Jing Yu Liu

1.4k total citations
43 papers, 988 citations indexed

About

Jing Yu Liu is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jing Yu Liu has authored 43 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jing Yu Liu's work include Ion channel regulation and function (6 papers), Pain Mechanisms and Treatments (5 papers) and Parathyroid Disorders and Treatments (4 papers). Jing Yu Liu is often cited by papers focused on Ion channel regulation and function (6 papers), Pain Mechanisms and Treatments (5 papers) and Parathyroid Disorders and Treatments (4 papers). Jing Yu Liu collaborates with scholars based in China, United States and United Kingdom. Jing Yu Liu's co-authors include John J. Schwartz, Robert Rosenberg, Zhang Li, Nicholas W. Shworak, Mugen Liu, Qing K. Wang, Cheng Wang, Junyu Luo, Xixiang Ma and Yulei Li and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Jing Yu Liu

43 papers receiving 977 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jing Yu Liu China 16 598 310 176 173 132 43 988
Huguette Debaix Belgium 19 814 1.4× 120 0.4× 261 1.5× 133 0.8× 159 1.2× 28 1.5k
Raphaela Schwappacher Germany 17 515 0.9× 95 0.3× 173 1.0× 75 0.4× 22 0.2× 23 870
Paul D. Walden United States 22 730 1.2× 124 0.4× 137 0.8× 170 1.0× 91 0.7× 45 1.5k
S. W. Manley Australia 17 440 0.7× 96 0.3× 111 0.6× 120 0.7× 83 0.6× 61 938
Maciej Pronicki Poland 21 795 1.3× 57 0.2× 115 0.7× 132 0.8× 45 0.3× 95 1.3k
Ramón Dı́az-Trelles Spain 14 639 1.1× 59 0.2× 107 0.6× 73 0.4× 116 0.9× 29 894
Ke Dong United States 19 1.1k 1.9× 101 0.3× 83 0.5× 390 2.3× 158 1.2× 31 1.4k
Kazushige Hanaoka Japan 17 1.0k 1.7× 120 0.4× 75 0.4× 1.1k 6.1× 118 0.9× 29 1.6k
Kazumichi Furuyama Japan 25 1.4k 2.3× 211 0.7× 235 1.3× 103 0.6× 60 0.5× 68 1.8k

Countries citing papers authored by Jing Yu Liu

Since Specialization
Citations

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

Fields of papers citing papers by Jing Yu Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jing Yu Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Jing Yu Liu. A scholar is included among the top collaborators of Jing Yu 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 Jing Yu Liu. Jing Yu 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.
Xu, Xuan, Hao Sun, Junyu Luo, et al.. (2022). The Pathology of Primary Familial Brain Calcification: Implications for Treatment. Neuroscience Bulletin. 39(4). 659–674. 15 indexed citations
2.
Xu, Xuan, Hao Sun, Zhijian Cao, et al.. (2022). Norbisabolane-type sesquiterpenoid derivatives, benzofuran lignans and a phenolic glycoside from the roots of Glochidion wilsonii Hutch. Phytochemistry. 204. 113447–113447. 3 indexed citations
3.
Liu, Kai, Junyu Luo, Zhe Xu, et al.. (2020). Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal–Regulated Kinase1/2 Cascade and TRPV6. Journal of Investigative Dermatology. 141(3). 533–544. 4 indexed citations
4.
Zhou, Xi, Shuijiao Peng, Lulu Li, et al.. (2020). Spider venom-derived peptide induces hyperalgesia in Nav1.7 knockout mice by activating Nav1.9 channels. Nature Communications. 11(1). 2293–2293. 27 indexed citations
5.
Jiang, Lei, Yulei Li, Yuping Wang, et al.. (2020). FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome. Investigative Ophthalmology & Visual Science. 61(5). 41–41. 7 indexed citations
6.
Li, Lulu, Guangyou Duan, Ningbo Li, et al.. (2020). Novel SCN9A missense mutations contribute to congenital insensitivity to pain: Unexpected correlation between electrophysiological characterization and clinical phenotype. Molecular Pain. 16. 2226727657–2226727657. 13 indexed citations
7.
Yang, Yujie, Junyu Luo, Teng Liu, et al.. (2019). A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate. Genetic Testing and Molecular Biomarkers. 23(11). 759–765. 7 indexed citations
8.
Duan, Guangyou, Ningbo Li, Yuhao Zhang, et al.. (2017). SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patients. Medicine. 96(39). e8149–e8149. 13 indexed citations
9.
Yu, Shanshan, Chang Li, Lincoln Biswas, et al.. (2017). CERKL gene knockout disturbs photoreceptor outer segment phagocytosis and causes rod-cone dystrophy in zebrafish. Human Molecular Genetics. 26(12). 2335–2345. 31 indexed citations
10.
Shi, Yi, Yan‐Jiun Huang, Ling Ni, et al.. (2016). Function and clinical implications of short‐chain fatty acids in patients with mixed refractory constipation. Colorectal Disease. 18(8). 803–810. 33 indexed citations
11.
Gao, Yong, Cheng Wang, Juan Liu, et al.. (2010). Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma. Molecular Genetics and Metabolism. 102(1). 107–109. 6 indexed citations
12.
Zhang, Su, Xiang Ren, Pengyun Wang, et al.. (2008). Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family. BMC Medical Genetics. 9(1). 24–24. 16 indexed citations
13.
Zhang, Shouyan, Qi Yao, Xiangyang Liu, et al.. (2008). Identification of a genetic locus for autosomal dominant disseminated superficial actinic porokeratosis on chromosome 1p31.3–p31.1. Human Genetics. 123(5). 507–513. 26 indexed citations
14.
Liu, Jing Yu, Xiaohua Dai, Xin Cui, et al.. (2008). Identification and functional characterization of a novel splicing mutation in RP gene PRPF31. Biochemical and Biophysical Research Communications. 367(2). 420–426. 19 indexed citations
15.
Liu, Jing Yu, Xiang Ren, Xiufeng Yang, et al.. (2007). Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation. Journal of Human Genetics. 52(6). 565–570. 45 indexed citations
16.
Diao, Ying, Lu Chen, Mingquan Zhou, et al.. (2006). Nuclear DNA C-values in 12 species in Nymphaeales. Caryologia. 59(1). 25–30. 19 indexed citations
17.
Liu, Mugen, Zhou Cai, Zhaohui Tang, et al.. (2006). A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family. Journal of Human Genetics. 51(8). 727–731. 25 indexed citations
18.
Li, Hua, et al.. (2006). Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.. PubMed. 23(2). 134–7. 15 indexed citations
19.
Huang, Changzheng, Qinbo Yang, Tie Ke, et al.. (2006). A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia. Journal of Human Genetics. 51(12). 1133–1137. 18 indexed citations
20.
Rosenberg, Robert, Nicholas W. Shworak, Jing Yu Liu, John J. Schwartz, & Zhang Li. (1997). Heparan sulfate proteoglycans of the cardiovascular system. Specific structures emerge but how is synthesis regulated?. Journal of Clinical Investigation. 99(9). 2062–2070. 309 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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