Aviad Tsherniak

25.2k total citations · 2 hit papers
30 papers, 3.1k citations indexed

About

Aviad Tsherniak is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Aviad Tsherniak has authored 30 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Aviad Tsherniak's work include CRISPR and Genetic Engineering (9 papers), Protein Degradation and Inhibitors (4 papers) and Genomics and Chromatin Dynamics (4 papers). Aviad Tsherniak is often cited by papers focused on CRISPR and Genetic Engineering (9 papers), Protein Degradation and Inhibitors (4 papers) and Genomics and Chromatin Dynamics (4 papers). Aviad Tsherniak collaborates with scholars based in United States, Netherlands and United Kingdom. Aviad Tsherniak's co-authors include William C. Hahn, Francisca Vázquez, David E. Root, James M. McFarland, Jesse S. Boehm, Joshua M. Dempster, Todd R. Golub, Sandro Santagata, Matthew Meyerson and Jill P. Mesirov and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Aviad Tsherniak

28 papers receiving 3.0k citations

Hit Papers

Mitochondrial metabolism promotes adaptation to proteotox... 2019 2026 2021 2023 2019 2021 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aviad Tsherniak United States 21 2.4k 696 492 400 356 30 3.1k
Antonella Papa United States 18 2.4k 1.0× 560 0.8× 855 1.7× 390 1.0× 247 0.7× 29 3.1k
Jung-Sik Kim United States 26 1.5k 0.6× 406 0.6× 596 1.2× 313 0.8× 303 0.9× 45 2.2k
Diana Mandelker United States 23 1.3k 0.5× 718 1.0× 867 1.8× 482 1.2× 319 0.9× 94 2.5k
Thomas Hattier United States 6 2.1k 0.9× 390 0.6× 488 1.0× 227 0.6× 333 0.9× 7 2.6k
Sidong Huang Canada 22 1.9k 0.8× 621 0.9× 1.2k 2.4× 404 1.0× 204 0.6× 44 2.9k
Joshua E. Allen United States 28 1.6k 0.7× 476 0.7× 671 1.4× 156 0.4× 393 1.1× 125 2.5k
Cheryl M. Koh United States 18 1.6k 0.7× 569 0.8× 583 1.2× 383 1.0× 251 0.7× 26 2.3k
Michalina Janiszewska United States 16 1.9k 0.8× 1.2k 1.7× 906 1.8× 416 1.0× 212 0.6× 25 2.9k
Dimpy Koul United States 33 2.6k 1.0× 892 1.3× 877 1.8× 537 1.3× 820 2.3× 63 3.7k
Kathryn O’Reilly United States 7 1.8k 0.7× 273 0.4× 563 1.1× 395 1.0× 220 0.6× 15 2.2k

Countries citing papers authored by Aviad Tsherniak

Since Specialization
Citations

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

Fields of papers citing papers by Aviad Tsherniak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aviad Tsherniak

