Robert K. Bradley

18.8k total citations · 3 hit papers
75 papers, 4.5k citations indexed

About

Robert K. Bradley is a scholar working on Molecular Biology, Hematology and Immunology. According to data from OpenAlex, Robert K. Bradley has authored 75 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 18 papers in Hematology and 7 papers in Immunology. Recurrent topics in Robert K. Bradley's work include RNA Research and Splicing (42 papers), RNA modifications and cancer (34 papers) and RNA and protein synthesis mechanisms (21 papers). Robert K. Bradley is often cited by papers focused on RNA Research and Splicing (42 papers), RNA modifications and cancer (34 papers) and RNA and protein synthesis mechanisms (21 papers). Robert K. Bradley collaborates with scholars based in United States, South Africa and United Kingdom. Robert K. Bradley's co-authors include Heidi Dvinge, Omar Abdel‐Wahab, Eun Hee Kim, Olga Anczuków, Christopher B. Burge, Lior Pachter, Sujatha Jagannathan, Ian Holmes, Jose Mario Bello Pineda and Simon Haas and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Robert K. Bradley

73 papers receiving 4.4k citations

Hit Papers

Braveheart, a Long Noncoding RNA Required for Cardiovascu... 2013 2026 2017 2021 2013 2016 2023 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert K. Bradley United States 36 3.8k 1.2k 393 325 304 75 4.5k
Vincent Schulz United States 34 2.6k 0.7× 368 0.3× 323 0.8× 392 1.2× 328 1.1× 76 3.9k
Keiko Akagi United States 33 2.9k 0.7× 612 0.5× 270 0.7× 1.1k 3.3× 423 1.4× 54 3.8k
Allen Delaney Canada 25 3.0k 0.8× 1.2k 1.0× 221 0.6× 588 1.8× 393 1.3× 41 4.2k
Xin Gao China 30 2.4k 0.6× 382 0.3× 295 0.8× 414 1.3× 145 0.5× 87 3.3k
Patrick J. Paddison United States 31 5.1k 1.3× 1.1k 1.0× 127 0.3× 1.1k 3.3× 222 0.7× 66 6.0k
Richard A. Young United States 11 5.5k 1.4× 792 0.7× 238 0.6× 611 1.9× 357 1.2× 11 6.2k
Peter B. Rahl United States 19 8.2k 2.1× 1.3k 1.1× 464 1.2× 714 2.2× 637 2.1× 28 9.3k
Peter N. Cockerill United Kingdom 37 3.4k 0.9× 582 0.5× 566 1.4× 532 1.6× 280 0.9× 90 4.6k
Alla A. Sigova United States 14 5.6k 1.5× 1.4k 1.2× 225 0.6× 591 1.8× 1.2k 3.8× 20 6.4k
Michael H. Kagey United States 15 5.1k 1.3× 624 0.5× 188 0.5× 549 1.7× 457 1.5× 34 5.8k

Countries citing papers authored by Robert K. Bradley

Since Specialization
Citations

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

Fields of papers citing papers by Robert K. Bradley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert K. Bradley. 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 Robert K. Bradley. The network helps show where Robert K. Bradley may publish in the future.

