Ayelet Erez

7.3k total citations
60 papers, 3.0k citations indexed

About

Ayelet Erez is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Ayelet Erez has authored 60 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 20 papers in Cancer Research and 19 papers in Genetics. Recurrent topics in Ayelet Erez's work include Cancer, Hypoxia, and Metabolism (17 papers), Metabolism and Genetic Disorders (14 papers) and Genomic variations and chromosomal abnormalities (13 papers). Ayelet Erez is often cited by papers focused on Cancer, Hypoxia, and Metabolism (17 papers), Metabolism and Genetic Disorders (14 papers) and Genomic variations and chromosomal abnormalities (13 papers). Ayelet Erez collaborates with scholars based in United States, Israel and United Kingdom. Ayelet Erez's co-authors include Rom Keshet, Christian Frezza, Sarah‐Maria Fendt, Peter W. Szlosarek, Arkaitz Carracedo, Brendan Lee, Sau Wai Cheung, Ralph J. DeBerardinis, Sandesh C.S. Nagamani and Sandesh C. Sreenath Nagamani and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Ayelet Erez

58 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ayelet Erez United States 31 1.6k 796 705 285 282 60 3.0k
Philippe M. Campeau Canada 33 1.8k 1.2× 466 0.6× 1.0k 1.5× 191 0.7× 303 1.1× 123 3.3k
Luisa Bonafé Switzerland 36 1.8k 1.2× 312 0.4× 1.4k 2.0× 723 2.5× 284 1.0× 97 3.5k
Janet L. Martin Australia 38 2.7k 1.7× 1.1k 1.4× 900 1.3× 164 0.6× 486 1.7× 75 5.0k
Yoko Aoki Japan 36 2.9k 1.9× 220 0.3× 777 1.1× 408 1.4× 277 1.0× 170 4.8k
Luc Schoonjans Belgium 24 2.3k 1.4× 1.5k 1.8× 643 0.9× 78 0.3× 426 1.5× 39 5.0k
Senén Vilaró Spain 39 2.0k 1.3× 438 0.6× 368 0.5× 116 0.4× 742 2.6× 108 4.3k
Robert Steinfeld Germany 29 1.6k 1.0× 197 0.2× 279 0.4× 418 1.5× 84 0.3× 56 2.8k
Ilkka Miinalainen Finland 28 1.4k 0.9× 455 0.6× 167 0.2× 114 0.4× 176 0.6× 85 2.1k
Hirofumi Fukumoto Japan 16 2.1k 1.4× 424 0.5× 425 0.6× 169 0.6× 1.0k 3.7× 29 3.3k
Lee‐Jun C. Wong United States 45 4.5k 2.9× 587 0.7× 786 1.1× 2.3k 8.1× 218 0.8× 180 5.9k

Countries citing papers authored by Ayelet Erez

Since Specialization
Citations

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

Fields of papers citing papers by Ayelet Erez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayelet Erez

This figure shows the co-authorship network connecting the top 25 collaborators of Ayelet Erez. A scholar is included among the top collaborators of Ayelet Erez 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 Ayelet Erez. Ayelet Erez 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.
Altea‐Manzano, Patricia, Amanda R. Decker-Farrell, Tobias Janowitz, & Ayelet Erez. (2025). Metabolic interplays between the tumour and the host shape the tumour macroenvironment. Nature reviews. Cancer. 25(4). 274–292. 16 indexed citations
2.
Furth, Noa, Avishay Spitzer, Tomer‐Meir Salame, et al.. (2024). Oncogenic IDH1 mut drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences. 122(1). e2403862122–e2403862122. 2 indexed citations
3.
Michaeli, Orli, Ayelet Erez, Shai Izraeli, et al.. (2021). Di‐genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predisposition. Clinical Genetics. 101(4). 442–447. 10 indexed citations
4.
Sinha, Sanju, Kuoyuan Cheng, Sanna Madan, et al.. (2021). Using a Recently Approved Tumor Mutational Burden Biomarker to Stratify Patients for Immunotherapy May Introduce a Sex Bias. JCO Precision Oncology. 5(5). 1147–1150. 3 indexed citations
5.
Fendt, Sarah‐Maria, Christian Frezza, & Ayelet Erez. (2020). Targeting Metabolic Plasticity and Flexibility Dynamics for Cancer Therapy. Cancer Discovery. 10(12). 1797–1807. 189 indexed citations
6.
Baruteau, Julien, Carmen Dı́ez-Fernández, Giusy Ranucci, et al.. (2019). Argininosuccinic aciduria: Recent pathophysiological insights and therapeutic prospects. Journal of Inherited Metabolic Disease. 42(6). 1147–1161. 26 indexed citations
7.
Bahat, Amir, Yehudit Zaltsman, Dilshad H. Khan, et al.. (2018). MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cells. Nature Communications. 9(1). 5132–5132. 64 indexed citations
8.
Koifman, Gabriela, Alon Silberman, Hilla Solomon, et al.. (2018). Mutant p53-dependent mitochondrial metabolic alterations in a mesenchymal stem cell-based model of progressive malignancy. Cell Death and Differentiation. 26(9). 1566–1581. 29 indexed citations
9.
Keshet, Rom & Ayelet Erez. (2018). Arginine and the metabolic regulation of nitric oxide synthesis in cancer. Disease Models & Mechanisms. 11(8). 109 indexed citations
10.
Rednam, Surya P., Ayelet Erez, Harriet Druker, et al.. (2017). Von Hippel–Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clinical Cancer Research. 23(12). e68–e75. 174 indexed citations
11.
Evans, D. Gareth, S.P. Hector, Vivian Y. Chang, et al.. (2017). Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 1. Clinical Cancer Research. 23(12). e46–e53. 114 indexed citations
12.
Peddibhotla, Sirisha, Sandesh C.S. Nagamani, Ayelet Erez, et al.. (2014). Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27. European Journal of Human Genetics. 23(1). 54–60. 32 indexed citations
13.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Frank J. Probst, et al.. (2012). Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function. Neurogenetics. 13(4). 333–339. 20 indexed citations
14.
Nagamani, Sandesh C.S., Ayelet Erez, & Brendan Lee. (2012). Response to Srilatha et al.. Genetics in Medicine. 14(6). 627–628. 1 indexed citations
15.
Bartnik, Magdalena, Katarzyna Derwińska, Monika Goś, et al.. (2011). Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females. Genetics in Medicine. 13(5). 447–452. 38 indexed citations
16.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Carolyn Bay, et al.. (2011). Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44. European Journal of Human Genetics. 20(2). 176–179. 38 indexed citations
17.
Brunetti‐Pierri, Nicola, Ayelet Erez, Oleg A. Shchelochkov, William Craigen, & Brendan Lee. (2009). Systemic hypertension in two patients with ASL deficiency: A result of nitric oxide deficiency?. Molecular Genetics and Metabolism. 98(1-2). 195–197. 26 indexed citations
18.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Joseph Shen, et al.. (2009). Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12. European Journal of Human Genetics. 18(3). 278–284. 103 indexed citations
19.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Christine M. Eng, et al.. (2008). Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss. European Journal of Human Genetics. 17(5). 573–581. 39 indexed citations
20.
Erez, Ayelet, Asher Castiel, Luba Trakhtenbrot, et al.. (2007). The SIL Gene Is Essential for Mitotic Entry and Survival of Cancer Cells. Cancer Research. 67(9). 4022–4027. 36 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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