Transcriptionally active chromatin recruits homologous recombination at DNA double-strand breaks

Mapping and analysis of chromatin state dynamics in nine human cell types

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53BP1 Inhibits Homologous Recombination in Brca1-Deficient Cells by Blocking Resection of DNA Breaks

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An auxin-based degron system for the rapid depletion of proteins in nonplant cells

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A User's Guide to the Encyclopedia of DNA Elements (ENCODE)

The ENCODE Project Consortium (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001046 · Cited by 1,515

Human CtIP promotes DNA end resection

Sartori, A. A., Lukas, C., Coates, J., Mistrik, M., Fu, S., Bartek, J., Baer, R., Lukas, J., & Jackson, S. P. (2007) · Nature · doi:10.1038/nature06337 · Cited by 1,362

Structural Basis for the Methylation State-Specific Recognition of Histone H4-K20 by 53BP1 and Crb2 in DNA Repair

Botuyan, M. V., Lee, J., Ward, I. M., Kim, J., Thompson, J. R., Chen, J., & Mer, G. (2006) · Cell · doi:10.1016/j.cell.2006.10.043 · Cited by 1,011

53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers

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A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice

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ATM-Dependent Chromatin Changes Silence Transcription In cis to DNA Double-Strand Breaks

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RIF1 Is Essential for 53BP1-Dependent Nonhomologous End Joining and Suppression of DNA Double-Strand Break Resection

Chapman, J. R., Barral, P., Vannier, J., Borel, V., Steger, M., Tomás‐Loba, A., Sartori, A. A., Adams, I. R., Batista, F. D., & Boulton, S. J. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.002 · Cited by 663

RAP80 suppresses the vulnerability of R-loops during DNA double-strand break repair

Yasuhara, T., Kato, R., Yamauchi, M., Uchihara, Y., Zou, L., Miyagawa, K., & Shibata, A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110335 · Cited by 12

Histone lysine methyltransferase-related neurodevelopmental disorders: current knowledge and saRNA future therapies

Roth, C., Kilpinen, H., Kurian, M. A., & Barral, S. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1090046 · Cited by 11

New facets in the chromatin-based regulation of genome maintenance

Dabin, J., Giacomini, G., Petit, E., & Polo, S. E. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103702 · Cited by 11

Emerging roles of cancer-associated histone mutations in genomic instabilities

Yadav, P., Jain, R., & Yadav, R. K. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1455572 · Cited by 11

Tetrameric INTS6-SOSS1 complex facilitates DNA:RNA hybrid autoregulation at double-strand breaks

Long, Q., Ajit, K., Šedová, K., Haluza, V., Štefl, R., Dokaneheifard, S., Beckedorff, F., Valencia, M. G., Šebesta, M., Shiekhattar, R., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae937 · Cited by 10

PARylation of GCN5 by PARP1 mediates its recruitment to DSBs and facilitates both HR and NHEJ Repair

Sarkar, D., Chakraborty, A., Mandi, S., & Dutt, S. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05469-9 · Cited by 12

Human RECQ helicases: roles in cancer, aging, and inherited disease

Monnat, R. J., & Sidorova, J. M. (2014) · Advances in Genomics and Genetics · doi:10.2147/agg.s54078 · Cited by 12

Collaborations between chromatin and nuclear architecture to optimize DNA repair fidelity

Mackenroth, B., & Alani, E. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.103018 · Cited by 11

MYC impairs resolution of site-specific DNA double-strand breaks repair

Ambrosio, S., Amente, S., Napolitano, G., Palo, G. D., Lania, L., & Majello, B. (2015) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2015.02.005 · Cited by 12

Quantifying site-specific chromatin mechanics and DNA damage response

Whitefield, D. B., Spagnol, S. T., Armiger, T. J., Lan, L., & Dahl, K. N. (2018) · Scientific Reports · doi:10.1038/s41598-018-36343-x · Cited by 12

