Xiaoling Yang

1.1k total citations
45 papers, 728 citations indexed

About

Xiaoling Yang is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Xiaoling Yang has authored 45 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 21 papers in Molecular Biology and 8 papers in Psychiatry and Mental health. Recurrent topics in Xiaoling Yang's work include Genetics and Neurodevelopmental Disorders (18 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (9 papers). Xiaoling Yang is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (9 papers). Xiaoling Yang collaborates with scholars based in China, United States and Australia. Xiaoling Yang's co-authors include Yuehua Zhang, Xiru Wu, Zhixian Yang, Aijie Liu, Liping Wei, Xiaoxu Yang, Qi Zeng, Qixi Wu, Yan Ruan and Jing Liu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Scientific Reports.

In The Last Decade

Xiaoling Yang

42 papers receiving 713 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiaoling Yang China 16 416 309 218 104 89 45 728
Haiheng Dong Canada 13 220 0.5× 449 1.5× 256 1.2× 354 3.4× 48 0.5× 20 894
Apostolos Papandreou United Kingdom 9 211 0.5× 196 0.6× 136 0.6× 108 1.0× 16 0.2× 24 560
Carl Friddle United States 7 256 0.6× 353 1.1× 122 0.6× 56 0.5× 27 0.3× 7 630
Hong Chang China 18 279 0.7× 400 1.3× 106 0.5× 87 0.8× 88 1.0× 62 833
Maarten Van Den Bossche Belgium 11 146 0.4× 160 0.5× 93 0.4× 47 0.5× 83 0.9× 33 470
Gabriela G. Cezar United States 10 129 0.3× 608 2.0× 41 0.2× 105 1.0× 82 0.9× 12 946
Rolando Meloni France 15 152 0.4× 346 1.1× 35 0.2× 231 2.2× 44 0.5× 35 715
Paula Martínez Spain 12 136 0.3× 295 1.0× 28 0.1× 122 1.2× 74 0.8× 16 851
Pornprot Limprasert Thailand 15 385 0.9× 288 0.9× 47 0.2× 175 1.7× 235 2.6× 50 854
Fatema Serajee United States 12 186 0.4× 177 0.6× 81 0.4× 59 0.6× 188 2.1× 19 459

Countries citing papers authored by Xiaoling Yang

Since Specialization
Citations

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

Fields of papers citing papers by Xiaoling Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoling Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaoling Yang. A scholar is included among the top collaborators of Xiaoling Yang 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 Xiaoling Yang. Xiaoling Yang 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.
Yang, Anning, Hongwen Zhang, Huiping Zhang, et al.. (2025). Pitavastatin and resveratrol bio-nanocomplexes against hyperhomocysteinemia-induced atherosclerosis via blocking ferroptosis-related lipid deposition. Journal of Controlled Release. 381. 113598–113598. 10 indexed citations
2.
Yang, Xiaolong, Qingan Wang, Xiaoling Yang, et al.. (2024). Association of plasma homocysteine with cardiometabolic multimorbidity: a cross-sectional study in northwest China. Lipids in Health and Disease. 23(1). 370–370. 1 indexed citations
3.
Bai, Ling, et al.. (2024). Novel copy number variations and phenotypes of infantile epileptic spasms syndrome. Clinical Genetics. 106(2). 161–179.
4.
Chen, Lan, et al.. (2023). The association of standard base excess upon emergency admission with outcomes in patients with heat stroke. The American Journal of Emergency Medicine. 72. 7–15. 4 indexed citations
5.
Wu, Hui, Zhen Li, Yali Yang, et al.. (2023). Rap1A accelerates homocysteine-induced ANA-1 cells inflammation via synergy of FoxO1 and DNMT3a. Cellular Signalling. 106. 110627–110627. 6 indexed citations
6.
Zhu, Ying, et al.. (2022). DYNC1H1‐related epilepsy: Genotype–phenotype correlation. Developmental Medicine & Child Neurology. 65(4). 534–543. 4 indexed citations
7.
Yang, Xiaoxu, Xiaoling Yang, Ying Yang, et al.. (2022). PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency. Frontiers in Neurology. 13. 1041509–1041509. 3 indexed citations
8.
Zeng, Qi, Ying Yang, Jing Duan, et al.. (2022). SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis. Frontiers in Molecular Neuroscience. 15. 809951–809951. 17 indexed citations
9.
Yang, Xiaoling, et al.. (2021). Phenotypes of GNAO1 Variants in a Chinese Cohort. Frontiers in Neurology. 12. 662162–662162. 15 indexed citations
10.
Shan, Wei, Xiaoling Yang, Qian Ren, & Qun Wang. (2021). Generation of SCN1A Knock out induced pluripotent stem cell (iPSC) line. Stem Cell Research. 55. 102452–102452. 2 indexed citations
11.
Yang, Ying, Qi Zeng, Wenshu XiangWei, et al.. (2021). GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications. Journal of Neurology. 269(5). 2649–2665. 10 indexed citations
12.
13.
Zeng, Qi, Xiaoling Yang, Jing Zhang, et al.. (2017). Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort. Journal of Human Genetics. 63(1). 9–18. 15 indexed citations
14.
Yang, Xiaoling, Ping Qian, Xiaoyan Liu, et al.. (2017). GRIN2A mutations in epilepsy-aphasia spectrum disorders. Brain and Development. 40(3). 205–210. 22 indexed citations
15.
Huang, August Yue, Xiaojing Xu, Adam Yongxin Ye, et al.. (2014). Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Research. 24(11). 1311–1327. 42 indexed citations
16.
Zhang, Yuehua, Xiaoyan Liu, Xiaoling Yang, et al.. (2013). Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations. Brain and Development. 36(8). 676–681. 36 indexed citations
17.
Qin, Jian, Meixiang Jia, Tianlan Lu, et al.. (2009). Association study of SHANK3 gene polymorphisms with autism in Chinese Han population. BMC Medical Genetics. 10(1). 61–61. 28 indexed citations
18.
Wu, Suping, Weihua Yue, Meixiang Jia, et al.. (2007). Association of the neuropilin‐2 (NRP2) gene polymorphisms with autism in Chinese Han population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(4). 492–495. 32 indexed citations
19.
Wu, Suping, Yanqing Guo, Meixiang Jia, et al.. (2005). Lack of evidence for association between the serotonin transporter gene (SLC6A4) polymorphisms and autism in the Chinese trios. Neuroscience Letters. 381(1-2). 1–5. 17 indexed citations
20.
Gong, Xiaohong, Meixiang Jia, Yan Ruan, et al.. (2004). Association between the FOXP2 gene and autistic disorder in Chinese population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 127B(1). 113–116. 64 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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