Ann Saada

11.9k citations

174 papers · 9.0k · 1 hit paper · h-index 53

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
- Biochemical and Molecular Research

Papers in

Molecular Biology 118
- Mitochondrial Function and Pathology 92
- ATP Synthase and ATPases Research 37
- RNA modifications and cancer 13
- Biochemical and Molecular Research 9
Clinical Biochemistry 67
- Metabolism and Genetic Disorders 67

Co-authors: Orly Elpeleg (55 shared papers)Avraham Shaag (44 shared papers)Hanna Mandel (17 shared papers)Simon Edvardson (18 shared papers)Chaya Miller (16 shared papers)Staffan Eriksson (3 shared papers)Shlomo Rotshenker (6 shared papers)Fanny Reichert (5 shared papers)
Journals: The American Journal of Human Genetics (14 papers)European Journal of Human Genetics (8 papers)Molecular Genetics and Metabolism (8 papers)Journal of Medical Genetics (6 papers)Biochemical and Biophysical Research Communications (5 papers)
Partner nations: Israel United States Germany

In The Last Decade

Ann Saada

167 papers receiving 8.8k citations

Ann Saada's Hit Papers

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Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy 2001 · 508 citations

Peers

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-authors

The 25 scholars most cited alongside Ann Saada, 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 Ann Saada Line = papers co-authored together Ann Saada links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 174 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy Nature Genetics ·Ann Saada, Avraham Shaag, Hanna Mandel, Yoram Nevo, Staffan Eriksson, Orly Elpeleg Hit paper breakdown →	2001	508
2	The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA Nature Genetics ·Hanna Mandel, Raymonde Szargel, Valentina Labay, Orly Elpeleg, Ann Saada, Adel Shalata, Yefim Anbinder, Drora Berkowitz, Corina Hartman, Mila Barak, Staffan Eriksson, Nadine Cohen	2001	480
3	Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia The American Journal of Human Genetics ·Simon Edvardson, Avraham Shaag, Olga A. Kolesnikova, John M. Gomori, Ivan Tarassov, Tom Einbinder, Ann Saada, Orly Elpeleg	2007	275
4	Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion The American Journal of Human Genetics ·Orly Elpeleg, Chaya Miller, Eli Hershkovitz, Maria Bitner‐Glindzicz, Gili Bondi-Rubinstein, Shamima Rahman, Alistair T. Pagnamenta, Sharon Eshhar, Ann Saada	2005	261
5	Control of Pancreatic β Cell Regeneration by Glucose Metabolism Cell Metabolism ·Shay Porat, Noa Weinberg-Corem, Sharona Tornovsky-Babaey, Rachel Ben‐Haroush Schyr, Ayat Hija, Miri Stolovich-Rain, Daniela Dadon, Zvi Granot, Vered Ben-Hur, Peter White, Christophe A. Girard, Rotem Karni, Klaus H. Kaestner, Frances M. Ashcroft, Mark A. Magnuson, Ann Saada, Joseph Grimsby, Benjamin Gläser, Yuval Dor	2011	255
6	Peripheral nerve injury induces Schwann cells to express two macrophage phenotypes: phagocytosis and the galactose-specific lectin MAC-2 Journal of Neuroscience ·Fanny Reichert, Ann Saada, Shlomo Rotshenker	1994	195
7	Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation Annals of Neurology ·Chaya Miller, Ann Saada, Nava Shaul, Naama Shabtai, Efrat Ben‐Shalom, Avraham Shaag, Eli Hershkovitz, Orly Elpeleg	2004	186
8	Acute Infantile Liver Failure Due to Mutations in the TRMU Gene The American Journal of Human Genetics ·Avraham Zeharia, Avraham Shaag, Orit Pappo, Anne-Marie Mager-Heckel, Ann Saada, Marine Beinat, Olga Karicheva, Hanna Mandel, Noa Ofek, Reeval Segel, Daphna Marom, Agnès Rötig, Ivan Tarassov, Orly Elpeleg	2009	182
9	Ablation of Ceramide Synthase 2 Causes Chronic Oxidative Stress Due to Disruption of the Mitochondrial Respiratory Chain Journal of Biological Chemistry ·Hila Zigdon, Aviram Kogot‐Levin, Joo‐Won Park, Ruth Goldschmidt, Samuel Kelly, Alfred H. Merrill, Avigdor Scherz, Yael Pewzner‐Jung, Ann Saada, Anthony H. Futerman	2013	178
10	Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood The American Journal of Human Genetics ·Avraham Zeharia, Avraham Shaag, Riekelt H. Houtkooper, Tareq Hindi, Pascale de Lonlay, Gilli Erez, Laurence Hubert, Ann Saada, Yves de Keyzer, Gideon Eshel, Frédéric M. Vaz, Ophry Pines, Orly Elpeleg	2008	174