Differences between the genomes of lymphoblastoid cell lines and blood-derived samples

Joesch-Cohen, L. M., & Glusman, G. (2017) · Advances in Genomics and Genetics · doi:10.2147/agg.s128824 · Cited by 11

Circular RNA Telomerase Reverses Endothelial Senescence in Progeria

Qin, W., Castillo, K., Li, H., Nguyen, T. K. C., Kiss, D., Cooke, J. P., & Mojiri, A. (2025) · Aging Cell · doi:10.1111/acel.70021 · Cited by 10

Homeodomain Proteins Directly Regulate ATM Kinase Activity

Johnson, T. E., Lee, J., Myler, L. R., Zhou, Y., Mosley, T. J., Yang, S.-H., Uprety, N., Kim, J., & Paull, T. T. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.089 · Cited by 12

CHD1 loss negatively influences metastasis-free survival in R0-resected prostate cancer patients and promotes spontaneous metastasis in vivo

Oh‐Hohenhorst, S. J., Derya Tilki, A., Ahlers, A., Suling, A. I., Hahn, O., Tennstedt, P., Matuszcak, C., Maar, H., Labitzky, V., Hanika, S., et al. (2021) · Cancer Gene Therapy · doi:10.1038/s41417-020-00288-z · Cited by 10

ATM suppresses c-Myc overexpression in the mammary epithelium in response to estrogen

Najnin, R. A., Mahmud, M. R. A., Rahman, M. M., Takeda, S., Sasanuma, H., Tanaka, H., Murakawa, Y., Shimizu, N., Akter, S., Takagi, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111909 · Cited by 10

XPF interacts with TOP2B for R-loop processing and DNA looping on actively transcribed genes

Chatzinikolaou, G., Stratigi, K., Siametis, A., Goulielmaki, E., Akalestou-Clocher, A., Tsamardinos, I., Topalis, P., Austin, C. A., Bouwman, B. A. M., Crosetto, N., et al. (2023) · Science Advances · doi:10.1126/sciadv.adi2095 · Cited by 10

The impact of chromatin on double-strand break repair: Imaging tools and discoveries

van Bueren, M. A. E., & Janssen, A. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103592 · Cited by 11

Deposition of onco‐histone H3 . 3‐G34W leads to DNA repair deficiency and activates cGAS / STING ‐mediated immune responses

Mancarella, D., Ellinghaus, H., Sigismondo, G., Veselinov, O., Kühn, A., Goyal, A., Hartmann, M., Fellenberg, J., Krijgsveld, J., Plass, C., et al. (2024) · International Journal of Cancer · doi:10.1002/ijc.34883 · Cited by 12

KDM5A demethylase: Erasing histone modifications to promote repair of DNA breaks

Price, B. D. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201705005 · Cited by 10

Proteomic analysis of H3K36me3 and PSIP1/p75 (LEDGF) complexes reveal their wider role in DNA repair

Pradeepa, M. M., Taylor, G. C. A., & von Kriegsheim, A. (2017) · Wellcome Open Research · doi:10.12688/wellcomeopenres.11589.1 · Cited by 8

Sir3 heterochromatin protein promotes non‐homologous end joining by direct inhibition of Sae2

Bordelet, H., Costa, R., Brocas, C., Dépagne, J., Veaute, X., Busso, D., Batté, A., Guérois, R., Marcand, S., & Dubrana, K. (2021) · The EMBO Journal · doi:10.15252/embj.2021108813 · Cited by 10

Transcription-dependent DNA double-strand breaks and human disease

Cristini, A., Gromak, N., & Sordet, O. (2020) · Molecular & Cellular Oncology · doi:10.1080/23723556.2019.1691905 · Cited by 10

A meeting at risk: Unrepaired DSBs go for broke

Guénolé, A., & Legube, G. (2017) · Nucleus · doi:10.1080/19491034.2017.1380138 · Cited by 14

