Wanshi Cai

1.2k total citations
27 papers, 785 citations indexed

About

Wanshi Cai is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Wanshi Cai has authored 27 papers receiving a total of 785 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Wanshi Cai's work include Epigenetics and DNA Methylation (9 papers), RNA modifications and cancer (7 papers) and Mitochondrial Function and Pathology (4 papers). Wanshi Cai is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), RNA modifications and cancer (7 papers) and Mitochondrial Function and Pathology (4 papers). Wanshi Cai collaborates with scholars based in China, United States and Ethiopia. Wanshi Cai's co-authors include Zhong Sheng Sun, Jialong Liang, Fengbiao Mao, Huajing Teng, Xianfeng Li, Jinyu Wu, Jia Qu, Tao Cai, Yi Tong and Xiangtian Zhou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Wanshi Cai

27 papers receiving 778 citations

Peers

Countries citing papers authored by Wanshi Cai

Since Specialization

Citations

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

Fields of papers citing papers by Wanshi Cai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wanshi Cai

This figure shows the co-authorship network connecting the top 25 collaborators of Wanshi Cai. A scholar is included among the top collaborators of Wanshi Cai 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 Wanshi Cai. Wanshi Cai 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

#	Work	Indexed citations
1	Inter- and intratumor DNA methylation heterogeneity associated with lymph node metastasis and prognosis of esophageal squamous cell carcinoma 2020 ·Theranostics ·Huajing Teng, (unknown), Jialong Liang, Xingxing Wang, Lu Wang, Wenqing Wei, Chao Li, Ze Zhang, Qinglan Li, Ran Xia, Xiaohui Shi, Wanshi Cai, Weihu Wang, Hengjun Gao, Zhong Sheng Sun	29
2	MFEprimer-3.0: quality control for PCR primers 2019 ·Nucleic Acids Research ·Kun Wang, Haiwei Li, Yue Xu, Qianzhi Shao, (unknown), Ruichao Wang, Wanshi Cai, Xingyi Hang, Chenggang Zhang, Haoyang Cai, Wubin Qu	59
3	Acetylation of hMOF Modulates H4K16ac to Regulate DNA Repair Genes in Response to Oxidative Stress 2017 ·International Journal of Biological Sciences ·Jianing Zhong, (unknown), Huiqian Chen, Xianfeng Li, Jianan Zhang, Xingxing Wang, Weilin Wu, Ying Xu, Fei Huang, Wanshi Cai, Zhong Sheng Sun	18
4	CirGRDB: a database for the genome-wide deciphering circadian genes and regulators 2017 ·Nucleic Acids Research ·Xianfeng Li, Leisheng Shi, Kun Zhang, Wenqing Wei, Qi Liu, Fengbiao Mao, Jinchen Li, Wanshi Cai, Huiqian Chen, Huajing Teng, Jia‐Da Li, Zhong Sheng Sun	23
5	TET1 modulates H4K16 acetylation by controlling auto-acetylation of hMOF to affect gene regulation and DNA repair function 2016 ·Nucleic Acids Research ·Jianing Zhong, Xianfeng Li, Wanshi Cai, Yan Wang, Shanshan Dong, Jie Yang, Jianan Zhang, (unknown), Yuanyuan Li, Fengbiao Mao, Cheng Zeng, Jinyu Wu, Xingzhi Xu, Zhong Sheng Sun	41
6	RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins 2015 ·Nucleic Acids Research ·Fengbiao Mao, (unknown), Xianfeng Li, Jialong Liang, Huajing Teng, Wanshi Cai, Zhong Sheng Sun	42
7	MBRidge: an accurate and cost-effective method for profiling DNA methylome at single-base resolution 2015 ·Journal of Molecular Cell Biology ·Wanshi Cai, Fengbiao Mao, Huajing Teng, Tao Cai, Fangqing Zhao, Jinyu Wu, Zhong Sheng Sun	5
