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Uri Ben‐David

Tel Aviv University · IL
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Area of research
Oncology · Cancer Research
Research interest
Research interests include Cancer Genomics and Diagnostics, CRISPR and Genetic Engineering, Microtubule and mitosis dynamics, and PARP inhibition in cancer therapy.
h-index
37
citations
10,230
works
206
NIH funding
primary concept
email

Recent publications

Feeder-free culture of human pluripotent stem cells drives MDM4-mediated gain of chromosome 1q
Stem Cell Reports 2024cited by 16position: middledoi
A palmitate-rich metastatic niche enables metastasis growth via p65 acetylation resulting in pro-metastatic NF-κB signaling
Nature Cancer 2023cited by 139position: middledoi
Acute expression of human APOBEC3B in mice results in RNA editing and lethality
Genome biology 2023cited by 21position: middledoi
Acute expression of human APOBEC3B in mice causes lethality associated with RNA editing
bioRxiv (Cold Spring Harbor Laboratory) 2022cited by 5position: middledoi
Acute expression of human APOBEC3B in mice causes lethality associated with RNA editing
Research Square 2022cited by 1position: middledoi
Aneuploid senescent cells activate NF-κB to promote their immune clearance by NK cells
EMBO Reports 2021cited by 80position: middledoi
Discovering the anticancer potential of non-oncology drugs by systematic viability profiling
Nature Cancer 2020cited by 872position: middledoi
Cas9 activates the p53 pathway and selects for p53-inactivating mutations
Nature Genetics 2020cited by 283position: lastdoi
Aneuploidy increases resistance to chemotherapeutics by antagonizing cell division
Proceedings of the National Academy of Sciences 2020cited by 115position: middledoi
Author Correction: Cas9 activates the p53 pathway and selects for p53-inactivating mutations
Nature Genetics 2020cited by 13position: lastdoi
Context is everything: aneuploidy in cancer
Nature Reviews Genetics 2019cited by 731position: firstdoi
Genetic and transcriptional evolution alters cancer cell line drug response
Nature 2018cited by 935position: firstdoi
Genomic evolution of cancer models: perils and opportunities
Nature reviews. Cancer 2018cited by 225position: firstdoi
Report of the Key Opinion Leaders Meeting on Stem Cell-derived Beta Cells
Transplantation 2018cited by 81position: middledoi
Somatic loss of WWOX is associated with TP53 perturbation in basal-like breast cancer
Cell Death and Disease 2018cited by 30position: middledoi
Patient-derived xenografts undergo mouse-specific tumor evolution
Nature Genetics 2017cited by 714position: firstdoi
Assessing the Safety of Human Pluripotent Stem Cells and Their Derivatives for Clinical Applications
Stem Cell Reports 2017cited by 137position: middledoi
Genomic Copy Number Dictates a Gene-Independent Cell Response to CRISPR/Cas9 Targeting
Cancer Discovery 2016cited by 630position: middledoi
Landscape of Genomic Alterations in Pituitary Adenomas
Clinical Cancer Research 2016cited by 131position: middledoi
The landscape of chromosomal aberrations in breast cancer mouse models reveals driver-specific routes to tumorigenesis
Nature Communications 2016cited by 54position: firstdoi
Concise Review: Workshop Review: Understanding and Assessing the Risks of Stem Cell-Based Therapies
Stem Cells Translational Medicine 2015cited by 136position: middledoi
Genomic Instability in Human Pluripotent Stem Cells Arises from Replicative Stress and Chromosome Condensation Defects
Cell stem cell 2015cited by 130position: middledoi
Aneuploidy induces profound changes in gene expression, proliferation and tumorigenicity of human pluripotent stem cells
Nature Communications 2014cited by 231position: firstdoi
Genome maintenance in pluripotent stem cells
The Journal of Cell Biology 2014cited by 151position: lastdoi
Chemical ablation of tumor-initiating human pluripotent stem cells
Nature Protocols 2014cited by 54position: firstdoi
Virtual Karyotyping Reveals Greater Chromosomal Stability in Neural Cells Derived by Transdifferentiation than Those from Stem Cells
Cell stem cell 2014cited by 27position: middledoi
Brief Reports: Controlling the Survival of Human Pluripotent Stem Cells by Small Molecule-Based Targeting of Topoisomerase II Alpha
Stem Cells 2014cited by 20position: firstdoi
Elimination of undifferentiated cancer cells by pluripotent stem cell inhibitors
Journal of Molecular Cell Biology 2014cited by 14position: firstdoi
Analyzing the genomic integrity of stem cells
StemBook 2014cited by 10position: firstdoi
Selective Elimination of Human Pluripotent Stem Cells by an Oleate Synthesis Inhibitor Discovered in a High-Throughput Screen
Cell stem cell 2013cited by 307position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Nissim Benvenisty · Hebrew University of Jerusalem15 papers (2012–2017)Rameen Beroukhim · Broad Institute5 papers (2016–2020)Todd R. Golub · Broad Institute5 papers (2016–2020)Reuben S. Harris · Howard Hughes Medical Institute3 papers (2022–2023)Rocı́o Sotillo · German Cancer Research Center3 papers (2022–2023)Tamar Golan‐Lev · Hebrew University of Jerusalem3 papers (2013–2015)Alicia Alonso de la Vega · The Francis Crick Institute3 papers (2022–2023)Eli Reuveni · Hebrew University of Jerusalem3 papers (2022–2023)Kálmán Somogyi · German Cancer Research Center3 papers (2022–2023)Uri Weissbein · Hebrew University of Jerusalem3 papers (2014–2014)Nuri A. Temiz · The University of Texas at Austin3 papers (2022–2023)Angelika Amon · Massachusetts Institute of Technology3 papers (2019–2021)Tanja Poth · Heidelberg University3 papers (2022–2023)Rafail Nikolaos Tasakis · Icahn School of Medicine at Mount Sinai3 papers (2022–2023)Albrecht Stenzinger · Chirurgische Universitätsklinik Heidelberg3 papers (2022–2023)Gavin Ha · Fred Hutch Cancer Center2 papers (2016–2017)Nina Papavasiliou · German Cancer Research Center2 papers (2022–2023)Francisca Vázquez · Universidade de Santiago de Compostela2 papers (2020–2020)Aaron R. Thorner · Dana-Farber Cancer Institute2 papers (2020–2020)John G. Doench · Broad Institute2 papers (2020–2020)
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