11	Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia The American Journal of Human Genetics ·Simon Edvardson, Hiroko Hama, Avraham Shaag, John M. Gomori, Itai Berger, Dov Soffer, Stanley H. Korman, I. Taustein, Ann Saada, Orly Elpeleg	2008	167
12	Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs The American Journal of Human Genetics ·Jan Smeıtınk, Orly Elpeleg, Hana Antonická, Heleen Diepstra, Ann Saada, P. Smits, Florin Sasarman, Gert Vriend, Jasmine Jacob‐Hirsch, Avraham Shaag, Gideon Rechavi, Brigitte Welling, Jürgen Horst, Richard J. Rodenburg, Bert van den Heuvel, Eric A. Shoubridge	2006	155
13	Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease The American Journal of Human Genetics ·Ann Saada, Rutger O. Vogel, Saskia J.G. Hoefs, Mariël A. van den Brand, Hans J. C. T. Wessels, Peter H.G.M. Willems, Hanka Venselaar, Avraham Shaag, Flora Barghuti, Orit Reish, Mordechai Shohat, Martijn A. Huynen, Jan Smeıtınk, Lambert P. van den Heuvel, Leo Nijtmans	2009	150
14	C6ORF66 Is an Assembly Factor of Mitochondrial Complex I The American Journal of Human Genetics ·Ann Saada, Simon Edvardson, Matan Rapoport, Avraham Shaag, Khaled Amry, Chaya Miller, Haya Lorberboum‐Galski, Orly Elpeleg	2008	144
15	Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation Journal of Medical Genetics ·Ann Saada, Avraham Shaag, Shmuel Arnon, T Dolfin, Carson C. Miller, Dana Fuchs‐Telem, Anne Lombès, Orly Elpeleg	2007	134
16	Type 2 Diabetes and Congenital Hyperinsulinism Cause DNA Double-Strand Breaks and p53 Activity in β Cells Cell Metabolism ·Sharona Tornovsky-Babeay, Daniela Dadon, Oren Ziv, Elhanan Tzipilevich, Tehila Kadosh, (unknown), Ayat Hija, Miri Stolovich-Rain, Judith Furth‐Lavi, Zvi Granot, Shay Porat, Louis H. Philipson, Kevan C. Herold, Tricia Bhatti, Charles A. Stanley, Frances M. Ashcroft, Pieter In 'T Veld, Ann Saada, Mark A. Magnuson, Benjamin Gläser, Yuval Dor	2013	132
17	Characteristics of Mitochondrial Transformation into Human Cells Scientific Reports ·Eyal E. Kesner, Ann Saada, Haya Lorberboum‐Galski	2016	130
18	Ceramide and the mitochondrial respiratory chain Biochimie ·Aviram Kogot‐Levin, Ann Saada	2013	129
19	Weaning Triggers a Maturation Step of Pancreatic β Cells Developmental Cell ·Miri Stolovich-Rain, Jonatan Enk, Jonas Vikeså, Finn Cilius Nielsen, Ann Saada, Benjamin Gläser, Yuval Dor	2015	122
20	Mitochondrial Transfer Ameliorates Cognitive Deficits, Neuronal Loss, and Gliosis in Alzheimer’s Disease Mice Journal of Alzheimer s Disease ·Keren Nitzan, Sandrine Benhamron, Michael Valitsky, Eyal E. Kesner, Michal Lichtenstein, Ayal Ben‐Zvi, Ezra Ella, Yehudit Segalstein, Ann Saada, Haya Lorberboum‐Galski, Hanna Rosenmann	2019	112

About Ann Saada

Ann Saada is a scholar working on Molecular Biology, Clinical Biochemistry, Physiology, Biochemistry and Genetics, having authored 174 papers that have together received 9.0k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (92 papers), Metabolism and Genetic Disorders (67 papers), ATP Synthase and ATPases Research (37 papers), Biochemical Acid Research Studies (14 papers), RNA modifications and cancer (13 papers), Pancreatic function and diabetes (10 papers), Biochemical and Molecular Research (9 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). The work is most often cited by research in Clinical Biochemistry (2.8k citations), Molecular Biology (6.4k citations), Biochemistry (485 citations), Neurology (403 citations) and Developmental Neuroscience (171 citations). Ann Saada has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Orly Elpeleg, Avraham Shaag, Hanna Mandel, Simon Edvardson, Chaya Miller, Staffan Eriksson, Shlomo Rotshenker, Fanny Reichert, Aviram Kogot‐Levin and Yoram Nevo. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Molecular Genetics and Metabolism, Journal of Medical Genetics and Biochemical and Biophysical Research Communications.

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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Ann Saada

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