Shih-Chieh Ti

1.5k total citations
24 papers, 1.1k citations indexed

About

Shih-Chieh Ti is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Shih-Chieh Ti has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Cell Biology and 2 papers in Genetics. Recurrent topics in Shih-Chieh Ti's work include Microtubule and mitosis dynamics (18 papers), Photosynthetic Processes and Mechanisms (7 papers) and Ubiquitin and proteasome pathways (6 papers). Shih-Chieh Ti is often cited by papers focused on Microtubule and mitosis dynamics (18 papers), Photosynthetic Processes and Mechanisms (7 papers) and Ubiquitin and proteasome pathways (6 papers). Shih-Chieh Ti collaborates with scholars based in United States, Hong Kong and Taiwan. Shih-Chieh Ti's co-authors include Tarun M. Kapoor, Thomas D. Pollard, Ting‐Fang Wang, Melissa C. Pamula, Gregory M. Alushin, Christopher T. Jurgenson, Brad J. Nolen, Han-Yi Huang, Feng-Ming Lin and Seth A. Darst and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Shih-Chieh Ti

22 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shih-Chieh Ti United States 12 875 688 99 73 68 24 1.1k
Jeffrey H. Stear Germany 12 993 1.1× 940 1.4× 158 1.6× 61 0.8× 63 0.9× 19 1.2k
Ryo Nitta Japan 16 669 0.8× 783 1.1× 81 0.8× 50 0.7× 64 0.9× 28 1.0k
Nikita B. Gudimchuk Russia 13 645 0.7× 698 1.0× 130 1.3× 33 0.5× 37 0.5× 37 933
Marija Žanić United States 17 1.1k 1.2× 1.2k 1.7× 131 1.3× 58 0.8× 57 0.8× 33 1.4k
Vlada Philimonenko Czechia 16 972 1.1× 350 0.5× 34 0.3× 58 0.8× 96 1.4× 24 1.2k
Manuel Hilbert Switzerland 14 777 0.9× 537 0.8× 101 1.0× 69 0.9× 137 2.0× 17 1.1k
William B. Redwine United States 7 688 0.8× 655 1.0× 29 0.3× 56 0.8× 104 1.5× 9 961
L. Urnavicius United States 11 852 1.0× 898 1.3× 27 0.3× 22 0.3× 95 1.4× 14 1.2k
Keith F. DeLuca United States 12 783 0.9× 539 0.8× 125 1.3× 98 1.3× 23 0.3× 19 996
Wei‐Lih Lee United States 20 1.1k 1.3× 1.1k 1.7× 127 1.3× 39 0.5× 50 0.7× 28 1.5k

Countries citing papers authored by Shih-Chieh Ti

Since Specialization
Citations

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

Fields of papers citing papers by Shih-Chieh Ti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shih-Chieh Ti. 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 Shih-Chieh Ti. The network helps show where Shih-Chieh Ti may publish in the future.

