Saba Tadesse

2.1k total citations
28 papers, 1.5k citations indexed

About

Saba Tadesse is a scholar working on Molecular Biology, Clinical Biochemistry and Electrical and Electronic Engineering. According to data from OpenAlex, Saba Tadesse has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 5 papers in Electrical and Electronic Engineering. Recurrent topics in Saba Tadesse's work include Mitochondrial Function and Pathology (17 papers), Coenzyme Q10 studies and effects (9 papers) and Metabolism and Genetic Disorders (9 papers). Saba Tadesse is often cited by papers focused on Mitochondrial Function and Pathology (17 papers), Coenzyme Q10 studies and effects (9 papers) and Metabolism and Genetic Disorders (9 papers). Saba Tadesse collaborates with scholars based in United States, Italy and Spain. Saba Tadesse's co-authors include Michio Hirano, Caterina Garone, Ramón Martí, Catarina M. Quinzii, Ichizo Nishino, Ali Naini, Luís C. López, Valentina Emmanuele, Antonella Spinazzola and Yutaka Nishigaki and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Brain.

In The Last Decade

Saba Tadesse

27 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saba Tadesse United States 20 1.3k 625 172 147 139 28 1.5k
Sindu Krishna United States 17 1.1k 0.9× 424 0.7× 113 0.7× 87 0.6× 70 0.5× 26 1.4k
Costanza Lamperti Italy 15 924 0.7× 134 0.2× 54 0.3× 152 1.0× 41 0.3× 23 1.2k
Langping He United Kingdom 25 1.8k 1.4× 959 1.5× 45 0.3× 172 1.2× 13 0.1× 52 2.0k
Emmanuelle Sarzi France 17 1.6k 1.2× 865 1.4× 46 0.3× 153 1.0× 9 0.1× 25 1.7k
Cristina Cerqua Italy 12 863 0.7× 94 0.2× 108 0.6× 53 0.4× 109 0.8× 14 1.1k
Teresa Rizza Italy 23 783 0.6× 338 0.5× 67 0.4× 84 0.6× 5 0.0× 43 1.1k
P. A. W. Mooyer Netherlands 14 1.4k 1.0× 526 0.8× 156 0.9× 106 0.7× 8 0.1× 19 1.5k
Alberto Blázquez Spain 18 750 0.6× 323 0.5× 22 0.1× 84 0.6× 7 0.1× 50 1.1k
Niels Gregersen Denmark 14 630 0.5× 535 0.9× 70 0.4× 40 0.3× 11 0.1× 28 935
Daria Diodato Italy 18 868 0.7× 535 0.9× 78 0.5× 84 0.6× 3 0.0× 44 1.2k

Countries citing papers authored by Saba Tadesse

Since Specialization
Citations

This map shows the geographic impact of Saba Tadesse'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 Saba Tadesse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Saba Tadesse more than expected).

Fields of papers citing papers by Saba Tadesse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Saba Tadesse. 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 Saba Tadesse. The network helps show where Saba Tadesse may publish in the future.