This figure shows the co-authorship network connecting the top 25 collaborators of Aviad Tsherniak. A scholar is included among the top collaborators of Aviad Tsherniak 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 Aviad Tsherniak. Aviad Tsherniak 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.
Krill-Burger, John M., Joshua M. Dempster, Ashir A. Borah, et al.. (2023). Partial gene suppression improves identification of cancer vulnerabilities when CRISPR-Cas9 knockout is pan-lethal. Genome biology. 24(1). 192–192. 13 indexed citations
2.
Pacini, Clare, Joshua M. Dempster, Isabella Boyle, et al.. (2021). Integrated cross-study datasets of genetic dependencies in cancer. Nature Communications. 12(1). 1661–1661. 145 indexed citations
3.
Warren, Allison, Andrew Jones, Tsukasa Shibue, et al.. (2021). Global computational alignment of tumor and cell line transcriptional profiles. Nature Communications. 12(1). 22–22. 72 indexed citations
4.
Dempster, Joshua M., Isabella Boyle, Francisca Vázquez, et al.. (2021). Chronos: a cell population dynamics model of CRISPR experiments that improves inference of gene fitness effects. Genome biology. 22(1). 343–343. 204 indexed citations breakdown →
5.
Price, Colles, Stanley Gill, Zandra V. Ho, et al.. (2019). Genome-Wide Interrogation of Human Cancers Identifies EGLN1 Dependency in Clear Cell Ovarian Cancers. Cancer Research. 79(10). 2564–2579. 28 indexed citations
6.
Tsvetkov, Peter, Alexandre Detappe, Kai Cai, et al.. (2019). Mitochondrial metabolism promotes adaptation to proteotoxic stress. Nature Chemical Biology. 15(7). 681–689. 436 indexed citations breakdown →
7.
Durbin, Adam D., Mark W. Zimmerman, Neekesh V. Dharia, et al.. (2018). Selective gene dependencies in MYCN-amplified neuroblastoma include the core transcriptional regulatory circuitry. Nature Genetics. 50(9). 1240–1246. 145 indexed citations
8.
Stolte, Björn, Amanda Balboni Iniguez, Neekesh V. Dharia, et al.. (2018). Genome-scale CRISPR-Cas9 screen identifies druggable dependencies in TP53 wild-type Ewing sarcoma. The Journal of Experimental Medicine. 215(8). 2137–2155. 46 indexed citations
9.
Gannon, Hugh, Tao Zou, Michael K. Kießling, et al.. (2018). Identification of ADAR1 adenosine deaminase dependency in a subset of cancer cells. Nature Communications. 9(1). 5450–5450. 159 indexed citations
10.
Pan, Joshua, Robin M. Meyers, Brittany C. Michel, et al.. (2018). Interrogation of Mammalian Protein Complex Structure, Function, and Membership Using Genome-Scale Fitness Screens. Cell Systems. 6(5). 555–568.e7. 92 indexed citations
11.
Zhang, Xiaoyang, Peter S. Choi, Joshua M. Francis, et al.. (2017). Somatic Superenhancer Duplications and Hotspot Mutations Lead to Oncogenic Activation of the KLF5 Transcription Factor. Cancer Discovery. 8(1). 108–125. 85 indexed citations
12.
Hsu, Jessie Hao-Ru, Guillaume Adelmant, Jialiang Huang, et al.. (2017). PRMT1-Mediated Translation Regulation Is a Crucial Vulnerability of Cancer. Cancer Research. 77(17). 4613–4625. 26 indexed citations
13.
Tóthová, Zuzana, John M. Krill-Burger, Katerina D. Popova, et al.. (2017). Multiplex CRISPR/Cas9-Based Genome Editing in Human Hematopoietic Stem Cells Models Clonal Hematopoiesis and Myeloid Neoplasia. Cell stem cell. 21(4). 547–555.e8. 63 indexed citations
14.
Rosenbluh, Joseph, Han Xu, William F. Harrington, et al.. (2017). Complementary information derived from CRISPR Cas9 mediated gene deletion and suppression. Nature Communications. 8(1). 15403–15403. 75 indexed citations
15.
Howard, Thomas P., Francisca Vázquez, Aviad Tsherniak, et al.. (2016). Functional Genomic Characterization of Cancer Genomes. Cold Spring Harbor Symposia on Quantitative Biology. 81. 237–246. 13 indexed citations
16.
Gannon, Hugh, Nathan O. Kaplan, Aviad Tsherniak, et al.. (2015). Identification of an “Exceptional Responder” Cell Line to MEK1 Inhibition: Clinical Implications for MEK-Targeted Therapy. Molecular Cancer Research. 14(2). 207–215. 19 indexed citations
17.
Kennedy, Alyssa L., Mounica Vallurupalli, Brian D. Crompton, et al.. (2015). Functional, chemical genomic, and super-enhancer screening identify sensitivity to cyclin D1/CDK4 pathway inhibition in Ewing sarcoma. Oncotarget. 6(30). 30178–30193. 71 indexed citations
18.
Nijhawan, Deepak, Travis Zack, Yin Ren, et al.. (2012). Cancer Vulnerabilities Unveiled by Genomic Loss. Cell. 150(4). 842–854. 161 indexed citations
19.
Shao, Diane D., Aviad Tsherniak, Shuba Gopal, et al.. (2012). ATARiS: Computational quantification of gene suppression phenotypes from multisample RNAi screens. Genome Research. 23(4). 665–678. 78 indexed citations
20.
Tamayo, Pablo, Yoon-Jae Cho, Aviad Tsherniak, et al.. (2011). Predicting Relapse in Patients With Medulloblastoma by Integrating Evidence From Clinical and Genomic Features. Journal of Clinical Oncology. 29(11). 1415–1423. 54 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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