Johanne M. Murray

4.7k total citations
66 papers, 3.7k citations indexed

About

Johanne M. Murray is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Johanne M. Murray has authored 66 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 10 papers in Cell Biology and 9 papers in Plant Science. Recurrent topics in Johanne M. Murray's work include DNA Repair Mechanisms (43 papers), Fungal and yeast genetics research (30 papers) and Genomics and Chromatin Dynamics (20 papers). Johanne M. Murray is often cited by papers focused on DNA Repair Mechanisms (43 papers), Fungal and yeast genetics research (30 papers) and Genomics and Chromatin Dynamics (20 papers). Johanne M. Murray collaborates with scholars based in United Kingdom, United States and Netherlands. Johanne M. Murray's co-authors include Antony M. Carr, Kazuko Nishikura, Jürg Kohli, Kinsey Maundrell, Christian Grimm, Ken‐ichi Mizuno, Alan R. Lehmann, Felicity Z. Watts, Matthew J. O’Connell and Anja Irmisch and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Johanne M. Murray

66 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Johanne M. Murray United Kingdom 31 3.4k 754 522 435 418 66 3.7k
Nancy M. Hollingsworth United States 32 4.0k 1.2× 1.2k 1.6× 631 1.2× 309 0.7× 353 0.8× 50 4.2k
Marco Muzi-Falconi Italy 31 3.2k 0.9× 712 0.9× 249 0.5× 287 0.7× 588 1.4× 70 3.4k
Tatiana García‐Muse Spain 16 3.1k 0.9× 398 0.5× 348 0.7× 368 0.8× 357 0.9× 19 3.3k
Haruhiko Takisawa Japan 24 3.3k 0.9× 854 1.1× 360 0.7× 323 0.7× 232 0.6× 46 3.5k
Andreas Hecht Germany 31 4.2k 1.2× 398 0.5× 490 0.9× 547 1.3× 287 0.7× 63 4.8k
Felicity Z. Watts United Kingdom 30 2.6k 0.8× 551 0.7× 335 0.6× 261 0.6× 220 0.5× 58 2.8k
Patrizia Lavia Italy 36 2.5k 0.7× 1.1k 1.4× 309 0.6× 349 0.8× 260 0.6× 80 3.1k
Albert Pastink Netherlands 30 3.6k 1.0× 312 0.4× 663 1.3× 551 1.3× 681 1.6× 56 3.9k
Masashige Bando Japan 20 2.7k 0.8× 481 0.6× 487 0.9× 388 0.9× 201 0.5× 29 3.0k
Bik K. Tye United States 26 2.7k 0.8× 588 0.8× 256 0.5× 445 1.0× 303 0.7× 36 3.0k

Countries citing papers authored by Johanne M. Murray

Since Specialization
Citations

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

Fields of papers citing papers by Johanne M. Murray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Johanne M. Murray. 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 Johanne M. Murray. The network helps show where Johanne M. Murray may publish in the future.

