Helen L. Yin

10.3k total citations · 3 hit papers
89 papers, 8.7k citations indexed

About

Helen L. Yin is a scholar working on Cell Biology, Molecular Biology and Physiology. According to data from OpenAlex, Helen L. Yin has authored 89 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Cell Biology, 43 papers in Molecular Biology and 11 papers in Physiology. Recurrent topics in Helen L. Yin's work include Cellular Mechanics and Interactions (40 papers), Cellular transport and secretion (33 papers) and Protein Kinase Regulation and GTPase Signaling (21 papers). Helen L. Yin is often cited by papers focused on Cellular Mechanics and Interactions (40 papers), Cellular transport and secretion (33 papers) and Protein Kinase Regulation and GTPase Signaling (21 papers). Helen L. Yin collaborates with scholars based in United States, France and Japan. Helen L. Yin's co-authors include Thomas P. Stossel, Paul A. Janmey, Masaya Yamamoto, Marisan Mejillano, Hui Sun, Joseph Albanesi, Hui-Qiao Sun, Andrew Rozelle, Jing Wang and Eric Macia and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Helen L. Yin

89 papers receiving 8.5k citations

Hit Papers

Control of cytoplasmic actin gel–sol transformation by ge... 1979 2026 1994 2010 1979 2003 1986 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helen L. Yin United States 51 5.0k 4.7k 1.0k 793 647 89 8.7k
Michael Schleicher Germany 53 4.3k 0.9× 4.1k 0.9× 755 0.8× 530 0.7× 516 0.8× 175 8.3k
Ichiro Yahara Japan 62 3.6k 0.7× 7.0k 1.5× 684 0.7× 1.6k 2.1× 594 0.9× 133 10.5k
John E. Heuser United States 54 6.1k 1.2× 8.0k 1.7× 1.7k 1.7× 1.1k 1.4× 547 0.8× 91 12.7k
Anthony I. Magee United Kingdom 52 2.7k 0.5× 7.4k 1.6× 566 0.6× 1.4k 1.8× 432 0.7× 144 10.3k
Christophe Lamaze France 41 4.2k 0.8× 4.9k 1.0× 1.1k 1.1× 1.2k 1.6× 512 0.8× 91 7.8k
Henry N. Higgs United States 52 6.3k 1.3× 6.3k 1.3× 602 0.6× 678 0.9× 1.4k 2.2× 104 11.6k
Ivan R. Nabi Canada 56 3.9k 0.8× 7.5k 1.6× 1.2k 1.2× 2.3k 2.9× 652 1.0× 140 11.1k
Toyoshi Fujimoto Japan 55 4.1k 0.8× 6.7k 1.4× 1.9k 1.9× 626 0.8× 261 0.4× 189 10.9k
Hans Georg Mannherz Germany 47 3.0k 0.6× 5.0k 1.1× 428 0.4× 1.6k 2.0× 510 0.8× 169 9.8k
Uno Lindberg Sweden 48 4.3k 0.9× 4.9k 1.0× 439 0.4× 478 0.6× 1.1k 1.7× 109 9.0k

Countries citing papers authored by Helen L. Yin

Since Specialization
Citations

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

Fields of papers citing papers by Helen L. Yin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helen L. Yin. 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 Helen L. Yin. The network helps show where Helen L. Yin may publish in the future.

