Alexis T. Weiner

675 total citations
17 papers, 424 citations indexed

About

Alexis T. Weiner is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alexis T. Weiner has authored 17 papers receiving a total of 424 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Cell Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alexis T. Weiner's work include Microtubule and mitosis dynamics (9 papers), Cellular transport and secretion (6 papers) and Ubiquitin and proteasome pathways (3 papers). Alexis T. Weiner is often cited by papers focused on Microtubule and mitosis dynamics (9 papers), Cellular transport and secretion (6 papers) and Ubiquitin and proteasome pathways (3 papers). Alexis T. Weiner collaborates with scholars based in United States, United Kingdom and Denmark. Alexis T. Weiner's co-authors include Melissa M. Rolls, Daniel J. Goetschius, Kavitha S. Rao, Richard M. Albertson, Michelle C. Stone, Melissa Long, Kyle W. Gheres, Sean Munro, Matthew Shorey and Michelle M. Nguyen and has published in prestigious journals such as Nature Communications, The Journal of Cell Biology and Journal of Cell Science.

In The Last Decade

Alexis T. Weiner

16 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexis T. Weiner United States 11 268 252 124 47 44 17 424
Taiichi Tsuyama Japan 6 219 0.8× 153 0.6× 168 1.4× 35 0.7× 34 0.8× 8 395
Noelia Pinal United Kingdom 12 339 1.3× 205 0.8× 194 1.6× 32 0.7× 29 0.7× 14 502
Joel M. Rawson United States 7 263 1.0× 111 0.4× 215 1.7× 28 0.6× 29 0.7× 7 393
Juan Tao United States 7 213 0.8× 232 0.9× 214 1.7× 14 0.3× 41 0.9× 8 416
Jack Jing Lin Wong Singapore 7 206 0.8× 114 0.5× 187 1.5× 42 0.9× 21 0.5× 7 364
Adriana Reuveny Israel 10 347 1.3× 124 0.5× 96 0.8× 28 0.6× 16 0.4× 12 454
Kah Wai Yau Netherlands 6 416 1.6× 540 2.1× 175 1.4× 54 1.1× 36 0.8× 6 719
Jingjun Li United States 9 193 0.7× 113 0.4× 215 1.7× 50 1.1× 44 1.0× 13 406
Shen Lin United States 10 276 1.0× 286 1.1× 169 1.4× 32 0.7× 17 0.4× 13 506
Anetta Konecna Austria 4 303 1.1× 153 0.6× 92 0.7× 35 0.7× 24 0.5× 5 413

Countries citing papers authored by Alexis T. Weiner

Since Specialization
Citations

This map shows the geographic impact of Alexis T. Weiner'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 Alexis T. Weiner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexis T. Weiner more than expected).

Fields of papers citing papers by Alexis T. Weiner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexis T. Weiner. 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 Alexis T. Weiner. The network helps show where Alexis T. Weiner may publish in the future.

Co-authorship network of co-authors of Alexis T. Weiner

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

All Works

17 of 17 papers shown
1.
Kothe, Gregory O., et al.. (2025). Endocytosis of Wnt ligands from surrounding epithelial cells positions microtubule nucleation sites at dendrite branch points. PLoS Biology. 23(1). e3002973–e3002973. 1 indexed citations
2.
Weiner, Alexis T., et al.. (2025). Cell autonomous polarization by the planar cell polarity signaling pathway. Nature Communications. 16(1). 9503–9503.
3.
Weiner, Alexis T., Silas Boye Nissen, Kaye Suyama, et al.. (2023). Protein phosphatase 1 regulates core PCP signaling. EMBO Reports. 24(12). e56997–e56997. 2 indexed citations
4.
Kunimoto, Koshi, Alexis T. Weiner, Jeffrey D. Axelrod, & Eszter K. Vladar. (2022). Distinct overlapping functions for Prickle1 and Prickle2 in the polarization of the airway epithelium. Frontiers in Cell and Developmental Biology. 10. 976182–976182. 4 indexed citations
5.
Pizzo, Lucilla, Micaela Lasser, Matthew Jensen, et al.. (2021). Functional assessment of the “two-hit” model for neurodevelopmental defects in Drosophila and X. laevis. PLoS Genetics. 17(4). e1009112–e1009112. 13 indexed citations
6.
Cleary, Joseph M., Gregory O. Kothe, Michelle C. Stone, et al.. (2021). Trim9 and Klp61F promote polymerization of new dendritic microtubules along parallel microtubules. Journal of Cell Science. 134(11). 9 indexed citations
7.
Weiner, Alexis T., et al.. (2021). To nucleate or not, that is the question in neurons. Neuroscience Letters. 751. 135806–135806. 13 indexed citations
8.
Albertson, Richard M., et al.. (2020). Kinetochore proteins suppress neuronal microtubule dynamics and promote dendrite regeneration. Molecular Biology of the Cell. 31(19). 2125–2138. 23 indexed citations
9.
Albertson, Richard M., Alexis T. Weiner, Matthew Shorey, et al.. (2020). The receptor tyrosine kinase Ror is required for dendrite regeneration in Drosophila neurons. PLoS Biology. 18(3). e3000657–e3000657. 25 indexed citations
10.
Weiner, Alexis T., Gregory O. Kothe, Christopher Kozlowski, et al.. (2020). Endosomal Wnt signaling proteins control microtubule nucleation in dendrites. PLoS Biology. 18(3). e3000647–e3000647. 40 indexed citations
11.
Shorey, Matthew, Alexis T. Weiner, Richard M. Albertson, et al.. (2019). Patronin-mediated minus end growth is required for dendritic microtubule polarity. The Journal of Cell Biology. 218(7). 2309–2328. 56 indexed citations
12.
Weiner, Alexis T., et al.. (2018). Identification of Proteins Required for Precise Positioning of Apc2 in Dendrites. G3 Genes Genomes Genetics. 8(5). 1841–1853. 10 indexed citations
13.
Iyer, Janani, Matthew Jensen, Payal T. Patel, et al.. (2018). Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster. Nature Communications. 9(1). 2548–2548. 40 indexed citations
14.
Chen, Li, Michelle C. Stone, Alexis T. Weiner, et al.. (2016). Mitochondria and Caspases Tune Nmnat-Mediated Stabilization to Promote Axon Regeneration. PLoS Genetics. 12(12). e1006503–e1006503. 30 indexed citations
15.
Rao, Kavitha S., Michelle C. Stone, Alexis T. Weiner, et al.. (2016). Spastin, atlastin, and ER relocalization are involved in axon but not dendrite regeneration. Molecular Biology of the Cell. 27(21). 3245–3256. 51 indexed citations
16.
Weiner, Alexis T., Michael C. Lanz, Daniel J. Goetschius, William O. Hancock, & Melissa M. Rolls. (2016). Kinesin‐2 and Apc function at dendrite branch points to resolve microtubule collisions. Cytoskeleton. 73(1). 35–44. 19 indexed citations
17.
Nguyen, Michelle M., Daniel J. Goetschius, Alexis T. Weiner, et al.. (2014). γ-Tubulin controls neuronal microtubule polarity independently of Golgi outposts. Molecular Biology of the Cell. 25(13). 2039–2050. 88 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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