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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Coenzyme Q10 deficiency disrupts lipid metabolism by altering cholesterol homeostasis in neurons 2025 ·Free Radical Biology and Medicine ·(unknown), Eliana Barriocanal‐Casado, Giacomo Monzio Compagnoni, Agustín Hidalgo‐Gutiérrez, (unknown), Mohammed Bakkali, Yashpal S. Chhonker, Giulio Kleiner, Delfina Larrea, Saba Tadesse, Luís C. López, Daryl J. Murry, Alessio Di Fonzo, (unknown), Catarina M. Quinzii	0
2	Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency 2023 ·Neurology Genetics ·Edoardo Monfrini, (unknown), (unknown), Cláudia Ferreira da Rosa Sobreira, Valentina Emmanuele, (unknown), Luís C. López, Saba Tadesse, Michio Hirano, Giacomo P. Comi, Catarina M. Quinzii, Alessio Di Fonzo	3
3	Thymidine Phosphorylase Intracellular Enzyme Replacement Therapy in a Murine Model of Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) (3975) 2020 ·Neurology ·Jonathan Shintaku, Wenlong Lian, Xiang Li, Saba Tadesse, (unknown), Xingfu Xu, (unknown), (unknown), Ziqing Qian, (unknown), Michio Hirano	3
4	Oral deoxynucleoside for the treatment of thymidine kinase 2 deficiency (P3.195) 2017 ·Neurology ·Carlos Lopez‐Gómez, Rebecca Levy, Maria J. Sanchez‐Quintero, Martí Juanola‐Falgarona, Emanuele Barca, Beatriz García-Díaz, Saba Tadesse, Caterina Garone, Michio Hirano	1
5	Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency 2017 ·Annals of Neurology ·Carlos Lopez‐Gómez, Rebecca J. Levy, Maria J. Sanchez‐Quintero, Martí Juanola‐Falgarona, Emanuele Barca, Beatriz García-Díaz, Saba Tadesse, Caterina Garone, Michio Hirano	70
6	Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum 2016 ·Journal of Neuropathology & Experimental Neurology ·Emanuele Barca, Giulio Kleiner, Guomei Tang, Marcello Ziosi, Saba Tadesse, Eliezer Masliah, Elan D. Louis, Phyllis L. Faust, Un Jung Kang, (unknown), Etty Cortés, Jean-Paul G. Vonsattel, Sheng‐Han Kuo, Catarina M. Quinzii	54
7	Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway 2016 ·EMBO Molecular Medicine ·Marcello Ziosi, Ivano Di Meo, Giulio Kleiner, Xing‐Huang Gao, Emanuele Barca, Maria J. Sanchez‐Quintero, Saba Tadesse, Hongfeng Jiang, (unknown), Richard J. Rodenburg, Emmanuel Scalais, Markus Schuelke, Belinda Willard, Maria Hatzoglou, Valeria Tiranti, Catarina M. Quinzii	57
8	Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency 2014 ·EMBO Molecular Medicine ·Caterina Garone, Beatriz García-Díaz, Valentina Emmanuele, Luís C. López, Saba Tadesse, Hasan O. Akman, Kurenai Tanji, Catarina M. Quinzii, Michio Hirano	68
9	Heterogeneity of Coenzyme Q₁₀Deficiency 2012 ·Archives of Neurology ·Valentina Emmanuele, Luís C. López, Andrés Berardo, Ali Naini, Saba Tadesse, Bing Wen, (unknown), Martha Solomon, Salvatore DiMauro, Catarina M. Quinzii, Michio Hirano	155
10	Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation 2012 ·The American Journal of Human Genetics ·Beatriz García-Díaz, Mário H. Barros, Simone Sanna‐Cherchi, Valentina Emmanuele, Hasan O. Akman, (unknown), Rita Horváth, Saba Tadesse, (unknown), Salvatore DiMauro, Darryl C. De Vivo, (unknown), Michio Hirano, Catarina M. Quinzii	33
11	Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy 2011 ·Brain ·Caterina Garone, Saba Tadesse, Michio Hirano	149
12	Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice 2008 ·Human Molecular Genetics ·Luís C. López, Hasan O. Akman, Ángeles García‐Cazorla, Beatriz Dorado, Ramón Martí, Ichizo Nishino, Saba Tadesse, Giuseppe Pizzorno, Dikoma C. Shungu, Eduardo Bonilla, Kurenai Tanji, Michio Hirano	117
13	Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) 2007 ·FEBS Letters ·Maria Lucia Valentino, Ramón Martí, Saba Tadesse, Luís C. López, (unknown), (unknown), Angelika F. Hahn, Valério Carelli, Michio Hirano	58
14	Late‐onset MNGIE due to partial loss of thymidine phosphorylase activity 2005 ·Annals of Neurology ·Ramón Martí, Jan J.G.M. Verschuuren, Alan L. Buchman, Ikuo Hirano, Saba Tadesse, André B. P. Kuilenburg, Albert H. Gennip, Ben J. H. M. Poorthuis, Michio Hirano	54
15	Definitive Diagnosis of Mitochondrial Neurogastrointestinal Encephalomyopathy by Biochemical Assays 2004 ·Clinical Chemistry ·Ramón Martí, Antonella Spinazzola, Saba Tadesse, Ichizo Nishino, Yutaka Nishigaki, Michio Hirano	87
16	A novel mitochondrial tRNALeu(UUR) mutation in a patient with features of MERRF and Kearns–Sayre syndrome 2003 ·Neuromuscular Disorders ·Yutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, Dikoma C. Shungu, Stephen P. Hersh, Bronya J.B. Keats, Charles I. Berlín, Morton F. Goldberg, Jerry Vockley, Salvatore DiMauro, Michio Hirano	50
17	Mitochondrial neurogastrointestinal encephalomyopathy and thymidine metabolism: results and hypotheses 2002 ·Mitochondrion ·Ramón Martí, Antonella Spinazzola, Ichizo Nishino, Antoni L. Andreu, Ali Naini, Saba Tadesse, Juan Oliver, Michio Hirano	9
18	Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase 2002 ·Journal of Biological Chemistry ·Antonella Spinazzola, Ramón Martí, Ichizo Nishino, Antoni L. Andreu, Ali Naini, Saba Tadesse, Ivana Pela, Enrico Zammarchi, Maria Alice Donati, Juan Oliver, Michio Hirano	180
19	Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma 2001 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·(unknown), Matthias Boehnke, Saba Tadesse, (unknown), Josef Flammer, Francis L. Munier, André Mermoud, Michio Hirano, (unknown), Daniel S. Mojon	19
20	Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA 2001 ·Seminars in Cell and Developmental Biology ·Michio Hirano, Ramón Martí, (unknown), (unknown), Saba Tadesse, Yutaka Nishigaki, Ichizo Nishino, Tuan Vu	89

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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