Avraham Zeharia

2.8k total citations
83 papers, 1.8k citations indexed

About

Avraham Zeharia is a scholar working on Molecular Biology, Psychiatry and Mental health and Surgery. According to data from OpenAlex, Avraham Zeharia has authored 83 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 22 papers in Psychiatry and Mental health and 21 papers in Surgery. Recurrent topics in Avraham Zeharia's work include Metabolism and Genetic Disorders (18 papers), Migraine and Headache Studies (16 papers) and Mitochondrial Function and Pathology (11 papers). Avraham Zeharia is often cited by papers focused on Metabolism and Genetic Disorders (18 papers), Migraine and Headache Studies (16 papers) and Mitochondrial Function and Pathology (11 papers). Avraham Zeharia collaborates with scholars based in Israel, United States and France. Avraham Zeharia's co-authors include Tal Eidlitz‐Markus, Y. Cohen, Marc Mimouni, Jacob Amir, Orly Elpeleg, Ann Saada, Avraham Shaag, Tal Eidlitz‐Markus, Tally Lerman‐Sagie and Dorit Lev and has published in prestigious journals such as New England Journal of Medicine, PEDIATRICS and Clinical Infectious Diseases.

In The Last Decade

Avraham Zeharia

83 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Avraham Zeharia Israel 25 721 433 358 335 274 83 1.8k
Ching‐Shiang Chi Taiwan 22 477 0.7× 211 0.5× 251 0.7× 293 0.9× 315 1.1× 134 1.5k
Li L United States 20 791 1.1× 513 1.2× 94 0.3× 69 0.2× 228 0.8× 58 3.1k
Manuel Castro‐Gago Spain 21 367 0.5× 201 0.5× 413 1.2× 257 0.8× 99 0.4× 105 1.4k
J. Lawrence Merritt United States 19 456 0.6× 174 0.4× 101 0.3× 346 1.0× 113 0.4× 46 1.3k
Christoph Baerwald Germany 27 527 0.7× 86 0.2× 169 0.5× 191 0.6× 205 0.7× 134 2.3k
Hans Hartmann Germany 23 441 0.6× 73 0.2× 252 0.7× 592 1.8× 118 0.4× 71 1.7k
Daniela Concolino Italy 24 630 0.9× 147 0.3× 142 0.4× 217 0.6× 328 1.2× 130 1.9k
Ashok Verma United States 23 258 0.4× 221 0.5× 97 0.3× 98 0.3× 218 0.8× 90 1.5k
J. Rodríguez Spain 24 291 0.4× 235 0.5× 83 0.2× 128 0.4× 152 0.6× 84 1.8k
N D Barnes United Kingdom 28 341 0.5× 485 1.1× 65 0.2× 183 0.5× 160 0.6× 67 1.8k

Countries citing papers authored by Avraham Zeharia

Since Specialization
Citations

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

Fields of papers citing papers by Avraham Zeharia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avraham Zeharia

This figure shows the co-authorship network connecting the top 25 collaborators of Avraham Zeharia. A scholar is included among the top collaborators of Avraham Zeharia 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 Avraham Zeharia. Avraham Zeharia 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.
Peretz, Hava, Ayala Lagziel, Florian Bittner, et al.. (2021). Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects. Biomedicines. 9(7). 788–788. 4 indexed citations
2.
Mozer‐Glassberg, Yael, et al.. (2018). [TRMU MUTATIONS - REVERSIBLE INFANTILE LIVER FAILURE OR MULTISYSTEM DISORDER?]. PubMed. 157(1). 52–57. 5 indexed citations
3.
Vivante, Asaf, Hadas Ityel, Ben Pode‐Shakked, et al.. (2017). Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatric Nephrology. 32(12). 2273–2282. 27 indexed citations
4.
Eidlitz‐Markus, Tal, Avraham Zeharia, Y. Cohen, & Osnat Konen. (2013). MRI white matter lesions in pediatric migraine. Cephalalgia. 33(11). 906–913. 27 indexed citations
5.
Behar, Doron M., Lina Basel‐Vanagaite, Fabian Glaser, et al.. (2013). Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency. Journal of Lipid Research. 55(2). 307–312. 24 indexed citations
6.
Basel‐Vanagaite, Lina, Noam Zevit, Liang Guo, et al.. (2012). Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1. The American Journal of Human Genetics. 90(1). 49–60. 73 indexed citations
7.
Eidlitz‐Markus, Tal, et al.. (2012). Nonpharmacologic Treatment of Migraine With Low-Dose Propranolol or Amitriptyline. Pediatric Neurology. 46(6). 345–349. 16 indexed citations
8.
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
9.
Eidlitz‐Markus, Tal, et al.. (2009). Effectiveness of Nonpharmacologic Treatment for Migraine in Young Children. Headache The Journal of Head and Face Pain. 50(2). 219–223. 31 indexed citations
10.
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
11.
Kramer, Uri, Bruria Ben‐Zeev, Eli Lahat, et al.. (2009). Multicenter long‐term follow‐up of children with idiopathic West syndrome: ACTH versus vigabatrin. European Journal of Neurology. 16(4). 482–487. 50 indexed citations
12.
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
13.
Amir, Jacob, et al.. (2008). Mycobacterium haemophilumand Lymphadenitis in Immunocompetent Children, Israel. Emerging infectious diseases. 14(9). 1437–1439. 18 indexed citations
14.
Aganna, Ebun, Avraham Zeharia, G. A. Hitman, et al.. (2002). An Israeli Arab patient with a de novoTNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome. Arthritis & Rheumatism. 46(1). 245–249. 23 indexed citations
15.
Shuper, Avinoam, et al.. (2000). 6th European Forum on Quality Improvement in Health Care. Journal of Medical Ethics. 26(6). 443–443. 2 indexed citations
16.
Mukamel, Masza, et al.. (1995). Prognosis of infantile seborrheic dermatitis. The Journal of Pediatrics. 127(5). 744–746. 14 indexed citations
17.
Zeharia, Avraham, Emmilia Hodak, Masza Mukamel, Y Danziger, & Marc Mimouni. (1994). Successful treatment of chronic bullous dermatosis of childhood with colchicine. Journal of the American Academy of Dermatology. 30(4). 660–661. 17 indexed citations
18.
Danziger, Y, M Mukamel, Avraham Zeharia, Gabriel Dinari, & Marc Mimouni. (1994). Stunting of growth in anorexia nervosa during the prepubertal and pubertal period.. PubMed. 30(8). 581–4. 26 indexed citations
19.
Zeharia, Avraham, Masza Mukamel, Yaacov Frishberg, Raphael Weitz, & Marc Mimouni. (1990). Benign plexus neuropathy in children. The Journal of Pediatrics. 116(2). 276–278. 12 indexed citations
20.
Rachmel, Avinoam, et al.. (1989). Alagille syndrome associated with Moyamoya disease. American Journal of Medical Genetics. 33(1). 89–91. 29 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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