NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease
2014 · Cell Metabolism · 340 citations
https://doi.org/10.1016/j.cmet.2014.04.001
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Costanza Lamperti
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Costanza Lamperti is an academic researcher from Fondazione IRCCS Istituto Neurologico Carlo Besta. The author has contributed to research in topics: Mitochondrial Function and Pathology & Metabolism and Genetic Disorders & ATP Synthase and ATPases Research. The author has an h-index of 46, co-authored 140 publications.
ORCID: 0000-0002-2280-2253Papers by this author
worksTranscription Factor EB Controls Metabolic Flexibility during Exercise
2016 · Cell Metabolism · 318 citations
https://doi.org/10.1016/j.cmet.2016.11.003
Clinical implementation of RNA sequencing for Mendelian disease diagnostics
2022 · Genome Medicine · 184 citations
https://doi.org/10.1186/s13073-022-01019-9
Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy
2013 · The American Journal of Human Genetics · 176 citations
https://doi.org/10.1016/j.ajhg.2013.07.016
Cowchock Syndrome Is Associated with a Mutation in Apoptosis-Inducing Factor
2012 · The American Journal of Human Genetics · 155 citations
https://doi.org/10.1016/j.ajhg.2012.10.008
Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency
2014 · The American Journal of Human Genetics · 76 citations
https://doi.org/10.1016/j.ajhg.2014.08.003
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