Travis H. Stracker

5.4k total citations · 1 hit paper
60 papers, 3.8k citations indexed

About

Travis H. Stracker is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Travis H. Stracker has authored 60 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 19 papers in Oncology and 16 papers in Cell Biology. Recurrent topics in Travis H. Stracker's work include DNA Repair Mechanisms (25 papers), Microtubule and mitosis dynamics (16 papers) and Cancer-related Molecular Pathways (12 papers). Travis H. Stracker is often cited by papers focused on DNA Repair Mechanisms (25 papers), Microtubule and mitosis dynamics (16 papers) and Cancer-related Molecular Pathways (12 papers). Travis H. Stracker collaborates with scholars based in Spain, United States and United Kingdom. Travis H. Stracker's co-authors include John H.J. Petrini, Matthew D. Weitzman, Christian T. Carson, Mónica Morales, Takehiko Usui, Philip A. Knobel, Marko Marjanović, Jan-Willem Theunissen, Felipe D. Araujo and Sandra Segura‐Bayona and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Travis H. Stracker

59 papers receiving 3.8k citations

Hit Papers

The MRE11 complex: starting from the ends 2011 2026 2016 2021 2011 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Travis H. Stracker Spain 31 3.1k 1.1k 990 524 487 60 3.8k
Annette M.G. Dirac Netherlands 17 3.7k 1.2× 1.2k 1.2× 473 0.5× 811 1.5× 477 1.0× 18 4.3k
Joseph T. Bruder United States 28 2.6k 0.8× 795 0.8× 913 0.9× 401 0.8× 324 0.7× 53 3.7k
Martijn S. Luijsterburg Netherlands 35 3.6k 1.2× 915 0.9× 653 0.7× 348 0.7× 226 0.5× 66 4.1k
Deanna M. Koepp United States 18 4.2k 1.4× 1.2k 1.2× 437 0.4× 548 1.0× 893 1.8× 33 4.8k
Jacob-S. Seeler France 30 3.8k 1.3× 1.0k 1.0× 744 0.8× 339 0.6× 295 0.6× 35 4.5k
Andrew C.G. Porter United Kingdom 32 2.8k 0.9× 999 0.9× 366 0.4× 283 0.5× 471 1.0× 83 3.6k
Vincent Moncollin France 25 3.9k 1.3× 873 0.8× 709 0.7× 535 1.0× 331 0.7× 38 4.5k
Jamal Tazi France 43 5.3k 1.7× 497 0.5× 457 0.5× 511 1.0× 284 0.6× 87 6.0k
Michael Meisterernst Germany 39 3.9k 1.3× 769 0.7× 720 0.7× 476 0.9× 165 0.3× 78 5.0k
Benoit Coulombe Canada 35 3.4k 1.1× 505 0.5× 545 0.6× 366 0.7× 282 0.6× 96 4.1k

Countries citing papers authored by Travis H. Stracker

Since Specialization
Citations

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

Fields of papers citing papers by Travis H. Stracker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Travis H. Stracker. 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 Travis H. Stracker. The network helps show where Travis H. Stracker may publish in the future.

