Carolyn M. Sue

Overview

Best Publications

• Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

  Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif

  10661
  Citations

• Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  8488
  Citations

• Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

  Ichizo Nishino;Jin Fu;Kurenai Tanji;Takeshi Yamada

  1058
  Citations

• Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  895
  Citations

• Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

  L C Papadopoulou;C M Sue;M M Davidson;K Tanji

  674
  Citations

• Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.

  Jin-Sung Park;Ryan L. Davis;Carolyn M. Sue;Carolyn M. Sue

  508
  Citations

• The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy

  Tom Cornelissen;Dominik Haddad;Fieke Wauters;Cindy Van Humbeeck

  337
  Citations

• Population prevalence of the MELAS A3243G mutation

  Neil Manwaring;Michael M. Jones;Jie Jin Wang;Elena Rochtchina

  334
  Citations

• Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

  Connie Marras;Anthony Lang;Bart P. van de Warrenburg;Carolyn M. Sue

  332
  Citations

• New insights into the complex role of mitochondria in Parkinson's disease.

  Anne Grünewald;Kishore R. Kumar;Carolyn M. Sue;Carolyn M. Sue;Carolyn M. Sue

  322
  Citations

• Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

  Sumit Parikh;Amy Goldstein;Amel Karaa;Mary Kay Koenig

  288
  Citations

• Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  287
  Citations

• Activation of β-Glucocerebrosidase Reduces Pathological α-Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons

  Joseph R. Mazzulli;Joseph R. Mazzulli;Friederike Zunke;Taiji Tsunemi;Taiji Tsunemi;Nicholas J. Toker

  257
  Citations

• Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes

  Stephanie M.Y. Kong;Brian K.K. Chan;Jin-Sung Park;Kathryn J. Hill

  253
  Citations

• Disease-specific, neurosphere-derived cells as models for brain disorders

  Nicholas Matigian;Greger Abrahamsen;Ratneswary Sutharsan;Anthony L. Cook

  230
  Citations

• Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNASer(UCN) gene

  C.M. Sue;K. Tanji;G. Hadjigeorgiou;A.L. Andreu

  224
  Citations

• Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned

  Roula Ghaoui;Sandra T. Cooper;Sandra T. Cooper;Monkol Lek;Kristi Jones;Kristi Jones

  209
  Citations

• Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

  Katja Lohmann;Robert A. Wilcox;Susen Winkler;Alfredo Ramirez;Alfredo Ramirez

  182
  Citations

• A Stop-Codon Mutation in the Human mtDNA Cytochrome c Oxidase I Gene Disrupts the Functional Structure of Complex IV

  Claudio Bruno;Claudio Bruno;Andrea Martinuzzi;Yingying Tang;Antoni L. Andreu

  173
  Citations

• The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms

  Jin-Sung Park;Nicholas F. Blair;Carolyn M. Sue

  172
  Citations