Eli Hershkovitz

5.5k citations

124 papers · 3.0k indexed · h-index 29

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Rheumatology top 2%
- Glycogen Storage Diseases and Myoclonus

Papers in ⓘ

Clinical Biochemistry 12
- Metabolism and Genetic Disorders 12
Endocrinology, Diabetes and Metabolism 23
- Growth Hormone and Insulin-like Growth Factors 9

Co-authors: Ruti Parvari (26 shared papers)Ann Saada (8 shared papers)Orly Elpeleg (6 shared papers)Shimon Moses (12 shared papers)Moshe Phillip (17 shared papers)Neta Loewenthal (19 shared papers)Avraham Shaag (5 shared papers)Chaya Miller (2 shared papers)
Journals: Hormone Research in Paediatrics (9 papers)Journal of Inherited Metabolic Disease (8 papers)The Journal of Clinical Endocrinology & Metabolism (6 papers)The American Journal of Human Genetics (5 papers)Acta Paediatrica (4 papers)
Partner nations: Israel United States United Kingdom

In The Last Decade

Eli Hershkovitz

121 papers receiving 2.9k citations

Peers

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-authors

The 25 scholars most cited alongside Eli Hershkovitz, 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 Eli Hershkovitz Line = papers co-authored together Eli Hershkovitz 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 124 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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	241
2	Autosomal-Recessive Hypophosphatemic Rickets Is Associated with an Inactivation Mutation in the ENPP1 Gene The American Journal of Human Genetics ·Varda Levy-Litan, Eli Hershkovitz, Luba Avizov, Neta Leventhal, Dani Bercovich, Vered Chalifa‐Caspi, Esther Manor, Sophia Buriakovsky, Yair Hadad, James W. Goding, Ruti Parvari	2010	205
3	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	175
4	Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease Genetics in Medicine ·Yoav H. Messinger, Nancy J. Mendelsohn, William J. Rhead, David Dimmock, Eli Hershkovitz, Michael Champion, Simon Jones, Rebecca Olson, Amy White, Cara Wells, Deeksha Bali, Laura E. Case, Sarah P. Young, Amy S. Rosenberg, Priya S. Kishnani	2012	166
5	Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: Genetic heterogeneity, novel mutations in theTRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies American Journal of Medical Genetics ·Sharon Shatzky, Shimon Moses, Jacov Levy, Vered Pinsk, Eli Hershkovitz, L. Herzog, Zamir Shorer, Anthony Luder, Ruti Parvari	2000	101
6	Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation Annals of Neurology ·Itai Berger, Eli Hershkovitz, Avraham Shaag, Simon Edvardson, Ann Saada, Orly Elpeleg	2008	93
7	The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23 The American Journal of Human Genetics ·Borhane Annabi, Brian C. Mansfield, Hisayuki Hiraiwa, Ke-Jian Lei, Tsuneyuki Ubagai, Mihael H. Polymeropoulos, Shimon Moses, Ruti Parvari, Eli Hershkovitz, Hanna Mandel, Moshe Fryman, Janice Y. Chou	1998	91
8	The utility of basal serum LH in prediction of central precocious puberty in girls European Journal of Endocrinology ·Yehonatan Pasternak, Michael Friger, Neta Loewenthal, Alon Haim, Eli Hershkovitz	2011	75
9	Effects of a Twelve-Week Randomized Intervention of Exercise and/or Diet on Weight Loss and Weight Maintenance, and Other Metabolic Parameters in Obese Preadolescent Children Hormone Research in Paediatrics ·Shlomit Shalitin, Liat Ashkenazi‐Hoffnung, Michal Yackobovitch‐Gavan, Nessia Nagelberg, Y. Karni, Eli Hershkovitz, Neta Loewenthal, Biana Shtaif, Galia Gat‐Yablonski, Moshe Phillip	2009	72
10	Homozygous Mutation G539R in the Gene for P450 Oxidoreductase in a Family Previously Diagnosed as Having 17,20-Lyase Deficiency The Journal of Clinical Endocrinology & Metabolism ·Eli Hershkovitz, Ruthi Parvari, Stefan A. Wudy, Michaela F. Hartmann, Larissa Garcia Gomes, Neta Loewental, Walter L. Miller	2008	62
11	The influence of diet and/or exercise and parental compliance on health-related quality of life in obese children Nutrition Research ·Michal Yackobovitch‐Gavan, Nessia Nagelberg, Moshe Phillip, Liat Ashkenazi‐Hoffnung, Eli Hershkovitz, Shlomit Shalitin	2009	53
12	Automated identification of RNA conformational motifs: theory and application to the HM LSU 23S rRNA Nucleic Acids Research ·Eli Hershkovitz	2003	52
13	TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome Journal of Medical Genetics ·Ronen Spiegel, Morad Khayat, Stavit A. Shalev, Y. Horovitz, Hanna Mandel, Eli Hershkovitz, Flora Barghuti, Avraham Shaag, Ann Saada, Stanley H. Korman, Orly Elpeleg, Ido Yatsiv	2010	52
14	A Single-Base Deletion in the 3'-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients European Journal of Human Genetics ·Ruti Parvari, Shimon Moses, Jianjun Shen, Eli Hershkovitz, Aaron Lerner, Yuan-Tsong Chen	1997	52
15	Luteinizing hormone-releasing hormone antagonists interfere with autocrine and paracrine growth stimulation of MCF-7 mammary cancer cells by insulin-like growth factors. The Journal of Clinical Endocrinology & Metabolism ·Eli Hershkovitz, Miriam Marbach, E Bosin, Jacob Levy, Charles T. Roberts, Derek LeRoith, Andrew V. Schally, Yoav Sharoni	1993	50
16	Multiple hops in multidimensional activated surface diffusion Surface Science ·Eli Hershkovitz, Peter Talkner, Eli Pollak, Yuri Georgievskii	1999	50
17	Lipoamide Dehydrogenase Deficiency Due to a Novel Mutation in the Interface Domain Biochemical and Biophysical Research Communications ·Eilon Shany, Ann Saada, Daniella Landau, Avraham Shaag, Eli Hershkovitz, Orly N. Elpeleg	1999	47
18	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 ·Ruti Parvari, Eli Hershkovitz, Adam B. Kanis, Rafael Gorodischer, Shlomit Shalitin, Val C. Sheffield, Rivka Carmi	1998	45
19	A Recessive Contiguous Gene Deletion of Chromosome 2p16 Associated with Cystinuria and a Mitochondrial Disease The American Journal of Human Genetics ·Ruti Parvari, Irena Brodyansky, Orly Elpeleg, Shimon Moses, Daniel Landau, Eli Hershkovitz	2001	44
20	Thyroglossal Duct Carcinoma in Children: Case Presentation and Review of the Literature Thyroid ·Asaf Peretz, Esther Leiberman, Joseph Kapelushnik, Eli Hershkovitz	2004	42

