Carlos T. Moraes

27.1k total citations · 3 hit papers
230 papers, 19.8k citations indexed

About

Carlos T. Moraes is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Carlos T. Moraes has authored 230 papers receiving a total of 19.8k indexed citations (citations by other indexed papers that have themselves been cited), including 207 papers in Molecular Biology, 110 papers in Clinical Biochemistry and 28 papers in Cellular and Molecular Neuroscience. Recurrent topics in Carlos T. Moraes's work include Mitochondrial Function and Pathology (187 papers), Metabolism and Genetic Disorders (110 papers) and ATP Synthase and ATPases Research (58 papers). Carlos T. Moraes is often cited by papers focused on Mitochondrial Function and Pathology (187 papers), Metabolism and Genetic Disorders (110 papers) and ATP Synthase and ATPases Research (58 papers). Carlos T. Moraes collaborates with scholars based in United States, Italy and Brazil. Carlos T. Moraes's co-authors include S. DiMauro, Eric A. Schon, Francisca Díaz, Sandra R. Bacman, Nadee Nissanka, Hirokazu Fukui, Milena Pinto, Sara Shanske, Antoni Barrientos and E. Bonilla and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Carlos T. Moraes

229 papers receiving 19.5k citations

Hit Papers

Glycolytic oligodendrocytes m... 1988 2026 2000 2013 2012 1989 1988 250 500 750 1000

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Carlos T. Moraes United States 77 16.0k 7.1k 2.3k 2.1k 1.2k 230 19.8k
Michio Hirano United States 82 16.4k 1.0× 7.8k 1.1× 2.1k 0.9× 1.6k 0.7× 1.3k 1.1× 341 20.5k
Nils‐Göran Larsson Sweden 85 19.8k 1.2× 6.5k 0.9× 2.2k 1.0× 3.9k 1.8× 1.4k 1.2× 193 24.2k
Anu Suomalainen Finland 63 12.7k 0.8× 5.4k 0.8× 1.5k 0.7× 2.1k 1.0× 1.3k 1.1× 189 15.7k
Eric A. Schon United States 85 19.7k 1.2× 8.9k 1.2× 2.8k 1.2× 3.1k 1.5× 1.5k 1.3× 221 23.5k
Massimo Zeviani Italy 92 28.0k 1.8× 13.0k 1.8× 3.2k 1.4× 2.4k 1.1× 2.3k 2.0× 411 33.4k
Valério Carelli Italy 71 12.4k 0.8× 3.4k 0.5× 1.7k 0.7× 1.2k 0.6× 621 0.5× 330 15.3k
Salvatore DiMauro United States 87 23.0k 1.4× 12.6k 1.8× 2.9k 1.3× 3.2k 1.5× 2.6k 2.1× 408 29.6k
Anders Oldfors Sweden 55 10.4k 0.6× 3.7k 0.5× 1.6k 0.7× 1.9k 0.9× 1.3k 1.1× 286 13.7k
Thomas Langer Germany 77 15.8k 1.0× 3.1k 0.4× 1.3k 0.6× 1.9k 0.9× 668 0.6× 175 18.5k
C. Angelini Italy 68 13.2k 0.8× 2.6k 0.4× 4.5k 2.0× 2.8k 1.3× 1.2k 1.0× 540 18.6k

Countries citing papers authored by Carlos T. Moraes

Since Specialization
Citations

This map shows the geographic impact of Carlos T. Moraes'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 Carlos T. Moraes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carlos T. Moraes more than expected).

Fields of papers citing papers by Carlos T. Moraes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos T. Moraes. 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 Carlos T. Moraes. The network helps show where Carlos T. Moraes may publish in the future.

