Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans

by Calvo, Sarah E., Pagliarini, David J., Mootha, Vamsi K.
Published 2009

Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOS

by Byrne, K., Calvo, S.E, Doench, J.G, Goldberger, O., Mootha, V.K, Reinstadler, B., Shah, H., Shen, H., Shi, X., Summer, L., To, T.-L
Published 2022

Comparative RNA editing in autistic and neurotypical cerebella

by Eran, A., Li, J. B., Vatalaro, K., McCarthy, J., Rahimov, F., Collins, C., Markianos, K., Margulies, David M., Calvo, Sarah E., Kohane, Isaac, Kunkel, Louis M., Brown, Emery N.
Published 2014

Mutations in MTFMT Underlie a Human Disorder of Formylation Causing Impaired Mitochondrial Translation

by Tucker, Elena J, Hershman, Steven G, Belcher-Timme, Casey A, Patel, Jinal, Goldberger, Olga A., Christodoulou, John, Silberstein, Jonathon M, McKenzie, Matthew, Ryan, Michael T, Compton, Alison G, Jaffe, Jacob D., Carr, Steven A., Calvo, Sarah E., RajBhandary, Uttam L, Thorburn, David R, Mootha, Vamsi K., Koehrer, Caroline
Published 2014