Methylation of histone H3 lysine 36 is a barrier for therapeutic interventions of head and neck squamous cell carcinomaPreprint

Caeiro, L. D., Nakata, Y., Borges, R. L., Zha, M., Garcia-Martinez, L., Bañuelos, C. P., Stransky, S., Liu, T., Chan, H. L., Brabson, J., et al. (2024) · Genes & Development · doi:10.1101/gad.351408.123 · Cited by 11

Roles for the 3D genome in the cell cycle, DNA replication, and double strand break repair

Giles, K. A., Taberlay, P. C., Cesare, A. J., & Jones, M. V. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1548946 · Cited by 11

CRISPR-Cas9 Direct Fusions for Improved Genome Editing via Enhanced Homologous Recombination

Tabassum, T., Pietrogrande, G., Healy, M. D., & Wolvetang, E. J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914701 · Cited by 9

Into the chromatin world: Role of nuclear architecture in epigenome regulation

Bianchi, A., & Lanzuolo, C. (2015) · AIMS Biophysics · doi:10.3934/biophy.2015.4.585 · Cited by 9

Quantifying DNA End Resection in Human Cells

Zhou, Y., & Paull, T. T. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0644-5_5 · Cited by 9

High-resolution, ultrasensitive and quantitative DNA double-strand break labeling in eukaryotic cells using i-BLESS

Biernacka, A., Skrzypczak, M., Zhu, Y., Pasero, P., Rowicka, M., & Ginalski, K. (2020) · Nature Protocols · doi:10.1038/s41596-020-00448-3 · Cited by 12

Systematic overview on the most widespread techniques for inducing and visualizing the DNA double-strand breaks

Berzsenyi, I., Pantazi, V., Borsos, B. N., & Pankotai, T. (2021) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2021.108397 · Cited by 13

Transcription–Replication Coordination

Saponaro, M. (2022) · Life · doi:10.3390/life12010108 · Cited by 9

Double-strand break repair and mis-repair in 3D

Zagelbaum, J., & Gautier, J. (2022) · DNA repair · doi:10.1016/j.dnarep.2022.103430 · Cited by 9

Independence between pre-mRNA splicing and DNA methylation in an isogenic minigene resource

Nanan, K. K., Ocheltree, C., Sturgill, D. M., Mandler, M. D., Prigge, M. F., Varma, G., & Oberdoerffer, S. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx900 · Cited by 7

ATM-dependent formation of a novel chromatin compartment regulates the Response to DNA Double Strand Breaks and the biogenesis of translocationsPreprint

Arnould, C., Rocher, V., Bader, A. S., Lesage, E., Puget, N., Clouaire, T., Mourad, R., Noordermeer, D., Bushell, M., & Legube, G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.07.467654 · Cited by 12

Regulation of eukaryotic transcription initiation in response to cellular stress

Ferdoush, J., Kadir, R. A., Ogle, M., & Saha, A. (2024) · Gene · doi:10.1016/j.gene.2024.148616 · Cited by 8

Transcription near arrested DNA replication forks triggers ribosomal DNA copy number changes

Sasaki, M., & Kobayashi, T. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf014 · Cited by 6

Transcription‐coupled repair: tangled up in convoluted repair

Schiffmacher, D. A. L., Pai, Y. J., Pines, A., & Vermeulen, W. (2025) · FEBS Journal · doi:10.1111/febs.70104 · Cited by 10

NSUN2 facilitates DICER cleavage of DNA damage-associated R-loops to promote repair

Alagia, A., Ajit, K., Fazio, A. D., Long, Q., & Gullerová, M. (2025) · Nature Communications · doi:10.1038/s41467-025-63220-9 · Cited by 8

DROSHA, DICER, and damage-induced long ncRNA control BMI1-dependent transcriptional repression at DNA double-strand break

Esposito, F., Capozzo, I., Riccardi, A., Gioia, U., Modafferi, S., Manfredi, L., Colantoni, A., Tavella, S., Cabrini, M., Iannelli, F., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116605 · Cited by 8

