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Carolyn Sue
Carolyn Sue
Professor and Kinghorn Chair, University of New South Wales, Sydney
Verified email at neura.edu.au - Homepage
Title
Cited by
Cited by
Year
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
13055*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
10582000
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
6761999
Mitochondrial dysfunction in Parkinson’s disease: new mechanistic insights and therapeutic perspectives
JS Park, RL Davis, CM Sue
Current neurology and neuroscience reports 18, 1-11, 2018
5142018
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
4901999
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
3302007
New insights into the complex role of mitochondria in Parkinson’s disease
A Grünewald, KR Kumar, CM Sue
Progress in neurobiology 177, 73-93, 2019
3202019
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
3162014
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
3082016
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society
S Parikh, A Goldstein, A Karaa, MK Koenig, I Anselm, C Brunel-Guitton, ...
Genetics in Medicine 19 (12), 1380-1397, 2017
2752017
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
2632016
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
2592014
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
2221999
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
2172010
Use of whole-exome sequencing for diagnosis of limb-girdle muscular dystrophy: outcomes and lessons learned
R Ghaoui, ST Cooper, M Lek, K Jones, A Corbett, SW Reddel, ...
JAMA neurology 72 (12), 1424-1432, 2015
2032015
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
1862010
The role of ATP13A2 in Parkinson's disease: clinical phenotypes and molecular mechanisms
JS Park, NF Blair, CM Sue
Movement Disorders 30 (6), 770-779, 2015
1842015
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
1752013
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
1751999
Nix restores mitophagy and mitochondrial function to protect against PINK1/Parkin-related Parkinson’s disease
B Koentjoro, JS Park, CM Sue
Scientific reports 7 (1), 44373, 2017
1712017
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