Limor Regev

2.4k total citations · 1 hit paper
18 papers, 1.7k citations indexed

About

Limor Regev is a scholar working on Behavioral Neuroscience, Social Psychology and Molecular Biology. According to data from OpenAlex, Limor Regev has authored 18 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Behavioral Neuroscience, 7 papers in Social Psychology and 5 papers in Molecular Biology. Recurrent topics in Limor Regev's work include Stress Responses and Cortisol (11 papers), Neuroendocrine regulation and behavior (7 papers) and Tryptophan and brain disorders (5 papers). Limor Regev is often cited by papers focused on Stress Responses and Cortisol (11 papers), Neuroendocrine regulation and behavior (7 papers) and Tryptophan and brain disorders (5 papers). Limor Regev collaborates with scholars based in Israel, United States and Bulgaria. Limor Regev's co-authors include Alon Chen, Adi Neufeld-Cohen, Tallie Z. Baram, Evan Elliott, Gili Ezra-Nevo, Shosh Gil, Jenny Molet, Inbal Goshen, Michael London and A. Doron and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Limor Regev

18 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Astrocytic Activation Generates De Novo Neuronal Potentiation and Memory Enhancement

2018 413 citations Tirzah Kreisel, A. Doron et al. Cell profile →

Peers

Limor Regev

CMN

Christian Mirescu United States

Marianne L. Seney United States

Immanuel Purushothaman United States

Deena M. Walker United States

Amy Mahan United States

Hannah M. Cates United States

Manabu Makinodan Japan

Dragoš Inta Germany

Arie Kaffman United States

Astrid Vallès Netherlands

Christian Mirescu United States

Limor Regev

611 ×0.9

370 ×0.8

233 ×0.5

381 ×0.8

CMN

184 ×0.7

Citations per year, relative to Limor Regev Limor Regev (= 1×) peers Christian Mirescu

Countries citing papers authored by Limor Regev

Since Specialization

Citations

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

Fields of papers citing papers by Limor Regev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Limor Regev

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

All Works

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18 of 18 papers shown

Petucci, Christopher, Hu Wang, Xianlin Han, et al.. (2025). MTCH2 controls energy demand and expenditure to fuel anabolism during adipogenesis. The EMBO Journal. 44(4). 1007–1038. 8 indexed citations

Mullokandov, Michael, et al.. (2023). MTCH2 cooperates with MFN2 and lysophosphatidic acid synthesis to sustain mitochondrial fusion. EMBO Reports. 25(1). 45–67. 13 indexed citations

Bolton, Jessica L., Anton Schulmann, Megan M. Curran, et al.. (2020). Unexpected Transcriptional Programs Contribute to Hippocampal Memory Deficits and Neuronal Stunting after Early-Life Adversity. Cell Reports. 33(11). 108511–108511. 27 indexed citations

Kreisel, Tirzah, A. Doron, Nofar Ozeri-Engelhard, et al.. (2018). Astrocytic Activation Generates De Novo Neuronal Potentiation and Memory Enhancement. Cell. 174(1). 59–71.e14. 413 indexed citations breakdown →

Schulmann, Anton, Jessica L. Bolton, Megan M. Curran, et al.. (2018). Blocking NRSF Function Rescues Spatial Memory Impaired by Early-Life Adversity and Reveals Unexpected Underlying Transcriptional Programs. SSRN Electronic Journal. 3 indexed citations

Bolton, Jessica L., Jenny Molet, Limor Regev, et al.. (2017). Anhedonia Following Early-Life Adversity Involves Aberrant Interaction of Reward and Anxiety Circuits and Is Reversed by Partial Silencing of Amygdala Corticotropin-Releasing Hormone Gene. Biological Psychiatry. 83(2). 137–147. 158 indexed citations

Frère, Samuel, Limor Regev, Amit Benbenishty, et al.. (2017). Sensory Deprivation Triggers Synaptic and Intrinsic Plasticity in the Hippocampus. Cerebral Cortex. 27(6). 3457–3470. 22 indexed citations

Molet, Jenny, et al.. (2016). Fragmentation and high entropy of neonatal experience predict adolescent emotional outcome. Translational Psychiatry. 6(1). e702–e702. 166 indexed citations

Regev, Limor, et al.. (2013). NMDA Receptor Activation and Calpain Contribute to Disruption of Dendritic Spines by the Stress Neuropeptide CRH. Journal of Neuroscience. 33(43). 16945–16960. 68 indexed citations

10.

Regev, Limor, Yuncai Chen, Anikó Kőrösi, et al.. (2013). Differential contribution of CBP:CREB binding to corticotropin-releasing hormone expression in the infant and adult hypothalamus. Stress. 17(1). 39–50. 7 indexed citations

11.

Regev, Limor & Tallie Z. Baram. (2013). Corticotropin releasing factor in neuroplasticity. Frontiers in Neuroendocrinology. 35(2). 171–179. 56 indexed citations

12.

Regev, Limor, Michael Tsoory, Shosh Gil, & Alon Chen. (2011). Site-Specific Genetic Manipulation of Amygdala Corticotropin-Releasing Factor Reveals Its Imperative Role in Mediating Behavioral Response to Challenge. Biological Psychiatry. 71(4). 317–326. 74 indexed citations

13.

Regev, Limor, Adi Neufeld-Cohen, Michael Tsoory, et al.. (2010). Prolonged and site-specific over-expression of corticotropin-releasing factor reveals differential roles for extended amygdala nuclei in emotional regulation. Molecular Psychiatry. 16(7). 714–728. 93 indexed citations

14.

Elliott, Evan, Gili Ezra-Nevo, Limor Regev, Adi Neufeld-Cohen, & Alon Chen. (2010). Resilience to social stress coincides with functional DNA methylation of the Crf gene in adult mice. Nature Neuroscience. 13(11). 1351–1353. 336 indexed citations

15.

Kuperman, Yael, Orna Issler, Limor Regev, et al.. (2010). Perifornical Urocortin-3 mediates the link between stress-induced anxiety and energy homeostasis. Proceedings of the National Academy of Sciences. 107(18). 8393–8398. 68 indexed citations

16.

Regev, Limor, et al.. (2010). Genetic approach for intracerebroventricular delivery. Proceedings of the National Academy of Sciences. 107(9). 4424–4429. 29 indexed citations

17.

Oberkovitz, Galia, Limor Regev, & Atan Gross. (2007). Nucleocytoplasmic shuttling of BID is involved in regulating its activities in the DNA-damage response. Cell Death and Differentiation. 14(9). 1628–1634. 13 indexed citations

18.

Kamer, Iris, Rachel Sarig, Yehudit Zaltsman, et al.. (2005). Proapoptotic BID Is an ATM Effector in the DNA-Damage Response. Cell. 122(4). 593–603. 178 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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