Ayelet Rahat

1.7k total citations
14 papers, 1.2k citations indexed

About

Ayelet Rahat is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ayelet Rahat has authored 14 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Ayelet Rahat's work include Genetics and Neurodevelopmental Disorders (5 papers), DNA Repair Mechanisms (4 papers) and Genomics and Chromatin Dynamics (4 papers). Ayelet Rahat is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), DNA Repair Mechanisms (4 papers) and Genomics and Chromatin Dynamics (4 papers). Ayelet Rahat collaborates with scholars based in Israel, United States and Canada. Ayelet Rahat's co-authors include Batsheva Kerem, Stephen W. Scherer, Nir Friedman, Hanah Margalit, Eitan Zlotorynski, Lap‐Chee Tsui, Assaf Weiner, Hsiuyi V. Chen, Oliver J. Rando and Assaf C. Bester and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and Molecular Cell.

In The Last Decade

Ayelet Rahat

14 papers receiving 1.2k 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 Rahat Israel 12 1.0k 545 167 103 60 14 1.2k
Jose I. de las Heras United Kingdom 21 1.3k 1.3× 180 0.3× 70 0.4× 171 1.7× 38 0.6× 33 1.4k
Barbara K. Lee United States 12 555 0.6× 401 0.7× 87 0.5× 45 0.4× 38 0.6× 15 786
Glenn Gundersen Norway 8 702 0.7× 203 0.4× 69 0.4× 26 0.3× 50 0.8× 9 913
Larry D. Mesner United States 20 902 0.9× 259 0.5× 108 0.6× 74 0.7× 59 1.0× 38 1.0k
Dachang Tao China 18 623 0.6× 239 0.4× 198 1.2× 38 0.4× 46 0.8× 67 1000
Robert D. Dredge United States 5 440 0.4× 398 0.7× 82 0.5× 25 0.2× 50 0.8× 5 832
Ercole Rao Germany 12 763 0.8× 777 1.4× 178 1.1× 19 0.2× 31 0.5× 19 1.1k
Son C. Nguyen United States 20 1.2k 1.2× 205 0.4× 336 2.0× 51 0.5× 70 1.2× 36 1.3k
Catherine M. Farrell United States 15 1.1k 1.1× 342 0.6× 132 0.8× 42 0.4× 39 0.7× 20 1.3k
Yacine Chérifi France 11 825 0.8× 282 0.5× 71 0.4× 30 0.3× 55 0.9× 21 1.0k

Countries citing papers authored by Ayelet Rahat

Since Specialization
Citations

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

Fields of papers citing papers by Ayelet Rahat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayelet Rahat

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

All Works

14 of 14 papers shown
1.
Joseph-Strauss, Daphna, Ayelet Rahat, Miriam Adam, et al.. (2021). Early sample tagging and pooling enables simultaneous SARS-CoV-2 detection and variant sequencing. Science Translational Medicine. 13(618). eabj2266–eabj2266. 9 indexed citations
2.
Sadeh, Ronen, et al.. (2016). Elucidating Combinatorial Chromatin States at Single-Nucleosome Resolution. Molecular Cell. 63(6). 1080–1088. 23 indexed citations
3.
4.
Weiner, Assaf, Tsung-Han S. Hsieh, Hsiuyi V. Chen, et al.. (2015). High-Resolution Chromatin Dynamics during a Yeast Stress Response. Molecular Cell. 58(2). 371–386. 139 indexed citations
5.
Weiner, Assaf, Hsiuyi V. Chen, Chih Long Liu, et al.. (2012). Systematic Dissection of Roles for Chromatin Regulators in a Yeast Stress Response. PLoS Biology. 10(7). e1001369–e1001369. 125 indexed citations
6.
Ozeri-Galai, E., Ronald Lebofsky, Ayelet Rahat, et al.. (2011). Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites. Molecular Cell. 43(1). 122–131. 137 indexed citations
7.
Schwartz, Michal, Yifat S. Oren, Assaf C. Bester, et al.. (2009). Impaired Replication Stress Response in Cells from Immunodeficiency Patients Carrying Cernunnos/XLF Mutations. PLoS ONE. 4(2). e4516–e4516. 16 indexed citations
8.
Schwartz, Michal, Eitan Zlotorynski, Michal Goldberg, et al.. (2005). Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability. Genes & Development. 19(22). 2715–2726. 110 indexed citations
9.
Zlotorynski, Eitan, Ayelet Rahat, Jennifer Skaug, et al.. (2003). Molecular Basis for Expression of Common and Rare Fragile Sites. Molecular and Cellular Biology. 23(20). 7143–7151. 199 indexed citations
10.
Hellman, Asaf, Ayelet Rahat, Stephen W. Scherer, et al.. (2000). Replication Delay along FRA7H, a Common Fragile Site on Human Chromosome 7, Leads to Chromosomal Instability. Molecular and Cellular Biology. 20(12). 4420–4427. 105 indexed citations
11.
Chiba‐Falek, Ornit, Eitan Kerem, Tzipora Shoshani, et al.. (1998). The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C→T Mutation. Genomics. 53(3). 276–283. 76 indexed citations
12.
Benhorin, Jesaia, Maya Goldmit, Jean W. MacCluer, et al.. (1998). Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Human Mutation. 12(1). 72–72. 3 indexed citations
13.
Benhorin, Jesaia, Maya Goldmit, Jean W. MacCluer, et al.. (1998). Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Human Mutation. 12(1). 72–72. 20 indexed citations
14.
Mishmar, Dan, Ayelet Rahat, Stephen W. Scherer, et al.. (1998). Molecular characterization of a common fragile site ( FRA7H ) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proceedings of the National Academy of Sciences. 95(14). 8141–8146. 189 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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