Susan M. Parkhurst

7.2k total citations
87 papers, 6.0k citations indexed

About

Susan M. Parkhurst is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Susan M. Parkhurst has authored 87 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 34 papers in Cell Biology and 13 papers in Plant Science. Recurrent topics in Susan M. Parkhurst's work include Cellular Mechanics and Interactions (28 papers), Genomics and Chromatin Dynamics (18 papers) and Developmental Biology and Gene Regulation (17 papers). Susan M. Parkhurst is often cited by papers focused on Cellular Mechanics and Interactions (28 papers), Genomics and Chromatin Dynamics (18 papers) and Developmental Biology and Gene Regulation (17 papers). Susan M. Parkhurst collaborates with scholars based in United States, South Africa and United Kingdom. Susan M. Parkhurst's co-authors include Victor G. Corces, Paul Martin, Jeffrey M. Verboon, Maria Teresa Abreu‐Blanco, Craig R. Magie, David Ish‐Horowicz, Howard D. Lipshitz, Gretchen Poortinga, Delia Pinto-Santini and Robert N. Eisenman and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Susan M. Parkhurst

85 papers receiving 5.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susan M. Parkhurst United States	44	4.4k	1.6k	935	818	716	87	6.0k
Alfonso Martínez-Arias United Kingdom	31	4.3k 1.0×	1.4k 0.9×	655 0.7×	1.0k 1.2×	837 1.2×	51	5.5k
Jean‐Paul Concordet France	41	8.4k 1.9×	1.1k 0.7×	633 0.7×	2.1k 2.6×	549 0.8×	102	10.8k
Pernille Rørth Germany	35	4.0k 0.9×	3.0k 1.8×	447 0.5×	479 0.6×	1.3k 1.8×	46	6.2k
Hannele Ruohola‐Baker United States	45	5.7k 1.3×	815 0.5×	592 0.6×	597 0.7×	689 1.0×	90	6.8k
Maria Novatchkova Austria	48	5.4k 1.2×	1.0k 0.6×	1.4k 1.5×	644 0.8×	434 0.6×	85	7.4k
Christian F. Lehner Germany	42	5.2k 1.2×	2.7k 1.7×	1.1k 1.2×	477 0.6×	463 0.6×	88	6.7k
John W. Tamkun United States	39	7.9k 1.8×	1.1k 0.7×	1.1k 1.2×	1.3k 1.6×	416 0.6×	54	9.6k
Susan M. Abmayr United States	40	5.0k 1.1×	936 0.6×	548 0.6×	918 1.1×	700 1.0×	72	6.0k
Stefan Baumgartner Switzerland	34	3.4k 0.8×	1.3k 0.8×	348 0.4×	753 0.9×	845 1.2×	78	4.9k
John Abrams United States	41	5.5k 1.2×	1.5k 0.9×	466 0.5×	431 0.5×	1.1k 1.5×	79	7.4k

Countries citing papers authored by Susan M. Parkhurst

Since Specialization

Citations

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

Fields of papers citing papers by Susan M. Parkhurst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan M. Parkhurst

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

All Works

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20 of 20 papers shown

Nakamura, Mitsutoshi & Susan M. Parkhurst. (2024). Calcium influx rapidly establishes distinct spatial recruitments of Annexins to cell wounds. Genetics. 227(4). 1 indexed citations

Nakamura, Mitsutoshi & Susan M. Parkhurst. (2024). Septin complexes: Ahead of the curve. Cytoskeleton. 82(4). 229–233.

