Sarah E. Calvo

23.1k citations

49 papers · 7.8k indexed · 4 hit papers · h-index 35

Impact in

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing

Papers in

Clinical Biochemistry 21
- Metabolism and Genetic Disorders 20
Molecular Biology 41
- Mitochondrial Function and Pathology 32
- RNA modifications and cancer 14
- ATP Synthase and ATPases Research 12
- RNA and protein synthesis mechanisms 7
- Metabolomics and Mass Spectrometry Studies 3
- Bioinformatics and Genomic Networks 3

Co-authors: Vamsi K. Mootha David J. Pagliarini Karl R. Clauser Steven A. Carr David R. Thorburn Betty Chang Sunil A. Sheth Canny Sugiana
Journals: Human Molecular Genetics (4 papers)Cell (4 papers)Mitochondrion (3 papers)Proceedings of the National Academy of Sciences (3 papers)Nature Genetics (3 papers)
Partner nations: United States Australia Italy

In The Last Decade

Sarah E. Calvo

46 papers receiving 7.7k citations

Hit Papers

align trajectories log scale

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins 2015 · 903 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2015 Nucleic Acids Research
2013 Science
2009 Proceedings of the National Academy of Sciences
2008 Cell

Peers

Countries citing papers authored by Sarah E. Calvo

Since Specialization

Citations

This map shows the geographic impact of Sarah E. Calvo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sarah E. Calvo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah E. Calvo more than expected).

