Bo Tan

592 total citations
28 papers, 441 citations indexed

About

Bo Tan is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Bo Tan has authored 28 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 9 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Bo Tan's work include Genomics and Rare Diseases (7 papers), MicroRNA in disease regulation (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Bo Tan is often cited by papers focused on Genomics and Rare Diseases (7 papers), MicroRNA in disease regulation (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Bo Tan collaborates with scholars based in China, United States and Israel. Bo Tan's co-authors include Sunil Badve, Zane T. Hammoud, Jinhui Yang, Bo Cheng, David K. O’Dell, Raphael Mechoulam, Jordyn Stuart, Vardit Kram, Hanchun Chen and Fei Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, International Journal of Biological Macromolecules and Medicine.

In The Last Decade

Bo Tan

26 papers receiving 439 citations

Peers

Bo Tan
Jiang-Zhou Yu United States
Andrea Watters United States
Hongyun Zheng China
Fan Xiao China
Hui‐Jun Mu China
Tania Islam Bangladesh
Philip M. Boone United States
Guowei Shi China
Isabelle Ernens Luxembourg
Yuan Hu China
Jiang-Zhou Yu United States
Bo Tan
Citations per year, relative to Bo Tan Bo Tan (= 1×) peers Jiang-Zhou Yu

Countries citing papers authored by Bo Tan

Since Specialization
Citations

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

Fields of papers citing papers by Bo Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bo Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Bo Tan. A scholar is included among the top collaborators of Bo Tan 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 Bo Tan. Bo Tan 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.
Yang, Nanyan, Mingze Zhang, Xin Pan, et al.. (2025). SNV/Indel and CNV Analysis in Trio‐WES for Intellectual and Developmental Disabilities: Diagnostic Yield & Cost‐Effectiveness. Clinical Genetics. 107(4). 402–412. 2 indexed citations
3.
Pan, Xin, Li Liu, Xu Zhang, et al.. (2024). FBXO11 variants are associated with intellectual disability and variable clinical manifestation in Chinese affected individuals. Journal of Human Genetics. 69(8). 391–400.
4.
Pan, Xin, Sihan Liu, Li Liu, et al.. (2023). Whole exome sequencing and transcriptome analysis in two unrelated patients with novel SET mutations. Journal of Human Genetics. 68(12). 867–874. 2 indexed citations
5.
Tan, Bo, Sihan Liu, Xin Pan, et al.. (2023). Expanding the mutational and clinical spectrum of Chinese intellectual disability patients with two novel CTCF variants. Frontiers in Pediatrics. 11. 1195862–1195862. 1 indexed citations
6.
Yang, Jinhui, Bo Tan, Guangcheng Dai, et al.. (2022). circSPECC1 promotes bladder cancer progression via regulating miR-136–5p/GNAS axis. Pathology - Research and Practice. 234. 153914–153914. 7 indexed citations
7.
Li, Xiaoduo, Li Liu, Xu Zhang, et al.. (2022). Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus. BMC Medical Genomics. 15(1). 202–202. 1 indexed citations
8.
Liu, Li, et al.. (2022). Whole-genome sequencing combined RNA-sequencing analysis of patients with mutations in SET binding protein 1. Frontiers in Neuroscience. 16. 980000–980000. 3 indexed citations
9.
Li, Dongmei, Xinyan Li, Haorong He, et al.. (2022). miR-10a-5p inhibits chicken granulosa cells proliferation and Progesterone(P4) synthesis by targeting MAPRE1 to suppress CDK2. Theriogenology. 192. 97–108. 14 indexed citations
10.
Pan, Xin, Sihan Liu, Li Liu, et al.. (2022). Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome. Frontiers in Genetics. 13. 853028–853028. 1 indexed citations
11.
Sun, Congjiao, Juan Li, Haorong He, et al.. (2022). Gga-miR-146b-3p promotes apoptosis and attenuate autophagy by targeting AKT1 in chicken granulosa cells. Theriogenology. 190. 52–64. 13 indexed citations
12.
Wang, Jing, Yu Lu, Xiaohong Yan, et al.. (2021). Identification of novel MITF mutations in Chinese families with Waardenburg syndrome type II. Molecular Genetics & Genomic Medicine. 9(9). e1770–e1770. 4 indexed citations
13.
Cheng, Ming, et al.. (2021). Gut Microbiota Is Involved in Alcohol-Induced Osteoporosis in Young and Old Rats Through Immune Regulation. Frontiers in Cellular and Infection Microbiology. 11. 636231–636231. 28 indexed citations
14.
15.
Cheng, Xueqing, Juan Li, Zirui Jiang, et al.. (2019). Preliminary study of real-time three-dimensional contrast-enhanced ultrasound of sentinel lymph nodes in breast cancer. European Radiology. 30(3). 1426–1435. 21 indexed citations
16.
Tan, Bo, Fu-Jun Ma, Bo Zhu, et al.. (2019). A Synthetic Light-switchable System based on CRISPR Cas13a Regulates the Expression of LncRNA MALAT1 and Affects the Malignant Phenotype of Bladder Cancer Cells. International Journal of Biological Sciences. 15(8). 1630–1636. 27 indexed citations
17.
Li, Juan, Man Lu, Xueqing Cheng, et al.. (2019). How Pre-operative Sentinel Lymph Node Contrast-Enhanced Ultrasound Helps Intra-operative Sentinel Lymph Node Biopsy in Breast Cancer: Initial Experience. Ultrasound in Medicine & Biology. 45(8). 1865–1873. 36 indexed citations
18.
Tan, Bo, et al.. (2017). Pathophysiology of refractory obsessive-compulsive disorder. Medicine. 96(1). e5655–e5655. 6 indexed citations
19.
Tan, Bo, et al.. (2015). Identification of a novel mutation of the EDA gene in X-linked hypohidrotic ectodermal dysplasia. Genetics and Molecular Research. 14(4). 15779–15782. 3 indexed citations
20.
Hammoud, Zane T., et al.. (2008). Estrogen promotes tumor progression in a genetically defined mouse model of lung adenocarcinoma. Endocrine Related Cancer. 15(2). 475–483. 91 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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