Co-authorship network of co-authors of Saba Tadesse

This figure shows the co-authorship network connecting the top 25 collaborators of Saba Tadesse. A scholar is included among the top collaborators of Saba Tadesse 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 Saba Tadesse. Saba Tadesse 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.
Barriocanal‐Casado, Eliana, Giacomo Monzio Compagnoni, Agustín Hidalgo‐Gutiérrez, et al.. (2025). Coenzyme Q10 deficiency disrupts lipid metabolism by altering cholesterol homeostasis in neurons. Free Radical Biology and Medicine. 229. 441–457.
2.
Monfrini, Edoardo, Cláudia Ferreira da Rosa Sobreira, Valentina Emmanuele, et al.. (2023). Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency. Neurology Genetics. 9(2). e200058–e200058. 3 indexed citations
3.
Shintaku, Jonathan, Wenlong Lian, Xiang Li, et al.. (2020). Thymidine Phosphorylase Intracellular Enzyme Replacement Therapy in a Murine Model of Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) (3975). Neurology. 94(15_supplement). 3 indexed citations
4.
Lopez‐Gómez, Carlos, Rebecca Levy, Maria J. Sanchez‐Quintero, et al.. (2017). Oral deoxynucleoside for the treatment of thymidine kinase 2 deficiency (P3.195). Neurology. 88(16_supplement). 1 indexed citations
5.
Lopez‐Gómez, Carlos, Rebecca J. Levy, Maria J. Sanchez‐Quintero, et al.. (2017). Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency. Annals of Neurology. 81(5). 641–652. 70 indexed citations
6.
Barca, Emanuele, Giulio Kleiner, Guomei Tang, et al.. (2016). Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum. Journal of Neuropathology & Experimental Neurology. 75(7). 663–672. 54 indexed citations
7.
Ziosi, Marcello, Ivano Di Meo, Giulio Kleiner, et al.. (2016). Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway. EMBO Molecular Medicine. 9(1). 96–111. 57 indexed citations
8.
Garone, Caterina, Beatriz García-Díaz, Valentina Emmanuele, et al.. (2014). Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency. EMBO Molecular Medicine. 6(8). 1016–1027. 68 indexed citations
9.
Emmanuele, Valentina, Luís C. López, Andrés Berardo, et al.. (2012). Heterogeneity of Coenzyme Q10Deficiency. Archives of Neurology. 69(8). 978–83. 155 indexed citations
10.
García-Díaz, Beatriz, Mário H. Barros, Simone Sanna‐Cherchi, et al.. (2012). Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation. The American Journal of Human Genetics. 91(4). 729–736. 33 indexed citations
11.
Garone, Caterina, Saba Tadesse, & Michio Hirano. (2011). Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. Brain. 134(11). 3326–3332. 149 indexed citations
12.
López, Luís C., Hasan O. Akman, Ángeles García‐Cazorla, et al.. (2008). Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice. Human Molecular Genetics. 18(4). 714–722. 117 indexed citations
13.
Valentino, Maria Lucia, Ramón Martí, Saba Tadesse, et al.. (2007). Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). FEBS Letters. 581(18). 3410–3414. 58 indexed citations
14.
Martí, Ramón, Jan J.G.M. Verschuuren, Alan L. Buchman, et al.. (2005). Late‐onset MNGIE due to partial loss of thymidine phosphorylase activity. Annals of Neurology. 58(4). 649–652. 54 indexed citations
15.
Martí, Ramón, Antonella Spinazzola, Saba Tadesse, et al.. (2004). Definitive Diagnosis of Mitochondrial Neurogastrointestinal Encephalomyopathy by Biochemical Assays. Clinical Chemistry. 50(1). 120–124. 87 indexed citations
16.
Nishigaki, Yutaka, Saba Tadesse, Eduardo Bonilla, et al.. (2003). A novel mitochondrial tRNALeu(UUR) mutation in a patient with features of MERRF and Kearns–Sayre syndrome. Neuromuscular Disorders. 13(4). 334–340. 50 indexed citations
17.
Martí, Ramón, Antonella Spinazzola, Ichizo Nishino, et al.. (2002). Mitochondrial neurogastrointestinal encephalomyopathy and thymidine metabolism: results and hypotheses. Mitochondrion. 2(1-2). 143–147. 9 indexed citations
18.
Spinazzola, Antonella, Ramón Martí, Ichizo Nishino, et al.. (2002). Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase. Journal of Biological Chemistry. 277(6). 4128–4133. 180 indexed citations
19.
Boehnke, Matthias, Saba Tadesse, Josef Flammer, et al.. (2001). Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma. Graefe s Archive for Clinical and Experimental Ophthalmology. 239(6). 437–440. 19 indexed citations
20.
Hirano, Michio, Ramón Martí, Saba Tadesse, et al.. (2001). Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA. Seminars in Cell and Developmental Biology. 12(6). 417–427. 89 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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