Yoon S. Chun

3.0k total citations · 1 hit paper
71 papers, 2.3k citations indexed

About

Yoon S. Chun is a scholar working on Surgery, Cancer Research and Molecular Biology. According to data from OpenAlex, Yoon S. Chun has authored 71 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Surgery, 14 papers in Cancer Research and 13 papers in Molecular Biology. Recurrent topics in Yoon S. Chun's work include Breast Implant and Reconstruction (36 papers), Reconstructive Surgery and Microvascular Techniques (35 papers) and Breast Cancer Treatment Studies (13 papers). Yoon S. Chun is often cited by papers focused on Breast Implant and Reconstruction (36 papers), Reconstructive Surgery and Microvascular Techniques (35 papers) and Breast Cancer Treatment Studies (13 papers). Yoon S. Chun collaborates with scholars based in United States, South Korea and China. Yoon S. Chun's co-authors include Stuart R. Lipsitz, Elof Eriksson, Kapil Verma, Heather Rosen, Donald J. Morris, Pardon R. Kenney, Hyunsuk Shim, Brian C. Lewis, Chi V. Dang and Sungkwon Chung and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Yoon S. Chun

71 papers receiving 2.3k citations

Hit Papers

Implant-Based Breast Reconstruction Using Acellular Derma... 2010 2026 2015 2020 2010 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoon S. Chun United States 25 1.4k 491 465 195 179 71 2.3k
Songqing He China 30 325 0.2× 622 1.3× 1.2k 2.6× 141 0.7× 8 0.0× 108 2.4k
Swasti Tiwari India 28 362 0.3× 320 0.7× 1.2k 2.7× 267 1.4× 5 0.0× 97 2.2k
Elisa Petrangeli Italy 27 166 0.1× 276 0.6× 625 1.3× 132 0.7× 5 0.0× 59 1.8k
Miguel Rivera Spain 25 213 0.2× 102 0.2× 580 1.2× 174 0.9× 6 0.0× 90 1.7k
Todd Holscher United States 13 104 0.1× 107 0.2× 319 0.7× 41 0.2× 65 0.4× 15 1.2k
Yuxin Tang China 24 231 0.2× 365 0.7× 670 1.4× 76 0.4× 52 0.3× 117 1.5k
Jennifer L. Gooch United States 28 142 0.1× 262 0.5× 1.2k 2.5× 179 0.9× 3 0.0× 51 2.1k
Helge Bruns Germany 19 565 0.4× 94 0.2× 259 0.6× 96 0.5× 2 0.0× 59 1.4k
Lindsey Kennedy United States 28 637 0.5× 250 0.5× 521 1.1× 262 1.3× 21 0.1× 96 2.2k

Countries citing papers authored by Yoon S. Chun

Since Specialization
Citations

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

Fields of papers citing papers by Yoon S. Chun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yoon S. Chun. 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 Yoon S. Chun. The network helps show where Yoon S. Chun may publish in the future.