8	Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmus 2015 ·Genetics in Medicine ·Ping Yu, Yun Cui, Wanshi Cai, (unknown), Xiaoqiang Xiao, Qianzhi Shao, Liang Ma, (unknown), (unknown), Zi‐Bing Jin, Yongjin Wang, Tao Cai, Zhong Sheng Sun, Jia Qu	12
9	Q-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analyses 2015 ·Epigenetics ·Kangli Wang, Xianfeng Li, Shanshan Dong, Jialong Liang, Fengbiao Mao, Cheng Zeng, (unknown), Jinyu Wu, Wanshi Cai, Zhong Sheng Sun	20
10	A Bayesian Framework to Identify Methylcytosines from High-Throughput Bisulfite Sequencing Data 2014 ·PLoS Computational Biology ·Qing Xie, Qi Liu, Fengbiao Mao, Wanshi Cai, (unknown), (unknown), Zhen Wang, Bingyu Chen, Zhongsheng Sun, Jinyu Wu	3
11	Single-Cell Sequencing Technologies: Current and Future 2014 ·Journal of genetics and genomics ·Jialong Liang, Wanshi Cai, Zhong Sheng Sun	62
12	Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree 2013 ·Neurobiology of Aging ·Zhanjun Wang, Wanshi Cai, Fang Cui, Tao Cai, Zhaohui Chen, Fengbiao Mao, Huajing Teng, Lin Chen, Jiesi Wang, Zhong Sheng Sun, Xusheng Huang, Ping Yü	6
13	Comparative RNA-seq analysis reveals potential mechanisms mediating the conversion to androgen independence in an LNCaP progression cell model 2013 ·Cancer Letters ·Yongqing Wang, Yan Wang, (unknown), Gang Xu, Fengbiao Mao, Tingting Qin, Huajing Teng, Wanshi Cai, Ping Yü, Tao Cai, Mei Zhao, Zhong Sheng Sun, Congying Xie	15
14	New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient 2013 ·Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Fang Cui, Wanshi Cai, Zhanjun Wang, Yuting Ren, Li Mao, Zhong Sheng Sun, Xusheng Huang	1
15	Genome-wide identification and divergent transcriptional expression of StAR-related lipid transfer (START) genes in teleosts 2013 ·Gene ·Huajing Teng, Wanshi Cai, Kun Zeng, Fengbiao Mao, (unknown), Tao Wang, Fangqing Zhao, Zhong Sheng Sun	5
16	Mutations ofANK3identified by exome sequencing are associated with autism susceptibility 2012 ·Human Mutation ·Cheng Bi, Jinyu Wu, Tao Jiang, Qi Liu, Wanshi Cai, Ping Yu, Tao Cai, (unknown), Yong‐hui Jiang, Zhong Sheng Sun	91
17	Evolutionary Mode and Functional Divergence of Vertebrate NMDA Receptor Subunit 2 Genes 2010 ·PLoS ONE ·Huajing Teng, Wanshi Cai, Zhou Linglin, Jing Zhang, Qi Liu, Yongqing Wang, Wei Dai, Mei Zhao, Zhong Sheng Sun	15
18	Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families 2010 ·Biochemical and Biophysical Research Communications ·Juanjuan Zhang, Xiangtian Zhou, Jian Zhou, Chengwu Li, Fuxin Zhao, Yan Wang, (unknown), Jiying Wang, (unknown), Wanshi Cai, Yi Tong, Yanhong Sun, Li Yang, Jia Qu, Min‐Xin Guan	25
19	Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation 2010 ·Molecular Genetics and Metabolism ·Minglian Zhang, Xiangtian Zhou, Chengwu Li, Fuxin Zhao, Juanjuan Zhang, (unknown), Yanhong Sun, Jingzheng Wang, Yi Tong, Min Liang, Li Yang, Wanshi Cai, Lifei Wang, Jia Qu, Min‐Xin Guan	31
20	The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy 2007 ·Biochemical and Biophysical Research Communications ·Yi Tong, (unknown), Xiangtian Zhou, Li Yang, Juanjuan Zhang, Wanshi Cai, Fuxin Zhao, Xinjian Wang, Fan Lü, Jia Qu, Min‐Xin Guan	28

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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