Statistical Enrichment of Epigenetic States Around Triplet Repeats that Can Undergo Expansions

Essebier, A., Wolf, P. V., Cao, M. D., Carroll, B. S., Balasubramanian, S., & Mikael Bodén, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00092 · Cited by 7

An Expanding Toolkit for Heterochromatin Repair Studies

Rawal, C. C., Butova, N. L., Mitra, A., & Chiolo, I. (2022) · Genes · doi:10.3390/genes13030529 · Cited by 8

iMUT-seq: high-resolution DSB-induced mutation profiling reveals prevalent homologous-recombination dependent mutagenesis

Bader, A. S., & Bushell, M. (2023) · Nature Communications · doi:10.1038/s41467-023-44167-1 · Cited by 11

Chromatin yo-yo: expansion and condensation during DNA repair

Covington, M. L., Yuan, G., & Greenberg, R. A. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.09.004 · Cited by 8

PWWP2B promotes DNA end resection and homologous recombination

Ju, M. K., Lee, J. R., Choi, Y., Park, S. Y., Sul, H. J., Chung, H. J., An, S., Lee, S., Jung, E. Y., Kim, B., et al. (2022) · EMBO Reports · doi:10.15252/embr.202153492 · Cited by 7

Networks and Islands of Genome Nano-architecture and Their Potential Relevance for Radiation Biology

Hausmann, M., Hildenbrand, G. L., & Pilarczyk, G. (2022) · Results and problems in cell differentiation · doi:10.1007/978-3-031-06573-6_1 · Cited by 8

Use of theHPRTgene to study nuclease-induced DNA double-strand break repair

Gravells, P., Ahrabi, S., Vangala, R. K., Tomita, K., Brash, J. T., Brustle, L. A., Chung, C. P., Hong, J. M., Kaloudi, A., Humphrey, T. C., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv409 · Cited by 8

Moving fast and breaking things: Incidence and repair of DNA damage within ribosomal DNA repeats

Blokhina, Y. P., & Buchwalter, A. L. (2020) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2020.111715 · Cited by 9

Site-specific targeting of a light activated dCas9-KillerRed fusion protein generates transient, localized regions of oxidative DNA damage

House, N. C. M., Parasuram, R., Layer, J. V., & Price, B. D. (2020) · PLoS ONE · doi:10.1371/journal.pone.0237759 · Cited by 8

Encounters in Three Dimensions: How Nuclear Topology Shapes Genome Integrity

Sebastian, R., Aladjem, M. I., & Oberdoerffer, P. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.746380 · Cited by 8

Nanorate sequencing reveals the Arabidopsis somatic mutation landscape

Meyer, C. A., Nelms, B. D., & Schmitz, R. J. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2514194122 · Cited by 9

Strategies and mechanisms of precision genome engineering: From gene editing to genome writing

Huang, K., Tian, J., Zhao, W., Zhang, S., Xiang, L., Yang, M., Ls, L., Huang, Y., Zhang, N., Sun, L., et al. (2026) · iMetaOmics. · doi:10.1002/imo2.70115 · Cited by 8

Disruption of Chromatin Dynamics by Hypotonic Stress Suppresses HR and Shifts DSB Processing to Error-Prone SSA

Krieger, L. M., Mladenov, E., Soni, A., Demond, M., Stuschke, M., & Iliakis, G. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222010957 · Cited by 7

Joining the PARty: PARP Regulation of KDM5A during DNA Repair (and Transcription?)

