Paul G. Young

1.2k total citations
22 papers, 955 citations indexed

About

Paul G. Young is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Paul G. Young has authored 22 papers receiving a total of 955 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Cell Biology and 5 papers in Plant Science. Recurrent topics in Paul G. Young's work include Fungal and yeast genetics research (12 papers), Microtubule and mitosis dynamics (8 papers) and RNA Research and Splicing (5 papers). Paul G. Young is often cited by papers focused on Fungal and yeast genetics research (12 papers), Microtubule and mitosis dynamics (8 papers) and RNA Research and Splicing (5 papers). Paul G. Young collaborates with scholars based in Canada, United States and Australia. Paul G. Young's co-authors include R. Rowley, Suresh Subramani, James D. Hudson, Jim Karagiannis, Ivan Rupeš, Helen Piwnica‐Worms, L L Parker, Zhengping Jia, Michael W. Gray and Murray N. Schnare and has published in prestigious journals such as Nature, Journal of Biological Chemistry and The EMBO Journal.

In The Last Decade

Paul G. Young

22 papers receiving 939 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul G. Young Canada 14 881 401 132 96 45 22 955
Derek L. Lindstrom United States 9 1.2k 1.4× 224 0.6× 177 1.3× 149 1.6× 44 1.0× 9 1.3k
Mahamadou Faty Switzerland 10 1.2k 1.4× 213 0.5× 152 1.2× 108 1.1× 27 0.6× 12 1.3k
Phuay‐Yee Goh Singapore 15 728 0.8× 500 1.2× 50 0.4× 199 2.1× 20 0.4× 18 1000
Kyung-Kwon Lee Japan 10 660 0.7× 282 0.7× 82 0.6× 26 0.3× 15 0.3× 12 813
Veena K. Parnaik India 22 1.5k 1.7× 208 0.5× 68 0.5× 49 0.5× 18 0.4× 57 1.6k
Janet Leatherwood United States 24 1.8k 2.0× 311 0.8× 158 1.2× 214 2.2× 30 0.7× 35 2.0k
Caroline R.M. Wilkinson United Kingdom 21 1.6k 1.8× 498 1.2× 279 2.1× 205 2.1× 26 0.6× 32 1.8k
Christine S. Weirich United States 9 989 1.1× 200 0.5× 37 0.3× 64 0.7× 31 0.7× 11 1.1k
Caroline Mas France 15 632 0.7× 274 0.7× 39 0.3× 56 0.6× 11 0.2× 35 905
Wen Deng China 13 534 0.6× 103 0.3× 73 0.6× 133 1.4× 35 0.8× 28 777

Countries citing papers authored by Paul G. Young

Since Specialization
Citations

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

Fields of papers citing papers by Paul G. Young

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul G. Young. 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 Paul G. Young. The network helps show where Paul G. Young may publish in the future.

Co-authorship network of co-authors of Paul G. Young

This figure shows the co-authorship network connecting the top 25 collaborators of Paul G. Young. A scholar is included among the top collaborators of Paul G. Young 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 Paul G. Young. Paul G. Young 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.
Leicher, Rachel, Adewola Osunsade, Sarah Faulkner, et al.. (2022). Single-stranded nucleic acid binding and coacervation by linker histone H1. Nature Structural & Molecular Biology. 29(5). 463–471. 41 indexed citations
2.
Eid, Rawan, et al.. (2017). Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast. PLoS ONE. 12(8). e0184151–e0184151. 8 indexed citations
3.
Young, Paul G., et al.. (2014). Genetic and physical interaction of Ssp1 CaMKK and Rad24 14-3-3 during low pH and osmotic stress in fission yeast. Open Biology. 4(1). 130127–130127. 13 indexed citations
4.
Frazer, Corey & Paul G. Young. (2011). Redundant Mechanisms Prevent Mitotic Entry Following Replication Arrest in the Absence of Cdc25 Hyper-Phosphorylation in Fission Yeast. PLoS ONE. 6(6). e21348–e21348. 6 indexed citations
5.
Benkő, Zsigmond, Dong Liang, Emmanuel Agbottah, et al.. (2007). Antagonistic interaction of HIV-1 Vpr with Hsf-mediated cellular heat shock response and Hsp16 in fission yeast (Schizosaccharomyces pombe). Retrovirology. 4(1). 16–16. 13 indexed citations
6.
Fliegel, Larry, Christine Wiebe, Gordon Chua, & Paul G. Young. (2005). Functional expression and cellular localization of the Na+/H+exchanger Sod2 of the fission yeastSchizosaccharomycespombe. Canadian Journal of Physiology and Pharmacology. 83(7). 565–572. 8 indexed citations
7.
Benkő, Zsigmond, Dong Liang, Emmanuel Agbottah, et al.. (2004). Anti-Vpr Activity of a Yeast Chaperone Protein. Journal of Virology. 78(20). 11016–11029. 25 indexed citations
8.
Taricani, Lorena, Max L. Tejada, & Paul G. Young. (2002). The Fission Yeast ES2 Homologue, Bis1, Interacts with the Ish1 Stress-responsive Nuclear Envelope Protein. Journal of Biological Chemistry. 277(12). 10562–10572. 27 indexed citations
9.
Karagiannis, Jim, et al.. (2002). The Scw1 RNA-Binding Domain Protein Regulates Septation and Cell-Wall Structure in Fission Yeast. Genetics. 162(1). 45–58. 23 indexed citations
10.
Rupeš, Ivan, Bradley A. Webb, Alan S. Mak, & Paul G. Young. (2001). G2/M Arrest Caused by Actin Disruption Is a Manifestation of the Cell Size Checkpoint in Fission Yeast. Molecular Biology of the Cell. 12(12). 3892–3903. 47 indexed citations
11.
Rupeš, Ivan, Zhengping Jia, & Paul G. Young. (1999). Ssp1 Promotes Actin Depolymerization and Is Involved in Stress Response and New End Take-Off Control in Fission Yeast. Molecular Biology of the Cell. 10(5). 1495–1510. 64 indexed citations
12.
Hudson, James D., et al.. (1998). Thecdr2+Gene Encodes a Regulator of G2/M Progression and Cytokinesis inSchizosaccharomyces pombe. Molecular Biology of the Cell. 9(12). 3399–3415. 83 indexed citations
13.
Rupeš, Ivan, et al.. (1997). Markers of cell polarity during and after nitrogen starvation in Schizosaccharomyces pombe. Biochemistry and Cell Biology. 75(6). 697–708. 2 indexed citations
14.
Parker, L L, et al.. (1993). Phosphorylation and inactivation of the mitotic inhibitor Weel by the nim1/cdr1 kinase. Nature. 363(6431). 736–738. 131 indexed citations
15.
Hudson, James D., et al.. (1992). The wee1 protein kinase is required for radiation-induced mitotic delay. Nature. 356(6367). 353–355. 124 indexed citations
16.
Rowley, R., Suresh Subramani, & Paul G. Young. (1992). Checkpoint controls in Schizosaccharomyces pombe: rad1.. The EMBO Journal. 11(4). 1335–1342. 205 indexed citations
17.
Hudson, James D., et al.. (1991). stf1: A New Suppressor of the Mitotic Control Gene, cdc25, in Schizosaccharomyces pombe. Cold Spring Harbor Symposia on Quantitative Biology. 56(0). 599–604. 6 indexed citations
18.
Schnare, Murray N., Taisto Y. K. Heinonen, Paul G. Young, & Michael W. Gray. (1986). A discontinuous small subunit ribosomal RNA in Tetrahymena pyriformis mitochondria.. Journal of Biological Chemistry. 261(11). 5187–5193. 58 indexed citations
19.
Young, Paul G., et al.. (1985). Changes in phosphoprotein pattern in Schizosaccharomyces pombe. Experimental Cell Research. 159(2). 495–509. 3 indexed citations
20.
Young, Paul G. & Arthur M. Zimmerman. (1973). Synthesis of mitochondrial RNA in disaggregated embryos of Xenopus laevis. Developmental Biology. 33(1). 196–205. 10 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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