Co-authorship network of co-authors of Johanne M. Murray

This figure shows the co-authorship network connecting the top 25 collaborators of Johanne M. Murray. A scholar is included among the top collaborators of Johanne M. Murray 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 Johanne M. Murray. Johanne M. Murray 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.
Pai, Chen‐Chun, Wei‐Chen Cheng, Carol Walker, et al.. (2023). Homologous recombination suppresses transgenerational DNA end resection and chromosomal instability in fission yeast. Nucleic Acids Research. 51(7). 3205–3222. 3 indexed citations
2.
Schellenberger, Pascale, Lihong Zhou, Nora Cronin, et al.. (2022). Cryo-EM structure of the Smc5/6 holo-complex. Nucleic Acids Research. 50(16). 9505–9520. 19 indexed citations
3.
Schellenberger, Pascale, Lihong Zhou, Fabienne Beuron, et al.. (2021). Nse5/6 is a negative regulator of the ATPase activity of the Smc5/6 complex. Nucleic Acids Research. 49(8). 4534–4549. 21 indexed citations
4.
Liu, Yang, Xin Xu, Yue Yuan, et al.. (2021). The intra-S phase checkpoint directly regulates replication elongation to preserve the integrity of stalled replisomes. Proceedings of the National Academy of Sciences. 118(24). 19 indexed citations
5.
Herbert, Alex, Anja Irmisch, Adam T. Watson, et al.. (2021). Live-cell single-molecule tracking highlights requirements for stable Smc5/6 chromatin association in vivo. Sussex Research Online (University of Sussex). 19 indexed citations
6.
7.
Murray, Johanne M., Adam T. Watson, & Antony M. Carr. (2016). Transformation of Schizosaccharomyces pombe: Electroporation Procedure. Cold Spring Harbor Protocols. 2016(4). pdb.prot090951–pdb.prot090951. 10 indexed citations
8.
Murray, Johanne M., et al.. (2013). Fission Yeast RecQ Helicase Rqh1 Is Required for the Maintenance of Circular Chromosomes. Molecular and Cellular Biology. 33(6). 1175–1187. 9 indexed citations
9.
Watson, Adam T., et al.. (2013). Optimisation of the Schizosaccharomyces pombe urg1 Expression System. PLoS ONE. 8(12). e83800–e83800. 19 indexed citations
10.
Murray, Johanne M., Tom Stiff, & Penny A. Jeggo. (2012). DNA double-strand break repair within heterochromatic regions. Biochemical Society Transactions. 40(1). 173–178. 24 indexed citations
11.
Luca, Maria De, et al.. (2011). LAMMER kinase Kic1 is involved in pre-mRNA processing. Experimental Cell Research. 317(16). 2308–2320. 9 indexed citations
12.
Mizuno, Ken‐ichi, Izumi Miyabe, Oliver Fleck, et al.. (2010). Schizosaccharomyces pombe Mms1 channels repair of perturbed replication into Rhp51 independent homologous recombination. DNA repair. 10(3). 283–295. 4 indexed citations
13.
Outwin, Emily, Anja Irmisch, Johanne M. Murray, & Matthew J. O’Connell. (2009). Smc5-Smc6-Dependent Removal of Cohesin from Mitotic Chromosomes. Molecular and Cellular Biology. 29(16). 4363–4375. 39 indexed citations
14.
Irmisch, Anja, et al.. (2009). Smc5/6 maintains stalled replication forks in a recombination‐competent conformation. The EMBO Journal. 28(2). 144–155. 83 indexed citations
15.
Jones, Rhiannon E., J. Ross Chapman, Chandrakala Puligilla, et al.. (2003). XRad17 Is Required for the Activation of XChk1 But Not XCds1 during Checkpoint Signaling inXenopus. Molecular Biology of the Cell. 14(9). 3898–3910. 23 indexed citations
16.
Laursen, Louise, et al.. (2003). Role for the Fission Yeast RecQ Helicase in DNA Repair in G2. Molecular and Cellular Biology. 23(10). 3692–3705. 59 indexed citations
17.
Mundt, Kirsten, Joanne Porte, Johanne M. Murray, et al.. (1999). The COP9/signalosome complex is conserved in fission yeast and has a role in S phase. Current Biology. 9(23). 1427–1433. 124 indexed citations
18.
Murray, Johanne M., et al.. (1997). Role of Schizosaccharomyces pombe RecQ Homolog, Recombination, and Checkpoint Genes in UV Damage Tolerance. Molecular and Cellular Biology. 17(12). 6868–6875. 167 indexed citations
19.
Lehmann, Alan R., M. Walicka, Dominic J. F. Griffiths, et al.. (1995). The rad18 Gene of Schizosaccharomyces pombe Defines a New Subgroup of the SMC Superfamily Involved in DNA Repair. Molecular and Cellular Biology. 15(12). 7067–7080. 182 indexed citations
20.
Lehmann, Alan R., Antony M. Carr, Felicity Z. Watts, & Johanne M. Murray. (1991). DNA repair in the fission yeast, Schizosaccharomyces pombe. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 250(1-2). 205–210. 34 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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