Eli Hershkovitz

5.5k total citations
124 papers, 3.0k citations indexed

About

Eli Hershkovitz is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Eli Hershkovitz has authored 124 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 23 papers in Endocrinology, Diabetes and Metabolism and 21 papers in Genetics. Recurrent topics in Eli Hershkovitz's work include Metabolism and Genetic Disorders (12 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Lysosomal Storage Disorders Research (10 papers). Eli Hershkovitz is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Lysosomal Storage Disorders Research (10 papers). Eli Hershkovitz collaborates with scholars based in Israel, United States and United Kingdom. Eli Hershkovitz's co-authors include Ruti Parvari, Ann Saada, Orly Elpeleg, Shimon Moses, Moshe Phillip, Neta Loewenthal, Avraham Shaag, Chaya Miller, Eli Pollak and Alon Haim and has published in prestigious journals such as Nucleic Acids Research, The Journal of Chemical Physics and PLoS ONE.

In The Last Decade

Eli Hershkovitz

121 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eli Hershkovitz Israel 29 1.4k 536 490 434 406 124 3.0k
Tom J. de Koning Netherlands 40 2.2k 1.6× 674 1.3× 1.2k 2.4× 522 1.2× 888 2.2× 153 4.6k
Risto Lapatto Finland 31 1.6k 1.2× 384 0.7× 211 0.4× 125 0.3× 386 1.0× 73 3.7k
Marie‐Cécile Nassogne Belgium 32 974 0.7× 388 0.7× 588 1.2× 197 0.5× 299 0.7× 103 3.1k
Saskia B. Wortmann Netherlands 32 1.9k 1.3× 539 1.0× 1.0k 2.1× 233 0.5× 302 0.7× 122 2.7k
Andreas Schulze Germany 43 2.2k 1.6× 559 1.0× 2.0k 4.0× 789 1.8× 712 1.8× 139 5.5k
Antònia Ribes Spain 38 2.5k 1.8× 395 0.7× 2.1k 4.4× 558 1.3× 586 1.4× 175 3.9k
Neil R.M. Buist United States 35 2.0k 1.5× 767 1.4× 1.6k 3.3× 492 1.1× 731 1.8× 111 5.4k
Hiroshi Mitsubuchi Japan 23 775 0.6× 207 0.4× 687 1.4× 188 0.4× 390 1.0× 92 2.0k
Pinar T. Ozand Saudi Arabia 34 2.2k 1.6× 496 0.9× 1.9k 3.9× 375 0.9× 923 2.3× 163 4.4k
Gregory M. Enns United States 36 2.5k 1.8× 732 1.4× 2.0k 4.1× 433 1.0× 687 1.7× 133 4.4k

Countries citing papers authored by Eli Hershkovitz

Since Specialization
Citations

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

Fields of papers citing papers by Eli Hershkovitz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eli Hershkovitz

