Lv Liu

625 total citations
54 papers, 461 citations indexed

About

Lv Liu is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Lv Liu has authored 54 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pulmonary and Respiratory Medicine, 9 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Lv Liu's work include Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (6 papers), Genomics and Rare Diseases (3 papers) and Plasmonic and Surface Plasmon Research (3 papers). Lv Liu is often cited by papers focused on Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (6 papers), Genomics and Rare Diseases (3 papers) and Plasmonic and Surface Plasmon Research (3 papers). Lv Liu collaborates with scholars based in China, Mexico and United Kingdom. Lv Liu's co-authors include Naifei Ren, Xiaoliang Xu, Quan Wang, Binfeng Yun, Zhiqiang Zhou, Jiawei Cong, Hong Luo, Yonghong Fu, Hongbing Yao and Leilei Jiang and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and Nanoscale.

In The Last Decade

Lv Liu

49 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lv Liu China 11 89 87 84 82 66 54 461
Qi Deng China 12 39 0.4× 99 1.1× 27 0.3× 171 2.1× 72 1.1× 37 459
Tetsuya Yano Japan 12 82 0.9× 92 1.1× 281 3.3× 83 1.0× 84 1.3× 52 590
Arshad Mehmood China 13 195 2.2× 56 0.6× 47 0.6× 102 1.2× 87 1.3× 69 586
William K. A. Sikkema United States 13 61 0.7× 188 2.2× 210 2.5× 194 2.4× 63 1.0× 16 735
Lalit Verma India 15 195 2.2× 103 1.2× 122 1.5× 82 1.0× 12 0.2× 71 1.1k
Jiang Chen China 14 54 0.6× 19 0.2× 83 1.0× 169 2.1× 79 1.2× 55 513
Yutong Chen China 15 35 0.4× 64 0.7× 33 0.4× 52 0.6× 207 3.1× 52 626
Jason Kim South Korea 10 68 0.8× 159 1.8× 22 0.3× 71 0.9× 36 0.5× 11 328
Ke Hu China 10 21 0.2× 90 1.0× 25 0.3× 60 0.7× 73 1.1× 20 364

Countries citing papers authored by Lv Liu

Since Specialization
Citations

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

Fields of papers citing papers by Lv Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lv Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Lv Liu. A scholar is included among the top collaborators of Lv Liu 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 Lv Liu. Lv Liu 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.
Wang, Chenyu, Yaqin Chen, Hao Huang, et al.. (2025). RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2. Molecular Medicine. 31(1). 63–63. 1 indexed citations
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Wang, Chen-Yu, Lv Liu, Hong Peng, & Hong Luo. (2024). A nonsense mutation (c.382C>T) of PARN in a patient with idiopathic pulmonary fibrosis. QJM. 117(8). 605–607. 1 indexed citations
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Wang, Wei, et al.. (2023). Image processing‐based Athletes' injury prevention mechanism. Internet Technology Letters. 7(6). 1 indexed citations
7.
Liu, Lv, Sheng Yue, Chen-Yu Wang, et al.. (2023). A novel mutation (p.Y24N) in NHP2 leads to idiopathic pulmonary fibrosis and lung carcinoma chronic obstructive lung disease by disrupting the expression and nucleocytoplasmic localization of NHP2. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1869(5). 166692–166692. 2 indexed citations
8.
Liu, Lv, et al.. (2023). Whole‐genome sequencing revealed a novel long‐range deletion mutation spanning GNAS in familial pseudohypoparathyroidism. Molecular Genetics & Genomic Medicine. 11(5). e2144–e2144. 1 indexed citations
9.
Liu, Lv, Sheng Yue, Xi Kang, et al.. (2023). A novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung disease. Hereditas. 160(1). 37–37. 3 indexed citations
10.
Dong, Yi, et al.. (2023). Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient. Frontiers in Genetics. 14. 1205052–1205052. 1 indexed citations
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Guo, Ting, Chaofeng Tu, Danhui Yang, et al.. (2021). Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Human Genetics. 140(5). 761–773. 26 indexed citations
14.
Liu, Lv, et al.. (2021). MITF p.Arg217Thr Variant Identified in a Han Chinese Family with Tietz/Waardenburg Syndrome. BioMed Research International. 2021(1). 4381272–4381272. 3 indexed citations
15.
Liu, Lv, Ting Guo, Ping Chen, et al.. (2020). Identification and functional characterization of a novel surfactant protein A2 mutation (p.N207Y) in a Chinese family with idiopathic pulmonary fibrosis. Molecular Genetics & Genomic Medicine. 8(9). e1393–e1393. 6 indexed citations
16.
Liu, Lv, et al.. (2020). Identification of a Missense Mutation in the Surfactant Protein A2 Gene in a Chinese Family with Interstitial Lung Disease. DNA and Cell Biology. 40(1). 126–131. 1 indexed citations
17.
Liu, Lv, et al.. (2017). Exome Sequencing Identifies a Novel <b><i>DES</i></b> Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family. Cardiology. 137(2). 78–82. 10 indexed citations
18.
Liu, Lv, Kai Yang, Xiang Wang, et al.. (2017). Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome. BioMed Research International. 2017. 1–6. 7 indexed citations
19.
Zhang, Xiaoying, Cuicui Zhu, Qiong Luo, et al.. (2016). Impact of siRNA targeting of β-catenin on differentiation of rat neural stem cells and gene expression of Ngn1 and BMP4 following in vitro hypoxic-ischemic brain damage. Molecular Medicine Reports. 14(4). 3595–3601. 10 indexed citations
20.
Gong, Maogang, et al.. (2009). A reticulate superhydrophobic self-assembly structure prepared by ZnO nanowires. Nanotechnology. 20(16). 165602–165602. 43 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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