Zachary T. Herbert

3.1k total citations · 1 hit paper
25 papers, 1.4k citations indexed

About

Zachary T. Herbert is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Zachary T. Herbert has authored 25 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Oncology and 7 papers in Immunology. Recurrent topics in Zachary T. Herbert's work include Epigenetics and DNA Methylation (4 papers), Immune Cell Function and Interaction (4 papers) and RNA modifications and cancer (4 papers). Zachary T. Herbert is often cited by papers focused on Epigenetics and DNA Methylation (4 papers), Immune Cell Function and Interaction (4 papers) and RNA modifications and cancer (4 papers). Zachary T. Herbert collaborates with scholars based in United States, Germany and Spain. Zachary T. Herbert's co-authors include Unmesh Jadhav, Nicholas K. O’Neill, Ramesh A. Shivdasani, Madhurima Saxena, Assieh Saadatpour, Guo‐Cheng Yuan, Kazutaka Murata, Michael Tolstorukov, Matthew A. Booker and Rameen Beroukhim and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Zachary T. Herbert

23 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate

2019 280 citations Abhishek A. Chakraborty, Matti Myllykoski et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zachary T. Herbert United States	14	722	451	329	289	175	25	1.4k
Lauri Miller United States	12	998 1.4×	444 1.0×	387 1.2×	348 1.2×	273 1.6×	16	2.1k
Yan Jin China	23	773 1.1×	262 0.6×	309 0.9×	104 0.4×	219 1.3×	74	1.3k
Giuseppe Fedele United States	13	1.0k 1.4×	445 1.0×	657 2.0×	277 1.0×	141 0.8×	15	1.6k
Klaudyna Kojder Poland	12	373 0.5×	330 0.7×	227 0.7×	149 0.5×	359 2.1×	29	1.2k
Selen C. Muratoglu United States	21	848 1.2×	244 0.5×	226 0.7×	231 0.8×	206 1.2×	33	1.5k
David I. Bellovin United States	16	991 1.4×	553 1.2×	448 1.4×	190 0.7×	164 0.9×	30	1.8k
Mahmut Yilmaz Switzerland	7	681 0.9×	435 1.0×	295 0.9×	106 0.4×	178 1.0×	7	1.3k
Kar‐Ming Fung United States	18	915 1.3×	207 0.5×	262 0.8×	128 0.4×	145 0.8×	39	1.6k
Qinchuan Wang China	22	757 1.0×	266 0.6×	288 0.9×	156 0.5×	191 1.1×	50	1.3k
Linda J. Metheny‐Barlow United States	21	755 1.0×	377 0.8×	434 1.3×	410 1.4×	151 0.9×	36	1.5k

Countries citing papers authored by Zachary T. Herbert

Since Specialization

Citations

This map shows the geographic impact of Zachary T. Herbert'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 Zachary T. Herbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zachary T. Herbert more than expected).

Fields of papers citing papers by Zachary T. Herbert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zachary T. Herbert. 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 Zachary T. Herbert. The network helps show where Zachary T. Herbert may publish in the future.

Co-authorship network of co-authors of Zachary T. Herbert

This figure shows the co-authorship network connecting the top 25 collaborators of Zachary T. Herbert. A scholar is included among the top collaborators of Zachary T. Herbert 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 Zachary T. Herbert. Zachary T. Herbert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Pantelidou, Constantia, et al.. (2025). BET Bromodomain Inhibition Reverses CDK4/6 Inhibitor Resistance in Estrogen Receptor–Positive Breast Cancer via Induction of miR-34a-5p. Clinical Cancer Research. 31(23). 5096–5110.

Venkadakrishnan, Varadha Balaji, Richa Singh, Matthew A. Booker, et al.. (2024). Lineage-specific canonical and non-canonical activity of EZH2 in advanced prostate cancer subtypes. Nature Communications. 15(1). 6779–6779. 20 indexed citations

Klonowska, Katarzyna, Krinio Giannikou, Aaron R. Thorner, et al.. (2023). Comprehensive genetic and phenotype analysis of 95 individuals with mosaic tuberous sclerosis complex. The American Journal of Human Genetics. 110(6). 979–988. 19 indexed citations

Landa, Iñigo, Bin Xu, Jacob Haase, et al.. (2023). Telomerase Upregulation Induces Progression of Mouse BrafV600E-Driven Thyroid Cancers and Triggers Nontelomeric Effects. Molecular Cancer Research. 21(11). 1163–1175. 12 indexed citations

