Bruria Ben Zeev

2.3k total citations
47 papers, 1.1k citations indexed

About

Bruria Ben Zeev is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Bruria Ben Zeev has authored 47 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 14 papers in Molecular Biology and 13 papers in Cognitive Neuroscience. Recurrent topics in Bruria Ben Zeev's work include Genetics and Neurodevelopmental Disorders (18 papers), Epilepsy research and treatment (12 papers) and Autism Spectrum Disorder Research (9 papers). Bruria Ben Zeev is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Epilepsy research and treatment (12 papers) and Autism Spectrum Disorder Research (9 papers). Bruria Ben Zeev collaborates with scholars based in Israel, United States and Australia. Bruria Ben Zeev's co-authors include Andreea Nissenkorn, Uri Kramer, Hadassa Goldberg‐Stern, Eva Gak, Nathanel Zelnik, Liora Sagi, Helen Leonard, Ami Bebbington, Nathan Watemberg and Shay Menascu and has published in prestigious journals such as PLoS ONE, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Bruria Ben Zeev

44 papers receiving 1.1k citations

Peers

Bruria Ben Zeev

GENET

PMH

CMN

Karen Weissbecker United States

Scott Demarest United States

Saul A. Mullen Australia

Giulia Barcia France

Humberto Arboleda Colombia

F. Andermann Canada

Alfredo D’Aniello Italy

Kenji Nakata Japan

Nicholas G. Irving United States

Maude L. Blundell United States

Karen Weissbecker United States

Bruria Ben Zeev

253 ×0.5

GENET

96 ×0.2

337 ×0.9

221 ×0.6

PMH

162 ×0.6

CMN

Citations per year, relative to Bruria Ben Zeev Bruria Ben Zeev (= 1×) peers Karen Weissbecker

Countries citing papers authored by Bruria Ben Zeev

Since Specialization

Citations

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

Fields of papers citing papers by Bruria Ben Zeev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bruria Ben Zeev. 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 Bruria Ben Zeev. The network helps show where Bruria Ben Zeev may publish in the future.

Co-authorship network of co-authors of Bruria Ben Zeev

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

All Works

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20 of 20 papers shown

Heimer, Gali, et al.. (2025). Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretation. npj Genomic Medicine. 10(1). 23–23. 1 indexed citations

Zeev, Bruria Ben, et al.. (2024). Autoimmune encephalitis in Israeli children – A retrospective nationwide study. European Journal of Paediatric Neurology. 50. 1–5.

Mor, Nofar, S. Raviv, Yoach Rais, et al.. (2024). Personalized allele-specific antisense oligonucleotides for GNAO1-neurodevelopmental disorder. Molecular Therapy — Nucleic Acids. 36(1). 102432–102432. 2 indexed citations

Danan-Gotthold, Miri, Tsviya Olender, Saurabh J. Pradhan, et al.. (2024). PRDM16 co-operates with LHX2 to shape the human brain. PubMed. 3. kvae001–kvae001. 2 indexed citations

Tzadok, Michal, Yael Michaeli, Tal Gilboa, et al.. (2023). Real-Life Experience With Purified Cannabidiol Treatment for Refractory Epilepsy: A Multicenter Retrospective Study. Pediatric Neurology. 150. 91–96. 10 indexed citations

Tzadok, Michal, et al.. (2022). The Long-Term Effectiveness and Safety of Cannabidiol-Enriched Oil in Children With Drug-Resistant Epilepsy. Pediatric Neurology. 136. 15–19. 4 indexed citations

Fattal‐Valevski, Aviva, Liat Ben‐Sira, Tally Lerman‐Sagie, et al.. (2021). Delineation of the phenotype of MED17-related disease in Caucasus-Jewish families. European Journal of Paediatric Neurology. 32. 40–45. 4 indexed citations

Ekstein, Dana, Iris Noyman, Firas Fahoum, et al.. (2020). Treating Epilepsy Patients with Investigational Anti-COVID-19 Drugs: Recommendations by the Israeli Chapter of the ILAE.. PubMed. 11(22). 665–672. 2 indexed citations

Waly, Bilal El, Cécile Mignon‐Ravix, Pierre Cacciagli, et al.. (2020). Molecular characterization of a 1p36 chromosomal duplication and in utero interference define ENO1 as a candidate gene for polymicrogyria. European Journal of Human Genetics. 28(12). 1703–1713. 4 indexed citations

10.

Zeev, Bruria Ben, et al.. (2017). Memory, Executive Skills, and Psychosocial Phenotype in Children with Pharmacoresponsive Epilepsy: Reactivity to Intervention. Frontiers in Neurology. 8. 86–86. 2 indexed citations

11.

Zeev, Bruria Ben, et al.. (2015). Auditory verbal memory and psychosocial symptoms are related in children with idiopathic epilepsy. Epilepsy & Behavior. 48. 53–60. 8 indexed citations

12.

Shorer, Zamir, Shay Menascu, Ilan Linder, et al.. (2012). Immunoglobulin Treatment for Severe Childhood Epilepsy. Pediatric Neurology. 46(6). 375–381. 20 indexed citations

13.

Goldberg‐Stern, Hadassa, Bruria Ben Zeev, Eli Heyman, et al.. (2011). The prevalence of atypical presentations and comorbidities of benign childhood epilepsy with centrotemporal spikes. Epilepsia. 52(8). 1483–1488. 94 indexed citations

14.

Zeev, Bruria Ben, Dorit Lev, Dan Su, et al.. (2010). Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy. The American Journal of Human Genetics. 87(4). 538–544. 107 indexed citations

15.

Bebbington, Ami, Alan K. Percy, John Christodoulou, et al.. (2009). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics. 47(4). 242–248. 54 indexed citations

16.

Fyfe, Sue, Ami Bebbington, Nadia Bahi‐Buisson, et al.. (2009). InterRett, a model for international data collection in a rare genetic disorder. Research in autism spectrum disorders. 3(3). 639–659. 45 indexed citations

17.

Abuhatzira, Liron, Kirill Makedonski, Eva Gak, et al.. (2005). Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis. Human Genetics. 118(1). 91–98. 12 indexed citations

18.

Kramer, Uri, et al.. (2001). Transient Oromotor Deficits in Children with Benign Childhood Epilepsy with Central Temporal Spikes. Epilepsia. 42(5). 616–620. 17 indexed citations

19.

Paret, Gideon, Reuven Tirosh, Bruria Ben Zeev, et al.. (1996). Intrathecal baclofen for severe torsion dystonia in a child. Acta Paediatrica. 85(5). 635–637. 16 indexed citations

20.

Tirosh, Reuven, et al.. (1995). Rhabdomyolysis due to hereditary torsion dystonia. Pediatric Neurology. 13(1). 83–84. 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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