Keqin Lin

461 total citations
42 papers, 322 citations indexed

About

Keqin Lin is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Keqin Lin has authored 42 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Immunology, 14 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Keqin Lin's work include T-cell and B-cell Immunology (7 papers), Immune Cell Function and Interaction (6 papers) and interferon and immune responses (5 papers). Keqin Lin is often cited by papers focused on T-cell and B-cell Immunology (7 papers), Immune Cell Function and Interaction (6 papers) and interferon and immune responses (5 papers). Keqin Lin collaborates with scholars based in China, Singapore and Japan. Keqin Lin's co-authors include Jiayou Chu, Hao Sun, Zhaoqing Yang, Shuyuan Liu, Lei Shi, Li Shi, Kai Huang, Xiaoqin Huang, Jiayou Chu and Xiaoqun Dong and has published in prestigious journals such as PLoS ONE, Applied and Environmental Microbiology and Scientific Reports.

In The Last Decade

Keqin Lin

39 papers receiving 317 citations

Peers

Keqin Lin
Andrea Rita Marrero Brazil
Gwo‐Chin Ma Taiwan
Georg Hemmrich‐Stanisak Germany
Céline Besse France
Inju Park South Korea
Cecil Han South Korea
Shan‐Shun Luo Japan
Warren W. Kretzschmar United Kingdom
Benjamin Etschmann Germany
Yanfei Wen China
Andrea Rita Marrero Brazil
Keqin Lin
Citations per year, relative to Keqin Lin Keqin Lin (= 1×) peers Andrea Rita Marrero

Countries citing papers authored by Keqin Lin

Since Specialization
Citations

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

Fields of papers citing papers by Keqin Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keqin Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Keqin Lin. A scholar is included among the top collaborators of Keqin Lin 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 Keqin Lin. Keqin Lin 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.
Y, Jin, Miao Zhao, Wanyu Zhao, et al.. (2024). Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 62–62. 1 indexed citations
2.
Li, Yufei, Wenwu Li, Yao Zhang, et al.. (2024). A novel mutation alters GNE bifunctional enzyme activity and leads to familial inherited GNE diseases. Gene. 927. 148750–148750.
3.
Zhang, Yunhan, Xiaoli Dong, Miao Zhao, et al.. (2024). FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population. BMC Medical Genomics. 17(1). 197–197.
4.
Lin, Keqin, et al.. (2023). Determination of the 3′UTR region of HLA‐B*53:01:03 sequence by next generation sequencing. HLA. 103(1). e15322–e15322. 4 indexed citations
5.
Zhang, Lin, Wen‐Wu Li, Yu‐Ting Weng, et al.. (2022). A novel splice site variant in the POPDC3 causes autosomal recessive limb‐girdle muscular dystrophy type 26. Clinical Genetics. 102(4). 345–349. 5 indexed citations
6.
Liu, Hongbo, et al.. (2020). Characterization of a novel echovirus 21 strain isolated from a healthy child in China in 2013. Archives of Virology. 165(3). 757–760. 1 indexed citations
7.
8.
Liu, Hongbo, Jie Zhang, Yilin Zhao, et al.. (2018). Molecular characterization of echovirus 12 strains isolated from healthy children in China. Scientific Reports. 8(1). 11716–11716. 3 indexed citations
9.
Sun, Hao, Keqin Lin, Kai Huang, et al.. (2017). Molecular evolution of two asymptomatic echovirus 6 strains that constitute a novel branch of recently epidemic echovirus 6 in China. Virology Journal. 14(1). 140–140. 3 indexed citations
10.
Sun, Hao, Hongxian Liu, Kai Huang, et al.. (2017). β-globin gene cluster haplotypes in ethnic minority populations of southwest China. Scientific Reports. 7(1). 42909–42909. 5 indexed citations
11.
Li, Qian, Keqin Lin, Hao Sun, et al.. (2016). Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans. Journal of Human Genetics. 61(12). 1021–1026. 20 indexed citations
12.
Yang, Zhaoqing, Shuyuan Liu, Chang-Jun Zhang, et al.. (2016). Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese. Asian Journal of Andrology. 19(4). 486–486. 22 indexed citations
13.
Sun, Hao, Zhaoqing Yang, Keqin Lin, et al.. (2015). The Adaptive Change of HLA-DRB1 Allele Frequencies Caused by Natural Selection in a Mongolian Population That Migrated to the South of China. PLoS ONE. 10(7). e0134334–e0134334. 9 indexed citations
14.
Li, Qian, Shuyuan Liu, Keqin Lin, et al.. (2013). Association between six single nucleotide polymorphisms of EGLN1 gene and adaptation to high-altitude hypoxia. Hereditas (Beijing). 35(8). 992–998. 4 indexed citations
15.
Sun, Hao, Chi Zhou, Xiaoqin Huang, et al.. (2013). Correlation between the linguistic affinity and genetic diversity of Chinese ethnic groups. Journal of Human Genetics. 58(10). 686–693. 16 indexed citations
16.
Yao, Yufeng, Lei Shi, Yufen Tao, et al.. (2011). Diversity of killer cell immunoglobulin-like receptor genes in four ethnic groups in China. Immunogenetics. 63(8). 475–483. 14 indexed citations
17.
Shi, Lei, Yufeng Yao, Li Shi, et al.. (2011). Polymorphic Alu insertions and their associations with HLAⅠalleles in Yugu and Zhuang ethnic populations. Hereditas (Beijing). 33(2). 138–146. 1 indexed citations
18.
Liu, Shuyuan, Chang-Jun Zhang, Peng Haiying, et al.. (2010). CAG-repeat variant in the polymerase γ gene and male infertility in the Chinese population: a meta-analysis. Asian Journal of Andrology. 13(2). 298–304. 7 indexed citations
19.
Qian, Yuan, Hao Sun, Keqin Lin, et al.. (2008). Distribution of CCR5-Δ32, CCR2-64I, SDF1-3′A, CX3CR1-249I, and CX3CR1-280M in Chinese Populations. AIDS Research and Human Retroviruses. 24(11). 1391–1397. 8 indexed citations
20.
Shi, Li, Jian Yu, Jun Ohashi, et al.. (2008). Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China. Human Immunology. 69(1). 58–65. 26 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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