Ying Su

2.2k total citations · 1 hit paper
24 papers, 1.4k citations indexed

About

Ying Su is a scholar working on Oncology, Molecular Biology and Genetics. According to data from OpenAlex, Ying Su has authored 24 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Oncology, 7 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Ying Su's work include Cancer Cells and Metastasis (5 papers), Phytoestrogen effects and research (4 papers) and Estrogen and related hormone effects (4 papers). Ying Su is often cited by papers focused on Cancer Cells and Metastasis (5 papers), Phytoestrogen effects and research (4 papers) and Estrogen and related hormone effects (4 papers). Ying Su collaborates with scholars based in China, United States and Australia. Ying Su's co-authors include Kornélia Polyák, Mary W. Brooks, Brian Bierie, Christine L. Chaffer, Lisa M. Arendt, Alicia J. Kaestli, Paul A. Wiggins, Charlotte Kuperwasser, Leonardo O. Rodrigues and Christina Scheel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer Research and Journal of Nutrition.

In The Last Decade

Ying Su

24 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state

2011 897 citations Christine L. Chaffer, Christina Scheel et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ying Su China	14	816	743	406	136	132	24	1.4k
Fiona Furlong Ireland	18	326 0.4×	887 1.2×	369 0.9×	67 0.5×	100 0.8×	34	1.3k
Katsuhide Yoshidome Japan	16	580 0.7×	610 0.8×	271 0.7×	160 1.2×	135 1.0×	61	1.3k
Letícia Batista Azevedo Rangel Brazil	14	284 0.3×	568 0.8×	280 0.7×	111 0.8×	106 0.8×	39	1.1k
Xian Lin China	23	476 0.6×	1.2k 1.7×	637 1.6×	60 0.4×	181 1.4×	63	1.7k
Xiangbing Meng United States	24	439 0.5×	912 1.2×	225 0.6×	152 1.1×	120 0.9×	58	1.3k
Yu-Mei Feng China	21	466 0.6×	847 1.1×	383 0.9×	83 0.6×	146 1.1×	41	1.3k
Noa Rivlin Israel	14	719 0.9×	982 1.3×	459 1.1×	86 0.6×	133 1.0×	15	1.6k
Géraldine Gentric France	13	752 0.9×	951 1.3×	602 1.5×	76 0.6×	180 1.4×	17	1.8k
Xiao-Feng Le United States	21	462 0.6×	910 1.2×	274 0.7×	105 0.8×	92 0.7×	23	1.3k
Nancy Klauber United States	6	403 0.5×	854 1.1×	293 0.7×	196 1.4×	124 0.9×	6	1.5k

Countries citing papers authored by Ying Su

Since Specialization

Citations

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

Fields of papers citing papers by Ying Su

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ying Su. 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 Ying Su. The network helps show where Ying Su may publish in the future.

Co-authorship network of co-authors of Ying Su

This figure shows the co-authorship network connecting the top 25 collaborators of Ying Su. A scholar is included among the top collaborators of Ying Su 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 Ying Su. Ying Su is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hao, Guang‐wei, Kai Liu, Yan Xue, et al.. (2024). Remifentanil vs. dexmedetomidine for cardiac surgery patients with noninvasive ventilation intolerance: a multicenter randomized controlled trial. Journal of Intensive Care. 12(1). 35–35. 2 indexed citations

Su, Ying, et al.. (2023). Assessment of iris volume in glaucoma patients with type 2 diabetes mellitus by AS-OCT. International Journal of Ophthalmology. 16(5). 743–747. 4 indexed citations

Wang, Huan, Qinyu Zhao, Jing‐chao Luo, et al.. (2022). Early prediction of noninvasive ventilation failure after extubation: development and validation of a machine-learning model. BMC Pulmonary Medicine. 22(1). 304–304. 13 indexed citations

Qin, Mengting, et al.. (2022). Corrigendum to “Global cognitive effects of second-generation antidepressants in patients with Alzheimer's disease: A systematic review and meta-analysis of randomized controlled trials” [J. Psychiatr. Res. 155 (2022) 371–379]. Journal of Psychiatric Research. 156. 44–44. 1 indexed citations

Wang, Qiang, Zhiyong He, Ying Su, et al.. (2020). <p>LHX6 Affects Erlotinib Resistance and Migration of <em>EGFR</em>-Mutant Non-Small-Cell Lung Cancer HCC827 Cells Through Suppressing Wnt/β-Catenin Signaling</p>. OncoTargets and Therapy. Volume 13. 10983–10994. 16 indexed citations

