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Eric A. Schon

Researcher at Columbia University Medical Center

Publications -  224
Citations -  32134

Eric A. Schon is an academic researcher from Columbia University Medical Center. The author has contributed to research in topics: Mitochondrial DNA & Respiratory chain. The author has an hindex of 88, co-authored 224 publications receiving 30129 citations. Previous affiliations of Eric A. Schon include University of Oregon & Osaka University.

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

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Mitochondrial respiratory-chain diseases

Salvatore DiMauro, +1 more
- 26 Jun 2003 - 
TL;DR: The mitochondrial respiratory chain has the crucial function of supplying the cell with energy in the form of ATP, and mutations affecting this chain can arise in mitochondrial or nuclear DNA and cause diseases known as mitochondrial encephalomyopathies.
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Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

Carlos T. Moraes, +19 more
- 18 May 1989 - 
TL;DR: It is concluded that deletions of muscle mitochondrial DNA are associated with ophthalmoplegia and may result in impaired mitochondrial function, however, the precise relation between clinical and biochemical phenotypes and deletions remains to be defined.
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Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

Massimo Zeviani, +6 more
- 01 Sep 1988 - 
TL;DR: Large-scale deletions in muscle mitochondrial DNA (mtDN A) in seven of seven patients with Kearns-Sayre syndrome (KSS) bolster arguments that KSS is a unique disorder and genetic in origin.
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Human mitochondrial DNA: roles of inherited and somatic mutations

Eric A. Schon, +2 more
- 01 Dec 2012 - 
TL;DR: Insight into the roles of mtDNA mutations in a wide variety of diseases is discussed, highlighting the interesting genetic characteristics of the mitochondrial genome and challenges in studying its contribution to pathogenesis.