Linghan Gao

592 total citations
23 papers, 462 citations indexed

About

Linghan Gao is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Linghan Gao has authored 23 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Linghan Gao's work include Connexins and lens biology (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Intraocular Surgery and Lenses (3 papers). Linghan Gao is often cited by papers focused on Connexins and lens biology (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Intraocular Surgery and Lenses (3 papers). Linghan Gao collaborates with scholars based in China, United States and Australia. Linghan Gao's co-authors include Guoyin Feng, Lin He, Chunling Wan, Baohu Ji, Zhao Zhang, Guang He, Jing Du, Jian Wang, Jinglei Yang and Zhaofeng Zhang and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and Schizophrenia Bulletin.

In The Last Decade

Linghan Gao

22 papers receiving 450 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Linghan Gao China 13 277 120 77 64 62 23 462
Joshua Atkins Australia 11 199 0.7× 104 0.9× 43 0.6× 15 0.2× 6 0.1× 22 360
Zhanwen He China 10 206 0.7× 47 0.4× 14 0.2× 15 0.2× 12 0.2× 33 360
Edward Daly United States 10 140 0.5× 35 0.3× 13 0.2× 27 0.4× 24 0.4× 11 316
Hidetoshi Taniguchi Japan 13 237 0.9× 58 0.5× 9 0.1× 56 0.9× 3 0.0× 19 550
William Craigen United States 9 290 1.0× 81 0.7× 11 0.1× 6 0.1× 8 0.1× 13 443
H. Peilot Sweden 5 242 0.9× 31 0.3× 22 0.3× 14 0.2× 4 0.1× 8 528
Beate Lubrich Germany 10 159 0.6× 57 0.5× 15 0.2× 14 0.2× 2 0.0× 12 508
Nannan Ning China 10 138 0.5× 8 0.1× 24 0.3× 20 0.3× 10 0.2× 16 316

Countries citing papers authored by Linghan Gao

Since Specialization
Citations

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

Fields of papers citing papers by Linghan Gao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linghan Gao

This figure shows the co-authorship network connecting the top 25 collaborators of Linghan Gao. A scholar is included among the top collaborators of Linghan Gao 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 Linghan Gao. Linghan Gao 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.
Shi, Yurong, et al.. (2025). Bone morphogenetic proteins (BMPs) at the forefront of ocular diseases and therapeutics. Eye and Vision. 12(1). 29–29.
2.
Zhang, Xibo, Gang Qin, Guilan Chen, et al.. (2015). Variants inTRIM44Cause Aniridia by ImpairingPAX6Expression. Human Mutation. 36(12). 1164–1167. 26 indexed citations
3.
Liu, Xudong, Linghan Gao, Rui Zhang, et al.. (2014). Identification of Duplication Downstream of BMP2 in a Chinese Family with Brachydactyly Type A2 (BDA2). PLoS ONE. 9(4). e94201–e94201. 10 indexed citations
4.
Li, Xingwang, Baocheng Liu, Yang Wang, et al.. (2013). Association study on the DLG4 gene and schizophrenia in the Chinese Han population. Psychiatric Genetics. 23(6). 247–250. 2 indexed citations
5.
Tian, Xiaoli, Minghao Yin, Linghan Gao, et al.. (2013). Analysis of ischemic neuronal injury in CaV2.1 channel α1 subunit mutant mice. Biochemical and Biophysical Research Communications. 434(1). 60–64. 11 indexed citations
6.
Jia, Xueyuan, Feng Zhang, Jing Bai, et al.. (2013). Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract. BMC Medical Genetics. 14(1). 107–107. 8 indexed citations
7.
Sun, Liya, Juan Li, Kejun Zhou, et al.. (2013). Metabolomic Analysis Reveals Metabolic Disturbance in the Cortex and Hippocampus of Subchronic MK-801 Treated Rats. PLoS ONE. 8(4). e60598–e60598. 29 indexed citations
8.
9.
Li, Daxu, Rui Zhang, Bo Shen, et al.. (2012). Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysis. Genomics. 99(4). 220–226. 17 indexed citations
10.
Zhao, Peiquan, Chunling Wan, Gang Ma, et al.. (2011). An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree.. PubMed. 17. 3200–7. 7 indexed citations
11.
Ma, Gang, Jiang Yu, Yue Xiao, et al.. (2011). Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels. Cell Research. 21(9). 1343–1357. 29 indexed citations
12.
Shen, Qi, Jing Zhang, Yang Wang, et al.. (2010). No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population. Neuroscience Letters. 487(1). 61–65. 2 indexed citations
13.
Zhou, Kejun, Yifeng Yang, Linghan Gao, et al.. (2010). NMDA Receptor Hypofunction Induces Dysfunctions of Energy Metabolism And Semaphorin Signaling in Rats: A Synaptic Proteome Study. Schizophrenia Bulletin. 38(3). 579–591. 22 indexed citations
14.
Zhang, Ming, Ke Huang, Zhao Zhang, et al.. (2010). Proteome alterations of cortex and hippocampus tissues in mice subjected to vitamin A depletion. The Journal of Nutritional Biochemistry. 22(11). 1003–1008. 12 indexed citations
15.
Du, Jing, Wenjing Zhang, Lingli Guo, et al.. (2010). Two FSHR variants, haplotypes and meta-analysis in Chinese women with premature ovarian failure and polycystic ovary syndrome. Molecular Genetics and Metabolism. 100(3). 292–295. 66 indexed citations
16.
Liu, Baocheng, Jing Zhang, Lei Wang, et al.. (2010). No association between EGR gene family polymorphisms and schizophrenia in the Chinese population. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 34(3). 506–509. 17 indexed citations
17.
Ji, Baohu, Yujuan La, Linghan Gao, et al.. (2009). A Comparative Proteomics Analysis of Rat Mitochondria from the Cerebral Cortex and Hippocampus in Response to Antipsychotic Medications. Journal of Proteome Research. 8(7). 3633–3641. 58 indexed citations
18.
Cui, Xiaobo, Linghan Gao, Yan Jin, et al.. (2007). The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese family.. PubMed. 13. 2023–9. 19 indexed citations
19.
Zhang, Lu, Linghan Gao, Zhijian Li, et al.. (2006). Progressive sutural cataract associated with a BFSP2 mutation in a Chinese family.. PubMed. 12. 1626–31. 20 indexed citations
20.
Gao, Linghan, Wei Qin, Hao Cui, et al.. (2005). A novel locus of coralliform cataract mapped to chromosome 2p24-pter. Journal of Human Genetics. 50(6). 305–310. 12 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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