Sanchez, A. R., Buck‐Koehntop, B. A., & Miller, K. M. (2022) · BioEssays · doi:10.1002/bies.202200015 · Cited by 8

Fanconi anemia associated protein 20 (FAAP20) plays an essential role in homology-directed repair of DNA double-strand breaks

Palovcak, A., Yuan, F., Verdún, R. E., Luo, L., & Zhang, Y. (2023) · Communications Biology · doi:10.1038/s42003-023-05252-9 · Cited by 6

Histone H3K36me3 mediates the genomic instability of Benzo[a]pyrene in human bronchial epithelial cells

Chen, S., Zhang, Z., Peng, H., Jiang, S., Xu, C., Ma, X., Zhang, L., Zhou, H., Xing, X., Chen, L., et al. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.123564 · Cited by 7

Nuclear F-actin assembly on damaged chromatin is regulated by DYRK1A and Spir1 phosphorylation

Li, J., Xiong, N., West, K. L., Leung, M. M. H., Ching, Y. P., Huang, J., Yuan, J., Yu, C., Leung, J. W. C., & Huen, M. S. Y. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae574 · Cited by 7

Double-strand breaks in facultative heterochromatin require specific movements and chromatin changes for efficient repair

Wensveen, M. R., Dixit, A. A., van Schendel, R., Kendek, A., Lambooij, J.-P., Tijsterman, M., Colmenares, S. U., & Janssen, A. (2024) · Nature Communications · doi:10.1038/s41467-024-53313-2 · Cited by 7

HDGF Knockout Suppresses Colorectal Cancer Progression and Drug Resistance by Modulating the DNA Damage Response

Su, R., Wang, Q., Hu, Q., Wendurige, Li, K., Wang, C., & Tao, L. (2025) · Biomolecules · doi:10.3390/biom15020282 · Cited by 7

Modulation of the Fanconi anemia pathway via chemically induced changes in chromatin structure

Vierra, D. A., Garzon, J. L., Rego, M. A., Adroved, M. M., Mauro, M., & Howlett, N. G. (2017) · Oncotarget · doi:10.18632/oncotarget.19470 · Cited by 7

A DNA Repair and Cell Cycle Gene Expression Signature in Pediatric High-Grade Gliomas: Prognostic and Therapeutic Value

Entz‐Werlé, N., Poidevin, L., Nazarov, P. V., Poch, O., Lhermitte, B., Chenard, M. P., Burckel, H., Guérin, É., Fuchs, Q., Castel, D., et al. (2021) · Cancers · doi:10.3390/cancers13092252 · Cited by 7

Epigenomic Analysis of RAD51 ChIP-seq Data Reveals cis-regulatory Elements Associated with Autophagy in Cancer Cell Lines

Kang, K., Choi, Y., Moon, H., You, C., Seo, M., Kwon, G., Yun, J., Beck, B. R., & Kang, K. (2021) · Cancers · doi:10.3390/cancers13112547 · Cited by 7

The Role of Drosophila CtIP in Homology-Directed Repair of DNA Double-Strand Breaks

Yannuzzi, I., Butler, M. A., Fernandez, J., & LaRocque, J. R. (2021) · Genes · doi:10.3390/genes12091430 · Cited by 8

Phasor Histone FLIM-FRET Microscopy Maps Nuclear-Wide Nanoscale Chromatin Architecture With Respect to Genetically Induced DNA Double-Strand Breaks

Lou, J., Solano, A. N., Liang, Z., & Hinde, E. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.770081 · Cited by 7

RNAPII response to transcription‐blocking DNA lesions in mammalian cells

Wang, J., Sadurnì, M. M., & Saponaro, M. (2022) · FEBS Journal · doi:10.1111/febs.16561 · Cited by 7

Report of mutation biases mirroring selection in Arabidopsis thaliana unlikely to be entirely due to variant calling errorsPreprint

Monroe, J. G., Murray, K., Xian, W., Carbonell‐Bejerano, P., Fenster, C. B., & Weigel, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.21.504682 · Cited by 7

Epigenetic targeting of MECOM/KRAS axis by JIB-04 impairs tumorigenesis and cisplatin resistance in MECOM-amplified ovarian cancer