He, Zhiyong, Qiang Wang, Ying Su, et al.. (2020). Spred-3 mutation and Ras/Raf/MAPK activation confer acquired resistance to EGFR tyrosine kinase inhibitor in an EGFR mutated NSCLC cell line. Translational Cancer Research. 9(4). 2542–2555. 6 indexed citations

Peluffo, Guillermo, Ashim Subedee, Nicholas W. Harper, et al.. (2019). EN1 Is a Transcriptional Dependency in Triple-Negative Breast Cancer Associated with Brain Metastasis. Cancer Research. 79(16). 4173–4183. 47 indexed citations

Martin, Lainie P., Jason Konner, Kathleen N. Moore, et al.. (2017). Characterization of folate receptor alpha (FRα) expression in archival tumor and biopsy samples from relapsed epithelial ovarian cancer patients: A phase I expansion study of the FRα-targeting antibody-drug conjugate mirvetuximab soravtansine. Gynecologic Oncology. 147(2). 402–407. 104 indexed citations

Cao, Shuyan, Leping Ye, Ying Wu, et al.. (2017). The Effects of Fungicides on Human 3β-Hydroxysteroid Dehydrogenase 1 and Aromatase in Human Placental Cell Line JEG-3. Pharmacology. 100(3-4). 139–147. 33 indexed citations

10.

Mao, Baiping, Senlin Li, Jianpeng Liu, et al.. (2016). Structure-activity relationships of phthalates in inhibition of human placental 3β-hydroxysteroid dehydrogenase 1 and aromatase. Reproductive Toxicology. 61. 151–161. 46 indexed citations

11.

Jin, Kideok, Sunju Park, Wei Wen Teo, et al.. (2015). HOXB7 Is an ERα Cofactor in the Activation of HER2 and Multiple ER Target Genes Leading to Endocrine Resistance. Cancer Discovery. 5(9). 944–959. 67 indexed citations

12.

Dong, Yaoyao, Baiping Mao, Linxi Li, et al.. (2015). Gossypol enantiomers potently inhibit human placental 3β-hydroxysteroid dehydrogenase 1 and aromatase activities. Fitoterapia. 109. 132–137. 15 indexed citations

13.

Li, Jiancheng, Di Liu, Yan Yang, et al.. (2013). Growth, Clonability, and Radiation Resistance of Esophageal Carcinoma-derived Stem-like Cells. Asian Pacific Journal of Cancer Prevention. 14(8). 4891–4896. 5 indexed citations

14.

Pabona, John Mark P., Bhuvanesh Dave, Ying Su, et al.. (2012). The soybean peptide lunasin promotes apoptosis of mammary epithelial cells via induction of tumor suppressor PTEN: similarities and distinct actions from soy isoflavone genistein. Genes & Nutrition. 8(1). 79–90. 42 indexed citations

15.

Su, Ying, Kartik Shankar, Omar Rahal, & Rosalia C.M. Simmen. (2011). Bidirectional signaling of mammary epithelium and stroma: implications for breast cancer—preventive actions of dietary factors. The Journal of Nutritional Biochemistry. 22(7). 605–611. 11 indexed citations

16.

Chaffer, Christine L., Christina Scheel, Alicia J. Kaestli, et al.. (2011). Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state. Proceedings of the National Academy of Sciences. 108(19). 7950–7955. 897 indexed citations breakdown →

17.

Dave, Bhuvanesh, Rebecca Wynne, Ying Su, et al.. (2010). Enhanced Mammary Progesterone Receptor-A Isoform Activity in the Promotion of Mammary Tumor Progression by Dietary Soy in Rats. Nutrition and Cancer. 62(6). 774–782. 6 indexed citations

18.

Su, Ying, Kartik Shankar, & Rosalia C.M. Simmen. (2009). Early Soy Exposure via Maternal Diet Regulates Rat Mammary Epithelial Differentiation by Paracrine Signaling from Stromal Adipocytes. Journal of Nutrition. 139(5). 945–951. 23 indexed citations

19.

Wang, Jianming, et al.. (2007). [Expression and significance of aPKC-iota and E-cadherin in cholangiocarcinoma].. PubMed. 26(7). 715–8. 2 indexed citations

20.

Su, Ying, Renea R. Eason, Yan Geng, et al.. (2006). In utero exposure to maternal diets containing soy protein isolate, but not genistein alone, protects young adult rat offspring from NMU-induced mammary tumorigenesis. Carcinogenesis. 28(5). 1046–1051. 32 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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