Catherine M. Drerup

1.5k total citations
22 papers, 642 citations indexed

About

Catherine M. Drerup is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Catherine M. Drerup has authored 22 papers receiving a total of 642 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Catherine M. Drerup's work include Microtubule and mitosis dynamics (8 papers), Cellular transport and secretion (6 papers) and Mitochondrial Function and Pathology (5 papers). Catherine M. Drerup is often cited by papers focused on Microtubule and mitosis dynamics (8 papers), Cellular transport and secretion (6 papers) and Mitochondrial Function and Pathology (5 papers). Catherine M. Drerup collaborates with scholars based in United States and Hungary. Catherine M. Drerup's co-authors include Alex Nechiporuk, Amrita Mandal, Jill A. Morris, Jacek Topczewski, Amy L Herbert, Kelly R. Monk, Hillary F. McGraw, Jules B. Panksepp, Robert Huber and David W. Raible and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Catherine M. Drerup

20 papers receiving 638 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine M. Drerup United States 12 400 215 179 83 66 22 642
Elizabeth M. McNeill United States 12 575 1.4× 101 0.5× 225 1.3× 68 0.8× 94 1.4× 22 877
Alejandra Kun Uruguay 15 393 1.0× 151 0.7× 275 1.5× 130 1.6× 66 1.0× 40 849
Νικόλαος Γιαγτζόγλου United States 16 568 1.4× 154 0.7× 232 1.3× 141 1.7× 34 0.5× 23 815
Chunlai Wu United States 12 559 1.4× 253 1.2× 301 1.7× 79 1.0× 32 0.5× 16 851
Kersti Lilleväli Estonia 18 448 1.1× 117 0.5× 160 0.9× 67 0.8× 91 1.4× 32 746
Andrea Ketschek United States 15 497 1.2× 429 2.0× 521 2.9× 56 0.7× 213 3.2× 22 1.0k
Minyeop Nahm South Korea 14 393 1.0× 282 1.3× 246 1.4× 99 1.2× 22 0.3× 34 704
Claire Haueter United States 12 713 1.8× 375 1.7× 311 1.7× 127 1.5× 27 0.4× 12 1.1k
Rossella Di Giaimo Italy 15 436 1.1× 153 0.7× 111 0.6× 127 1.5× 179 2.7× 34 848
Kai Murk Germany 11 276 0.7× 178 0.8× 193 1.1× 53 0.6× 76 1.2× 13 597

Countries citing papers authored by Catherine M. Drerup

Since Specialization
Citations

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

Fields of papers citing papers by Catherine M. Drerup

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine M. Drerup

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine M. Drerup. A scholar is included among the top collaborators of Catherine M. Drerup 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 Catherine M. Drerup. Catherine M. Drerup 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.
Stein, C. Michael, et al.. (2025). CCSer2 gates dynein activity at the cell periphery. The Journal of Cell Biology. 224(6).
2.
Brewer, Melissa, et al.. (2024). Gut microbiota regulate maturation and mitochondrial function of the nutrient-sensing enteroendocrine cell. Development. 151(8). 4 indexed citations
3.
Wong, Hiu-Tung, et al.. (2024). ALS-Linked VapB P56S Mutation Alters Neuronal Mitochondrial Turnover at the Synapse. Journal of Neuroscience. 44(35). e0879242024–e0879242024. 3 indexed citations
4.
Mandal, Amrita, et al.. (2024). An initial HOPS-mediated fusion event is critical for autophagosome transport initiation from the axon terminal. Autophagy. 20(10). 2275–2296. 1 indexed citations
5.
Wong, Hiu-Tung, et al.. (2023). In vivo investigation of mitochondria in lateral line afferent neurons and hair cells. Hearing Research. 431. 108740–108740. 1 indexed citations
6.
Petralia, Ronald S., et al.. (2022). NudC regulated Lis1 stability is essential for the maintenance of dynamic microtubule ends in axon terminals. iScience. 25(10). 105072–105072. 10 indexed citations
7.
8.
Mandal, Amrita, Hiu-Tung Wong, Alisha Beirl, et al.. (2020). Retrograde Mitochondrial Transport Is Essential for Organelle Distribution and Health in Zebrafish Neurons. Journal of Neuroscience. 41(7). 1371–1392. 40 indexed citations
9.
Drerup, Catherine M., et al.. (2020). A Conserved Role for Vezatin Proteins in Cargo-Specific Regulation of Retrograde Axonal Transport. Genetics. 216(2). 431–445. 5 indexed citations
10.
Mandal, Amrita & Catherine M. Drerup. (2019). Axonal Transport and Mitochondrial Function in Neurons. Frontiers in Cellular Neuroscience. 13. 373–373. 114 indexed citations
11.
Mandal, Amrita, et al.. (2018). Analyzing Neuronal Mitochondria in vivo Using Fluorescent Reporters in Zebrafish. Frontiers in Cell and Developmental Biology. 6. 144–144. 37 indexed citations
12.
Herbert, Amy L, Meng‐meng Fu, Catherine M. Drerup, et al.. (2017). Dynein/dynactin is necessary for anterograde transport of Mbp mRNA in oligodendrocytes and for myelination in vivo. Proceedings of the National Academy of Sciences. 114(43). E9153–E9162. 43 indexed citations
13.
Drerup, Catherine M., Amy L Herbert, Kelly R. Monk, & Alex Nechiporuk. (2017). Regulation of mitochondria-dynactin interaction and mitochondrial retrograde transport in axons. eLife. 6. 53 indexed citations
14.
Drerup, Catherine M., et al.. (2016). Kif1B Interacts with KBP to Promote Axon Elongation by Localizing a Microtubule Regulator to Growth Cones. Journal of Neuroscience. 36(26). 7014–7026. 24 indexed citations
15.
Drerup, Catherine M. & Alex Nechiporuk. (2015). In vivo analysis of axonal transport in zebrafish. Methods in cell biology. 131. 311–329. 19 indexed citations
16.
Drerup, Catherine M. & Alex Nechiporuk. (2013). JNK-Interacting Protein 3 Mediates the Retrograde Transport of Activated c-Jun N-Terminal Kinase and Lysosomes. PLoS Genetics. 9(2). e1003303–e1003303. 108 indexed citations
17.
Drerup, Catherine M., et al.. (2009). Disc1 regulatesfoxd3andsox10expression, affecting neural crest migration and differentiation. Development. 136(15). 2623–2632. 71 indexed citations
18.
Drerup, Catherine M., et al.. (2009). Characterization of the overlapping expression patterns of the zebrafish LIS1 orthologs. Gene Expression Patterns. 10(1). 75–85. 4 indexed citations
19.
Drerup, Catherine M., Sara Ahlgren, & Jill A. Morris. (2007). Expression profiles of ndel1a and ndel1b, two orthologs of the NudE-Like gene, in the zebrafish. Gene Expression Patterns. 7(6). 672–679. 11 indexed citations
20.
Panksepp, Jules B., et al.. (2003). Amine neurochemistry and aggression in crayfish. Microscopy Research and Technique. 60(3). 360–368. 37 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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