Weihong Gu

866 total citations
27 papers, 331 citations indexed

About

Weihong Gu is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Weihong Gu has authored 27 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 16 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Weihong Gu's work include Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (12 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Weihong Gu is often cited by papers focused on Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (12 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Weihong Gu collaborates with scholars based in China and United States. Weihong Gu's co-authors include Jian Xing, Qian Liu, Kai Wang, Li Dai, Peng Zhang, Wenlong Song, Bo Peng, Depeng Wang, R.S. Rana and Guoxiang Wang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Optics Express and Journal of the Neurological Sciences.

In The Last Decade

Weihong Gu

24 papers receiving 308 citations

Peers

Weihong Gu
Timo Kühn Germany
Junpei Yamashita Japan
Ivan A. Kuznetsov United States
Jae-Joon Park South Korea
Fumiaki Yamamoto Japan
Claudia Bianchini Italy
Timo Kühn Germany
Weihong Gu
Citations per year, relative to Weihong Gu Weihong Gu (= 1×) peers Timo Kühn

Countries citing papers authored by Weihong Gu

Since Specialization
Citations

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

Fields of papers citing papers by Weihong Gu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Weihong Gu

This figure shows the co-authorship network connecting the top 25 collaborators of Weihong Gu. A scholar is included among the top collaborators of Weihong Gu 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 Weihong Gu. Weihong Gu 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.
2.
Duan, Xiaohui, Xiaoxuan Liu, Guochun Wang, et al.. (2021). Characterization of genotype–phenotype correlation with MORC2 mutated Axonal Charcot–Marie–Tooth disease in a cohort of Chinese patients. Orphanet Journal of Rare Diseases. 16(1). 244–244. 5 indexed citations
3.
Duan, Xiaohui, Zhenhua Cao, Chao Zhou, et al.. (2020). Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants. The Cerebellum. 20(1). 74–82. 8 indexed citations
4.
Dai, Li, Weihong Gu, Bo Peng, et al.. (2018). Generalized inverse matrix-exterior penalty function (GIM-EPF) algorithm for data processing of multi-wavelength pyrometer (MWP). Optics Express. 26(20). 25706–25706. 38 indexed citations
5.
Liu, Qian, Peng Zhang, Depeng Wang, Weihong Gu, & Kai Wang. (2017). Interrogating the “unsequenceable” genomic trinucleotide repeat disorders by long-read sequencing. Genome Medicine. 9(1). 65–65. 59 indexed citations
6.
Wang, Li, Peng Yu, Zhenhua Cao, et al.. (2017). Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family. The Cerebellum. 17(3). 294–299. 12 indexed citations
7.
Xing, Jian, Bo Peng, Zhao Ma, et al.. (2017). Directly data processing algorithm for multi-wavelength pyrometer (MWP). Optics Express. 25(24). 30560–30560. 50 indexed citations
8.
Wang, Li, et al.. (2016). Nervous system disorder caused by nitrous oxide intoxication: one case report. SHILAP Revista de lepidopterología. 2 indexed citations
9.
10.
Xing, Jian, R.S. Rana, & Weihong Gu. (2016). Emissivity range constraints algorithm for multi-wavelength pyrometer (MWP). Optics Express. 24(17). 19185–19185. 33 indexed citations
11.
Liu, Zunjing, et al.. (2015). Myotonic Dystrophy Type 1 Associated with White Matter Hyperintense Lesions. Chinese Medical Journal. 128(10). 1412–1414. 2 indexed citations
12.
McFarland, Karen N., Jilin Liu, Guangbin Xia, et al.. (2015). Spinocerebellar ataxia type 10 in Chinese Han. Neurology Genetics. 1(3). e26–e26. 21 indexed citations
13.
Zhang, Linwei, Weihong Gu, Guoxiang Wang, et al.. (2013). [Analysis of fragile X mental retardation 1 gene premutation in multiple system atrophy patients].. PubMed. 93(47). 3744–7. 1 indexed citations
14.
Gu, Weihong. (2012). Transcranial brain parenchyma sonography in movement disorders.
15.
Ying, Zhengxin, Fankai Lin, Weihong Gu, et al.. (2011). α-Synuclein increases U251 cells vulnerability to hydrogen peroxide by disrupting calcium homeostasis. Journal of Neural Transmission. 118(8). 1165–1172. 10 indexed citations
16.
Liu, Yang, et al.. (2011). Clinical Manifestation, Imaging, and Genotype Analysis of Two Pedigrees with Spinocerebellar Ataxia. Cell Biochemistry and Biophysics. 61(3). 691–698.
17.
Jin, Miao, Jinsong Jiao, Weihong Gu, et al.. (2005). [A study on PARKIN gene in three pedigrees with autosomal recessive early-onset Parkinson's disease].. PubMed. 22(5). 514–7. 2 indexed citations
18.
Gu, Weihong, Huizi Ma, Miao Jin, et al.. (2004). The Shortest Expanded Allele of the MJD1 Gene in a Chinese MJD Kindred with Autonomic Dysfunction. European Neurology. 52(2). 107–111. 24 indexed citations
19.
Qiao, Wenhui, Weihong Gu, Yoshihisa Takiyama, et al.. (2001). Spinocerebellar Ataxia Type 1 in China. Archives of Neurology. 58(5). 789–789. 18 indexed citations
20.
Gu, Weihong, et al.. (2000). Molecular and Clinical Study of Spinocerebellar Ataxia Type 7 in Chinese Kindreds. Archives of Neurology. 57(10). 1513–8. 20 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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