Vamsi Mootha

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Cell Biology, Bioinformatics Biology
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"Vamsi Mootha"

Children

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Joshua M. Baughman grad student 2011 Harvard
Steven G. Hershman grad student 2013 Harvard
Daniel S. Lieber grad student 2013 Harvard
Tslil Ast post-doc Harvard
Owen S Skinner post-doc 2017- Harvard (Chemistry Tree)
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Publications

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Jain IH, Calvo SE, Markhard AL, et al. (2020) Genetic Screen for Cell Fitness in High or Low Oxygen Highlights Mitochondrial and Lipid Metabolism. Cell
To TL, Cuadros AM, Shah H, et al. (2019) A Compendium of Genetic Modifiers of Mitochondrial Dysfunction Reveals Intra-organelle Buffering. Cell. 179: 1222-1238.e17
Ast T, Meisel JD, Patra S, et al. (2019) Hypoxia Rescues Frataxin Loss by Restoring Iron Sulfur Cluster Biogenesis. Cell
Lake NJ, Formosa LE, Stroud DA, et al. (2019) A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant. Human Mutation
Gopal RK, Kübler K, Calvo SE, et al. (2018) Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma. Cancer Cell. 34: 242-255.e5
Gopal RK, Calvo SE, Shih AR, et al. (2018) Early loss of mitochondrial complex I and rewiring of glutathione metabolism in renal oncocytoma. Proceedings of the National Academy of Sciences of the United States of America
Lake NJ, Webb BD, Stroud DA, et al. (2018) Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. American Journal of Human Genetics. 102: 713
Garone C, D'Souza AR, Dallabona C, et al. (2017) Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome. Human Molecular Genetics
Feichtinger RG, Oláhová M, Kishita Y, et al. (2017) Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies. American Journal of Human Genetics
Lake NJ, Webb BD, Stroud DA, et al. (2017) Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. American Journal of Human Genetics. 101: 239-254
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