Co-authorship network of co-authors of Yoon S. Chun

This figure shows the co-authorship network connecting the top 25 collaborators of Yoon S. Chun. A scholar is included among the top collaborators of Yoon S. Chun 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 Yoon S. Chun. Yoon S. Chun 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.
Chun, Yoon S., Mi‐Yeon Kim, Sun‐Young Lee, et al.. (2022). MEK1/2 inhibition rescues neurodegeneration by TFEB-mediated activation of autophagic lysosomal function in a model of Alzheimer’s Disease. Molecular Psychiatry. 27(11). 4770–4780. 28 indexed citations
2.
Atkins, Katelyn M., Linh Truong, Bhupendra Rawal, et al.. (2019). Effects of Postmastectomy Radiation Therapy on Immediate Tissue Expander and Acellular Dermal Matrix Reconstruction: Results of a Prospective Clinical Trial. Practical Radiation Oncology. 9(5). 338–346. 8 indexed citations
3.
Guo, Hao, Yoon S. Chun, Suzanne B. Coopey, et al.. (2017). Patient experience with breast reconstruction process following bilateral mastectomy in BRCA mutation carriers. The American Journal of Surgery. 214(4). 687–694. 9 indexed citations
4.
Roh, Danny S., et al.. (2017). Technique to Promote Symmetry in 2-Staged Bilateral Breast Reconstruction in the Setting of Unilateral Postmastectomy Radiation. Annals of Plastic Surgery. 78(4). 386–391. 4 indexed citations
5.
Xu, Mary Jue, Srinivas M. Susarla, Wei Jiang, et al.. (2016). Impact of Prior Unilateral Chest Wall Radiotherapy on Outcomes in Bilateral Breast Reconstruction. Plastic & Reconstructive Surgery. 138(4). 575e–580e. 12 indexed citations
6.
Sinha, Indranil, Andrea L. Pusic, Edwin G. Wilkins, et al.. (2016). Late Surgical-Site Infection in Immediate Implant-Based Breast Reconstruction. Plastic & Reconstructive Surgery. 139(1). 20–28. 74 indexed citations
7.
Ricci, Joseph A., Matthew D. Treiser, Ran Tao, et al.. (2016). Predictors of Complications and Comparison of Outcomes Using SurgiMend Fetal Bovine and AlloDerm Human Cadaveric Acellular Dermal Matrices in Implant-Based Breast Reconstruction. Plastic & Reconstructive Surgery. 138(4). 583e–591e. 33 indexed citations
8.
Susarla, Srinivas M., et al.. (2015). Comparison of Clinical Outcomes and Patient Satisfaction in Immediate Single-Stage versus Two-Stage Implant-Based Breast Reconstruction. Plastic & Reconstructive Surgery. 135(1). 1e–8e. 66 indexed citations
9.
Carty, Matthew J., Edward J. Caterson, Stephanie A. Caterson, et al.. (2013). Why We Are Here. Plastic & Reconstructive Surgery. 132(6). 1623–1627. 4 indexed citations
10.
Chun, Yoon S., et al.. (2013). Cholesterol regulates HERG K+channel activation by increasing phospholipase C β1 expression. Channels. 7(4). 275–287. 9 indexed citations
11.
Ganske, Ingrid M., Kapil Verma, Heather Rosen, Elof Eriksson, & Yoon S. Chun. (2013). Minimizing Complications With the Use of Acellular Dermal Matrix for Immediate Implant-Based Breast Reconstruction. Annals of Plastic Surgery. 71(5). 464–470. 58 indexed citations
12.
Hu, Yue‐Yung, Haejin In, Christopher Dodgion, et al.. (2011). Impact of neoadjuvant chemotherapy on breast reconstruction. Cancer. 117(13). 2833–2841. 45 indexed citations
13.
Chun, Yoon S., Yonjung Kim, Sora Shin, et al.. (2011). Modulation of transient receptor potential melastatin related 7 channel by presenilins. Developmental Neurobiology. 72(6). 865–877. 20 indexed citations
15.
Chun, Yoon S., Indranil Sinha, Janet H. Yueh, et al.. (2010). Comparison of Morbidity, Functional Outcome, and Satisfaction following Bilateral TRAM versus Bilateral DIEP Flap Breast Reconstruction. Plastic & Reconstructive Surgery. 126(4). 1133–1141. 61 indexed citations
16.
Chun, Yoon S., Sora Shin, Yonjung Kim, et al.. (2009). Cholesterol modulates ion channels via down‐regulation of phosphatidylinositol 4,5‐bisphosphate. Journal of Neurochemistry. 112(5). 1286–1294. 38 indexed citations
17.
Chun, Yoon S., et al.. (2009). Outcomes and Patient Satisfaction following Breast Reconstruction with Bilateral Pedicled TRAM Flaps in 105 Consecutive Patients. Plastic & Reconstructive Surgery. 125(1). 1–9. 38 indexed citations
18.
Chun, Yoon S. & Amir H. Taghinia. (2009). Hyperprolactinemia and Galactocele Formation After Augmentation Mammoplasty. Annals of Plastic Surgery. 62(2). 122–123. 17 indexed citations
19.
Chun, Yoon S. & Julian J. Pribaz. (2005). A Simple Guide to Inframammary-Fold Reconstruction. Annals of Plastic Surgery. 55(1). 8–11. 16 indexed citations
20.
Chun, Yoon S., Motoyasu Saji, & Martha A. Zeiger. (1998). Overexpression of TTF-1 and PAX-8 restores thyroglobulin gene promoter activity in ARO and WRO cell lines. Surgery. 124(6). 1100–1105. 26 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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