This figure shows the co-authorship network connecting the top 25 collaborators of Eli Hershkovitz. A scholar is included among the top collaborators of Eli Hershkovitz 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 Eli Hershkovitz. Eli Hershkovitz 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.
Pode‐Shakked, Ben, Yuval E. Landau, Eli Hershkovitz, et al.. (2024). The natural history of dihydrolipoamide dehydrogenase deficiency in Israel. Journal of Inherited Metabolic Disease. 47(5). 895–902. 1 indexed citations
2.
Hershkovitz, Eli, et al.. (2023). Comparison of glucagon stimulation test and low dose ACTH test in assessing hypothalamic‐pituitary‐adrenal (HPA) axis in children. Clinical Endocrinology. 98(5). 678–681. 4 indexed citations
3.
Yackobovitch‐Gavan, Michal, Liora Lazar, Marianna Rachmiel, et al.. (2022). The Effect of a Nutritional Supplement on Growth and Body Composition in Short and Lean Preadolescent Boys following One Year of Intervention. Hormone Research in Paediatrics. 96(3). 278–288. 3 indexed citations
4.
Anzi, Shira, Inbar Plaschkes, Hadar Benyamini, et al.. (2022). P450 oxidoreductase regulates barrier maturation by mediating retinoic acid metabolism in a model of the human BBB. Stem Cell Reports. 17(9). 2050–2063. 3 indexed citations
5.
Hazan, Guy, Eli Hershkovitz, & Orna Staretz‐Chacham. (2020). Incidence of inherited metabolic disorders in southern Israel: a comparison between consanguinity and non-consanguinity communities. Orphanet Journal of Rare Diseases. 15(1). 13 indexed citations
6.
Haim, Alon, Yisrael Parmet, Neta Loewenthal, et al.. (2020). Acute hyperglycaemia can impair driving skill in young type 1 diabetes mellitus patients. Diabetes & Metabolism. 47(2). 101176–101176. 1 indexed citations
7.
Radovick, Sally, et al.. (2018). Gamification Concepts to Promote and Maintain Therapy Adherence in Children with Growth Hormone Deficiency. J — Multidisciplinary Scientific Journal. 1(1). 71–80. 11 indexed citations
8.
Loewenthal, Neta, Alon Haim, Ruti Parvari, & Eli Hershkovitz. (2015). Phosphoglucomutase‐1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiency. American Journal of Medical Genetics Part A. 167(12). 3139–3143. 21 indexed citations
9.
Feinstein, Yael, Baruch Yerushalmi, Neta Loewenthal, et al.. (2014). Natural History and Clinical Manifestations of Hyponatremia and Hyperchlorhidrosis due to Carbonic Anhydrase XII Deficiency. Hormone Research in Paediatrics. 81(5). 336–342. 11 indexed citations
10.
Pasternak, Yehonatan, et al.. (2013). Ethnic differences in glycemic control and diabetic ketoacidosis rate among children with diabetes mellitus type 1 in the Negev area.. PubMed. 15(6). 267–70. 11 indexed citations
11.
Athavale, Shreyas S., J. Jared Gossett, Chiaolong Hsiao, et al.. (2012). Domain III of the T. thermophilus 23S rRNA folds independently to a near-native state. RNA. 18(4). 752–758. 18 indexed citations
12.
Yardeni, David, et al.. (2011). Ethnic and Gender Inequities in the Evaluation of Referred Short Children. Hormone Research in Paediatrics. 76(1). 50–55. 8 indexed citations
13.
Berger, Itai, Eli Hershkovitz, Avraham Shaag, et al.. (2008). Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation. Annals of Neurology. 63(3). 405–408. 93 indexed citations
14.
Galron, Dalia, et al.. (2004). Carnitine‐acylcarnitine translocase deficiency: Identification of a novel molecular defect in a Bedouin patient. Journal of Inherited Metabolic Disease. 27(2). 267–273. 5 indexed citations
15.
Díaz, George A., Bruce D. Gelb, Marios Kambouris, et al.. (2002). Mutation of a tubulin folding gene, TCFE, causes the autosomal recessive Kenny-Caffey syndrome. Journal of Investigative Medicine. 50(2). 161. 1 indexed citations
16.
Hershkovitz, Eli, et al.. (2001). Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disorders. European Radiology. 11(6). 1070–1072. 4 indexed citations
17.
Shorer, Zamir, Shimon Moses, Eli Hershkovitz, Vered Pinsk, & Jacov Levy. (2001). Neurophysiologic studies in congenital insensitivity to pain with anhidrosis. Pediatric Neurology. 25(5). 397–400. 31 indexed citations
18.
Miura, Yoshitaka, Eli Hershkovitz, Akemi Inagaki, et al.. (2000). A Novel Mutation Causing Complete Thyroxine-Binding Globulin Deficiency (TBG-CD-Negev) among the Bedouins in Southern Israel. The Journal of Clinical Endocrinology & Metabolism. 85(10). 3687–3689. 15 indexed citations
19.
Parvari, Ruti, Eli Hershkovitz, Adam B. Kanis, et al.. (1998). Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43. The American Journal of Human Genetics. 63(1). 163–169. 45 indexed citations
20.
Hershkovitz, Eli, et al.. (1996). Short-Term Growth Hormone Therapy Increases Serum Lipoprotein (a) Levels in Normal Short Children without Growth Hormone Deficiency. Hormone Research. 46(1). 38–40. 11 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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