Qian Luo

1.8k total citations
39 papers, 1.4k citations indexed

About

Qian Luo is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Qian Luo has authored 39 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Plant Science and 9 papers in Cancer Research. Recurrent topics in Qian Luo's work include RNA modifications and cancer (10 papers), Cancer-related molecular mechanisms research (9 papers) and Plant Reproductive Biology (6 papers). Qian Luo is often cited by papers focused on RNA modifications and cancer (10 papers), Cancer-related molecular mechanisms research (9 papers) and Plant Reproductive Biology (6 papers). Qian Luo collaborates with scholars based in China, Germany and Australia. Qian Luo's co-authors include Hong‐Quan Yang, Long Wang, Yanchun Zhang, Yan‐Xia Mai, Jianxin Shi, Dabing Zhang, Lukas Schreiber, Shengbo He, Kun‐Peng Jia and Xuedan Lu and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PLANT PHYSIOLOGY and Bioresource Technology.

In The Last Decade

Qian Luo

35 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Qian Luo China 17 879 721 163 106 83 39 1.4k
Xiaoxia Li China 26 888 1.0× 782 1.1× 123 0.8× 39 0.4× 72 0.9× 95 1.7k
Chaonan Li China 25 1.1k 1.2× 571 0.8× 98 0.6× 81 0.8× 138 1.7× 63 1.6k
Sakihito Kitajima Japan 23 842 1.0× 855 1.2× 183 1.1× 85 0.8× 26 0.3× 61 1.6k
Baolong Zhang China 26 1.5k 1.7× 950 1.3× 128 0.8× 58 0.5× 26 0.3× 69 2.4k
Andrea Nolte Germany 11 532 0.6× 228 0.3× 66 0.4× 98 0.9× 74 0.9× 22 922
A. M. Ismail Egypt 18 1.0k 1.2× 438 0.6× 239 1.5× 53 0.5× 78 0.9× 55 1.5k
Guowei Li China 18 1.3k 1.5× 702 1.0× 83 0.5× 57 0.5× 39 0.5× 36 1.7k
Zhiqiang Gao China 19 494 0.6× 261 0.4× 164 1.0× 35 0.3× 50 0.6× 82 1.1k
Zhiqiang Xu China 19 323 0.4× 425 0.6× 70 0.4× 156 1.5× 133 1.6× 79 1.2k

Countries citing papers authored by Qian Luo

Since Specialization
Citations

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

Fields of papers citing papers by Qian Luo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qian Luo

This figure shows the co-authorship network connecting the top 25 collaborators of Qian Luo. A scholar is included among the top collaborators of Qian Luo 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 Qian Luo. Qian Luo 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.
Li, Jie, Qian Luo, Minjie Lu, et al.. (2025). METTL16 Promotes Lipid Metabolic Reprogramming and Colorectal Cancer Progression. International Journal of Biological Sciences. 21(11). 4782–4797.
2.
Luo, Qian, et al.. (2024). Aflatoxin B1 induces ROS‐dependent mitophagy by modulating the PINK1/Parkin pathway in HepG2 cells. Basic & Clinical Pharmacology & Toxicology. 135(2). 195–209. 4 indexed citations
3.
Tan, Qian, Xu Dong Zhang, Qian Luo, et al.. (2024). The RING Domain of Rice HEI10 is Essential for Male, But Not Female Fertility. Rice. 17(1). 3–3. 1 indexed citations
4.
Ding, Jie, Juan Pu, Qian Luo, et al.. (2024). A novel lncRNA LOC101928222 promotes colorectal cancer angiogenesis by stabilizing HMGCS2 mRNA and increasing cholesterol synthesis. Journal of Experimental & Clinical Cancer Research. 43(1). 185–185. 16 indexed citations
5.
6.
Mu, Rong, et al.. (2023). Diagnostic value of FibroTouch in identifying hepatic steatosis in NAFLD with MRI‐PDFF as the reference standard. Journal of Digestive Diseases. 24(12). 691–701.
7.
Luo, Qian, et al.. (2023). Pan-cancer analysis of PCAT6 and its effect on oesophageal squamous cell carcinoma cell proliferation and migration. Medical Oncology. 40(4). 125–125. 3 indexed citations
8.
Chen, Xuyu, et al.. (2022). LINC00467: an oncogenic long noncoding RNA. Cancer Cell International. 22(1). 303–303. 5 indexed citations
9.
Liu, Yang, Mingyang Yu, Qian Luo, et al.. (2022). A novel LUAD prognosis prediction model based on immune checkpoint-related lncRNAs. Frontiers in Genetics. 13. 1016449–1016449. 2 indexed citations
10.
Luo, Qian, et al.. (2022). WTAP promotes oesophageal squamous cell carcinoma development by decreasing CPSF4 expression in an m6A-dependent manner. Medical Oncology. 39(12). 231–231. 6 indexed citations
11.
Xu, Shaoqing, Xiaodong Yang, Yiwei Qian, et al.. (2021). Analysis of serum levels of organochlorine pesticides and related factors in Parkinson’s disease. NeuroToxicology. 88. 216–223. 14 indexed citations
12.
13.
Zafar, Syed Adeel, S. B. Patil, Muhammad Uzair, et al.. (2019). DEGENERATED PANICLE AND PARTIAL STERILITY 1 (DPS1) encodes a cystathionine β‐synthase domain containing protein required for anther cuticle and panicle development in rice. New Phytologist. 225(1). 356–375. 80 indexed citations
14.
Chen, Huiqiong, Zhiguo Zhang, Erdong Ni, et al.. (2019). HMS1 interacts with HMS1I to regulate very‐long‐chain fatty acid biosynthesis and the humidity‐sensitive genic male sterility in rice (Oryza sativa). New Phytologist. 225(5). 2077–2093. 41 indexed citations
15.
Hu, Chaoyang, Quan‐Lin Li, Sheng Quan, et al.. (2016). Characterization of factors underlying the metabolic shifts in developing kernels of colored maize. Scientific Reports. 6(1). 35479–35479. 26 indexed citations
16.
Zhao, Guochao, Jianxin Shi, Wanqi Liang, et al.. (2015). Two ATP Binding Cassette G (ABCG) Transporters, OsABCG26 and OsABCG15, Collaboratively Regulate Rice Male Reproduction. PLANT PHYSIOLOGY. 169(3). pp.00262.2015–pp.00262.2015. 81 indexed citations
17.
Cai, Wenjuan, Weihua Huang, Xin Zhou, et al.. (2014). Arabidopsis miR171-Targeted Scarecrow-Like Proteins Bind to GT cis-Elements and Mediate Gibberellin-Regulated Chlorophyll Biosynthesis under Light Conditions. PLoS Genetics. 10(8). e1004519–e1004519. 159 indexed citations
18.
Luo, Qian, et al.. (2013). Effect of 6-BA on the Plant Regeneration via Organogenesis from Cotyledonary Node of Cowpea (Vigna unguiculata L. Walp). Journal of Agricultural Science. 5(5). 5 indexed citations
19.
Tao, Fei, Yanhua Liu, Qian Luo, et al.. (2011). Novel organic solvent-responsive expression vectors for biocatalysis: Application for development of an organic solvent-tolerant biodesulfurizing strain. Bioresource Technology. 102(20). 9380–9387. 23 indexed citations
20.
Wang, Long, Yan‐Xia Mai, Yanchun Zhang, Qian Luo, & Hong‐Quan Yang. (2010). MicroRNA171c-Targeted SCL6-II, SCL6-III, and SCL6-IV Genes Regulate Shoot Branching in Arabidopsis. Molecular Plant. 3(5). 794–806. 209 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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