Devorah Soiferman

703 total citations
10 papers, 531 citations indexed

About

Devorah Soiferman is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Devorah Soiferman has authored 10 papers receiving a total of 531 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Devorah Soiferman's work include Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). Devorah Soiferman is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). Devorah Soiferman collaborates with scholars based in Israel, United Kingdom and Sweden. Devorah Soiferman's co-authors include Ann Saada, Avraham Shaag, Liza Douiev, Simon Edvardson, Orly Elpeleg, Patrick Yu‐Wai‐Man, Florence Burté, Ronen Spiegel, Morad Khayat and Stavit A. Shalev and has published in prestigious journals such as PLoS ONE, Journal of Medical Genetics and Biochimie.

In The Last Decade

Devorah Soiferman

10 papers receiving 525 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Devorah Soiferman Israel 10 426 173 49 46 43 10 531
François‐Guillaume Debray Belgium 14 305 0.7× 211 1.2× 84 1.7× 55 1.2× 23 0.5× 26 507
Jorida Çoku United States 12 459 1.1× 204 1.2× 37 0.8× 15 0.3× 26 0.6× 18 525
R. Nair Finland 10 265 0.6× 84 0.5× 41 0.8× 25 0.5× 26 0.6× 12 380
Catherine Brunel‐Guitton Canada 14 454 1.1× 203 1.2× 66 1.3× 27 0.6× 20 0.5× 28 621
Karolina Szczepanowska Germany 14 586 1.4× 123 0.7× 117 2.4× 78 1.7× 53 1.2× 19 726
Andrew A.M. Morris United Kingdom 11 701 1.6× 606 3.5× 107 2.2× 18 0.4× 38 0.9× 16 851
Joyeeta Rahman United Kingdom 6 389 0.9× 226 1.3× 38 0.8× 21 0.5× 26 0.6× 7 458
A. E. M. Stroomer Netherlands 10 271 0.6× 185 1.1× 61 1.2× 30 0.7× 22 0.5× 13 445
Célia Nogueira Portugal 11 249 0.6× 216 1.2× 27 0.6× 20 0.4× 15 0.3× 36 385
Magalie Barth France 12 274 0.6× 171 1.0× 92 1.9× 11 0.2× 25 0.6× 32 378

Countries citing papers authored by Devorah Soiferman

Since Specialization
Citations

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

Fields of papers citing papers by Devorah Soiferman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Devorah Soiferman

This figure shows the co-authorship network connecting the top 25 collaborators of Devorah Soiferman. A scholar is included among the top collaborators of Devorah Soiferman 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 Devorah Soiferman. Devorah Soiferman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Yu‐Wai‐Man, Patrick, Devorah Soiferman, David Moore, Florence Burté, & Ann Saada. (2017). Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy. Mitochondrion. 36. 36–42. 52 indexed citations
2.
Kogot‐Levin, Aviram, Ann Saada, Gil Leibowitz, et al.. (2016). Upregulation of Mitochondrial Content in Cytochrome c Oxidase Deficient Fibroblasts. PLoS ONE. 11(10). e0165417–e0165417. 28 indexed citations
3.
Douiev, Liza, et al.. (2016). The Effects of Ascorbate, N-Acetylcysteine, and Resveratrol on Fibroblasts from Patients with Mitochondrial Disorders. Journal of Clinical Medicine. 6(1). 1–1. 60 indexed citations
4.
Spiegel, Ronen, Devorah Soiferman, Avraham Shaag, et al.. (2016). Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency. JIMD Reports. 33. 55–60. 15 indexed citations
5.
Sheffer, Ruth, Liza Douiev, Simon Edvardson, et al.. (2016). Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function. American Journal of Medical Genetics Part A. 170(6). 1603–1607. 78 indexed citations
6.
Spiegel, Ronen, Ann Saada, Padraig J. Flannery, et al.. (2015). Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation. Journal of Medical Genetics. 53(2). 127–131. 82 indexed citations
7.
Soiferman, Devorah, Ora Schueler‐Furman, Chaya Miller, et al.. (2014). Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy. European Journal of Human Genetics. 23(2). 159–164. 75 indexed citations
8.
Spiegel, Ronen, Ann Saada, Jonatan Halvardson, et al.. (2013). Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy. European Journal of Human Genetics. 22(7). 902–906. 66 indexed citations
9.
Edvardson, Simon, Vito Porcelli, Chaim Jalas, et al.. (2013). Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter. Journal of Medical Genetics. 50(4). 240–245. 53 indexed citations
10.
Soiferman, Devorah, et al.. (2013). The effect of small molecules on nuclear-encoded translation diseases. Biochimie. 100. 184–191. 22 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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