Singh, I., Karna, A., Prajapati, A., Solanki, U., Mukherjee, A., Uppal, S., Malhotra, P., Kumar, M., & Agarwal, P. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02618-2 · Cited by 6

Current Status of Production of Transgenic Livestock by Genome Editing Technology

Park, D. S., Kim, S., Koo, D., & Kang, M. (2019) · Journal of Animal Reproduciton and Biotechnology · doi:10.12750/jarb.34.3.148 · Cited by 6

CRISPR/Cas9-Induced Breaks in Heterochromatin, Visualized by Immunofluorescence

Mitrentsi, I., & Soutoglou, E. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0644-5_30 · Cited by 6

Radial pair correlation of molecular brightness fluctuations maps protein diffusion as a function of oligomeric state within live-cell nuclear architecture

Solano, A. N., Lou, J., Scipioni, L., Gratton, E., & Hinde, E. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.04.030 · Cited by 6

Development of a simple multiple mutation detection system using seed-coat flavonoid pigments in irradiated Arabidopsis M1 plants

Kitamura, S., Hirata, S., Satoh, K., Rie, I., Narumi, I., & Oono, Y. (2022) · Scientific Reports · doi:10.1038/s41598-022-26989-z · Cited by 6

Rapid profiling of DNA replication dynamics using mass spectrometry–based analysis of nascent DNA

Ashour, M. E., Byrum, A. K., Meroni, A., Xia, J., Singh, S. S., Galletto, R., Rosenberg, S. M., Vindigni, A., & Mosammaparast, N. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202207121 · Cited by 6

Efficient CRISPR/Cas9-mediated gene editing in mammalian cells by the novel selectable traffic light reporters

Lyu, M., Sun, Y., Yan, N., Chen, Q., Wang, X., Wei, Z., Zhang, Z., & Xu, K. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.124926 · Cited by 6

Adaptive changes in the DNA damage response during skeletal muscle cell differentiation

Faleiro, I., Afonso, A., Balsinha, A., Lucas, B., Martin, R. M., Gomes, E. R., & de Almeida, S. F. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1239138 · Cited by 6

LC3B drives transcription-associated homologous recombination via direct interaction with R-loops

Yoon, J., Hwang, Y., Yun, H., Chung, J. M., Kim, S., Kim, G., Lee, Y., Lee, B. D., & Kang, H. C. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae156 · Cited by 7

Chromatin control in double strand break repair

Gospodinov, A. G., & Ugrinova, I. (2018) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2018.11.003 · Cited by 6

The γH2AX DSB marker may not be a suitable biodosimeter to measure the biological MRT valley dose

Ventura, J. A., Donoghue, J. F., Nowell, C. J., Cann, L. M., Day, L. R. J., Smyth, L. M. L., Forrester, H. B., Rogers, P. A. W., & Crosbie, J. C. (2021) · International Journal of Radiation Biology · doi:10.1080/09553002.2021.1893854 · Cited by 6

Mammalian RAD51 prevents non-conservative alternative end-joining and single strand annealing through non-catalytic mechanismsPreprint

So, A., Muhammad, A. A., Chailleux, C., Sesma-Sanz, L., Ragu, S., Cam, É. L., Canitrot, Y., Masson, J., Pauline, D., López, B. S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/768887 · Cited by 6

C8orf33 dictates DNA double-strand break repair choice by modulating KAT8-mediated H4K16 acetylation

Bishara, L. A., Abu‐Zhayia, E. R., Nicola, M., & Ayoub, N. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-08194-8 · Cited by 6

Histone H2A variants play a key role at DNA double-strand breaks during repair pathway choice

Clerf, E., Galloy, M., Fradet‐Turcotte, A., & Côté, J. (2024) · Frontiers in Epigenetics and Epigenomics · doi:10.3389/freae.2024.1445765 · Cited by 5

PARP1-TRIM44-MRN loop dictates the response to PARP inhibitors

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Interplay and Dynamics of Chromatin Architecture and DNA Damage Response: An Overview

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