About Eli Hershkovitz

Eli Hershkovitz is a scholar working on Clinical Biochemistry, Endocrinology, Diabetes and Metabolism, Rheumatology, Pediatrics, Perinatology and Child Health and Genetics, having authored 124 papers that have together received 3.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (12 papers), Glycogen Storage Diseases and Myoclonus (11 papers), Carbohydrate Chemistry and Synthesis (10 papers), Lysosomal Storage Disorders Research (10 papers), Growth Hormone and Insulin-like Growth Factors (9 papers), Congenital heart defects research (7 papers), Mitochondrial Function and Pathology (7 papers) and stochastic dynamics and bifurcation (7 papers). The work is most often cited by research in Clinical Biochemistry (490 citations), Rheumatology (434 citations), Nephrology (171 citations), Endocrinology, Diabetes and Metabolism (368 citations) and Molecular Biology (1.4k citations). Eli Hershkovitz has collaborated with scholars based in Israel, United States and United Kingdom. Frequent co-authors include Ruti Parvari, Ann Saada, Orly Elpeleg, Shimon Moses, Moshe Phillip, Neta Loewenthal, Avraham Shaag, Chaya Miller, Eli Pollak and Alon Haim. Their work appears in journals such as Hormone Research in Paediatrics, Journal of Inherited Metabolic Disease, The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Acta Paediatrica.

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