Yalan Liu

1.2k total citations
54 papers, 745 citations indexed

About

Yalan Liu is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Yalan Liu has authored 54 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 16 papers in Sensory Systems and 12 papers in Genetics. Recurrent topics in Yalan Liu's work include Hearing, Cochlea, Tinnitus, Genetics (16 papers), RNA regulation and disease (12 papers) and melanin and skin pigmentation (9 papers). Yalan Liu is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (16 papers), RNA regulation and disease (12 papers) and melanin and skin pigmentation (9 papers). Yalan Liu collaborates with scholars based in China, United States and France. Yalan Liu's co-authors include Yong Feng, Lingyun Mei, Chufeng He, Yuhua Fan, Yaoyun Tang, Xing Fang, Hongsheng Chen, Zhengmao Hu, Wei Wang and Xin Li and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Yalan Liu

54 papers receiving 731 citations

Peers

Yalan Liu

GENET

Matías Morin Spain

Paolo E. Forni United States

Yunbo Qiao China

Cong Tian China

Teresa Rivera Spain

Bryan Kuo United States

Mary D’Souza United States

Luo Guo China

Yoojin Choi United States

Matías Morin Spain

Yalan Liu

529 ×1.4

262 ×1.8

83 ×0.6

GENET

323 ×2.5

57 ×0.6

Citations per year, relative to Yalan Liu Yalan Liu (= 1×) peers Matías Morin

Countries citing papers authored by Yalan Liu

Since Specialization

Citations

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

Fields of papers citing papers by Yalan Liu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yalan Liu

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

All Works

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20 of 20 papers shown

Hu, Huamei, et al.. (2023). Xp22.31 copy number variations in 87 fetuses: refined genotype–phenotype correlations by prenatal and postnatal follow-up. BMC Medical Genomics. 16(1). 69–69. 3 indexed citations

Liu, Yalan, et al.. (2022). Arylalkylamine N-acetyltransferase 1 gene (AANAT1) regulates cuticle pigmentation and ovary development of the adult oriental fruit fly, Bactrocera dorsalis. Insect Biochemistry and Molecular Biology. 150. 103850–103850. 7 indexed citations

Li, Jianfang, Xiaoyu Zhang, Xue Bai, et al.. (2021). Identification of putative muscarinic acetylcholine receptor genes in Bactrocera dorsalis and functional analysis of Bdor-mAChR-B. Insect Biochemistry and Molecular Biology. 139. 103657–103657. 14 indexed citations

Liu, Yalan, Lu Shen, Yaowen Zhang, et al.. (2021). Rare NRXN1 missense variants identified in autism interfered protein degradation and Drosophila sleeping. Journal of Psychiatric Research. 143. 113–122. 3 indexed citations

Wen, Jie, Jian Song, Chufeng He, et al.. (2021). Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation. Stem Cell Research. 51. 102157–102157. 5 indexed citations

Li, Xin, Ping Wu, Yaoyun Tang, et al.. (2020). Down-Regulation of MiR-181c-5p Promotes Epithelial-to-Mesenchymal Transition in Laryngeal Squamous Cell Carcinoma via Targeting SERPINE1. Frontiers in Oncology. 10. 544476–544476. 14 indexed citations

Mei, Lingyun, Hongsheng Chen, Xinzhang Cai, et al.. (2019). New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing. Neural Plasticity. 2019. 1–12. 18 indexed citations

Liu, Yalan, Chang Liu, Deyuan Liu, et al.. (2019). A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss. PLoS ONE. 14(4). e0215212–e0215212. 13 indexed citations

Feng, Yong, Yalan Liu, Chufeng He, et al.. (2019). A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review. Gene. 704. 113–120. 13 indexed citations

10.

Wen, Jie, Yalan Liu, Jie Ling, et al.. (2018). Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families. International Journal of Pediatric Otorhinolaryngology. 115. 114–119. 2 indexed citations

11.

Feng, Yong, Denise Yan, M’hamed Grati, et al.. (2018). A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss. Human Genetics. 137(6-7). 437–446. 13 indexed citations

12.

Liu, Yalan, Lingyun Mei, Chufeng He, et al.. (2017). Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II. Biochemical and Biophysical Research Communications. 493(1). 258–262. 3 indexed citations

13.

Feng, Yong, Zhengmao Hu, Jia‐Da Li, et al.. (2017). Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family. International Journal of Pediatric Otorhinolaryngology. 100. 1–7. 8 indexed citations

14.

Li, Jia‐Da, Fen Tang, Jie Sun, et al.. (2017). Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I. Gene. 642. 362–366. 5 indexed citations

15.

Pan, Yongcheng, Jingjing Chen, Hui Guo, et al.. (2015). Association of genetic variants of GRIN2B with autism. Scientific Reports. 5(1). 8296–8296. 38 indexed citations

16.

Lu, Lina, Hui Guo, Peng Yu, et al.. (2014). Common and rare variants of the THBS1 gene associated with the risk for autism. Psychiatric Genetics. 24(6). 235–240. 13 indexed citations

17.

Xu, Xiaojuan, Zhimin Xiong, Lusi Zhang, et al.. (2014). Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients. Molecular Biology Reports. 41(6). 4133–4140. 30 indexed citations

18.

Guo, Hui, Guanglei Xun, Peng Yu, et al.. (2012). Disruption of Contactin 4 in two subjects with autism in Chinese population. Gene. 505(2). 201–205. 23 indexed citations

19.

Jiang, Lu, Honghan Wang, Yalan Liu, et al.. (2011). Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation. Acta Oto-Laryngologica. 131(9). 970–975. 3 indexed citations

20.

Jiang, Lu, Yalan Liu, Yong Feng, et al.. (2011). Gene localization in a Chinese family with autosomal dominant non-syndromic deafness. Acta Oto-Laryngologica. 131(10). 1061–1068. 2 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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