Nakamura, Mitsutoshi, et al.. (2023). Centralspindlin proteins Pavarotti and Tumbleweed along with WASH regulate nuclear envelope budding. The Journal of Cell Biology. 222(8). 1 indexed citations

Nakamura, Mitsutoshi, et al.. (2023). Coordinated efforts of different actin filament populations are needed for optimal cell wound repair. Molecular Biology of the Cell. 34(3). ar15–ar15. 8 indexed citations

Verboon, Jeffrey M., et al.. (2020). Drosophila Wash and the Wash regulatory complex function in nuclear envelope budding. Journal of Cell Science. 133(13). 7 indexed citations

Nakamura, Mitsutoshi, et al.. (2020). The kinesin-like protein Pavarotti functions noncanonically to regulate actin dynamics. The Journal of Cell Biology. 219(9). 12 indexed citations

Nakamura, Mitsutoshi, et al.. (2020). Autocrine insulin pathway signaling regulates actin dynamics in cell wound repair. PLoS Genetics. 16(12). e1009186–e1009186. 8 indexed citations

Abreu‐Blanco, Maria Teresa, et al.. (2012). Drosophila embryos close epithelial wounds using a combination of cellular protrusions and an actomyosin purse string. Journal of Cell Science. 125(24). 5984–5997. 120 indexed citations

Abreu‐Blanco, Maria Teresa, Jeffrey M. Verboon, & Susan M. Parkhurst. (2011). Cell wound repair in Drosophila occurs through three distinct phases of membrane and cytoskeletal remodeling. The Journal of Cell Biology. 193(3). 455–464. 115 indexed citations

10.

Barry, Kevin C., et al.. (2011). TheDrosophilaSTUbL protein Degringolade limits HES functions during embryogenesis. Development. 138(9). 1759–1769. 24 indexed citations

11.

Abreu‐Blanco, Maria Teresa, Jeffrey M. Verboon, & Susan M. Parkhurst. (2011). Single cell wound repair. PubMed. 1(3). 114–121. 39 indexed citations

12.

Liu, Raymond, et al.. (2008). Sisyphus, the Drosophila myosin XV homolog, traffics within filopodia transporting key sensory and adhesion cargos. Journal of Cell Science. 121(1). 5 indexed citations

13.

Liu, Raymond, Elena V. Linardopoulou, Gregory E. Osborn, & Susan M. Parkhurst. (2008). Formins in development: Orchestrating body plan origami. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1803(2). 207–225. 33 indexed citations

14.

Orian, Amir, Jeffrey J. Delrow, Alicia E. Rosales‐Nieves, et al.. (2007). A Myc–Groucho complex integrates EGF and Notch signaling to regulate neural development. Proceedings of the National Academy of Sciences. 104(40). 15771–15776. 48 indexed citations

15.

Secombe, Julie & Susan M. Parkhurst. (2004). Drosophila Topors Is a RING Finger-containing Protein That Functions as a Ubiquitin-protein Isopeptide Ligase for the Hairy Basic Helix-Loop-Helix Repressor Protein. Journal of Biological Chemistry. 279(17). 17126–17133. 14 indexed citations

16.

Bianchi‐Frias, Daniella, Amir Orian, Jeffrey J. Delrow, et al.. (2004). Hairy Transcriptional Repression Targets and Cofactor Recruitment in Drosophila. PLoS Biology. 2(7). e178–e178. 86 indexed citations

17.

Phippen, T., Andrea L. Sweigart, Mariko Moniwa, et al.. (2000). Drosophila C-terminal Binding Protein Functions as a Context-dependent Transcriptional Co-factor and Interferes with Both Mad and Groucho Transcriptional Repression. Journal of Biological Chemistry. 275(48). 37628–37637. 72 indexed citations

18.

Parkhurst, Susan M.. (1998). Groucho: making its Marx as a transcriptional co-repressor. Trends in Genetics. 14(4). 130–132. 68 indexed citations

19.

Alifragis, Pavlos, Gretchen Poortinga, Susan M. Parkhurst, & Christos Delidakis. (1997). A network of interacting transcriptional regulators involved in Drosophila neural fate specification revealed by the yeast two-hybrid system. Proceedings of the National Academy of Sciences. 94(24). 13099–13104. 69 indexed citations

20.

Parkhurst, Susan M., et al.. (1986). The Drosophila melanogaster Gypsy Transposable Element Encodes Putative Gene Products Homologous to Retroviral Proteins. Molecular and Cellular Biology. 6(4). 1129–1134. 94 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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