Chang‐Lung Lee

2.0k total citations
42 papers, 1.0k citations indexed

About

Chang‐Lung Lee is a scholar working on Oncology, Radiology, Nuclear Medicine and Imaging and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Chang‐Lung Lee has authored 42 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Oncology, 16 papers in Radiology, Nuclear Medicine and Imaging and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Chang‐Lung Lee's work include Cancer-related Molecular Pathways (12 papers), Effects of Radiation Exposure (12 papers) and Cancer Cells and Metastasis (8 papers). Chang‐Lung Lee is often cited by papers focused on Cancer-related Molecular Pathways (12 papers), Effects of Radiation Exposure (12 papers) and Cancer Cells and Metastasis (8 papers). Chang‐Lung Lee collaborates with scholars based in United States, South Korea and Canada. Chang‐Lung Lee's co-authors include David G. Kirsch, Yan Ma, Everett J. Moding, Jordan M. Blum, Katherine D. Castle, Lixia Luo, Yongbaek Kim, Jei‐Fu Shaw, Chien‐Chih Yang and Po-Hsuan Chen and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and PLoS ONE.

In The Last Decade

Chang‐Lung Lee

40 papers receiving 987 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chang‐Lung Lee United States 20 411 276 268 255 223 42 1.0k
Seung Ah Choi South Korea 19 549 1.3× 148 0.5× 63 0.2× 81 0.3× 196 0.9× 52 957
David F. Meoli United States 14 586 1.4× 110 0.4× 190 0.7× 231 0.9× 115 0.5× 19 1.1k
Suhn K. Rhie United States 19 909 2.2× 184 0.7× 90 0.3× 226 0.9× 352 1.6× 41 1.3k
Julia Huber Austria 17 377 0.9× 362 1.3× 76 0.3× 71 0.3× 154 0.7× 31 1.1k
Kyoko Arai Japan 18 595 1.4× 250 0.9× 113 0.4× 188 0.7× 112 0.5× 53 1.0k
Callie A.S. Corsa United States 11 790 1.9× 393 1.4× 52 0.2× 81 0.3× 204 0.9× 12 1.4k
Julia Gilhodes France 19 513 1.2× 459 1.7× 78 0.3× 170 0.7× 218 1.0× 38 1.2k
Chenghua Luo China 15 283 0.7× 118 0.4× 55 0.2× 96 0.4× 84 0.4× 59 749
Ciara Metcalfe United States 14 1.1k 2.6× 588 2.1× 108 0.4× 196 0.8× 197 0.9× 33 1.6k
Ichidai Tanaka Japan 14 421 1.0× 310 1.1× 58 0.2× 218 0.9× 175 0.8× 42 899

Countries citing papers authored by Chang‐Lung Lee

Since Specialization
Citations

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

Fields of papers citing papers by Chang‐Lung Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chang‐Lung Lee. 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 Chang‐Lung Lee. The network helps show where Chang‐Lung Lee may publish in the future.