Co-authorship network of co-authors of Travis H. Stracker

This figure shows the co-authorship network connecting the top 25 collaborators of Travis H. Stracker. A scholar is included among the top collaborators of Travis H. Stracker 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 Travis H. Stracker. Travis H. Stracker 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.
Sagar, Md Abdul Kader, et al.. (2025). Optical pooled screening for the discovery of regulators of the alternative lengthening of telomeres pathway. Methods. 241. 1–12. 1 indexed citations
2.
Stracker, Travis H., et al.. (2023). Exploiting the DNA Damage Response for Prostate Cancer Therapy. Cancers. 16(1). 83–83. 4 indexed citations
3.
García‐Cao, Isabel, et al.. (2021). Loss of the abasic site sensor HMCES is synthetic lethal with the activity of the APOBEC3A cytosine deaminase in cancer cells. PLoS Biology. 19(3). e3001176–e3001176. 23 indexed citations
4.
Segura‐Bayona, Sandra, et al.. (2020). Tousled-Like Kinases Suppress Innate Immune Signaling Triggered by Alternative Lengthening of Telomeres. Cell Reports. 32(5). 107983–107983. 21 indexed citations
5.
Segura‐Bayona, Sandra & Travis H. Stracker. (2019). The Tousled-like kinases regulate genome and epigenome stability: implications in development and disease. Cellular and Molecular Life Sciences. 76(19). 3827–3841. 31 indexed citations
6.
Lee, Sung‐Bau, Sandra Segura‐Bayona, Giulia Saredi, et al.. (2018). Tousled-like kinases stabilize replication forks and show synthetic lethality with checkpoint and PARP inhibitors. Science Advances. 4(8). eaat4985–eaat4985. 39 indexed citations
7.
Cánovas, Begoña, Ana Igea, Alessandro A. Sartori, et al.. (2018). Targeting p38α Increases DNA Damage, Chromosome Instability, and the Anti-tumoral Response to Taxanes in Breast Cancer Cells. Cancer Cell. 33(6). 1094–1110.e8. 70 indexed citations
8.
Stracker, Travis H.. (2018). E2F4/5-mediated transcriptional control of multiciliated cell differentiation: redundancy or fine-tuning?. Developmental Biology. 446(1). 20–21. 4 indexed citations
9.
Picart‐Armada, Sergio, Francesc Fernández-Albert, María Vinaixa, et al.. (2017). Null diffusion-based enrichment for metabolomics data. PLoS ONE. 12(12). e0189012–e0189012. 30 indexed citations
10.
Terré, Berta, Sandra Segura‐Bayona, Gabriel Gil‐Gómez, et al.. (2016). GEMC 1 is a critical regulator of multiciliated cell differentiation. The EMBO Journal. 35(9). 942–960. 76 indexed citations
11.
Marjanović, Marko, Carlos Sánchez-Huertas, Berta Terré, et al.. (2015). CEP63 deficiency promotes p53-dependent microcephaly and reveals a role for the centrosome in meiotic recombination. Nature Communications. 6(1). 7676–7676. 84 indexed citations
12.
Yanez, Diana A., Berta Terré, Lluís Palenzuela, et al.. (2015). EXO1 is critical for embryogenesis and the DNA damage response in mice with a hypomorphicNbs1allele. Nucleic Acids Research. 43(15). 7371–7387. 14 indexed citations
13.
Torres, Adrián Gabriel, David Piñeyro, Liudmila Filonava, et al.. (2014). A‐to‐I editing on tRNAs: Biochemical, biological and evolutionary implications. FEBS Letters. 588(23). 4279–4286. 117 indexed citations
14.
Stracker, Travis H., Ignasi Roig, Philip A. Knobel, & Marko Marjanović. (2013). The ATM signaling network in development and disease. Frontiers in Genetics. 4. 37–37. 117 indexed citations
15.
Bianchi, Julie, Sean G. Rudd, Stanisław K. Jóźwiakowski, et al.. (2013). PrimPol Bypasses UV Photoproducts during Eukaryotic Chromosomal DNA Replication. Molecular Cell. 52(4). 566–573. 221 indexed citations
16.
Foster, Steven S., Saurav De, Linda K. Johnson, John H.J. Petrini, & Travis H. Stracker. (2012). Cell cycle- and DNA repair pathway-specific effects of apoptosis on tumor suppression. Proceedings of the National Academy of Sciences. 109(25). 9953–9958. 48 indexed citations
17.
Stracker, Travis H., Takehiko Usui, & John H.J. Petrini. (2009). Taking the time to make important decisions: The checkpoint effector kinases Chk1 and Chk2 and the DNA damage response. DNA repair. 8(9). 1047–1054. 182 indexed citations
18.
Lee, Youngsoo, Hironobu Nakane, Travis H. Stracker, et al.. (2009). Differential DNA damage signaling accounts for distinct neural apoptotic responses in ATLD and NBS. Genes & Development. 23(2). 171–180. 83 indexed citations
19.
Stracker, Travis H., Suzana S. Couto, Carlos Cordon‐Cardo, Tulio Matos, & John H.J. Petrini. (2008). Chk2 Suppresses the Oncogenic Potential of DNA Replication-Associated DNA Damage. Molecular Cell. 32(6). 889–889. 3 indexed citations
20.
Stracker, Travis H., et al.. (2003). Roles of host cell factors in circularization of retroviral dna. Virology. 314(1). 460–467. 96 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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