Rosemary Williams

4.1k total citations · 1 hit paper
18 papers, 2.7k citations indexed

About

Rosemary Williams is a scholar working on Molecular Biology, Cell Biology and Nephrology. According to data from OpenAlex, Rosemary Williams has authored 18 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Cell Biology and 1 paper in Nephrology. Recurrent topics in Rosemary Williams's work include RNA Research and Splicing (12 papers), Nuclear Structure and Function (11 papers) and RNA modifications and cancer (3 papers). Rosemary Williams is often cited by papers focused on RNA Research and Splicing (12 papers), Nuclear Structure and Function (11 papers) and RNA modifications and cancer (3 papers). Rosemary Williams collaborates with scholars based in United States, France and Germany. Rosemary Williams's co-authors include Michael P. Rout, Brian T. Chait, Andrej Săli, Svetlana Dokudovskaya, Damien P. Devos, Frank Alber, Wenzhu Zhang, Orit Karni-Schmidt, Liesbeth M. Veenhoff and Ileana M. Cristea and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Rosemary Williams

17 papers receiving 2.7k citations

Hit Papers

The molecular architecture of the nuclear pore complex 2007 2026 2013 2019 2007 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. The molecular architecture of the nuclear pore complex
    2007 814 citations Frank Alber, Svetlana Dokudovskaya et al. Nature profile →

Peers

Rosemary Williams
Svetlana Dokudovskaya France
Dan Simpson United States
Stefan Bohn Germany
Michael Rexach United States
Marjolaine Noirclerc‐Savoye France
Jeffrey K. Noel United States
Anastasia S. Politou Greece
Alexander von Appen Germany
Nicholas R. Guydosh United States
Susan E. Tsutakawa United States
Svetlana Dokudovskaya France
Rosemary Williams
Citations per year, relative to Rosemary Williams Rosemary Williams (= 1×) peers Svetlana Dokudovskaya

Countries citing papers authored by Rosemary Williams

Since Specialization
Citations

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

Fields of papers citing papers by Rosemary Williams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosemary Williams. 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 Rosemary Williams. The network helps show where Rosemary Williams may publish in the future.

Co-authorship network of co-authors of Rosemary Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Rosemary Williams. A scholar is included among the top collaborators of Rosemary Williams 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 Rosemary Williams. Rosemary Williams is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Upla, Paula, Seung Joong Kim, Parthasarathy Sampathkumar, et al.. (2017). Molecular Architecture of the Major Membrane Ring Component of the Nuclear Pore Complex. Structure. 25(3). 434–445. 43 indexed citations
2.
Fernández-Martı́nez, Javier, Seung Joong Kim, Yi Shi, et al.. (2016). Structure and Function of the Nuclear Pore Complex Cytoplasmic mRNA Export Platform. Cell. 167(5). 1215–1228.e25. 113 indexed citations
3.
Williams, Rosemary, et al.. (2015). Using Data Analytics for Oversight and Efficiency. 64(2). 18. 5 indexed citations
4.
Shi, Yi, Javier Fernández-Martı́nez, Elina Tjioe, et al.. (2014). Structural Characterization by Cross-linking Reveals the Detailed Architecture of a Coatomer-related Heptameric Module from the Nuclear Pore Complex. Molecular & Cellular Proteomics. 13(11). 2927–2943. 130 indexed citations
5.
Williams, Rosemary, et al.. (2013). Workforce Planning and Management. 62(4). 34.
6.
Niepel, Mario, Kelly R. Molloy, Rosemary Williams, et al.. (2013). The nuclear basket proteins Mlp1p and Mlp2p are part of a dynamic interactome including Esc1p and the proteasome. Molecular Biology of the Cell. 24(24). 3920–3938. 91 indexed citations
7.
Fernández-Martı́nez, Javier, Jeremy Phillips, Matthew D. Sekedat, et al.. (2012). Structure–function mapping of a heptameric module in the nuclear pore complex. The Journal of Cell Biology. 196(4). 419–434. 88 indexed citations
8.
Dokudovskaya, Svetlana, François Waharte, Avner Schlessinger, et al.. (2011). A Conserved Coatomer-related Complex Containing Sec13 and Seh1 Dynamically Associates With the Vacuole in Saccharomyces cerevisiae. Molecular & Cellular Proteomics. 10(6). M110.006478–M110.006478. 113 indexed citations
9.
Alber, Frank, Svetlana Dokudovskaya, Liesbeth M. Veenhoff, et al.. (2007). The molecular architecture of the nuclear pore complex. Nature. 450(7170). 695–701. 814 indexed citations breakdown →
10.
Alber, Frank, Svetlana Dokudovskaya, Liesbeth M. Veenhoff, et al.. (2007). Determining the architectures of macromolecular assemblies. Nature. 450(7170). 683–694. 417 indexed citations
11.
Devos, Damien P., Svetlana Dokudovskaya, Rosemary Williams, et al.. (2006). Simple fold composition and modular architecture of the nuclear pore complex. Proceedings of the National Academy of Sciences. 103(7). 2172–2177. 215 indexed citations
12.
Dokudovskaya, Svetlana, Rosemary Williams, Damien P. Devos, et al.. (2006). Protease Accessibility Laddering: A Proteomic Tool for Probing Protein Structure. Structure. 14(4). 653–660. 27 indexed citations
13.
Dokudovskaya, Svetlana, Rosemary Williams, Damien P. Devos, et al.. (2006). Technical Advance Protease Accessibility Laddering: A Proteomic Tool for Probing Protein Structure. 1 indexed citations
14.
Timney, Benjamin L., Jaclyn Tetenbaum-Novatt, Rosemary Williams, et al.. (2006). Simple kinetic relationships and nonspecific competition govern nuclear import rates in vivo. The Journal of Cell Biology. 175(4). 579–593. 121 indexed citations
15.
Cristea, Ileana M., Rosemary Williams, Brian T. Chait, & Michael P. Rout. (2005). Fluorescent Proteins as Proteomic Probes. Molecular & Cellular Proteomics. 4(12). 1933–1941. 208 indexed citations
16.
Devos, Damien P., Svetlana Dokudovskaya, Frank Alber, et al.. (2005). Correction: Components of Coated Vesicles and Nuclear Pore Complexes Share a Common Molecular Architecture. PLoS Biology. 3(2). e80–e80. 1 indexed citations
17.
Devos, Damien P., Svetlana Dokudovskaya, Frank Alber, et al.. (2004). Components of Coated Vesicles and Nuclear Pore Complexes Share a Common Molecular Architecture. PLoS Biology. 2(12). e380–e380. 317 indexed citations
18.
Topham, Richard W., et al.. (1982). Evidence for the participation of intestinal xanthine oxidase in the mucosal processing of iron. Biochemistry. 21(19). 4529–4535. 32 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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