Costanzo-Garvey, Diane, Benjamin A. Teply, Zachary T. Herbert, et al.. (2023). Androgen receptor inhibition suppresses anti-tumor neutrophil response against bone metastatic prostate cancer via regulation of TβRI expression. Cancer Letters. 579. 216468–216468. 15 indexed citations

Koch, Marilin, Mykola Zdioruk, Michal O. Nowicki, et al.. (2023). Uncovering transcriptomic landscape alterations of CAN-2409 in in vitro and in vivo glioma models. Frontiers in Medicine. 10. 1140352–1140352. 4 indexed citations

Herbert, Zachary T., et al.. (2022). Splicing factor SRSF1 controls autoimmune-related molecular pathways in regulatory T cells distinct from FoxP3. Molecular Immunology. 152. 140–152. 5 indexed citations

Juárez, Ignacio, Shi Su, Zachary T. Herbert, John R. Teijaro, & Vaishali R. Moulton. (2022). Splicing factor SRSF1 is essential for CD8 T cell function and host antigen-specific viral immunity. Frontiers in Immunology. 13. 906355–906355. 3 indexed citations

Canesin, Giacomo, Linda Feldbrügge, Guangyan Wei, et al.. (2022). Heme oxygenase-1 mitigates liver injury and fibrosis via modulation of LNX1/Notch1 pathway in myeloid cells. iScience. 25(9). 104983–104983. 8 indexed citations

10.

Xie, Yajun, Aaron T. Kuan, Wengang Wang, et al.. (2022). Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development. Cell Reports. 38(8). 110416–110416. 53 indexed citations

11.

Herbert, Zachary T., et al.. (2021). Splicing factor SRSF1 controls distinct molecular programs in regulatory and effector T cells implicated in systemic autoimmune disease. Molecular Immunology. 141. 94–103. 10 indexed citations

12.

Herbert, Zachary T., Vladimir Vrbanac, Maud Déruaz, et al.. (2021). Intra- and extra-cellular environments contribute to the fate of HIV-1 infection. Cell Reports. 36(9). 109622–109622. 17 indexed citations

13.

Sadow, Peter M., et al.. (2020). Therapeutic Targeting of the Secreted Lysophospholipase D Autotaxin Suppresses Tuberous Sclerosis Complex-Associated Tumorigenesis. Cancer Research. 80(13). 2751–2763. 7 indexed citations

14.

Chakraborty, Abhishek A., Matti Myllykoski, Alison E. Ringel, et al.. (2019). Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate. Science. 363(6432). 1217–1222. 280 indexed citations breakdown →

15.

Feng, Xudong, Dongxian Guan, Jae Won Choi, et al.. (2019). IL1R1 is required for celastrol’s leptin-sensitization and antiobesity effects. Nature Medicine. 25(4). 575–582. 105 indexed citations

16.

Jadhav, Unmesh, Alessia Cavazza, Kushal K. Banerjee, et al.. (2019). Extensive Recovery of Embryonic Enhancer and Gene Memory Stored in Hypomethylated Enhancer DNA. Molecular Cell. 74(3). 542–554.e5. 55 indexed citations

17.

Cornwell, MacIntosh, Mahesh Vangala, Len Taing, et al.. (2018). VIPER: Visualization Pipeline for RNA-seq, a Snakemake workflow for efficient and complete RNA-seq analysis. BMC Bioinformatics. 19(1). 135–135. 109 indexed citations

18.

Castaño, Zafira, Beatriz P. San Juan, Asaf Spiegel, et al.. (2018). IL-1β inflammatory response driven by primary breast cancer prevents metastasis-initiating cell colonization. Nature Cell Biology. 20(9). 1084–1097. 130 indexed citations

19.

Jadhav, Unmesh, Madhurima Saxena, Nicholas K. O’Neill, et al.. (2017). Dynamic Reorganization of Chromatin Accessibility Signatures during Dedifferentiation of Secretory Precursors into Lgr5+ Intestinal Stem Cells. Cell stem cell. 21(1). 65–77.e5. 179 indexed citations

20.

Herbert, Zachary T., Nicholas Beckloff, Sridar V. Chittur, et al.. (2013). Nucleic Acids Research Group (NRG): The Importance of DNA Extraction in Metagenomics: The Gatekeeper to Accurate Results!. Europe PMC (PubMed Central). 24.

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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