Carolyn Sue
Carolyn Sue
Professor and Director of Neurogenetics, University of Sydney
Verified email at med.usyd.edu.au
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
73622021
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
8922000
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
6141999
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
4251999
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
2702007
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
2132014
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
2121999
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
1992018
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
1782016
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
1752014
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
1752010
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
1561999
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
1511998
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
1492016
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
1472011
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
1452013
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
1452010
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
1421998
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
1412000
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
1332004
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Articles 1–20