Co-authorship network of co-authors of Shih-Chieh Ti

This figure shows the co-authorship network connecting the top 25 collaborators of Shih-Chieh Ti. A scholar is included among the top collaborators of Shih-Chieh Ti 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 Shih-Chieh Ti. Shih-Chieh Ti 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.
Makino, Shigeru, Liqin Zheng, Guocheng Lan, et al.. (2025). The kinesin-4 protein KIF27 forms a cytoskeletal scaffold at the transition zone to promote motile cilia structural integrity. Proceedings of the National Academy of Sciences. 122(51). e2515392122–e2515392122.
2.
3.
4.
Luo, Jingyi, Daqi Yu, Chang Zhao, et al.. (2024). Tubulin acetyltransferases access and modify the microtubule luminal K40 residue through anchors in taxane-binding pockets. Nature Structural & Molecular Biology. 32(2). 358–368. 5 indexed citations
5.
Tan, Daisylyn Senna, Ya Gao, Liyang Shi, et al.. (2023). The homeodomain of Oct4 is a dimeric binder of methylated CpG elements. Nucleic Acids Research. 51(3). 1120–1138. 6 indexed citations
6.
Yan, Shan, et al.. (2023). Integrated regulation of tubulin tyrosination and microtubule stability by human α-tubulin isotypes. Cell Reports. 42(6). 112653–112653. 7 indexed citations
7.
Ti, Shih-Chieh. (2022). Reconstituting Microtubules: A Decades-Long Effort From Building Block Identification to the Generation of Recombinant α/β-Tubulin. Frontiers in Cell and Developmental Biology. 10. 861648–861648. 1 indexed citations
8.
Tanaka, Masahito, Kei Saito, Shih-Chieh Ti, et al.. (2022). Morphological growth dynamics, mechanical stability, and active microtubule mechanics underlying spindle self-organization. Proceedings of the National Academy of Sciences. 119(44). e2209053119–e2209053119. 5 indexed citations
9.
Wieczorek, Michał W., Shih-Chieh Ti, L. Urnavicius, et al.. (2021). Biochemical reconstitutions reveal principles of human γ-TuRC assembly and function. The Journal of Cell Biology. 220(3). 23 indexed citations
10.
Ti, Shih-Chieh, Michał W. Wieczorek, & Tarun M. Kapoor. (2020). Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells. STAR Protocols. 1(1). 100011–100011. 17 indexed citations
11.
Wieczorek, Michał W., L. Urnavicius, Shih-Chieh Ti, et al.. (2019). Asymmetric Molecular Architecture of the Human γ-Tubulin Ring Complex. Cell. 180(1). 165–175.e16. 92 indexed citations
12.
Ti, Shih-Chieh, Gregory M. Alushin, & Tarun M. Kapoor. (2018). Human β-Tubulin Isotypes Can Regulate Microtubule Protofilament Number and Stability. Developmental Cell. 47(2). 175–190.e5. 95 indexed citations
13.
Ti, Shih-Chieh, Melissa C. Pamula, Stuart C. Howes, et al.. (2016). Mutations in Human Tubulin Proximal to the Kinesin-Binding Site Alter Dynamic Instability at Microtubule Plus- and Minus-Ends. Developmental Cell. 37(1). 72–84. 81 indexed citations
14.
Subramanian, Radhika, Shih-Chieh Ti, Lei Tan, Seth A. Darst, & Tarun M. Kapoor. (2013). Marking and Measuring Single Microtubules by PRC1 and Kinesin-4. Cell. 154(2). 377–390. 118 indexed citations
15.
Subramanian, Radhika, Shih-Chieh Ti, Lei Tan, Seth A. Darst, & Tarun M. Kapoor. (2013). Marking and Measuring Single Microtubules by PRC1 and Kinesin-4. Cell. 155(5). 1188–1188. 8 indexed citations
16.
McCormick, Chad D., Matthew Akamatsu, Shih-Chieh Ti, & Thomas D. Pollard. (2013). Measuring Affinities of Fission Yeast Spindle Pole Body Proteins in Live Cells across the Cell Cycle. Biophysical Journal. 105(6). 1324–1335. 11 indexed citations
17.
Ti, Shih-Chieh, Christopher T. Jurgenson, Brad J. Nolen, & Thomas D. Pollard. (2011). Structural and biochemical characterization of two binding sites for nucleation-promoting factor WASp-VCA on Arp2/3 complex. Proceedings of the National Academy of Sciences. 108(33). E463–71. 119 indexed citations
18.
Ti, Shih-Chieh & Thomas D. Pollard. (2010). Purification of Actin from Fission Yeast Schizosaccharomyces pombe and Characterization of Functional Differences from Muscle Actin. Journal of Biological Chemistry. 286(7). 5784–5792. 22 indexed citations
19.
Ti, Shih-Chieh, et al.. (2006). SUMO modifications control assembly of synaptonemal complex and polycomplex in meiosis of Saccharomyces cerevisiae. Genes & Development. 20(15). 2067–2081. 213 indexed citations
20.
Chen, Yi‐Kai, Chih‐Hsiang Leng, Heidi Olivares, et al.. (2004). Heterodimeric complexes of Hop2 and Mnd1 function with Dmc1 to promote meiotic homolog juxtaposition and strand assimilation. Proceedings of the National Academy of Sciences. 101(29). 10572–10577. 87 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jeffrey H. Stear Breakdown of academic impact, for papers by Ryo Nitta Breakdown of academic impact, for papers by Nikita B. Gudimchuk Breakdown of academic impact, for papers by Marija Žanić Breakdown of academic impact, for papers by Vlada Philimonenko Breakdown of academic impact, for papers by Manuel Hilbert Breakdown of academic impact, for papers by William B. Redwine Breakdown of academic impact, for papers by L. Urnavicius Breakdown of academic impact, for papers by Keith F. DeLuca Breakdown of academic impact, for papers by Wei‐Lih Lee
Rankless by CCL
2026