Vamsi Mootha

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


Sign in to add mentor
Robert Stephen Balaban grad student NIH (Physiology Academic Tree)
Eric Lander post-doc Whitehead Institute (MathTree)


Sign in to add trainee
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
Vishal Gohil post-doc Harvard
Toshimori Kitami post-doc Harvard
David J. Pagliarini post-doc Harvard (Chemistry Tree)
Owen S Skinner post-doc 2017- Harvard (Chemistry Tree)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Rath S, Sharma R, Gupta R, et al. (2020) MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations. Nucleic Acids Research
Ghosh S, Basu Ball W, Madaris TR, et al. (2020) An essential role for cardiolipin in the stability and function of the mitochondrial calcium uniporter. Proceedings of the National Academy of Sciences of the United States of America
Gohil VM, Nilsson R, Belcher-Timme CA, et al. (2020) Correction: Mitochondrial and nuclear genomic responses to loss of expression. The Journal of Biological Chemistry. 295: 5533
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
See more...