Chenhong Guo

629 total citations
13 papers, 426 citations indexed

About

Chenhong Guo is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Chenhong Guo has authored 13 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Chenhong Guo's work include Ubiquitin and proteasome pathways (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Epigenetics and DNA Methylation (3 papers). Chenhong Guo is often cited by papers focused on Ubiquitin and proteasome pathways (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Epigenetics and DNA Methylation (3 papers). Chenhong Guo collaborates with scholars based in China, United States and Ireland. Chenhong Guo's co-authors include Yaoqin Gong, Changshun Shao, Yongxin Zou, Guimin Gao, Bingxi Chen, Qiji Liu, Xiyu Zhang, Haibin Zhou, Jiangxia Li and Jun Mi and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Chenhong Guo

13 papers receiving 422 citations

Peers

Chenhong Guo

GENET

ONCOL

IMMUN

Kunhua Qin United States

Natalia de Olano Spain

Henri A. Kester Netherlands

Diana Z. Ye United States

Adam G. Evertts United States

Ioulia B. Appelskog Sweden

Anwesh Kamireddy United States

Aarti D. Rohira United States

Yaiza Núñez‐Álvarez Spain

Müge Öğrünç United States

Kunhua Qin United States

Chenhong Guo

325 ×0.9

50 ×0.6

GENET

57 ×1.0

ONCOL

22 ×0.5

IMMUN

38 ×1.0

Citations per year, relative to Chenhong Guo Chenhong Guo (= 1×) peers Kunhua Qin

Countries citing papers authored by Chenhong Guo

Since Specialization

Citations

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

Fields of papers citing papers by Chenhong Guo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chenhong Guo

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

All Works

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13 of 13 papers shown

Guo, Chenhong, Ting Cao, Long Tai Zheng, John L. Waddington, & Xuechu Zhen. (2020). Development and characterization of an inducible Dicer conditional knockout mouse model of Parkinson’s disease: validation of the antiparkinsonian effects of a sigma-1 receptor agonist and dihydromyricetin. Acta Pharmacologica Sinica. 41(4). 499–507. 30 indexed citations

Jiang, Baichun, Wei Zhao, Jupeng Yuan, et al.. (2012). Lack of Cul4b, an E3 Ubiquitin Ligase Component, Leads to Embryonic Lethality and Abnormal Placental Development. PLoS ONE. 7(5). e37070–e37070. 67 indexed citations

Li, Lin, Jiangxia Li, Rongfang Qiu, et al.. (2012). Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly. Gene. 499(1). 48–51. 8 indexed citations

Wang, Hui, Haibin Zhou, Yongxin Zou, et al.. (2010). Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells. Biochemical Pharmacology. 80(9). 1386–1395. 61 indexed citations

Zou, Yongxin, Jun Mi, Defen Lu, et al.. (2009). Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role in Cyclin E Degradation and Cell Cycle Progression. Journal of Biological Chemistry. 284(48). 33320–33332. 102 indexed citations

Zou, Yongxin, Qiji Liu, Bingxi Chen, et al.. (2007). Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation. The American Journal of Human Genetics. 80(3). 561–566. 123 indexed citations

Zhang, Xiyu, Qiji Liu, Bingxi Chen, et al.. (2004). A locus for nonspecific X‐linked mental retardation mapped to a 22.3 cM region of Xp11.3‐q22.3. American Journal of Medical Genetics Part A. 129A(3). 286–289. 3 indexed citations

Lu, Yong, Chenhong Guo, Qiji Liu, et al.. (2003). A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads. American Journal of Medical Genetics Part A. 120A(3). 345–349. 12 indexed citations

Cheng, Lin, Yaoqin Gong, Qiji Liu, et al.. (2003). [Gene mapping of a nonsyndromic hearing impairmint family].. PubMed. 20(2). 89–93. 3 indexed citations

10.

Liu, Qiji, et al.. (2002). [Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome].. PubMed. 19(1). 22–5. 2 indexed citations

11.

Guo, Chenhong, et al.. (2002). [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].. PubMed. 19(4). 295–7. 4 indexed citations

12.

Lei, Dapeng, Xinliang Pan, Chenhong Guo, et al.. (2002). [Relationship between polymorphism of N-acetyltransferase 2 and genetic susceptibility to laryngeal carcinoma].. PubMed. 24(2). 154–6. 5 indexed citations

13.

Lei, Dapeng, Xinliang Pan, Chenhong Guo, et al.. (2002). [Genetic polymorphism of cytochrome P4501A1 and susceptibility to laryngeal carcinoma].. PubMed. 37(5). 373–6. 6 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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