Anli Shu

431 total citations
9 papers, 280 citations indexed

About

Anli Shu is a scholar working on Molecular Biology, Pharmacology and Developmental Biology. According to data from OpenAlex, Anli Shu has authored 9 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pharmacology and 2 papers in Developmental Biology. Recurrent topics in Anli Shu's work include Pharmacogenetics and Drug Metabolism (3 papers), Congenital limb and hand anomalies (2 papers) and Genetic Neurodegenerative Diseases (1 paper). Anli Shu is often cited by papers focused on Pharmacogenetics and Drug Metabolism (3 papers), Congenital limb and hand anomalies (2 papers) and Genetic Neurodegenerative Diseases (1 paper). Anli Shu collaborates with scholars based in China. Anli Shu's co-authors include Lin He, Zheng Tan, Bo Gao, Guoying Feng, Xinping Yang, Chao‐Wen She, Shengzhen Guo, Guoyin Feng, Qinghe Xing and Yongyong Shi and has published in prestigious journals such as Nature Genetics, Neurobiology of Aging and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

Anli Shu

9 papers receiving 274 citations

Peers

Anli Shu

MB

GENET

DB

ONCOL

PHARM

Boris Zagradišnik Slovenia

Naeimeh Tayebi Singapore

F Pascu Germany

Kristen Wigby United States

A. Jeannette M. Hoogeboom Netherlands

Miguel Angel Alcántara‐Ortigoza Mexico

Wilfried Müller Austria

S. Ashbel Israel

David Mossman Australia

Ilhem Ben Charfeddine Tunisia

Boris Zagradišnik Slovenia

Anli Shu

113 ×0.7

MB

131 ×1.1

GENET

3 ×0.1

DB

12 ×0.3

ONCOL

18 ×0.5

PHARM

Citations per year, relative to Anli Shu Anli Shu (= 1×) peers Boris Zagradišnik

Countries citing papers authored by Anli Shu

Since Specialization

Citations

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

Fields of papers citing papers by Anli Shu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anli Shu

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

All Works

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9 of 9 papers shown

1.

Shu, Anli, Yi‐Min Sun, Wanli Yang, et al.. (2022). DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients. Neurobiology of Aging. 113. 1–6. 3 indexed citations

2.

Yang, Lun, Lei Wang, Zhiyun Wei, et al.. (2009). Systematic Screening for Polymorphisms Within theUGT1A6Gene in Three Chinese Populations and Function Prediction Through Structural Modeling. Pharmacogenomics. 10(5). 741–752. 11 indexed citations

3.

Du, Jing, Yongyong Shi, Aiping Zhang, et al.. (2007). Screening for SNPs and Haplotypes in theCYP3A7Gene in Chinese Populations. Pharmacogenomics. 8(6). 559–566. 7 indexed citations

4.

Du, Jing, Qinghe Xing, Mingsheng Xu, et al.. (2006). Systematic Screening for Polymorphisms in theCYP3A4Gene in the Chinese Population. Pharmacogenomics. 7(6). 831–841. 53 indexed citations

5.

Qin, Wei, Anli Shu, Xueqing Qian, et al.. (2006). A novel mutation of PAX3 in a Chinese family with Waardenburg syndrome.. PubMed. 12. 1001–8. 8 indexed citations

6.

Qin, Wei, Jin Shi, Qinghe Xing, et al.. (2005). [Mutation detection of COL1A1 gene in a pedigree with osteogenesis imperfecta].. PubMed. 32(3). 248–52. 4 indexed citations

7.

Qian, Xueqing, Anli Shu, Wei Qin, et al.. (2004). A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis–ptosis–epicanthus inversus. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 554(1-2). 19–22. 15 indexed citations

8.

Qin, Wei, et al.. (2003). [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].. PubMed. 30(10). 973–7. 1 indexed citations

9.

Gao, Bo, Chao‐Wen She, Anli Shu, et al.. (2001). Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1. Nature Genetics. 28(4). 386–388. 178 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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