Lian‐He Yang

948 total citations
41 papers, 673 citations indexed

About

Lian‐He Yang is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lian‐He Yang has authored 41 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Oncology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lian‐He Yang's work include Wnt/β-catenin signaling in development and cancer (15 papers), Cancer-related gene regulation (14 papers) and Viral-associated cancers and disorders (4 papers). Lian‐He Yang is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (15 papers), Cancer-related gene regulation (14 papers) and Viral-associated cancers and disorders (4 papers). Lian‐He Yang collaborates with scholars based in China, United States and Sweden. Lian‐He Yang's co-authors include Enhua Wang, Hong‐Tao Xu, Yuan Miao, Yang Han, Guiyang Jiang, Shun‐Dong Dai, Chuifeng Fan, Xuyong Lin, Juan‐Han Yu and Liang Wang and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and International Journal of Radiation Oncology*Biology*Physics.

In The Last Decade

Lian‐He Yang

41 papers receiving 662 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lian‐He Yang China 16 383 148 147 107 82 41 673
Jan Sun United States 8 317 0.8× 142 1.0× 171 1.2× 83 0.8× 89 1.1× 12 620
Luca Ventura Italy 16 378 1.0× 142 1.0× 239 1.6× 132 1.2× 102 1.2× 59 735
Hyoun Wook Lee South Korea 16 281 0.7× 117 0.8× 196 1.3× 130 1.2× 95 1.2× 57 631
Alissa Minkovsky United States 6 258 0.7× 112 0.8× 123 0.8× 114 1.1× 61 0.7× 7 542
Angela Queisser Germany 15 240 0.6× 114 0.8× 180 1.2× 96 0.9× 186 2.3× 18 603
Erna Raja Japan 13 476 1.2× 65 0.4× 154 1.0× 111 1.0× 41 0.5× 17 628
Shariq S. Khwaja United States 11 306 0.8× 98 0.7× 342 2.3× 180 1.7× 140 1.7× 24 671
Lucia Nappi Canada 13 405 1.1× 240 1.6× 153 1.0× 186 1.7× 191 2.3× 78 734
Juqun Shen United States 11 527 1.4× 134 0.9× 175 1.2× 66 0.6× 66 0.8× 11 814
Yoshinori Kodama Japan 14 221 0.6× 150 1.0× 190 1.3× 109 1.0× 60 0.7× 51 681

Countries citing papers authored by Lian‐He Yang

Since Specialization
Citations

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

Fields of papers citing papers by Lian‐He Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lian‐He Yang. 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 Lian‐He Yang. The network helps show where Lian‐He Yang may publish in the future.

