Hsueh‐Ning Liu

1.1k total citations
16 papers, 891 citations indexed

About

Hsueh‐Ning Liu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Developmental Neuroscience. According to data from OpenAlex, Hsueh‐Ning Liu has authored 16 papers receiving a total of 891 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Developmental Neuroscience. Recurrent topics in Hsueh‐Ning Liu's work include Neuroscience and Neuropharmacology Research (6 papers), Neurogenesis and neuroplasticity mechanisms (4 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Hsueh‐Ning Liu is often cited by papers focused on Neuroscience and Neuropharmacology Research (6 papers), Neurogenesis and neuroplasticity mechanisms (4 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Hsueh‐Ning Liu collaborates with scholars based in Canada, United States and Spain. Hsueh‐Ning Liu's co-authors include Guillermina Almazán, Janice Robertson, Lorne Zinman, Ekaterina Rogaeva, Walter E. Mushynski, Juan M. Bilbao, Daniel Larocque, Sylvain Chemtob, André Galarneau and Eduardo Molina‐Holgado and has published in prestigious journals such as Nature Neuroscience, Annals of Neurology and Free Radical Biology and Medicine.

In The Last Decade

Hsueh‐Ning Liu

16 papers receiving 872 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hsueh‐Ning Liu Canada 15 420 234 207 176 159 16 891
Gye Sun Jeon South Korea 18 506 1.2× 250 1.1× 241 1.2× 69 0.4× 129 0.8× 47 891
Merja Jaronen Finland 14 246 0.6× 180 0.8× 123 0.6× 61 0.3× 249 1.6× 17 834
Tomoko Tashiro Japan 20 497 1.2× 81 0.3× 395 1.9× 79 0.4× 77 0.5× 62 1.1k
Laura A. Pasquini Argentina 21 638 1.5× 84 0.4× 175 0.8× 255 1.4× 386 2.4× 41 1.3k
Mia Emgård Sweden 17 454 1.1× 117 0.5× 490 2.4× 274 1.6× 61 0.4× 20 874
Hitoshi Nagara Japan 21 491 1.2× 103 0.4× 172 0.8× 100 0.6× 197 1.2× 52 992
Sa Sun Cho South Korea 19 424 1.0× 56 0.2× 278 1.3× 119 0.7× 198 1.2× 57 871
Hisae Sumi Japan 11 311 0.7× 289 1.2× 142 0.7× 24 0.1× 159 1.0× 15 707
Morgan G. Stykel Canada 12 306 0.7× 182 0.8× 284 1.4× 140 0.8× 88 0.6× 21 690
Yimin Yuan China 18 328 0.8× 61 0.3× 415 2.0× 356 2.0× 257 1.6× 32 993

Countries citing papers authored by Hsueh‐Ning Liu

Since Specialization
Citations

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

Fields of papers citing papers by Hsueh‐Ning Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hsueh‐Ning Liu. 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 Hsueh‐Ning Liu. The network helps show where Hsueh‐Ning Liu may publish in the future.

Co-authorship network of co-authors of Hsueh‐Ning Liu

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

All Works

16 of 16 papers shown
1.
Hossain, Shireen, Hsueh‐Ning Liu, Gabriela Fragoso, & Guillermina Almazán. (2014). Agonist-induced down-regulation of AMPA receptors in oligodendrocyte progenitors. Neuropharmacology. 79. 506–514. 12 indexed citations
2.
McLean, Jesse R., Hsueh‐Ning Liu, Yuan Cheng Weng, et al.. (2010). Distinct biochemical signatures characterize peripherin isoform expression in both traumatic neuronal injury and motor neuron disease. Journal of Neurochemistry. 114(4). 1177–1192. 17 indexed citations
3.
Liu, Hsueh‐Ning, Sidney Croul, Juan M. Bilbao, et al.. (2010). Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form. Acta Neuropathologica. 119(3). 335–344. 163 indexed citations
4.
Hossain, Shireen, et al.. (2009). Cadmium exposure induces mitochondria-dependent apoptosis in oligodendrocytes. NeuroToxicology. 30(4). 544–554. 55 indexed citations
5.
Silvertown, Josh D., Anton Neschadim, Hsueh‐Ning Liu, et al.. (2009). Relaxin-3 and receptors in the human and rhesus brain and reproductive tissues. Regulatory Peptides. 159(1-3). 44–53. 24 indexed citations
6.
Liu, Hsueh‐Ning, Teresa Sanelli, Patrick Horne, et al.. (2009). Lack of evidence of monomer/misfolded superoxide dismutase‐1 in sporadic amyotrophic lateral sclerosis. Annals of Neurology. 66(1). 75–80. 69 indexed citations
7.
Fragoso, Gabriela, et al.. (2004). Developmental differences in H2O2‐induced oligodendrocyte cell death: role of glutathione, mitogen‐activated protein kinases and caspase 3. Journal of Neurochemistry. 90(2). 392–404. 69 indexed citations
8.
Larocque, Daniel, André Galarneau, Hsueh‐Ning Liu, et al.. (2004). Protection of p27Kip1 mRNA by quaking RNA binding proteins promotes oligodendrocyte differentiation. Nature Neuroscience. 8(1). 27–33. 140 indexed citations
9.
Brault, Sonia, Jackson Roberts, Qiao‐Ling Cui, et al.. (2004). Cytotoxicity of the E 2 -isoprostane 15-E 2t -IsoP on oligodendrocyte progenitors. Free Radical Biology and Medicine. 37(3). 358–366. 26 indexed citations
10.
Molina‐Holgado, Eduardo, et al.. (2003). Regulation of muscarinic receptor function in developing oligodendrocytes by agonist exposure. British Journal of Pharmacology. 138(1). 47–56. 25 indexed citations
11.
Liu, Hsueh‐Ning, Benoit I. Giasson, Walter E. Mushynski, & Guillermina Almazán. (2002). AMPA receptor‐mediated toxicity in oligodendrocyte progenitors involves free radical generation and activation of JNK, calpain and caspase 3. Journal of Neurochemistry. 82(2). 398–409. 71 indexed citations
12.
Molina‐Holgado, Eduardo, et al.. (2001). Pharmacological and functional characterization of muscarinic receptor subtypes in developing oligodendrocytes. Journal of Neurochemistry. 77(5). 1396–1406. 45 indexed citations
13.
Almazán, Guillermina, et al.. (2000). Exposure of developing oligodendrocytes to cadmium causes HSP72 induction, free radical generation, reduction in glutathione levels, and cell death. Free Radical Biology and Medicine. 29(9). 858–869. 66 indexed citations
14.
Liu, Hsueh‐Ning, Jorge N. Larocca, & Guillermina Almazán. (1999). Molecular pathways mediating activation by kainate of mitogen-activated protein kinase in oligodendrocyte progenitors. Molecular Brain Research. 66(1-2). 50–61. 28 indexed citations
15.
Liu, Hsueh‐Ning, Eduardo Molina‐Holgado, & Guillermina Almazán. (1997). Glutamate-stimulated production of inositol phosphates is mediated by Ca2+ influx in oligodendrocyte progenitors. European Journal of Pharmacology. 338(3). 277–287. 31 indexed citations
16.
Liu, Hsueh‐Ning & Guillermina Almazán. (1995). Glutamate Induces c‐fos Proto‐oncogene Expression and Inhibits Proliferation in Oligodendrocyte Progenitors: Receptor Characterization. European Journal of Neuroscience. 7(12). 2355–2363. 50 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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