Xianli Bian

475 total citations
16 papers, 367 citations indexed

About

Xianli Bian is a scholar working on Molecular Biology, Epidemiology and Rheumatology. According to data from OpenAlex, Xianli Bian has authored 16 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Epidemiology and 4 papers in Rheumatology. Recurrent topics in Xianli Bian's work include RNA regulation and disease (3 papers), Autophagy in Disease and Therapy (3 papers) and Neurological diseases and metabolism (2 papers). Xianli Bian is often cited by papers focused on RNA regulation and disease (3 papers), Autophagy in Disease and Therapy (3 papers) and Neurological diseases and metabolism (2 papers). Xianli Bian collaborates with scholars based in China, United States and Hong Kong. Xianli Bian's co-authors include Qiji Liu, Jiangxia Li, Qianqian Yuan, Jie Dang, Xiaochun Ma, Shan Shan, Fei Gao, Yaoqin Gong, Yan Li and Na Liu and has published in prestigious journals such as The Journal of Immunology, Scientific Reports and Arthritis Research & Therapy.

In The Last Decade

Xianli Bian

16 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xianli Bian China	11	207	101	96	61	46	16	367
Yujun Pan China	11	146 0.7×	157 1.6×	40 0.4×	79 1.3×	30 0.7×	16	433
Jiyeon Han South Korea	5	319 1.5×	60 0.6×	268 2.8×	89 1.5×	45 1.0×	10	507
Kip D. Zimmerman United States	9	156 0.8×	94 0.9×	33 0.3×	51 0.8×	10 0.2×	25	309
Gabriela Carreno United Kingdom	12	219 1.1×	30 0.3×	35 0.4×	23 0.4×	31 0.7×	18	415
Y.K Semra United Kingdom	14	255 1.2×	214 2.1×	32 0.3×	64 1.0×	23 0.5×	19	606
Lorea Blázquez Spain	13	533 2.6×	51 0.5×	78 0.8×	14 0.2×	23 0.5×	21	676
Yihang Shen China	12	258 1.2×	66 0.7×	80 0.8×	15 0.2×	15 0.3×	32	399
Sakina Zaïdi France	9	152 0.7×	39 0.4×	29 0.3×	30 0.5×	90 2.0×	11	441
A. Rocchini United States	5	184 0.9×	196 1.9×	59 0.6×	16 0.3×	21 0.5×	5	431
Francesca Tagliavini Italy	12	418 2.0×	49 0.5×	26 0.3×	16 0.3×	54 1.2×	14	522

Countries citing papers authored by Xianli Bian

Since Specialization

Citations

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

Fields of papers citing papers by Xianli Bian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xianli Bian

This figure shows the co-authorship network connecting the top 25 collaborators of Xianli Bian. A scholar is included among the top collaborators of Xianli Bian 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 Xianli Bian. Xianli Bian is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Chang, Zhenyu, Zhiyang Wang, Li Luo, et al.. (2024). Case report: Double mutations in a patient with early-onset Alzheimer’s disease in China, PSEN2 and IDE variants. Frontiers in Neuroscience. 18. 1423892–1423892. 2 indexed citations

Yin, Hongqiang, Xiao‐Jing Wang, Xianli Bian, et al.. (2022). Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice. Frontiers in Molecular Neuroscience. 15. 822129–822129. 6 indexed citations

Bian, Xianli, Shang Wang, Suqin Jin, et al.. (2021). Two novel missense variants in SPTBN2 likely associated with spinocerebellar ataxia type 5. Neurological Sciences. 42(12). 5195–5203. 10 indexed citations

Ding, Shouluan, et al.. (2021). Diagnostic value of amygdala volume on structural magnetic resonance imaging in Alzheimer’s disease. World Journal of Clinical Cases. 9(18). 4627–4636. 13 indexed citations

Li, Yan, Jiangxia Li, Qianqian Yuan, et al.. (2021). Deficiency in WDFY4 reduces the number of CD8+ T cells via reactive oxygen species-induced apoptosis. Molecular Immunology. 139. 131–138. 10 indexed citations

Wang, Dewei, Ping Wang, Xianli Bian, et al.. (2020). Elevated plasma levels of exosomal BACE1‑AS combined with the volume and thickness of the right entorhinal cortex may serve as a biomarker for the detection of Alzheimer's disease. Molecular Medicine Reports. 22(1). 227–238. 62 indexed citations

Liu, Qi, Jiangxia Li, Xianli Bian, et al.. (2019). A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus. Journal of Clinical Immunology. 39(8). 795–804. 18 indexed citations

Bian, Xianli, Pengfei Lin, Jiangxia Li, et al.. (2018). Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2. Neurodegenerative Diseases. 18(2-3). 74–83. 7 indexed citations

Yuan, Qianqian, Yan Li, Jiangxia Li, et al.. (2018). WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy. The Journal of Immunology. 201(9). 2570–2578. 25 indexed citations

10.

Dang, Jie, Xianli Bian, Xiaochun Ma, et al.. (2017). ORMDL3 Facilitates the Survival of Splenic B Cells via an ATF6α–Endoplasmic Reticulum Stress–Beclin1 Autophagy Regulatory Pathway. The Journal of Immunology. 199(5). 1647–1659. 27 indexed citations

11.

Dang, Jie, Jiangxia Li, Shan Shan, et al.. (2015). Gene–gene interaction of ATG5, ATG7, BLK and BANK1 in systemic lupus erythematosus. International Journal of Rheumatic Diseases. 19(12). 1284–1293. 30 indexed citations

12.

Ma, Xiaochun, Rongfang Qiu, Jie Dang, et al.. (2015). ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells. Scientific Reports. 5(1). 17194–17194. 25 indexed citations

13.

Li, Jiangxia, Jie Dang, Xianli Bian, et al.. (2015). miR-155 Deficiency Ameliorates Autoimmune Inflammation of Systemic Lupus Erythematosus by Targeting S1pr1 in Faslpr/lpr Mice. The Journal of Immunology. 194(11). 5437–5445. 83 indexed citations

14.

Wang, Xue, Lin Li, Jiangxia Li, et al.. (2014). Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation. European Journal of Human Genetics. 22(9). 1105–1110. 27 indexed citations

15.

Shan, Shan, Jie Dang, Jiangxia Li, et al.. (2014). ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese. Arthritis Research & Therapy. 16(2). R87–R87. 19 indexed citations

16.

Liu, Yongchao, Hua Zhang, Jiangxia Li, et al.. (2013). Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study. Immunogenetics. 65(12). 835–839. 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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