Noélia Che

606 total citations
10 papers, 424 citations indexed

About

Noélia Che is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Noélia Che has authored 10 papers receiving a total of 424 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Cancer Research and 2 papers in Oncology. Recurrent topics in Noélia Che's work include Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (3 papers) and Acute Myeloid Leukemia Research (2 papers). Noélia Che is often cited by papers focused on Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (3 papers) and Acute Myeloid Leukemia Research (2 papers). Noélia Che collaborates with scholars based in China, Hong Kong and United Kingdom. Noélia Che's co-authors include Stephanie Ma, Tin Lok Wong, Terence K. Lee, Man Tong, Lei Zhou, Kwan Man, Chung Mau Lo, Jin Ding, Esw Ngan and Kel Vin Tan and has published in prestigious journals such as Hepatology, Cancer Research and Gut.

In The Last Decade

Noélia Che

10 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Noélia Che China 7 282 167 103 82 58 10 424
Kai‐Yu Ng Hong Kong 9 402 1.4× 235 1.4× 130 1.3× 59 0.7× 46 0.8× 11 542
Yuquan Tao China 11 313 1.1× 230 1.4× 98 1.0× 49 0.6× 48 0.8× 14 524
Suk Mei Wang Singapore 6 223 0.8× 133 0.8× 105 1.0× 60 0.7× 46 0.8× 6 403
Marco Seehawer United States 6 242 0.9× 152 0.9× 144 1.4× 70 0.9× 97 1.7× 8 512
Manqing Cao China 11 421 1.5× 309 1.9× 125 1.2× 50 0.6× 40 0.7× 17 601
Mitsuhiro Hishida Japan 12 309 1.1× 152 0.9× 91 0.9× 65 0.8× 40 0.7× 23 484
Shinji Oie Japan 12 315 1.1× 88 0.5× 140 1.4× 48 0.6× 44 0.8× 22 515
Jiongqiang Huang China 10 272 1.0× 153 0.9× 116 1.1× 54 0.7× 28 0.5× 15 425
Jiawen Tian China 7 171 0.6× 87 0.5× 91 0.9× 64 0.8× 33 0.6× 10 315
Jason T. Godfrey United States 4 224 0.8× 100 0.6× 153 1.5× 53 0.6× 40 0.7× 5 404

Countries citing papers authored by Noélia Che

Since Specialization
Citations

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

Fields of papers citing papers by Noélia Che

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Noélia Che

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

All Works

10 of 10 papers shown
1.
Cantilena, Sandra, et al.. (2024). Synergistic Strategies for KMT2A-Rearranged Leukemias: Beyond Menin Inhibitor. Cancers. 16(23). 4017–4017. 2 indexed citations
2.
Gasparoli, Luca, Clémence Virely, Noélia Che, et al.. (2023). Susceptibility of pediatric acute lymphoblastic leukemia to STAT3 inhibition depends on p53 induction. Haematologica. 109(4). 1069–1081. 2 indexed citations
3.
Tong, Man, Tin Lok Wong, Hongzhi Zhao, et al.. (2021). Loss of tyrosine catabolic enzyme HPD promotes glutamine anaplerosis through mTOR signaling in liver cancer. Cell Reports. 36(8). 109617–109617. 27 indexed citations
5.
Che, Noélia, Kai‐Yu Ng, Tin Lok Wong, et al.. (2020). PRMT6 deficiency induces autophagy in hostile microenvironments of hepatocellular carcinoma tumors by regulating BAG5-associated HSC70 stability. Cancer Letters. 501. 247–262. 23 indexed citations
6.
Leung, Carmen Oi Ning, Man Tong, Noélia Che, et al.. (2019). Overriding Adaptive Resistance to Sorafenib Through Combination Therapy With Src Homology 2 Domain–Containing Phosphatase 2 Blockade in Hepatocellular Carcinoma. Hepatology. 72(1). 155–168. 73 indexed citations
7.
Wong, Tin Lok, Kai‐Yu Ng, Kel Vin Tan, et al.. (2019). CRAF Methylation by PRMT6 Regulates Aerobic Glycolysis–Driven Hepatocarcinogenesis via ERK‐Dependent PKM2 Nuclear Relocalization and Activation. Hepatology. 71(4). 1279–1296. 91 indexed citations
8.
Tong, Man, Noélia Che, Lei Zhou, et al.. (2018). Efficacy of annexin A3 blockade in sensitizing hepatocellular carcinoma to sorafenib and regorafenib. Journal of Hepatology. 69(4). 826–839. 99 indexed citations
9.
Tong, Man, Tin Lok Wong, Noélia Che, et al.. (2018). Abstract 1432: Deranged tyrosine metabolism drives tumorigenesis in liver cancer. Cancer Research. 78(13_Supplement). 1432–1432. 1 indexed citations
10.
Wong, Tin Lok, Noélia Che, & Stephanie Ma. (2017). Reprogramming of central carbon metabolism in cancer stem cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(7). 1728–1738. 64 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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