Niu Li

1.3k total citations
84 papers, 806 citations indexed

About

Niu Li is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Niu Li has authored 84 papers receiving a total of 806 indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 42 papers in Genetics and 9 papers in Immunology. Recurrent topics in Niu Li's work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and RNA modifications and cancer (9 papers). Niu Li is often cited by papers focused on Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and RNA modifications and cancer (9 papers). Niu Li collaborates with scholars based in China, United States and Saudi Arabia. Niu Li's co-authors include Jian Wang, Tingting Yu, Ruen Yao, Yiping Shen, Xiumin Wang, Yufei Xu, Yu Ding, Xuyun Hu, Xiumin Wang and Guoying Chang and has published in prestigious journals such as Nucleic Acids Research, Advanced Materials and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Niu Li

76 papers receiving 796 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Niu Li China 15 442 356 79 73 57 84 806
Babak Behnam Iran 17 353 0.8× 129 0.4× 112 1.4× 57 0.8× 55 1.0× 51 783
Virginie Millet France 15 481 1.1× 145 0.4× 86 1.1× 40 0.5× 137 2.4× 21 958
Zinger Yang United States 15 1.0k 2.3× 254 0.7× 105 1.3× 22 0.3× 74 1.3× 20 1.4k
Xiaoyan Tian United States 12 605 1.4× 98 0.3× 98 1.2× 35 0.5× 44 0.8× 22 836
Xi Luo China 11 467 1.1× 253 0.7× 113 1.4× 48 0.7× 67 1.2× 23 933
Jiangming Luo Canada 10 721 1.6× 411 1.2× 63 0.8× 12 0.2× 79 1.4× 14 1.1k
Paola Sena Italy 18 335 0.8× 73 0.2× 78 1.0× 43 0.6× 121 2.1× 49 857
Luyi Sen United States 19 548 1.2× 131 0.4× 49 0.6× 55 0.8× 75 1.3× 37 1.2k
Shuting Yang United States 15 373 0.8× 82 0.2× 95 1.2× 39 0.5× 49 0.9× 40 605

Countries citing papers authored by Niu Li

Since Specialization
Citations

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

Fields of papers citing papers by Niu Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niu Li

This figure shows the co-authorship network connecting the top 25 collaborators of Niu Li. A scholar is included among the top collaborators of Niu Li 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 Niu Li. Niu Li 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.
Ding, Yu, Shiyang Gao, Guoying Chang, et al.. (2025). Focusing on Rare Variants Related to Maturity‐Onset Diabetes of the Young in Children. Pediatric Diabetes. 2025(1). 8155443–8155443.
4.
Wang, Xiuling, Niu Li, Xucun Jia, et al.. (2024). Integrated transcriptomics and metabolomics analysis provide insights into the alleviation of waterlogging stress in maize by exogenous spermidine application. Journal of Integrative Agriculture. 24(12). 4546–4560.
5.
Yu, Tingting, et al.. (2023). Two patients with KDM3B variants and new presentations of Diets–Jongmans syndrome. Neurogenetics. 24(2). 95–101. 2 indexed citations
6.
Zhang, Jiasheng, et al.. (2023). SINE-VNTR-Alu retrotransposon insertion as a novel mutational event underlying Glanzmann thrombasthenia. Journal of Thrombosis and Haemostasis. 21(12). 3597–3607. 3 indexed citations
7.
Li, Xin, Yirou Wang, Ruen Yao, et al.. (2023). Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients. Orphanet Journal of Rare Diseases. 18(1). 284–284. 3 indexed citations
8.
Ding, Yu, Niu Li, Dan Lou, et al.. (2020). Clinical and genetic analysis in a Chinese cohort of children and adolescents with diabetes/persistent hyperglycemia. Journal of Diabetes Investigation. 12(1). 48–62. 7 indexed citations
9.
Sun, Li‐Ying, Qun Li, Yijun Tang, et al.. (2020). A novel PIK3R1 mutation of SHORT syndrome in a Chinese female with diffuse thyroid disease: a case report and review of literature. BMC Medical Genetics. 21(1). 215–215. 11 indexed citations
10.
Xu, Yufei, et al.. (2020). TRPS1 mutation detection in Chinese patients with Tricho‐rhino‐phalangeal syndrome and identification of four novel mutations. Molecular Genetics & Genomic Medicine. 8(10). e1417–e1417. 6 indexed citations
11.
Liu, Jie, Jiwen Wang, Yufei Xu, et al.. (2020). Clinical and Molecular Characterization of Three Novel ARHGEF9 Mutations in Patients with Developmental Delay and Epilepsy. Journal of Molecular Neuroscience. 70(6). 908–915. 9 indexed citations
12.
Li, Niu, Jing Wu, Yufen Wu, et al.. (2020). Further delineation of primary B cell immunodeficiency caused by novel variants of the BLNK gene in two Chinese patients. Clinical Immunology. 214. 108387–108387. 2 indexed citations
13.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients. Clinical Genetics. 96(4). 290–299. 32 indexed citations
14.
Wang, Yirou, Niu Li, Zhe Su, et al.. (2019). The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series. American Journal of Medical Genetics Part A. 182(4). 640–651. 10 indexed citations
15.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients. 2 indexed citations
16.
Xu, Yufei, Yirou Wang, Niu Li, et al.. (2019). New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development. European Journal of Endocrinology. 181(3). 311–323. 20 indexed citations
17.
Zeng, Ting, Niu Li, Jian Wang, et al.. (2018). Familial short stature caused by ACAN gene mutation:a familial case report. The Journal of clinical Pediatrics. 463–466. 2 indexed citations
19.
Yao, Ruen, Cheng Zhang, Tingting Yu, et al.. (2017). Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data. Molecular Cytogenetics. 10(1). 30–30. 67 indexed citations
20.
Zhou, Huimin, et al.. (2016). Variation Trends of Atmospheric Visibility and Its Influence Factors in Nanjing. 55(18). 4698. 1 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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