Matthew J. Gamble

3.3k total citations · 1 hit paper
27 papers, 2.7k citations indexed

About

Matthew J. Gamble is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Matthew J. Gamble has authored 27 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Oncology and 3 papers in Genetics. Recurrent topics in Matthew J. Gamble's work include Genomics and Chromatin Dynamics (12 papers), Epigenetics and DNA Methylation (7 papers) and DNA Repair Mechanisms (6 papers). Matthew J. Gamble is often cited by papers focused on Genomics and Chromatin Dynamics (12 papers), Epigenetics and DNA Methylation (7 papers) and DNA Repair Mechanisms (6 papers). Matthew J. Gamble collaborates with scholars based in United States, Switzerland and South Korea. Matthew J. Gamble's co-authors include W. Lee Kraus, Leonard P. Freedman, Raga Krishnakumar, Kristine M. Frizzell, Christophe Rachez, Hediye Erdjument‐Bromage, Paul Tempst, Penelope D. Ruiz, Hongshan Chen and Anders M. Näär and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Matthew J. Gamble

27 papers receiving 2.7k citations

Hit Papers

Ligand-dependent transcription activation by nuclear rece... 1999 2026 2008 2017 1999 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
Matthew J. Gamble United States 22 2.0k 732 504 247 232 27 2.7k
Alida M.M. de Vries-Smits Netherlands 11 2.6k 1.3× 522 0.7× 152 0.3× 275 1.1× 176 0.8× 12 3.2k
Qihuang Jin China 17 1.8k 0.9× 306 0.4× 189 0.4× 220 0.9× 80 0.3× 20 2.3k
Denis Biard France 31 2.5k 1.3× 1.2k 1.6× 250 0.5× 255 1.0× 105 0.5× 73 3.1k
Qingyuan Ge United States 17 1.9k 1.0× 360 0.5× 204 0.4× 168 0.7× 58 0.3× 19 2.5k
Zhihu Ding United States 14 2.1k 1.0× 452 0.6× 111 0.2× 172 0.7× 115 0.5× 21 2.7k
Jingxiang Huang Singapore 15 1.9k 0.9× 390 0.5× 227 0.5× 264 1.1× 157 0.7× 22 2.8k
Elisabeth Fayard France 13 1.3k 0.6× 545 0.7× 488 1.0× 258 1.0× 97 0.4× 15 2.1k
Rita A. Busuttil Australia 22 1.7k 0.8× 577 0.8× 173 0.3× 376 1.5× 179 0.8× 39 2.5k
Nada Y. Kalaany United States 12 2.0k 1.0× 548 0.7× 158 0.3× 284 1.1× 87 0.4× 14 3.1k
Peter Ordentlich United States 29 2.9k 1.5× 1.2k 1.6× 725 1.4× 806 3.3× 105 0.5× 67 4.2k

Countries citing papers authored by Matthew J. Gamble

Since Specialization
Citations

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

Fields of papers citing papers by Matthew J. Gamble

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew J. Gamble. 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 Matthew J. Gamble. The network helps show where Matthew J. Gamble may publish in the future.

