Xiaocai Gao

412 total citations
47 papers, 314 citations indexed

About

Xiaocai Gao is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Xiaocai Gao has authored 47 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 18 papers in Molecular Biology and 16 papers in Cognitive Neuroscience. Recurrent topics in Xiaocai Gao's work include Genetics and Neurodevelopmental Disorders (24 papers), Cognitive Abilities and Testing (6 papers) and Genetic Associations and Epidemiology (6 papers). Xiaocai Gao is often cited by papers focused on Genetics and Neurodevelopmental Disorders (24 papers), Cognitive Abilities and Testing (6 papers) and Genetic Associations and Epidemiology (6 papers). Xiaocai Gao collaborates with scholars based in China, Canada and United States. Xiaocai Gao's co-authors include Kejin Zhang, Fuchang Zhang, Pingyuan Gong, Dongmei Chen, Xing Yang, Shaoping Huang, Junlin Li, Lei Xu, Jianjun Gao and Guifang Zhao and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Personality and Individual Differences.

In The Last Decade

Xiaocai Gao

46 papers receiving 309 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Xiaocai Gao China 11 107 99 90 68 35 47 314
Darina Roeske Germany 9 112 1.0× 72 0.7× 138 1.5× 82 1.2× 25 0.7× 11 478
Guanghan Chen United States 6 92 0.9× 61 0.6× 86 1.0× 77 1.1× 16 0.5× 12 311
Hannah Loke Australia 6 93 0.9× 53 0.5× 73 0.8× 62 0.9× 14 0.4× 7 360
H. Tagaya Japan 5 120 1.1× 68 0.7× 80 0.9× 113 1.7× 56 1.6× 6 527
Réka Kovács-Nagy Hungary 13 168 1.6× 56 0.6× 82 0.9× 37 0.5× 17 0.5× 22 363
Kathryn M. Harper United States 13 162 1.5× 72 0.7× 89 1.0× 71 1.0× 17 0.5× 30 441
Jared V. Goodman United States 7 149 1.4× 64 0.6× 50 0.6× 61 0.9× 11 0.3× 8 376
Dae-Yeon Cho South Korea 10 110 1.0× 122 1.2× 88 1.0× 87 1.3× 14 0.4× 12 415
Dea Adamsen Denmark 9 85 0.8× 65 0.7× 57 0.6× 102 1.5× 9 0.3× 11 279
Margaret Czesak Canada 9 197 1.8× 70 0.7× 81 0.9× 278 4.1× 42 1.2× 11 568

Countries citing papers authored by Xiaocai Gao

Since Specialization
Citations

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

Fields of papers citing papers by Xiaocai Gao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaocai Gao

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaocai Gao. A scholar is included among the top collaborators of Xiaocai Gao 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 Xiaocai Gao. Xiaocai Gao 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.
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.
3.
Yang, Xing, Guomin Shen, Kejin Zhang, et al.. (2017). Independent self-construal mediates the association between CYP19A1 gene variant and subjective well-being. Consciousness and Cognition. 55. 205–213. 3 indexed citations
4.
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
5.
Li, Junlin, Guifang Zhao, & Xiaocai Gao. (2013). Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins. Journal of Neurodevelopmental Disorders. 5(1). 4–4. 9 indexed citations
6.
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
7.
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
8.
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
9.
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
10.
Han, Ning, Kejin Zhang, Xiaocai Gao, et al.. (2011). Polymorphisms in the DLG3 Gene is not Associated with Non-Syndromic Mental Retardation in the Chinese Han Population of Qin-Ba Mountain. Cellular and Molecular Neurobiology. 31(5). 695–700. 1 indexed citations
11.
Zhang, Kejin, et al.. (2010). Genetic variations of FACL4 have no obvious influence on cognitive ability in young Chinese children. Psychiatry Research. 178(1). 202–204. 1 indexed citations
12.
Gong, Pingyuan, et al.. (2009). Effect of BDNF Val66Met Polymorphism on Digital Working Memory and Spatial Localization in a Healthy Chinese Han Population. Journal of Molecular Neuroscience. 38(3). 250–256. 37 indexed citations
13.
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
14.
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
15.
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
16.
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
17.
Sun, Yun, Fuchang Zhang, Jianjun Gao, et al.. (2006). Variants in the RAB3A gene are not associated with mental retardation in the Chinese population. Neuroscience Letters. 401(1-2). 114–118. 1 indexed citations
18.
Gao, Jianjun, Xiaocai Gao, Wei Qin, et al.. (2006). No Observable Relationship between the ACE Gene Insertion/Deletion Polymorphism and Psychometric IQ and Psychomotor Ability in Chinese Children. Neuropsychobiology. 53(4). 196–202. 1 indexed citations
19.
Li, Junjie, Jianjun Gao, Qinghe Xing, et al.. (2005). An association study between the transthyretin (TTR) gene and mental retardation. European Archives of Psychiatry and Clinical Neuroscience. 256(4). 230–235. 2 indexed citations
20.
Gao, Jianjun, Fuchang Zhang, Tingwei Guo, et al.. (2004). Distribution of apolipoprotein E allele frequencies of the Han Chinese in an iodine-deficient mountainous area. Annals of Human Biology. 31(5). 578–585. 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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