Co-authorship network of co-authors of Lian‐He Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Lian‐He Yang. A scholar is included among the top collaborators of Lian‐He Yang 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 Lian‐He Yang. Lian‐He Yang 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.
Ding, Jinli, Yunyun Duan, Zhizheng Zhuo, et al.. (2021). Acceleration of Brain TOF-MRA with Compressed Sensitivity Encoding: A Multicenter Clinical Study. American Journal of Neuroradiology. 42(7). 1208–1215. 16 indexed citations
2.
3.
Ma, Shuang, Rachel Jug, Shuai Shen, et al.. (2018). Marginal zone lymphoma of palatine tonsil with prominent plasmacytic differentiation. Medicine. 97(2). e9648–e9648. 4 indexed citations
4.
Li, Xin, Jianping Zhou, Ming Dong, & Lian‐He Yang. (2018). Management and prognosis of low-grade appendiceal mucinous neoplasms: A clinicopathologic analysis of 50 cases. European Journal of Surgical Oncology. 44(10). 1640–1645. 30 indexed citations
5.
Zhang, Wanlin, Shuang Ma, Rachel Jug, et al.. (2018). Primary testicular natural killer/T-cell lymphoma. Medicine. 97(12). e0181–e0181. 3 indexed citations
6.
Ma, Shuang, Xuefeng Zhang, Wanlin Zhang, et al.. (2018). Primary central nervous system histiocytic sarcoma. Medicine. 97(26). e11271–e11271. 10 indexed citations
7.
Ma, Shuang, et al.. (2018). X-ray irradiation induced Disabled-2 gene promoter de-methylation enhances radiosensitivity of non-small-cell lung carcinoma cells. Journal of Experimental & Clinical Cancer Research. 37(1). 315–315. 8 indexed citations
8.
Zhang, Wanlin, Shuang Ma, Lin Cai, et al.. (2017). Primary thyroid-like low-grade nasopharyngeal papillary adenocarcinoma. Medicine. 96(47). e8851–e8851. 15 indexed citations
9.
Yu, Juan‐Han, Lian‐He Yang, Xuyong Lin, et al.. (2015). Neurocytoma arising from a mature ovary teratoma: a case report. Diagnostic Pathology. 10(1). 171–171. 2 indexed citations
10.
Xie, Chengyao, Guiyang Jiang, Chuifeng Fan, et al.. (2014). ARMC8α promotes proliferation and invasion of non-small cell lung cancer cells by activating the canonical Wnt signaling pathway. Tumor Biology. 35(9). 8903–8911. 28 indexed citations
11.
Xie, Xuemei, Ziyin Zhang, Lian‐He Yang, et al.. (2013). Aberrant hypermethylation and reduced expression of disabled-2 promote the development of lung cancers. International Journal of Oncology. 43(5). 1636–1642. 24 indexed citations
12.
Yang, Lian‐He, Yang Han, Guang Li, et al.. (2013). Axin gene methylation status correlates with radiosensitivity of lung cancer cells. BMC Cancer. 13(1). 368–368. 14 indexed citations
13.
Jiang, Guiyang, Chuifeng Fan, Xiupeng Zhang, et al.. (2013). Ascertaining an Appropriate Diagnostic Algorithm Using EGFR Mutation-Specific Antibodies to Detect EGFR Status in Non-Small-Cell Lung Cancer. PLoS ONE. 8(3). e59183–e59183. 25 indexed citations
14.
Yang, Lian‐He, Hong‐Tao Xu, Qingchang Li, et al.. (2012). Abnormal hypermethylation and clinicopathological significance of Axin gene in lung cancer. Tumor Biology. 34(2). 749–757. 16 indexed citations
15.
Han, Yang, Yong Zhang, Lian‐He Yang, et al.. (2012). X-radiation inhibits histone deacetylase 1 and 2, upregulates Axin expression and induces apoptosis in non-small cell lung cancer. Radiation Oncology. 7(1). 183–183. 16 indexed citations
16.
Miao, Yuan, Ailin Li, Liang Wang, et al.. (2012). Overexpression of NEDD9 is Associated with Altered Expression of E-Cadherin, β-Catenin and N-Cadherin and Predictive of Poor Prognosis in non-Small Cell Lung Cancer. Pathology & Oncology Research. 19(2). 281–286. 41 indexed citations
17.
Yang, Lian‐He, Hong‐Tao Xu, Yang Han, et al.. (2010). Axin downregulates TCF-4 transcription via β-catenin, but not p53, and inhibits the proliferation and invasion of lung cancer cells. Molecular Cancer. 9(1). 25–25. 33 indexed citations
18.
Han, Yang, Yan Wang, Hong‐Tao Xu, et al.. (2009). X-Radiation Induces Non-Small-Cell Lung Cancer Apoptosis by Upregulation of Axin Expression. International Journal of Radiation Oncology*Biology*Physics. 75(2). 518–526. 22 indexed citations
19.
Liu, Yang, Yan Wang, Yuan Miao, et al.. (2009). Abnormal expression of p120-catenin, E-cadherin, and small GTPases is significantly associated with malignant phenotype of human lung cancer. Lung Cancer. 63(3). 375–382. 87 indexed citations
20.
Xu, Hong‐Tao, Qiang Wei, Yang Liu, et al.. (2007). Overexpression of Axin Downregulates TCF-4 and Inhibits the Development of Lung Cancer. Annals of Surgical Oncology. 14(11). 3251–3259. 39 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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