Co-authorship network of co-authors of Robert K. Bradley

This figure shows the co-authorship network connecting the top 25 collaborators of Robert K. Bradley. A scholar is included among the top collaborators of Robert K. Bradley 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 Robert K. Bradley. Robert K. Bradley 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.
Clough, Courtnee, Anna Gallì, Cristina Picone, et al.. (2025). Distinct routes of clonal progression in SF3B1-mutant myelodysplastic syndromes. Blood Advances. 9(12). 3044–3055.
2.
Clough, Courtnee, Jason Kim, Anna Gallì, et al.. (2024). Mis-splicing of Mitotic Regulators Sensitizes SF3B1-Mutated Human HSCs to CHK1 Inhibition. Blood Cancer Discovery. 5(5). 353–370. 8 indexed citations
3.
Gabel, Austin M., et al.. (2024). Multiplexed screening reveals how cancer-specific alternative polyadenylation shapes tumor growth in vivo. Nature Communications. 15(1). 959–959. 6 indexed citations
4.
Pineda, Jose Mario Bello & Robert K. Bradley. (2023). DUX4 is a common driver of immune evasion and immunotherapy failure in metastatic cancers. eLife. 12. 5 indexed citations
5.
Dunker, William, et al.. (2023). The proto-oncogene SRC phosphorylates cGAS to inhibit an antitumor immune response. JCI Insight. 8(12). 6 indexed citations
6.
Wang, Eric, et al.. (2023). Abstract A04: Modulation of RNA splicing enhances response to BCL2 inhibition in leukemia. Blood Cancer Discovery. 4(3_Supplement). A04–A04. 1 indexed citations
7.
Benbarche, Salima, Bo Liu, Jeetayu Biswas, et al.. (2023). Synthetic Introns Identify the Novel RNA Splicing Factor GPATCH8 As Required for Mis-Splicing Induced By SF3B1 Mutations. Blood. 142(Supplement 1). 3–3. 1 indexed citations
8.
North, Khrystyna, Salima Benbarche, Bo Liu, et al.. (2022). Synthetic introns enable splicing factor mutation-dependent targeting of cancer cells. Nature Biotechnology. 40(7). 1103–1113. 38 indexed citations
9.
Takao, Sumiko, Lauren Forbes, Shuyuan Cheng, et al.. (2021). Convergent organization of aberrant MYB complex controls oncogenic gene expression in acute myeloid leukemia. eLife. 10. 34 indexed citations
10.
Clough, Courtnee, Joseph Pangallo, Janine O. Ilagan, et al.. (2021). Coordinated missplicing of TMEM14C and ABCB7 causes ring sideroblast formation in SF3B1-mutant myelodysplastic syndrome. Blood. 139(13). 2038–2049. 45 indexed citations
11.
Pangallo, Joseph, Jean‐Jacques Kiladjian, Bruno Cassinat, et al.. (2020). Rare and private spliceosomal gene mutations drive partial, complete, and dual phenocopies of hotspot alterations. Blood. 135(13). 1032–1043. 11 indexed citations
12.
Taylor, Justin, Xiaoli Mi, Khrystyna North, et al.. (2020). Single-cell genomics reveals the genetic and molecular bases for escape from mutational epistasis in myeloid neoplasms. Blood. 136(13). 1477–1486. 38 indexed citations
13.
Thomas, James D., Jacob T. Polaski, Qing Feng, et al.. (2020). RNA isoform screens uncover the essentiality and tumor-suppressor activity of ultraconserved poison exons. Nature Genetics. 52(1). 84–94. 72 indexed citations
14.
Dvinge, Heidi, Jamie Guenthoer, Peggy L. Porter, & Robert K. Bradley. (2019). RNA components of the spliceosome regulate tissue- and cancer-specific alternative splicing. Genome Research. 29(10). 1591–1604. 105 indexed citations
15.
Palangat, Murali, Dimitrios G. Anastasakis, Dennis Liang Fei, et al.. (2019). The splicing factor U2AF1 contributes to cancer progression through a noncanonical role in translation regulation. Genes & Development. 33(9-10). 482–497. 66 indexed citations
16.
Fei, Dennis Liang, Tao Zhen, Benjamin H. Durham, et al.. (2018). Impaired hematopoiesis and leukemia development in mice with a conditional knock-in allele of a mutant splicing factor gene U2af1. Proceedings of the National Academy of Sciences. 115(44). E10437–E10446. 58 indexed citations
17.
Dvinge, Heidi, Rhonda E. Ries, Janine O. Ilagan, et al.. (2014). Sample processing obscures cancer-specific alterations in leukemic transcriptomes. Proceedings of the National Academy of Sciences. 111(47). 16802–16807. 52 indexed citations
18.
Ilagan, Janine O., Aravind Ramakrishnan, Brian Hayes, et al.. (2014). U2AF1 mutations alter splice site recognition in hematological malignancies. Genome Research. 25(1). 14–26. 210 indexed citations
19.
Klattenhoff, Carla, Johanna C. Scheuermann, Lauren E. Surface, et al.. (2013). Braveheart, a Long Noncoding RNA Required for Cardiovascular Lineage Commitment. Cell. 152(3). 570–583. 733 indexed citations breakdown →
20.
Bradley, Robert K., et al.. (2009). Evolutionary Modeling and Prediction of Non-Coding RNAs in Drosophila. PLoS ONE. 4(8). e6478–e6478. 11 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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