Co-authorship network of co-authors of Chang‐Lung Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Chang‐Lung Lee. A scholar is included among the top collaborators of Chang‐Lung Lee 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 Chang‐Lung Lee. Chang‐Lung Lee 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.
2.
Nead, Kevin T., Tae‐Beom Kim, Jing Zhao, et al.. (2024). Impact of cancer therapy on clonal hematopoiesis mutations and subsequent clinical outcomes. Blood Advances. 8(19). 5215–5224. 9 indexed citations
3.
Morral, Clara, Arshad Ayyaz, Hsuan-Cheng Kuo, et al.. (2024). p53 promotes revival stem cells in the regenerating intestine after severe radiation injury. Nature Communications. 15(1). 3018–3018. 22 indexed citations
4.
Daniel, Andrea R., Chang Su, Nerissa T. Williams, et al.. (2023). Temporary Knockdown of p53 During Focal Limb Irradiation Increases the Development of Sarcomas. Cancer Research Communications. 3(12). 2455–2467.
5.
6.
Kam, Angel Y.F., Chang‐Lung Lee, David A. Rizzieri, et al.. (2021). Selective ERBB2 and BCL2 Inhibition Is Synergistic for Mitochondrial-Mediated Apoptosis in MDS and AML Cells. Molecular Cancer Research. 19(5). 886–899. 4 indexed citations
7.
Lee, Chang‐Lung, Andrea R. Daniel, Matt Holbrook, et al.. (2021). Characterization of cardiovascular injury in mice following partial-heart irradiation with clinically relevant dose and fractionation. Radiotherapy and Oncology. 157. 155–162. 12 indexed citations
8.
Lee, Chang‐Lung, Dadong Zhang, Alexander B. Sibley, et al.. (2021). Whole-Exome Sequencing of Radiation-Induced Thymic Lymphoma in Mouse Models Identifies Notch1 Activation as a Driver of p53 Wild-Type Lymphoma. Cancer Research. 81(14). 3777–3790. 12 indexed citations
9.
Lee, Chang‐Lung, Yvonne M. Mowery, Andrea R. Daniel, et al.. (2019). Mutational landscape in genetically engineered, carcinogen-induced, and radiation-induced mouse sarcoma. JCI Insight. 4(13). 37 indexed citations
10.
Torok, Jordan A., Katherine D. Castle, Yan Ma, et al.. (2018). Deletion of Atm in Tumor but not Endothelial Cells Improves Radiation Response in a Primary Mouse Model of Lung Adenocarcinoma. Cancer Research. 79(4). 773–782. 25 indexed citations
11.
Cheung, Phyllis F., Sven‐Thorsten Liffers, Kristina Althoff, et al.. (2018). Notch-Induced Myeloid Reprogramming in Spontaneous Pancreatic Ductal Adenocarcinoma by Dual Genetic Targeting. Cancer Research. 78(17). 4997–5010. 8 indexed citations
12.
Wisdom, Amy J., Katherine D. Castle, Yvonne M. Mowery, et al.. (2018). Characterizing the Potency and Impact of Carbon Ion Therapy in a Primary Mouse Model of Soft Tissue Sarcoma. Molecular Cancer Therapeutics. 17(4). 858–868. 23 indexed citations
13.
Lee, Chang‐Lung, Eric S. Xu, Yan Ma, et al.. (2018). Blocking Cyclin-Dependent Kinase 4/6 During Single Dose Versus Fractionated Radiation Therapy Leads to Opposite Effects on Acute Gastrointestinal Toxicity in Mice. International Journal of Radiation Oncology*Biology*Physics. 102(5). 1569–1576. 32 indexed citations
14.
Dodd, Rebecca D., Chang‐Lung Lee, Wesley Huang, et al.. (2017). NF1+/− Hematopoietic Cells Accelerate Malignant Peripheral Nerve Sheath Tumor Development without Altering Chemotherapy Response. Cancer Research. 77(16). 4486–4497. 21 indexed citations
15.
Moding, Everett J., Hooney Min, Katherine D. Castle, et al.. (2016). An extra copy of p53 suppresses development of spontaneous Kras-driven but not radiation-induced cancer. JCI Insight. 1(10). 14 indexed citations
16.
Lee, Chang‐Lung, Katherine D. Castle, Everett J. Moding, et al.. (2015). Acute DNA damage activates the tumour suppressor p53 to promote radiation-induced lymphoma. Nature Communications. 6(1). 8477–8477. 36 indexed citations
17.
Clark, Darin P., Chang‐Lung Lee, David G. Kirsch, & Cristian T. Badea. (2015). Spectrotemporal CT data acquisition and reconstruction at low dose. Medical Physics. 42(11). 6317–6336. 20 indexed citations
18.
Sachdeva, Mohit, Jeffrey K. Mito, Chang‐Lung Lee, et al.. (2014). MicroRNA-182 drives metastasis of primary sarcomas by targeting multiple genes. Journal of Clinical Investigation. 124(10). 4305–4319. 84 indexed citations
19.
Lee, Chang‐Lung, William Lento, Katherine D. Castle, Nelson J. Chao, & David G. Kirsch. (2014). Inhibiting Glycogen Synthase Kinase-3 Mitigates the Hematopoietic Acute Radiation Syndrome in Mice. Radiation Research. 181(5). 445–451. 11 indexed citations
20.
Sullivan, Julie M., et al.. (2012). p21 Protects “Super p53” Mice from the Radiation-Induced Gastrointestinal Syndrome. Radiation Research. 177(3). 307–310. 19 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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