Emily Cybulla
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
19
Citations
965
Est. group size
—
Recurring co-author estimate
Active years
9
Publishing since 2018
Emily Cybulla's research focuses on how cells respond to DNA damage during replication, particularly in cancers with defects in DNA repair genes like BRCA1. Her work examines molecular pathways (such as PRIMPOL, RAD18, and GAS6/AXL signaling) that allow cancer cells to tolerate replication stress, and explores how targeting these pathways with drugs like PARP inhibitors, chemotherapy, or other agents could make cancer treatment more effective. Much of her research uses laboratory models of breast, ovarian, and prostate cancers to study these mechanisms and their potential clinical applications.
Publication output has grown from roughly zero to one paper per year in the late 2010s to a steadier pace of about two to five papers annually in recent years, suggesting increasing research activity over the past decade.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Correction: GAS6/AXL Inhibition Enhances Ovarian Cancer Sensitivity to Chemotherapy and PARP Inhibition through Increased DNA Damage and Enhanced Replication Stress
Molecular Cancer Research · 2026
- CDK4/6 inhibitor ribociclib and doxorubicin combination treatment inhibits breast cancer bone metastasis and enhances T-cell targeted therapy
Journal of bone oncology · 2026
- Circulating DNA tumor fraction as a biomarker for advanced breast cancer
Frontiers in Oncology · 2025
- A RAD18–UBC13–PALB2–RNF168 axis mediates replication fork recovery in BRCA1-deficient cancer cells
Nucleic Acids Research · 2024
- Number of Prescription Medications and Overall Survival in Metastatic Castrate‐Resistant Prostate Cancer
Prostate Cancer · 2024
- Abstract P2-17-03: Preclinical study of trastuzumab deruxtecan (T-Dxd; DS-8201a) in combination with DNA damage response pathway inhibitors in HER2-low/Hormone receptor negative breast cancer patient-derived xenograft models
Cancer Research · 2023
- Supplementary Data from GAS6/AXL Inhibition Enhances Ovarian Cancer Sensitivity to Chemotherapy and PARP Inhibition through Increased DNA Damage and Enhanced Replication Stress
2023
- Data from GAS6/AXL Inhibition Enhances Ovarian Cancer Sensitivity to Chemotherapy and PARP Inhibition through Increased DNA Damage and Enhanced Replication Stress
2023
- Supplementary Data from GAS6/AXL Inhibition Enhances Ovarian Cancer Sensitivity to Chemotherapy and PARP Inhibition through Increased DNA Damage and Enhanced Replication Stress
2023
- Data from GAS6/AXL Inhibition Enhances Ovarian Cancer Sensitivity to Chemotherapy and PARP Inhibition through Increased DNA Damage and Enhanced Replication Stress
2023
- Leveraging the replication stress response to optimize cancer therapy
Nature reviews. Cancer · 2022
- Abstract 803: Identifying a RAD18/UBC13-dependent mechanism of replication fork recovery to modulate chemoresponse in BRCA1-deficient cancers
Cancer Research · 2022
- Temporally distinct post-replicative repair mechanisms fill PRIMPOL-dependent ssDNA gaps in human cells
Molecular Cell · 2021
- To skip or not to skip: choosing repriming to tolerate DNA damage
Molecular Cell · 2021
- Entinostat, a selective HDAC1/2 inhibitor, potentiates the effects of olaparib in homologous recombination proficient ovarian cancer
Gynecologic Oncology · 2021
- Molecular Cell×3
- Cancer Research×2
- Nature reviews. Cancer×1
- Cell Reports×1
- Critical Reviews in Biochemistry and Molecular Biology×1
- Jeffrey D. Parvin
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Hannah L. Klein
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Hengyao Niu
Biochemistry, Genetics and Molecular Biology · Indiana University
- Alexander J.R. Bishop
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Ruben C. Petreaca
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile