John L. Woolford

8.9k total citations · 2 hit papers
109 papers, 7.4k citations indexed

About

John L. Woolford is a scholar working on Molecular Biology, Oncology and Plant Science. According to data from OpenAlex, John L. Woolford has authored 109 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Molecular Biology, 12 papers in Oncology and 7 papers in Plant Science. Recurrent topics in John L. Woolford's work include RNA and protein synthesis mechanisms (92 papers), RNA modifications and cancer (73 papers) and RNA Research and Splicing (69 papers). John L. Woolford is often cited by papers focused on RNA and protein synthesis mechanisms (92 papers), RNA modifications and cancer (73 papers) and RNA Research and Splicing (69 papers). John L. Woolford collaborates with scholars based in United States, China and Germany. John L. Woolford's co-authors include Susan J. Baserga, Michael Rosbash, Jelena Jakovljevic, Sebastian Klinge, Mitch O. Rotenberg, Jesús de la Cruz, Michelle Moritz, Yi‐Fang Tsay, Katrin Karbstein and Amanda G. Paulovich and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

John L. Woolford

108 papers receiving 7.2k citations

Hit Papers

Ribosome Biogenesis in... 1979 2026 1994 2010 2013 1979 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
John L. Woolford United States 50 7.0k 673 433 415 253 109 7.4k
Arno L. Greenleaf United States 41 4.8k 0.7× 656 1.0× 420 1.0× 426 1.0× 306 1.2× 65 5.4k
Lev L. Kisselev Russia 42 5.7k 0.8× 417 0.6× 461 1.1× 941 2.3× 152 0.6× 191 6.2k
Claire Moore United States 42 6.8k 1.0× 250 0.4× 424 1.0× 642 1.5× 190 0.8× 93 7.4k
Claiborne V.C. Glover United States 37 3.8k 0.5× 332 0.5× 610 1.4× 632 1.5× 548 2.2× 62 4.3k
Dieter Kressler Switzerland 34 3.7k 0.5× 520 0.8× 213 0.5× 295 0.7× 186 0.7× 63 4.1k
Klaus Scherrer France 41 5.7k 0.8× 558 0.8× 529 1.2× 846 2.0× 517 2.0× 159 6.7k
Giuseppe Biamonti Italy 47 5.5k 0.8× 525 0.8× 457 1.1× 445 1.1× 346 1.4× 114 6.3k
Stephen M. Dilworth United Kingdom 31 2.4k 0.3× 920 1.4× 412 1.0× 588 1.4× 340 1.3× 47 3.5k
Jorge E. Allende Chile 36 2.8k 0.4× 429 0.6× 308 0.7× 344 0.8× 448 1.8× 121 3.6k
Richard A. Padgett United States 38 6.9k 1.0× 373 0.6× 476 1.1× 758 1.8× 267 1.1× 72 7.9k

Countries citing papers authored by John L. Woolford

Since Specialization
Citations

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

Fields of papers citing papers by John L. Woolford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John L. Woolford. 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 John L. Woolford. The network helps show where John L. Woolford may publish in the future.

Co-authorship network of co-authors of John L. Woolford

This figure shows the co-authorship network connecting the top 25 collaborators of John L. Woolford. A scholar is included among the top collaborators of John L. Woolford 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 John L. Woolford. John L. Woolford 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
2.
Rodríguez‐Galán, Olga, et al.. (2022). Ribosomal protein eL39 is important for maturation of the nascent polypeptide exit tunnel and proper protein folding during translation. Nucleic Acids Research. 50(11). 6453–6473. 11 indexed citations
3.
Woolford, John L., et al.. (2022). Additional principles that govern the release of pre-ribosomes from the nucleolus into the nucleoplasm in yeast. Nucleic Acids Research. 51(20). 10867–10883. 10 indexed citations
4.
Tartakoff, Alan M., et al.. (2021). The nucleolus as a polarized coaxial cable in which the rDNA axis is surrounded by dynamic subunit-specific phases. Current Biology. 31(12). 2507–2519.e4. 13 indexed citations
5.
Wilson, Daniel M., et al.. (2020). Structural insights into assembly of the ribosomal nascent polypeptide exit tunnel. Nature Communications. 11(1). 5111–5111. 23 indexed citations
6.
Talkish, Jason, Jelena Jakovljevic, Jingyu Zhang, et al.. (2016). Disruption of ribosome assembly in yeast blocks cotranscriptional pre-rRNA processing and affects the global hierarchy of ribosome biogenesis. RNA. 22(6). 852–866. 31 indexed citations
7.
Woolford, John L.. (2015). Assembly of ribosomes in eukaryotes. RNA. 21(4). 766–768. 2 indexed citations
8.
Talkish, Jason, Gemma E. May, Yizhu Lin, John L. Woolford, & C. Joel McManus. (2014). Mod-seq: high-throughput sequencing for chemical probing of RNA structure. RNA. 20(5). 713–720. 149 indexed citations
9.
Ohmayer, Uli, Michael Gamalinda, Martina Sauert, et al.. (2013). Studies on the Assembly Characteristics of Large Subunit Ribosomal Proteins in S. cerevisae. PLoS ONE. 8(7). e68412–e68412. 53 indexed citations
10.
Dembowski, Jill A., et al.. (2013). Identification of the binding site of Rlp7 on assembling 60S ribosomal subunits in Saccharomyces cerevisiae. RNA. 19(12). 1639–1647. 23 indexed citations
11.
Jakovljevic, Jelena, Uli Ohmayer, Michael Gamalinda, et al.. (2012). Ribosomal proteins L7 and L8 function in concert with six A3 assembly factors to propagate assembly of domains I and II of 25S rRNA in yeast 60S ribosomal subunits. RNA. 18(10). 1805–1822. 55 indexed citations
12.
Pöll, Gisela, Tobias Braun, Jelena Jakovljevic, et al.. (2009). rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins. PLoS ONE. 4(12). e8249–e8249. 88 indexed citations
13.
Wacheul, Ludivine, Marc Thiry, Adam C. Berger, et al.. (2008). Identification of Genes That Function in the Biogenesis and Localization of Small Nucleolar RNAs in Saccharomyces cerevisiae. Molecular and Cellular Biology. 28(11). 3686–3699. 17 indexed citations
14.
Horsey, Edward, et al.. (2004). Role of the yeast Rrp1 protein in the dynamics of pre-ribosome maturation. RNA. 10(5). 813–827. 84 indexed citations
15.
Harnpicharnchai, Piyanun, Jelena Jakovljevic, Edward Horsey, et al.. (2001). Composition and Functional Characterization of Yeast 66S Ribosome Assembly Intermediates. Molecular Cell. 8(3). 505–515. 259 indexed citations
16.
Woolford, John L., et al.. (1997). Prp31p Promotes the Association of the U4/U6 · U5 Tri-snRNP with Prespliceosomes To Form Spliceosomes in Saccharomyces cerevisiae. Molecular and Cellular Biology. 17(7). 3580–3588. 52 indexed citations
17.
Kim, Kyong‐Tai, et al.. (1995). The final stages of spliceosome maturation require Spp2p that can interact with the DEAH box protein Prp2p and promote step 1 of splicing.. PubMed Central. 1(4). 375–90. 83 indexed citations
18.
Woolford, John L. & Jonathan R. Warner. (1991). 10 The Ribosome and Its Synthesis. Cold Spring Harbor Monograph Archive. 587–626. 15 indexed citations
19.
Moritz, Michelle, Beth A. Pulaski, & John L. Woolford. (1991). Assembly of 60S Ribosomal Subunits Is Perturbed in Temperature-Sensitive Yeast Mutants Defective in Ribosomal Protein L16. Molecular and Cellular Biology. 11(11). 5681–5692. 70 indexed citations
20.
Rotenberg, Mitch O. & John L. Woolford. (1986). Tripartite Upstream Promoter Element Essential for Expression of Saccharomyces cerevisiae Ribosomal Protein Genes. Molecular and Cellular Biology. 6(2). 674–687. 126 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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