Fields of papers citing papers by Sarah E. Calvo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah E. Calvo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sarah E. Calvo. The network helps show where Sarah E. Calvo may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Sarah E. Calvo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sarah E. Calvo Line = papers co-authored together Sarah E. Calvo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mitochondrial genome copy number variation across tissues in mice and humans Proceedings of the National Academy of Sciences ·Sneha Rath, Rahul Gupta, Ellen Todres, Hong Wang, Alexis A. Jourdain, Kristin Ardlie, Sarah E. Calvo, Vamsi K. Mootha	2024	9
2	Nuclear genetic control of mtDNA copy number and heteroplasmy in humans Nature ·Rahul Gupta, Masahiro Kanai, Timothy Durham, Kristin Tsuo, Jason G. McCoy, Anna V. Kotrys, Wei Zhou, Patrick F. Chinnery, Konrad J. Karczewski, Sarah E. Calvo, Benjamin M. Neale, Vamsi K. Mootha	2023	84
3	Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease Human Molecular Genetics ·Erik M. S. Ocean, Daniella H. Hock, Nicole J. Lake, Sarah E. Calvo, Sabine Grønborg, Emma Krzesinski, David J. Amor, Michael Fahey, Cas Simons, Flemming Wibrand, Vamsi K. Mootha, Monkol Lek, Sebastian Lunke, Zornitza Stark, Elsebet Østergaard, John Christodoulou, David R. Thorburn, David A. Stroud, Alison G. Compton	2023	13
4	Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOS Nature Communications ·Xiaojian Shi, Wenlu Che, Hardik Shah, Tsz‐Leung To, João Ribeiro da Silva, Maurice Carité, Sarah E. Calvo, Olga Goldberger, John G. Doench, Vamsi K. Mootha, Hongying Shen	2022	60
5	Mitochondrial DNA variation across 56,434 individuals in gnomAD Genome Research ·Kristen M. Laricchia, Nicole J. Lake, Nicholas A. Watts, Megan Shand, Andrea Haessly, Laura D. Gauthier, David Benjamin, Eric Banks, José Soto, Kiran Garimella, K. C. Sales, Heidi L. Rehm, Daniel G. MacArthur, Grace Tiao, Monkol Lek, Vamsi K. Mootha, Sarah E. Calvo	2022	53
6	Loss of LUC7L2 and U1 snRNP subunits shifts energy metabolism from glycolysis to OXPHOS Molecular Cell ·Alexis A. Jourdain, Bridget E. Begg, Eran Mick, Hardik Shah, Sarah E. Calvo, Owen S. Skinner, Rohit Sharma, Steven M. Blue, G Yeo, Christopher B. Burge, Vamsi K. Mootha	2021	56
7	A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein‐truncating variant Human Mutation ·Nicole J. Lake, Luke E. Formosa, David A. Stroud, Michael T. Ryan, Sarah E. Calvo, Vamsi K. Mootha, Bharti Morar, Peter G. Procopis, John Christodoulou, Alison G. Compton, David R. Thorburn	2019	7
8	Early loss of mitochondrial complex I and rewiring of glutathione metabolism in renal oncocytoma Proceedings of the National Academy of Sciences ·Raj K. Gopal, Sarah E. Calvo, Angela Shih, Frances Cháves, Declan McGuone, Eran Mick, Kerry A. Pierce, Yang Li, Andrea Garofalo, Eliezer M. Van Allen, Clary B. Clish, Esther Oliva, Vamsi K. Mootha	2018	69
9	Spatiotemporal compartmentalization of hepatic NADH and NADPH metabolism Journal of Biological Chemistry ·Russell P. Goodman, Sarah E. Calvo, Vamsi K. Mootha	2018	98
10	Comparative Analysis of Mitochondrial N-Termini from Mouse, Human, and Yeast Molecular & Cellular Proteomics ·Sarah E. Calvo, Olivier Julien, Karl R. Clauser, Hongying Shen, Kimberli J. Kamer, James A. Wells, Vamsi K. Mootha	2017	66
11	CLIC, a tool for expanding biological pathways based on co-expression across thousands of datasets PLoS Computational Biology ·Yang Li, Alexis A. Jourdain, Sarah E. Calvo, Jun S. Liu, Vamsi K. Mootha	2017	29
12	A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation Cell Metabolism ·Jason D. Arroyo, Alexis A. Jourdain, Sarah E. Calvo, J. A. Aruldoss, John G. Doench, David E. Root, Vamsi K. Mootha	2016	221
13	Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency BMC Medical Genetics ·Daniel S. Lieber, Steven G. Hershman, Nancy G. Slate, Sarah E. Calvo, Katherine B. Sims, Jeremy D. Schmahmann, Vamsi K. Mootha	2014	35
14	Mitochondrial Encephalomyopathy Due to a Novel Mutation inACAD9 JAMA Neurology ·Caterina Garone, Maria Alice Donati, Michele Sacchini, Beatriz García-Díaz, Claudio Bruno, Sarah E. Calvo, Vamsi K. Mootha, Salvatore DiMauro	2013	34
15	Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions Brain ·Dario Ronchi, Caterina Garone, Andrea Bordoni, Qiuxuan Li, Sarah E. Calvo, Michela Ripolone, Michela Ranieri, Mafalda Rizzuti, Luísa Villa, Francesca Magri, Stefania Corti, Nereo Bresolin, Vamsi K. Mootha, Laura Uberti Hughes, S. DiMauro, Giacomo P. Comi, Monica Sciacco	2012	73
16	Comparative RNA editing in autistic and neurotypical cerebella Molecular Psychiatry ·Alal Eran, Jin Billy Li, Anna Löfgren Burström, Jillian McCarthy, Fedik Rahimov, Christin Collins, Kyriacos Markianos, David Margulies, Emery N. Brown, Sarah E. Calvo, Isaac S. Kohane, Louis M. Kunkel	2012	56
17	Mutations in MTFMT Underlie a Human Disorder of Formylation Causing Impaired Mitochondrial Translation Cell Metabolism ·Elena J. Tucker, Steven G. Hershman, Caroline Köhrer, Ibnu Faldi, Jinal Patel, Olga Goldberger, John Christodoulou, ماجدة ابراهيم الأسود, Matthew McKenzie, Michael T. Ryan, Alison G. Compton, Jacob D. Jaffe, Steven A. Carr, Sarah E. Calvo, Uttam L. RajBhandary, David R. Thorburn, Vamsi K. Mootha	2011	125
18	FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy Human Molecular Genetics ·Elisa Fassone, Andrew Duncan, Jan‐Willem Taanman, Alistair T. Pagnamenta, Michael I. Sadowski, 余佳益 YU Jiayi, Waseem Qasim, Paul Rutland, Sarah E. Calvo, Vamsi K. Mootha, Maria Bitner‐Glindzicz, Shamima Rahman	2010	78
19	Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans Proceedings of the National Academy of Sciences ·Sarah E. Calvo, David J. Pagliarini, Vamsi K. Mootha Hit paper breakdown →	2009	664
20	The Complete Genome and Proteome of Mycoplasma mobile Genome Research ·Jacob D. Jaffe, Nicole Stange-Thomann, N Priyadharshini, David DeCaprio, Sheila Fisher, Jonathan A. Butler, Sarah E. Calvo, T. Ebel, Michael G. FitzGerald, Nabil Hafez, Chinnappa D. Kodira, John E. Major, Shunguang Wang, Jane Wilkinson, Robert Nicol, Chad Nusbaum, Bruce W. Birren, Howard C. Berg, George M. Church	2004	201

About Sarah E. Calvo

Sarah E. Calvo is a scholar working on Clinical Biochemistry, Molecular Biology, Cancer Research, Endocrinology and Microbiology, having authored 49 papers that have together received 7.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (32 papers), Metabolism and Genetic Disorders (20 papers), RNA modifications and cancer (14 papers), ATP Synthase and ATPases Research (12 papers), RNA and protein synthesis mechanisms (7 papers), Metabolomics and Mass Spectrometry Studies (3 papers), Cancer, Hypoxia, and Metabolism (3 papers) and Bioinformatics and Genomic Networks (3 papers). The work is most often cited by research in Clinical Biochemistry (2.0k citations), Molecular Biology (6.7k citations), Aging (106 citations), Cancer Research (622 citations) and Cell Biology (517 citations). Sarah E. Calvo has collaborated with scholars based in United States, Australia and Italy. Frequent co-authors include Vamsi K. Mootha, David J. Pagliarini, Karl R. Clauser, Steven A. Carr, David R. Thorburn, Betty Chang, Sunil A. Sheth, Canny Sugiana, Scott B. Vafai and David E. Hill. Their work appears in journals such as Human Molecular Genetics, Cell, Mitochondrion, Proceedings of the National Academy of Sciences and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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