Co-authorship network of co-authors of Carlos T. Moraes

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos T. Moraes. A scholar is included among the top collaborators of Carlos T. Moraes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Carlos T. Moraes. Carlos T. Moraes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Michell, Craig, Carlos T. Moraes, Smaranda Willcox, et al.. (2024). Linear DNA-driven recombination in mammalian mitochondria. Nucleic Acids Research. 52(6). 3088–3105. 3 indexed citations
2.
Arguello, Tania, Sandra R. Bacman, Roger F. Castilho, et al.. (2024). NEK10 kinase ablation affects mitochondrial morphology, function and protein phosphorylation status. Proteome Science. 22(1). 8–8. 1 indexed citations
3.
Nissanka, Nadee, et al.. (2024). Absence of both MGME1 and POLG EXO abolishes mtDNA whereas absence of either creates unique mtDNA duplications. Journal of Biological Chemistry. 300(4). 107128–107128. 3 indexed citations
4.
Lape, Janel, Sandra R. Bacman, Flavia Fontanesi, et al.. (2023). Efficient elimination of MELAS-associated m.3243G mutant mitochondrial DNA by an engineered mitoARCUS nuclease. Nature Metabolism. 5(12). 2169–2183. 20 indexed citations
5.
Lang, Anna L., Nadee Nissanka, Ruy A. Louzada, et al.. (2023). A Defect in Mitochondrial Complex III but Not in Complexes I or IV Causes Early β-Cell Dysfunction and Hyperglycemia in Mice. Diabetes. 72(9). 1262–1276. 13 indexed citations
6.
Protasoni, Margherita, Rafael Pérez‐Pérez, Teresa Lobo‐Jarne, et al.. (2020). Respiratory supercomplexes act as a platform for complex III ‐mediated maturation of human mitochondrial complexes I and IV. The EMBO Journal. 39(3). e102817–e102817. 103 indexed citations
7.
Wan, Junmei, Hasini A. Kalpage, Asmita Vaishnav, et al.. (2019). Regulation of Respiration and Apoptosis by Cytochrome c Threonine 58 Phosphorylation. Scientific Reports. 9(1). 15815–15815. 46 indexed citations
8.
Gammage, Payam A., Carlos T. Moraes, & Michal Minczuk. (2017). Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized. Trends in Genetics. 34(2). 101–110. 254 indexed citations
9.
Wang, Xiao, Alicia M. Pickrell, Susana G. Rossi, et al.. (2013). Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool. Human Molecular Genetics. 22(19). 3976–3986. 45 indexed citations
10.
Rocco, Daniela De, Cristina Cerqua, P Goffrini, et al.. (2013). Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(2). 269–274. 65 indexed citations
11.
Pickrell, Alicia M., Milena Pinto, Aline Hida, & Carlos T. Moraes. (2011). Striatal Dysfunctions Associated with Mitochondrial DNA Damage in Dopaminergic Neurons in a Mouse Model of Parkinson's Disease. Journal of Neuroscience. 31(48). 17649–17658. 96 indexed citations
12.
Wenz, Tina, Xiao Wang, Matteo Marini, & Carlos T. Moraes. (2010). A metabolic shift induced by a PPAR panagonist markedly reduces the effects of pathogenic mitochondrial tRNA mutations. Journal of Cellular and Molecular Medicine. 15(11). 2317–2325. 22 indexed citations
13.
Vempati, Uma D., Francisca Díaz, Antoni Barrientos, et al.. (2007). Role of Cytochrome c in Apoptosis: Increased Sensitivity to Tumor Necrosis Factor Alpha Is Associated with Respiratory Defects but Not with Lack of Cytochrome c Release. Molecular and Cellular Biology. 27(5). 1771–1783. 51 indexed citations
14.
Bacman, Sandra R., Dayami Hernandez, Jose Oca‐Cossio, et al.. (2005). CytochromecAssociation with the Inner Mitochondrial Membrane Is Impaired in the CNS of G93A-SOD1 Mice. Journal of Neuroscience. 25(1). 164–172. 165 indexed citations
15.
Lanza, Robert, José B. Cibelli, Francisca Díaz, et al.. (2000). Cloning of an Endangered Species ( Bos gaurus ) Using Interspecies Nuclear Transfer. PubMed. 2(2). 79–90. 263 indexed citations
16.
Barrientos, Antoni & Carlos T. Moraes. (1999). Titrating the Effects of Mitochondrial Complex I Impairment in the Cell Physiology. Journal of Biological Chemistry. 274(23). 16188–16197. 332 indexed citations
17.
Tengan, Célia Harumi, et al.. (1998). Mitochondrial Encephalomyopathy and Hypoparathyrodism Associated with a Duplication and a Deletion of Mitochondrial Deoxyribonucleic Acid1. The Journal of Clinical Endocrinology & Metabolism. 83(1). 125–129. 19 indexed citations
18.
Tersariol, Ivarne L.S., Marimélia Porcionatto, Carlos T. Moraes, et al.. (1994). Sequencing of heparan sulfate proteoglycans: identification of variable and constant oligosaccharide regions in eight heparan sulfate proteoglycans of different origins.. PubMed. 27(9). 2097–102. 7 indexed citations
19.
Moraes, Carlos T.. (1993). Mitochondrial DNA depletion in human pathology. 8(1). 40–44. 3 indexed citations
20.
Arnaudo, E., et al.. (1991). Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy. The Lancet. 337(8740). 508–510. 399 indexed citations

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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