Yi Guo

1.7k total citations
77 papers, 1.1k citations indexed

About

Yi Guo is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Yi Guo has authored 77 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Neurology, 29 papers in Molecular Biology and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Yi Guo's work include Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological disorders and treatments (15 papers) and Nuclear Receptors and Signaling (8 papers). Yi Guo is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological disorders and treatments (15 papers) and Nuclear Receptors and Signaling (8 papers). Yi Guo collaborates with scholars based in China, United States and Japan. Yi Guo's co-authors include Hao Deng, Joseph Jankovic, Weidong Le, Wenjie Xie, Hongbo Xu, Xiong Deng, Lamei Yuan, Zhijian Yang, Zhi Song and Dehua Hu and has published in prestigious journals such as Nature Communications, PLoS ONE and Neurology.

In The Last Decade

Yi Guo

76 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yi Guo China 18 494 372 272 155 145 77 1.1k
Cengiz Yalçınkaya Türkiye 22 131 0.3× 470 1.3× 168 0.6× 81 0.5× 155 1.1× 79 1.2k
Marta Radaelli Italy 25 482 1.0× 199 0.5× 104 0.4× 140 0.9× 26 0.2× 61 1.6k
Irene Pichler Italy 21 386 0.8× 401 1.1× 145 0.5× 83 0.5× 273 1.9× 45 1.2k
Wouter van Rheenen Netherlands 17 741 1.5× 356 1.0× 147 0.5× 239 1.5× 213 1.5× 30 1.2k
Stacey Clardy United States 18 819 1.7× 173 0.5× 137 0.5× 82 0.5× 120 0.8× 75 1.2k
Emilio Di Maria Italy 22 461 0.9× 565 1.5× 500 1.8× 215 1.4× 243 1.7× 66 1.4k
Milena De Riz Italy 24 317 0.6× 552 1.5× 136 0.5× 312 2.0× 55 0.4× 52 1.6k
Tomoko Okamoto Japan 18 659 1.3× 636 1.7× 169 0.6× 180 1.2× 86 0.6× 85 1.9k
Anna M. Pietroboni Italy 22 266 0.5× 331 0.9× 110 0.4× 185 1.2× 31 0.2× 52 1.1k
Clara de Andrés Spain 22 481 1.0× 182 0.5× 212 0.8× 94 0.6× 95 0.7× 61 1.4k

Countries citing papers authored by Yi Guo

Since Specialization
Citations

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

Fields of papers citing papers by Yi Guo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yi Guo

This figure shows the co-authorship network connecting the top 25 collaborators of Yi Guo. A scholar is included among the top collaborators of Yi Guo 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 Yi Guo. Yi Guo 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.
Shi, Xue, Lin Jiang, Lin Zhu, et al.. (2024). Prediction of rTMS Efficacy in Patients With Essential Tremor: Biomarkers From Individual Resting-State EEG Network. IEEE Transactions on Neural Systems and Rehabilitation Engineering. 32. 3719–3728. 1 indexed citations
2.
3.
Yuan, Meng, Yi Guo, Xia Hong, et al.. (2021). Novel SCN5A and GPD1L Variants Identified in Two Unrelated Han-Chinese Patients With Clinically Suspected Brugada Syndrome. Frontiers in Cardiovascular Medicine. 8. 758903–758903. 6 indexed citations
4.
Liu, Qi, Qiao Yang, Yi Guo, et al.. (2020). Comparison of seizure outcomes and safety between anterior temporal lobotomy and lobectomy in patients with temporal lobe epilepsy. Neurological Research. 42(2). 164–169. 4 indexed citations
5.
Yan, Yuxiang, Louisa Dahmani, Jianxun Ren, et al.. (2020). Reconstructing lost BOLD signal in individual participants using deep machine learning. Nature Communications. 11(1). 5046–5046. 22 indexed citations
6.
Zeng, Ting, Niu Li, Jian Wang, et al.. (2018). Familial short stature caused by ACAN gene mutation:a familial case report. The Journal of clinical Pediatrics. 463–466. 2 indexed citations
7.
Qin, Xiang, Yi Guo, Wei Xiong, et al.. (2018). Identification of a CNGB1 Frameshift Mutation in a Han Chinese Family with Retinitis Pigmentosa. Optometry and Vision Science. 95(12). 1155–1161. 4 indexed citations
8.
Guo, Yi, Xia Hong, Hongbo Xu, et al.. (2018). Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma. Cellular Physiology and Biochemistry. 46(5). 1919–1929. 13 indexed citations
9.
Liu, Ziyuan, Yang Liu, Lin Wang, et al.. (2018). Pallidal Deep Brain Stimulation in Patients With Chorea-Acanthocytosis. Neuromodulation Technology at the Neural Interface. 21(8). 741–747. 6 indexed citations
10.
Deng, Hao, Quanyong He, Zhijian Yang, et al.. (2017). Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing. Molecular Medicine Reports. 16(1). 473–477. 11 indexed citations
11.
Deng, Hao, Sheng Deng, Hongbo Xu, et al.. (2016). Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly. PLoS ONE. 11(5). e0155180–e0155180. 8 indexed citations
12.
Hao, Hongwei, Fangang Meng, Yi Guo, et al.. (2015). Patient perspectives on the efficacy of a new kind of rechargeable deep brain stimulators1. International Journal of Neuroscience. 126(11). 996–1001. 13 indexed citations
13.
Guo, Yi, Zhi Song, Hongbo Xu, et al.. (2014). Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation. Canadian Journal of Ophthalmology. 49(1). 50–53. 7 indexed citations
14.
Yang, Huarong, Yong Qi, Xiong Deng, et al.. (2013). Novel ATPase Cu2+ Transporting Beta Polypeptide Mutations in Chinese Families with Wilson's Disease. PLoS ONE. 8(7). e66526–e66526. 6 indexed citations
15.
Guo, Yi, Huarong Yang, Xiong Deng, et al.. (2013). Genetic analysis of the S100B gene in Chinese patients with Parkinson disease. Neuroscience Letters. 555. 134–136. 23 indexed citations
16.
Guo, Yi, Linyan Su, Jie Zhang, et al.. (2012). Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome. Psychiatric Genetics. 22(6). 300–303. 14 indexed citations
17.
Guo, Yi, Hua Lin, Kai Gao, et al.. (2011). Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease. Biochemical and Biophysical Research Communications. 415(2). 284–287. 22 indexed citations
18.
Guo, Yi, Wei-Dong Le, Joseph Jankovic, et al.. (2011). Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease. Movement Disorders. 26(9). 1729–1732. 20 indexed citations
19.
Guo, Yi, Xiong Deng, Wen Zheng, et al.. (2011). HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease. Neuroscience Letters. 501(3). 185–187. 40 indexed citations
20.
Deng, Hao, Joseph Jankovic, Yi Guo, Wenjie Xie, & Weidong Le. (2005). Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y. Biochemical and Biophysical Research Communications. 337(4). 1133–1138. 128 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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