Co-authorship network of co-authors of Matthew J. Gamble

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew J. Gamble. A scholar is included among the top collaborators of Matthew J. Gamble 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 Matthew J. Gamble. Matthew J. Gamble 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.
DeAngelo, Joseph D., Maxim I. Maron, Jacob S. Roth, et al.. (2025). Productive mRNA chromatin escape is promoted by PRMT5 activity. Molecular Cell. 85(21). 4016–4031.e9. 1 indexed citations
2.
Gamble, Matthew J., et al.. (2021). MacroH2A1.1 has evolved to let PARP1 do more by loosening its grip on PAR. Nature Structural & Molecular Biology. 28(12). 961–962. 1 indexed citations
3.
Pinto, Hugo, Laxmi Mishra, Justin C. Wheat, et al.. (2020). H1 linker histones silence repetitive elements by promoting both histone H3K9 methylation and chromatin compaction. Proceedings of the National Academy of Sciences. 117(25). 14251–14258. 53 indexed citations
4.
Kim, Jeongkyu, Chongkui Sun, Andy D. Tran, et al.. (2019). The macroH2A1.2 histone variant links ATRX loss to alternative telomere lengthening. Nature Structural & Molecular Biology. 26(3). 213–219. 40 indexed citations
5.
Cui, Jihong, et al.. (2018). Histone Variant MacroH2A1 Plays an Isoform-Specific Role in Suppressing Epithelial-Mesenchymal Transition. Scientific Reports. 8(1). 841–841. 26 indexed citations
6.
Ruiz, Penelope D. & Matthew J. Gamble. (2018). MacroH2A1 chromatin specification requires its docking domain and acetylation of H2B lysine 20. Nature Communications. 9(1). 5143–5143. 21 indexed citations
7.
Dulyaninova, Natalya G., Penelope D. Ruiz, Matthew J. Gamble, Jonathan Backer, & Anne R. Bresnick. (2017). S100A4 regulates macrophage invasion by distinct myosin-dependent and myosin-independent mechanisms. Molecular Biology of the Cell. 29(5). 632–642. 20 indexed citations
8.
Wang, Wei–Lin, Lissa C. Anderson, Joshua J. Nicklay, et al.. (2014). Phosphorylation and arginine methylation mark histone H2A prior to deposition during Xenopus laevis development. Epigenetics & Chromatin. 7(1). 22–22. 26 indexed citations
9.
Chen, Hongshan, et al.. (2014). MacroH2A1.1 and PARP-1 cooperate to regulate transcription by promoting CBP-mediated H2B acetylation. Nature Structural & Molecular Biology. 21(11). 981–989. 92 indexed citations
10.
Zhang, Tong, Jie Yao, Raga Krishnakumar, et al.. (2012). Regulation of Poly(ADP-ribose) Polymerase-1-dependent Gene Expression through Promoter-directed Recruitment of a Nuclear NAD+ Synthase. Journal of Biological Chemistry. 287(15). 12405–12416. 88 indexed citations
11.
Zhang, Xuesen, Matthew J. Gamble, Sonja C. Stadler, et al.. (2011). Genome-Wide Analysis Reveals PADI4 Cooperates with Elk-1 to Activate c-Fos Expression in Breast Cancer Cells. PLoS Genetics. 7(6). e1002112–e1002112. 92 indexed citations
12.
Gamble, Matthew J. & W. Lee Kraus. (2010). Multiple facets of the unique histone variant macroH2A: From genomics to cell biology. Cell Cycle. 9(13). 2568–2574. 73 indexed citations
13.
Frizzell, Kristine M., Matthew J. Gamble, Tong Zhang, et al.. (2009). Global Analysis of Transcriptional Regulation by Poly(ADP-ribose) Polymerase-1 and Poly(ADP-ribose) Glycohydrolase in MCF-7 Human Breast Cancer Cells. Journal of Biological Chemistry. 284(49). 33926–33938. 94 indexed citations
14.
Zhang, Tong, Kristine M. Frizzell, Matthew J. Gamble, et al.. (2009). Enzymes in the NAD+ Salvage Pathway Regulate SIRT1 Activity at Target Gene Promoters. Journal of Biological Chemistry. 284(30). 20408–20417. 196 indexed citations
15.
Gamble, Matthew J., Kristine M. Frizzell, Christine Yang, Raga Krishnakumar, & W. Lee Kraus. (2009). The histone variant macroH2A1 marks repressed autosomal chromatin, but protects a subset of its target genes from silencing. Genes & Development. 24(1). 21–32. 136 indexed citations
16.
Gamble, Matthew J. & Robert P. Fisher. (2007). SET and PARP1 remove DEK from chromatin to permit access by the transcription machinery. Nature Structural & Molecular Biology. 14(6). 548–555. 84 indexed citations
17.
Gamble, Matthew J., Hediye Erdjument‐Bromage, Paul Tempst, Leonard P. Freedman, & Robert P. Fisher. (2005). The Histone Chaperone TAF-I/SET/INHAT Is Required for Transcription In Vitro of Chromatin Templates. Molecular and Cellular Biology. 25(2). 797–807. 59 indexed citations
18.
Larochelle, Stéphane, Jasmin Batliner, Matthew J. Gamble, et al.. (2005). Dichotomous but stringent substrate selection by the dual-function Cdk7 complex revealed by chemical genetics. Nature Structural & Molecular Biology. 13(1). 55–62. 90 indexed citations
19.
Rachez, Christophe, Matthew J. Gamble, Chao-Pei Betty Chang, et al.. (2000). The DRIP Complex and SRC-1/p160 Coactivators Share Similar Nuclear Receptor Binding Determinants but Constitute Functionally Distinct Complexes. Molecular and Cellular Biology. 20(8). 2718–2726. 158 indexed citations
20.
Rachez, Christophe, Bryan D. Lemon, Zalman Suldan, et al.. (1999). Ligand-dependent transcription activation by nuclear receptors requires the DRIP complex. Nature. 398(6730). 824–828. 591 indexed citations breakdown →

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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