Carolyn Sue
Carolyn Sue
Professor and Director of Neurogenetics, University of Sydney
Verified email at
Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
I Nishino, J Fu, K Tanji, T Yamada, S Shimojo, T Koori, M Mora, JE Riggs, ...
Nature 406 (6798), 906-910, 2000
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
LC Papadopoulou, CM Sue, MM Davidson, K Tanji, I Nishino, JE Sadlock, ...
Nature genetics 23 (3), 333-337, 1999
Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
AL Andreu, MG Hanna, H Reichmann, C Bruno, AS Penn, K Tanji, ...
New England Journal of Medicine 341 (14), 1037-1044, 1999
Population prevalence of the MELAS A3243G mutation
N Manwaring, MM Jones, JJ Wang, E Rochtchina, C Howard, P Mitchell, ...
Mitochondrion 7 (3), 230-233, 2007
The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy
T Cornelissen, D Haddad, F Wauters, C Van Humbeeck, W Mandemakers, ...
Human molecular genetics 23 (19), 5227-5242, 2014
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNASer (UCN) gene
CM Sue, K Tanji, G Hadjigeorgiou, AL Andreu, I Nishino, S Krishna, ...
Neurology 52 (9), 1905-1905, 1999
Mitochondrial dysfunction in Parkinson’s disease: new mechanistic insights and therapeutic perspectives
JS Park, RL Davis, CM Sue
Current neurology and neuroscience reports 18 (5), 1-11, 2018
N omenclature of genetic movement disorders: R ecommendations of the international P arkinson and movement disorder society task force
C Marras, A Lang, BP van de Warrenburg, CM Sue, SJ Tabrizi, L Bertram, ...
Movement Disorders 31 (4), 436-457, 2016
Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes
SMY Kong, BKK Chan, JS Park, KJ Hill, JB Aitken, L Cottle, H Farghaian, ...
Human molecular genetics 23 (11), 2816-2833, 2014
Disease-specific, neurosphere-derived cells as models for brain disorders
N Matigian, G Abrahamsen, R Sutharsan, AL Cook, AM Vitale, ...
Disease models & mechanisms 3 (11-12), 785-798, 2010
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
C Bruno, A Martinuzzi, Y Tang, AL Andreu, F Pallotti, E Bonilla, S Shanske, ...
The American Journal of Human Genetics 65 (3), 611-620, 1999
Neuroradiological features of six kindreds with MELAS tRNALeu A3243G point mutation: implications for pathogenesis
CM Sue, DS Crimmins, YS Soo, R Pamphlett, CM Presgrave, ...
Journal of Neurology, Neurosurgery & Psychiatry 65 (2), 233-240, 1998
Activation of β-glucocerebrosidase reduces pathological α-synuclein and restores lysosomal function in Parkinson's patient midbrain neurons
JR Mazzulli, F Zunke, T Tsunemi, NJ Toker, S Jeon, LF Burbulla, ...
Journal of Neuroscience 36 (29), 7693-7706, 2016
Mechanical thrombectomy with a self-expanding retrievable intracranial stent (Solitaire AB): experience in 26 patients with acute cerebral artery occlusion
F Miteff, KC Faulder, ACC Goh, BS Steinfort, C Sue, TJ Harrington
American journal of neuroradiology 32 (6), 1078-1081, 2011
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
K Lohmann, RA Wilcox, S Winkler, A Ramirez, A Rakovic, JS Park, B Arns, ...
Annals of neurology 73 (4), 537-545, 2013
Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts
A Grünewald, L Voges, A Rakovic, M Kasten, H Vandebona, ...
PloS one 5 (9), e12962, 2010
Cochlear origin of hearing loss in MELAS syndrome
CM Sue, LJ Lipsett, DS Crimmins, CST DipAud, SC Boyages, ...
Annals of neurology 43 (3), 350-359, 1998
Differential features of patients with mutations in two COX assembly genes, SURF‐1 and SCO2
CM Sue, C Karadimas, N Checcarelli, K Tanji, LC Papadopoulou, ...
Annals of neurology 47 (5), 589-595, 2000
Mitochondrial DNA abnormalities and autistic spectrum disorders
R Pons, AL Andreu, N Checcarelli, MR Vilà, K Engelstad, CM Sue, ...
The Journal of pediatrics 144 (1), 81-85, 2004
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