Yo‐Tsen Liu

1.2k total citations
30 papers, 792 citations indexed

About

Yo‐Tsen Liu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Yo‐Tsen Liu has authored 30 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Yo‐Tsen Liu's work include Genetic Neurodegenerative Diseases (8 papers), Neurological diseases and metabolism (6 papers) and Cellular transport and secretion (6 papers). Yo‐Tsen Liu is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Neurological diseases and metabolism (6 papers) and Cellular transport and secretion (6 papers). Yo‐Tsen Liu collaborates with scholars based in Taiwan, United Kingdom and United States. Yo‐Tsen Liu's co-authors include Yi‐Chung Lee, Henry Houlden, Bing‐Wen Soong, Mary M. Reilly, Yi‐Chu Liao, Sinéad M. Murphy, Matilde Laurá, Julian Blake, Katherine A. Fawcett and Amelie Pandraud and has published in prestigious journals such as PLoS ONE, Journal of Neurology Neurosurgery & Psychiatry and Epilepsia.

In The Last Decade

Yo‐Tsen Liu

29 papers receiving 771 citations

Peers

Yo‐Tsen Liu

CMN

NEURO

Moreno Ferrarini Italy

Alessandro Malandrini Italy

G Fabrizi Italy

Luigi Pianese Italy

Emil Ylikallio Finland

Xinghua Luan China

Emeline Mundwiller France

Annabelle Chaussenot France

Sandra Gill United States

T. Sprovieri Italy

Moreno Ferrarini Italy

Yo‐Tsen Liu

353 ×0.9

CMN

249 ×0.8

223 ×0.8

NEURO

105 ×0.5

NEURO

168 ×1.6

Citations per year, relative to Yo‐Tsen Liu Yo‐Tsen Liu (= 1×) peers Moreno Ferrarini

Countries citing papers authored by Yo‐Tsen Liu

Since Specialization

Citations

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

Fields of papers citing papers by Yo‐Tsen Liu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yo‐Tsen Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Yo‐Tsen Liu. A scholar is included among the top collaborators of Yo‐Tsen 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 Yo‐Tsen Liu. Yo‐Tsen Liu 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

Kuo, Ling, et al.. (2024). The Structural and Dynamic Insights into the Ala97Ser Amyloidogenic Mutation in Transthyretin. Chemistry - An Asian Journal. 20(4). e202401438–e202401438.

Lu, Chia‐Feng, Yong-Sin Hu, Huai‐Che Yang, et al.. (2023). Magnetic resonance radiomics-derived sphericity correlates with seizure in brain arteriovenous malformations. European Radiology. 34(1). 588–599. 2 indexed citations

Liu, Yo‐Tsen, et al.. (2022). Novel lissencephaly‐associated DCX variants in the C‐terminal DCX domain affect microtubule binding and dynamics. Epilepsia. 63(5). 1253–1265. 8 indexed citations

Chi, Nai‐Fang, Chun‐Yu Chen, Yung‐Shuan Lin, et al.. (2022). Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing. Cellular and Molecular Neurobiology. 43(6). 2769–2783. 6 indexed citations

Chou, Chien‐Chen, Syu‐Jyun Peng, Hsiang‐Yu Yu, et al.. (2022). Clinical characteristics and long‐term outcome of cerebral cavernous malformations‐related epilepsy. Epilepsia. 63(8). 2056–2067. 10 indexed citations

Liu, Yo‐Tsen, et al.. (2022). Precise Motor Function Monitor for Parkinson Disease using Low Power and Wearable IMU Body Area Network. 1–5. 1 indexed citations

Chou, Chien‐Chen, Der‐Jen Yen, Hsiang‐Yu Yu, et al.. (2021). Acute withdrawal of new-generation antiepileptic drugs in epilepsy monitoring units: Safety and efficacy. Epilepsy & Behavior. 117. 107846–107846. 1 indexed citations

Lu, Yanting, Chung‐Yao Hsu, Yo‐Tsen Liu, et al.. (2021). The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia. Biomedical Journal. 45(3). 542–548. 4 indexed citations

Tsai, Meng‐Han, Mei‐Hsin Hsu, Wei‐Szu Liu, et al.. (2019). PRRT2 missense mutations cluster near C‐terminus and frequently lead to protein mislocalization. Epilepsia. 60(5). 807–817. 17 indexed citations

10.

Liu, Yo‐Tsen, et al.. (2017). Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias. PLoS ONE. 12(11). e0187503–e0187503. 12 indexed citations

11.

Wiethoff, Sarah, Conceição Bettencourt, Reema Paudel, et al.. (2016). Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene. The Cerebellum. 16(1). 262–267. 20 indexed citations

12.

Tsai, Pei‐Chien, Yi‐Chien Liu, Kon‐Ping Lin, et al.. (2016). Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of Aging. 40. 191.e11–191.e16. 41 indexed citations

13.

Ernst, Daniela, Sinéad M. Murphy, Wei Yu, et al.. (2015). Novel HSAN1 Mutation in Serine Palmitoyltransferase Resides at a Putative Phosphorylation Site That Is Involved in Regulating Substrate Specificity. NeuroMolecular Medicine. 17(1). 47–57. 25 indexed citations

14.

Liao, Yi‐Chu, Jong‐Ling Fuh, Chang‐Ming Chern, et al.. (2015). Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles. PLoS ONE. 10(8). e0136501–e0136501. 80 indexed citations

15.

Gonzalez, Michael, Heather M. McLaughlin, Henry Houlden, et al.. (2013). Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2. Journal of Neurology Neurosurgery & Psychiatry. 84(11). 1247–1249. 99 indexed citations

16.

Murphy, Sinéad M., Matilde Laurá, Katherine A. Fawcett, et al.. (2012). Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. Journal of Neurology Neurosurgery & Psychiatry. 83(7). 706–710. 257 indexed citations

17.

Fawcett, Katherine A., Mohadeseh Mehrabian, Yo‐Tsen Liu, et al.. (2012). The frequency of spinocerebellar ataxia type 23 in a UK population. Journal of Neurology. 260(3). 856–859. 9 indexed citations

18.

Liu, Yo‐Tsen, et al.. (2007). Transthyretin Ala97Ser in Chinese–Taiwanese patients with familial amyloid polyneuropathy: Genetic studies and phenotype expression. Journal of the Neurological Sciences. 267(1-2). 91–99. 32 indexed citations

19.

Liu, Yo‐Tsen, et al.. (2007). A Novel ABCD1 Gene Mutation in a Chinese-Taiwanese Patient with Adrenomyeloneuropathy. Pediatric Neurology. 36(5). 348–350. 3 indexed citations

20.

Lee, Yi‐Chung, et al.. (2005). Median nerve motor conduction velocity is concordant with myelin protein zero gene mutation. Journal of Neurology. 252(2). 151–155. 9 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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