Zamir Shorer

3.0k total citations
67 papers, 2.1k citations indexed

About

Zamir Shorer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Psychiatry and Mental health. According to data from OpenAlex, Zamir Shorer has authored 67 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 16 papers in Psychiatry and Mental health. Recurrent topics in Zamir Shorer's work include Hereditary Neurological Disorders (13 papers), Epilepsy research and treatment (13 papers) and Pharmacological Effects and Toxicity Studies (7 papers). Zamir Shorer is often cited by papers focused on Hereditary Neurological Disorders (13 papers), Epilepsy research and treatment (13 papers) and Pharmacological Effects and Toxicity Studies (7 papers). Zamir Shorer collaborates with scholars based in Israel, United States and Canada. Zamir Shorer's co-authors include Ohad S. Birk, Jacov Levy, Hagit Flusser, Rivka Ofir, Ilan Shelef, Bruria Ben‐Zeev, Uri Kramer, Giora Pillar, Nir Peled and Eli Hershkovitz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Brain.

In The Last Decade

Zamir Shorer

67 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zamir Shorer Israel 25 790 534 348 289 258 67 2.1k
Robert Surtees United Kingdom 23 848 1.1× 384 0.7× 294 0.8× 380 1.3× 246 1.0× 45 2.2k
Jari Honkaniemi Finland 32 974 1.2× 1.0k 1.9× 335 1.0× 370 1.3× 261 1.0× 49 2.7k
Johanna Palmio Finland 27 851 1.1× 638 1.2× 570 1.6× 465 1.6× 168 0.7× 76 2.0k
Ming Ren China 24 1.3k 1.6× 539 1.0× 245 0.7× 573 2.0× 285 1.1× 77 2.7k
William T. O’Brien United States 26 1.1k 1.4× 401 0.8× 272 0.8× 377 1.3× 248 1.0× 89 2.7k
Martin H. Maurer Germany 29 1.1k 1.4× 537 1.0× 136 0.4× 253 0.9× 336 1.3× 70 2.9k
Eiji Nakagawa Japan 25 900 1.1× 547 1.0× 682 2.0× 219 0.8× 249 1.0× 177 2.6k
Zsolt Csaba France 26 791 1.0× 468 0.9× 94 0.3× 186 0.6× 162 0.6× 63 2.2k
Philipp von Rosenstiel United States 20 845 1.1× 307 0.6× 386 1.1× 519 1.8× 157 0.6× 55 2.4k
László Vutskits Switzerland 38 783 1.0× 1.2k 2.3× 159 0.5× 216 0.7× 190 0.7× 89 4.2k

Countries citing papers authored by Zamir Shorer

Since Specialization
Citations

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

Fields of papers citing papers by Zamir Shorer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zamir Shorer

This figure shows the co-authorship network connecting the top 25 collaborators of Zamir Shorer. A scholar is included among the top collaborators of Zamir Shorer 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 Zamir Shorer. Zamir Shorer 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.
Shorer, Zamir, et al.. (2022). Correlates of Caregiving Burden among Bedouin-Muslim Mothers of Children Diagnosed with Epilepsy. International Journal of Environmental Research and Public Health. 19(18). 11595–11595. 3 indexed citations
2.
Halpérin, Daniel, Ohad Wormser, Yuval Yogev, et al.. (2020). Phenotypic variability and mutation hotspot in COX15‐related Leigh syndrome. American Journal of Medical Genetics Part A. 182(6). 1506–1512. 9 indexed citations
3.
Shorer, Zamir, et al.. (2019). Correlates of quality of life in mothers of children with diagnosed epilepsy. Epilepsy & Behavior. 93. 80–86. 7 indexed citations
4.
Flusser, Hagit, Daniel Halpérin, Rotem Kadir, et al.. (2018). Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease. Clinical Genetics. 94(5). 473–479. 11 indexed citations
5.
Halpérin, Daniel, Rotem Kadir, Yonatan Perez, et al.. (2018). SEC31A mutation affects ER homeostasis, causing a neurological syndrome. Journal of Medical Genetics. 56(3). 139–148. 27 indexed citations
6.
Benifla, Mony, et al.. (2017). Temporal lobe surgery for intractable epilepsy in children: What to do with the hippocampus?. Seizure. 52. 81–88. 7 indexed citations
7.
Perez, Yonatan, Zamir Shorer, Pauline Chabosseau, et al.. (2017). SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome. Brain. 140(4). 928–939. 71 indexed citations
8.
Volodarsky, Michael, Hava Lichtig, Tom Leibson, et al.. (2015). CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay. Human Molecular Genetics. 24(22). 6485–6491. 12 indexed citations
9.
Nevo, Yoram, Bruria Ben‐Zeev, Adi Tabib, et al.. (2012). CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood. 121(1). 129–135. 111 indexed citations
10.
Cox, James J., Jony Sheynin, Zamir Shorer, et al.. (2010). Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations. Human Mutation. 31(9). E1670–E1686. 84 indexed citations
11.
Barel, Ortal, Stavit A. Shalev, Rivka Ofir, et al.. (2008). Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9. The American Journal of Human Genetics. 83(2). 193–199. 137 indexed citations
12.
Barel, Ortal, Zamir Shorer, Hagit Flusser, et al.. (2008). Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ. The American Journal of Human Genetics. 82(5). 1211–1216. 92 indexed citations
13.
14.
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
15.
Shorer, Zamir, et al.. (2001). Congenital insensitivity to pain with anhidrosis (CIPA): the spectrum of radiological findings. Pediatric Radiology. 31(10). 701–705. 28 indexed citations
16.
Moses, Shimon, Jacov Levy, Vered Pinsk, et al.. (2000). 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. 92(5). 353–360. 101 indexed citations
17.
Kramer, Uri, et al.. (2000). Alternating Hemiplegia of Childhood in Half-Sisters. Journal of Child Neurology. 15(2). 128–130. 11 indexed citations
18.
Warner, Laura E., Mordechai Shohat, Zamir Shorer, & James R. Lupski. (1997). Multiplede novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case. Human Mutation. 10(1). 21–24. 21 indexed citations
19.
Shahar, Eli, Zamir Shorer, Chaim M. Roifman, et al.. (1997). Immune globulins are effective in severe pediatric Guillain-Barre syndrome. Pediatric Neurology. 16(1). 32–36. 16 indexed citations
20.
Hershkovitz, Eli, et al.. (1996). Status epilepticus following intravenous N-acetylcysteine therapy.. PubMed. 32(11). 1102–4. 19 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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