Ann Saada

11.9k total citations
170 papers, 8.3k citations indexed

About

Ann Saada is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Ann Saada has authored 170 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 126 papers in Molecular Biology, 69 papers in Clinical Biochemistry and 21 papers in Physiology. Recurrent topics in Ann Saada's work include Mitochondrial Function and Pathology (95 papers), Metabolism and Genetic Disorders (69 papers) and ATP Synthase and ATPases Research (39 papers). Ann Saada is often cited by papers focused on Mitochondrial Function and Pathology (95 papers), Metabolism and Genetic Disorders (69 papers) and ATP Synthase and ATPases Research (39 papers). Ann Saada collaborates with scholars based in Israel, United States and Germany. Ann Saada's co-authors include Orly Elpeleg, Avraham Shaag, Hanna Mandel, Simon Edvardson, Chaya Miller, Shlomo Rotshenker, Staffan Eriksson, Fanny Reichert, Aviram Kogot‐Levin and Haya Lorberboum‐Galski and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Ann Saada

164 papers receiving 8.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Ann Saada 6.2k 2.8k 796 780 695 170 8.3k
Anne Lombès 7.1k 1.1× 3.5k 1.3× 982 1.2× 1.0k 1.3× 431 0.6× 145 9.5k
Stephan Kemp 6.3k 1.0× 1.6k 0.6× 1.5k 1.9× 515 0.7× 573 0.8× 110 7.5k
Sara Shanske 9.6k 1.5× 6.2k 2.2× 1.1k 1.4× 1.3k 1.6× 1.2k 1.7× 188 12.1k
William J. Craigen 5.1k 0.8× 1.3k 0.5× 620 0.8× 535 0.7× 851 1.2× 104 6.8k
Valeria Tiranti 7.1k 1.1× 3.5k 1.3× 622 0.8× 773 1.0× 588 0.8× 134 8.7k
Shamima Rahman 4.7k 0.8× 2.8k 1.0× 561 0.7× 438 0.6× 641 0.9× 160 6.3k
Yisang Yoon 7.7k 1.2× 1.5k 0.5× 1.8k 2.3× 714 0.9× 258 0.4× 69 9.9k
S. DiMauro 12.7k 2.1× 8.0k 2.8× 1.5k 1.9× 1.8k 2.3× 1.2k 1.8× 237 15.9k
Nancy Braverman 4.6k 0.7× 1.4k 0.5× 1.1k 1.4× 196 0.3× 458 0.7× 113 6.0k
Gino Cortopassi 4.8k 0.8× 1.3k 0.5× 645 0.8× 689 0.9× 434 0.6× 64 6.5k

Countries citing papers authored by Ann Saada

Since Specialization
Citations

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

Fields of papers citing papers by Ann Saada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Saada

This figure shows the co-authorship network connecting the top 25 collaborators of Ann Saada. A scholar is included among the top collaborators of Ann Saada 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 Ann Saada. Ann Saada 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.
Morelli, A., Ann Saada, & Felix Scholkmann. (2025). Extra-mitochondrial ATP synthesis, proton dynamics at the membrane, and mitochondria-derived vesicles: Current findings and considerations. SHILAP Revista de lepidopterología. 3. 47–51.
2.
Sweetat, Sahar, Paschalis Theotokis, Oded Abramsky, et al.. (2024). Ovariectomy and High Fat-Sugar-Salt Diet Induced Alzheimer's Disease/Vascular Dementia Features in Mice. Aging and Disease. 15(5). 2284–2284. 1 indexed citations
3.
4.
Mor‐Shaked, Hagar, Simona Ben‐Haim, Zvi Israel, et al.. (2021). Levodopa-responsive dystonia caused by biallelic PRKN exon inversion invisible to exome sequencing. Brain Communications. 3(3). fcab197–fcab197. 9 indexed citations
5.
Douiev, Liza & Ann Saada. (2018). The pathomechanism of cytochrome c oxidase deficiency includes nuclear DNA damage. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859(9). 893–900. 10 indexed citations
6.
Stolovich-Rain, Miri, Jonatan Enk, Jonas Vikeså, et al.. (2015). Weaning Triggers a Maturation Step of Pancreatic β Cells. Developmental Cell. 33(2). 238–239. 2 indexed citations
7.
Kay, Gillian, Sagi Tshori, Hovav Nechushtan, et al.. (2014). Mitochondrial STAT3 plays a major role in IgE-antigen–mediated mast cell exocytosis. Journal of Allergy and Clinical Immunology. 134(2). 460–469.e10. 67 indexed citations
8.
Saada, Ann, et al.. (2014). Apoptosis-Like Death, an Extreme SOS Response in Escherichia coli. mBio. 5(4). e01426–14. 100 indexed citations
9.
Tenenbaum, Ariel, et al.. (2013). Mitochondrial OXPHOS function is unaffected by chronic azithromycin treatment. Journal of Cystic Fibrosis. 12(6). 682–687. 9 indexed citations
10.
Spiegel, Ronen, Ophry Pines, Asaf Ta‐Shma, et al.. (2012). Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2. The American Journal of Human Genetics. 90(3). 518–523. 76 indexed citations
11.
Zeharia, Avraham, Avraham Shaag, Orit Pappo, et al.. (2010). Acute Infantile Liver Failure Due to Mutations in the TRMU Gene. The American Journal of Human Genetics. 86(2). 295–295. 4 indexed citations
12.
Zeharia, Avraham, Avraham Shaag, Orit Pappo, et al.. (2009). Acute Infantile Liver Failure Due to Mutations in the TRMU Gene. The American Journal of Human Genetics. 85(3). 401–407. 161 indexed citations
13.
Saada, Ann, Simon Edvardson, Avraham Shaag, et al.. (2008). C6ORF66 Is an Assembly Factor of Mitochondrial Complex I. The American Journal of Human Genetics. 82(1). 32–38. 134 indexed citations
14.
Barel, Ortal, Zamir Shorer, Hagit Flusser, et al.. (2008). Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ. The American Journal of Human Genetics. 82(5). 1211–1216. 92 indexed citations
15.
Zeharia, Avraham, Avraham Shaag, Riekelt H. Houtkooper, et al.. (2008). Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood. The American Journal of Human Genetics. 83(4). 489–494. 163 indexed citations
16.
Edvardson, Simon, Hiroko Hama, Avraham Shaag, et al.. (2008). Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia. The American Journal of Human Genetics. 83(5). 643–648. 154 indexed citations
17.
Edvardson, Simon, Avraham Shaag, Olga A. Kolesnikova, et al.. (2007). Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 81(4). 857–862. 258 indexed citations
18.
Elpeleg, Orly, Chaya Miller, Eli Hershkovitz, et al.. (2005). Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion. The American Journal of Human Genetics. 76(6). 1081–1086. 241 indexed citations
19.
Saada, Ann. (2004). Deoxyribonucleotides and Disorders of Mitochondrial DNA Integrity. DNA and Cell Biology. 23(12). 797–806. 38 indexed citations
20.
Saada, Ann, et al.. (1997). Liver Disease in the Ashkenazi‐Jewish Lipoamide Dehydrogenase Deficiency. Journal of Pediatric Gastroenterology and Nutrition. 24(5). 599–601. 1 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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