Co-authorship network of co-authors of Helen L. Yin

This figure shows the co-authorship network connecting the top 25 collaborators of Helen L. Yin. A scholar is included among the top collaborators of Helen L. Yin 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 Helen L. Yin. Helen L. Yin 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.
Chen, Yan, et al.. (2022). PI4P-Dependent Targeting of ATG14 to Mature Autophagosomes. Biochemistry. 61(8). 722–729. 6 indexed citations
2.
Wang, Hanzhi, Xiaohui Zhu, Li Zhang, et al.. (2015). GABARAPs regulate PI4P-dependent autophagosome:lysosome fusion. Proceedings of the National Academy of Sciences. 112(22). 7015–7020. 159 indexed citations
4.
Sun, Hui & Helen L. Yin. (2007). The β‐Thymosin Enigma. Annals of the New York Academy of Sciences. 1112(1). 45–55. 18 indexed citations
5.
Feng, Siyi, Chengcheng Shen, Vincenzo Lariccia, et al.. (2007). Dual control of cardiac Na+–Ca2+ exchange by PIP2: electrophysiological analysis of direct and indirect mechanisms. The Journal of Physiology. 582(3). 991–1010. 52 indexed citations
6.
Wang, Jing, Hui-Qiao Sun, Eric Macia, et al.. (2007). PI4P Promotes the Recruitment of the GGA Adaptor Proteins to the Trans-Golgi Network and Regulates Their Recognition of the Ubiquitin Sorting Signal. Molecular Biology of the Cell. 18(7). 2646–2655. 138 indexed citations
7.
Yang, Xiaojing, et al.. (2007). RhoA required for acid-induced stress fiber formation and trafficking and activation of NHE3. American Journal of Physiology-Renal Physiology. 293(4). F1054–F1064. 14 indexed citations
8.
Mao, Yuntao S. & Helen L. Yin. (2007). Regulation of the actin cytoskeleton by phosphatidylinositol 4-phosphate 5 kinases. Pflügers Archiv - European Journal of Physiology. 455(1). 5–18. 65 indexed citations
9.
Yang, Lin, et al.. (2007). Global Structure Changes Associated with Ca2+ Activation of Full-length Human Plasma Gelsolin. Journal of Biological Chemistry. 282(35). 25884–25892. 50 indexed citations
10.
Wang, Tianyi, Tsung‐Hsien Chuang, Tapani Ronni, et al.. (2006). Flightless I Homolog Negatively Modulates the TLR Pathway. The Journal of Immunology. 176(3). 1355–1362. 56 indexed citations
11.
Aguda, A.H., Mårten Larsson, Christophe Guérin, et al.. (2004). Structural basis of actin sequestration by thymosin‐β4: implications for WH2 proteins. The EMBO Journal. 23(18). 3599–3608. 99 indexed citations
12.
Rozelle, Andrew, et al.. (2003). Regulation of Sustained Actin Dynamics by the TCR and Costimulation as a Mechanism of Receptor Localization. The Journal of Immunology. 171(5). 2287–2295. 83 indexed citations
13.
Turnage, Richard H., Fiemu E. Nwariaku, Joseph Murphy, et al.. (2002). Mechanisms of Pulmonary Microvascular Dysfunction during Severe Burn Injury. World Journal of Surgery. 26(7). 848–853. 47 indexed citations
14.
Feng, Siyi, Masaya Yamamoto, Helen L. Yin, et al.. (2002). Nonradioactive Analysis of Phosphatidylinositides and Other Anionic Phospholipids by Anion-Exchange High-Performance Liquid Chromatography with Suppressed Conductivity Detection. Analytical Biochemistry. 301(2). 243–254. 120 indexed citations
15.
Wright, Keith, Fiemu E. Nwariaku, Nabil Halaihel, et al.. (2000). Burn-activated neutrophils and tumor necrosis factor-α alter endothelial cell actin cytoskeleton and enhance monolayer permeability. Surgery. 128(2). 259–265. 15 indexed citations
16.
Sun, Hui, Masaya Yamamoto, Marisan Mejillano, & Helen L. Yin. (1999). Gelsolin, a Multifunctional Actin Regulatory Protein. Journal of Biological Chemistry. 274(47). 33179–33182. 483 indexed citations
17.
Baryłko, Barbara, Derk D. Binns, Keng-Mean Lin, et al.. (1998). Synergistic Activation of Dynamin GTPase by Grb2 and Phosphoinositides. Journal of Biological Chemistry. 273(6). 3791–3797. 111 indexed citations
18.
Liu, Yu-Tsueng & Helen L. Yin. (1998). Identification of the Binding Partners for Flightless I, A Novel Protein Bridging the Leucine-rich Repeat and the Gelsolin Superfamilies. Journal of Biological Chemistry. 273(14). 7920–7927. 75 indexed citations
19.
Lin, Keng, et al.. (1997). Gelsolin Binding to Phosphatidylinositol 4,5-Bisphosphate Is Modulated by Calcium and pH. Journal of Biological Chemistry. 272(33). 20443–20450. 67 indexed citations
20.
Yin, Helen L.. (1989). Calcium and Polyphosphoinositide Regulation of Actin Network Structure by Gelsolin. Advances in experimental medicine and biology. 255. 315–323. 6 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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