Kejin Zhang

895 total citations
63 papers, 671 citations indexed

About

Kejin Zhang is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Kejin Zhang has authored 63 papers receiving a total of 671 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 28 papers in Molecular Biology and 11 papers in Cognitive Neuroscience. Recurrent topics in Kejin Zhang's work include Genetics and Neurodevelopmental Disorders (23 papers), Genetic Associations and Epidemiology (9 papers) and Epigenetics and DNA Methylation (7 papers). Kejin Zhang is often cited by papers focused on Genetics and Neurodevelopmental Disorders (23 papers), Genetic Associations and Epidemiology (9 papers) and Epigenetics and DNA Methylation (7 papers). Kejin Zhang collaborates with scholars based in China, United States and Canada. Kejin Zhang's co-authors include Pingyuan Gong, Xiaocai Gao, Fuchang Zhang, Ling Guo, Xing Yang, Jinting Liu, Xiaolin Zhou, Huiyong Fan, Hushan Yang and Ronald E. Myers and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Kejin Zhang

61 papers receiving 663 citations

Peers

Kejin Zhang

ONCOL

GENET

Ayako Inoue Japan

Lisa Yang United Kingdom

Gabriela Rodrı́guez United States

Tiina Saanijoki Finland

Sara Moruzzi Italy

Jeannie F Todd United Kingdom

Reza Ahadi Iran

Nasim Ahmadiyeh United States

Shinobu Takayasu Japan

Victoria Scott New Zealand

Ayako Inoue Japan

Kejin Zhang

255 ×1.2

97 ×0.8

199 ×1.8

ONCOL

44 ×0.4

GENET

56 ×0.7

Citations per year, relative to Kejin Zhang Kejin Zhang (= 1×) peers Ayako Inoue

Countries citing papers authored by Kejin Zhang

Since Specialization

Citations

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

Fields of papers citing papers by Kejin Zhang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kejin Zhang

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

Deng, Heran, Liying Wang, Na Wang, et al.. (2023). Neoadjuvant checkpoint blockade in combination with Chemotherapy in patients with tripe-negative breast cancer: exploratory analysis of real-world, multicenter data. BMC Cancer. 23(1). 29–29. 9 indexed citations

Zhang, Kejin, et al.. (2023). Types of milk consumed and risk of essential hypertension: A 2-sample Mendelian randomization analysis. Journal of Dairy Science. 106(7). 4516–4523. 5 indexed citations

Wu, Yufei, et al.. (2021). Association between the ABCA1 (R219K) polymorphism and lipid profiles: a meta-analysis. Scientific Reports. 11(1). 21718–21718. 10 indexed citations

Liu, Xiaofen, Yanan Liu, Fuchang Zhang, et al.. (2020). Genetic Variants of the MTMR 9 Gene Are Associated with Nonspecific Intellectual Disability: A Family-Based Association Study. Genetic Testing and Molecular Biomarkers. 24(10). 625–631.

Liang, Junqing, et al.. (2018). Genetic variants of SLC12A3 modulate serum lipid profiles in a group of Mongolian pedigree population. Lipids in Health and Disease. 17(1). 83–83. 2 indexed citations

He, Hongjuan, Lei Lei, Erfei Chen, et al.. (2016). The c.553G>T Genetic Variant of the APOA5 Gene and Altered Triglyceride Levels in the Asian Population: A Meta-Analysis of Case–Control Studies. Genetic Testing and Molecular Biomarkers. 20(12). 758–765. 7 indexed citations

Cui, Meng, Junlin Li, Fuchang Zhang, et al.. (2015). A New Role for LOC101928437 in Non-Syndromic Intellectual Disability: Findings from a Family-Based Association Test. PLoS ONE. 10(8). e0135669–e0135669. 4 indexed citations

Wang, Chun, Jesse Civan, Yinzhi Lai, et al.. (2014). Racial disparity in breast cancer survival: the impact of pre-treatment hematologic variables. Cancer Causes & Control. 26(1). 45–56. 16 indexed citations

Zhang, Kejin. (2014). Genetic variations in colorectal cancer risk and clinical outcome. World Journal of Gastroenterology. 20(15). 4167–4167. 34 indexed citations

10.

Li, Meili, et al.. (2013). Molecular cloning and characterization of the pseudorabies virus US1 gene. Genetics and Molecular Research. 12(1). 85–98. 5 indexed citations

11.

Gong, Pingyuan, et al.. (2012). An Association Study on the Polymorphisms of Dopaminergic Genes with Working Memory in a Healthy Chinese Han Population. Cellular and Molecular Neurobiology. 32(6). 1011–1019. 10 indexed citations

12.

Li, Yajing, et al.. (2011). Positive Association of CC2D1A and CC2D2A Gene Haplotypes with Mental Retardation in a Han Chinese Population. DNA and Cell Biology. 31(1). 80–87. 8 indexed citations

13.

Gong, Pingyuan, Fuchang Zhang, Lei Xu, et al.. (2011). No Observable Relationship Between the 12 Genes of Nervous System and Reasoning Skill in a Young Chinese Han Population. Cellular and Molecular Neurobiology. 31(4). 519–526. 5 indexed citations

14.

Zhang, Kejin, et al.. (2011). A modified protocol for the comet assay allowing the processing of multiple samples. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 721(2). 153–156. 14 indexed citations

15.

Gong, Pingyuan, Lei Xu, Xiaodong Wu, et al.. (2011). An Association Study of the Genetic Polymorphisms in 13 Neural Plasticity-Related Genes with Semantic and Episodic Memories. Journal of Molecular Neuroscience. 46(2). 352–361. 15 indexed citations

16.

Zhang, Kejin, et al.. (2008). Non-syndromic Mental Retardation is not expressed in RAC1 Gene Polymorphisms. Neuroscience Letters. 437(2). 71–75. 1 indexed citations

17.

Zhang, Kejin. (2008). Relationship between the polymorphisms of <I>GDI1</I>, chil-dren NSMR and their intelligence in Qinba region. Hereditas (Beijing). 30(5). 590–594. 1 indexed citations

18.

Zhang, Kejin, et al.. (2007). Possible Relationship between the COMT Gene Vel<sup>158</sup>Met Polymorphism and Psychometric IQ in Girls of the Qinba Region in China. Neuropsychobiology. 56(2-3). 98–103. 9 indexed citations

19.

Zhang, Kejin, Jianjun Gao, Xiaocai Gao, et al.. (2007). An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population. Neuroscience Letters. 419(1). 83–87. 12 indexed citations

20.

Zhang, Kejin, Xiaocai Gao, Ruilin Li, et al.. (2006). Association Between a Functional COMT Polymorphism, Mental Retardation and Cognition in Qinba Area Children. Acta Genetica Sinica. 33(6). 495–500. 3 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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