell, CA McLean, D Thyagarajan, WP Gai, RM Kapsa, ... Journal of Alzheimer's Disease 4 (4), 309-315, 2002 | 64 | 2002 |
| Dominantly‐inherited adult‐onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene D Thyagarajan, T Chataway, R Li, WP Gai, M Brenner Movement disorders: official journal of the Movement Disorder Society 19 (10 …, 2004 | 57 | 2004 |
| Meningoencephalomyelitis with vasculitis due to varicella zoster virus: a case report and review of the literature PA McKelvie, S Collins, D Thyagarajan, N Trost, H Sheorey, E Byrne Pathology 34 (1), 88-93, 2002 | 57 | 2002 |
| Clinical and molecular features of adPEO due to mutations in the Twinkle gene S Lewis, W Hutchison, D Thyagarajan, HHM Dahl Journal of the neurological sciences 201 (1-2), 39-44, 2002 | 55 | 2002 |
| Parkinson's disease alters multisensory perception: Insights from the Rubber Hand Illusion C Ding, CJ Palmer, J Hohwy, GJ Youssef, B Paton, N Tsuchiya, JC Stout, ... Neuropsychologia 97, 38-45, 2017 | 41 | 2017 |
| Abnormal vocal cord movement treated with botulinum toxin in patients with asthma resistant to optimised management M Baxter, N Uddin, S Raghav, P Leong, K Low, K Hamza, PW Holmes, ... Respirology 19 (4), 531-537, 2014 | 38 | 2014 |
| “He’s Back so I’m Not Alone”: the impact of deep brain stimulation on personality, self, and relationships in Parkinson’s disease CJ Thomson, RA Segrave, E Racine, N Warren, D Thyagarajan, A Carter Qualitative Health Research 30 (14), 2217-2233, 2020 | 33 | 2020 |
| The mitochondrial T1095C mutation increases gentamicin-mediated apoptosis H Muyderman, NR Sims, M Tanaka, N Fuku, R Raghupathi, ... Mitochondrion 12 (4), 465-471, 2012 | 33 | 2012 |
