Can Liao

1.5k total citations
81 papers, 923 citations indexed

About

Can Liao is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Can Liao has authored 81 papers receiving a total of 923 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 38 papers in Pediatrics, Perinatology and Child Health and 28 papers in Genetics. Recurrent topics in Can Liao's work include Prenatal Screening and Diagnostics (37 papers), Genomic variations and chromosomal abnormalities (22 papers) and Congenital heart defects research (11 papers). Can Liao is often cited by papers focused on Prenatal Screening and Diagnostics (37 papers), Genomic variations and chromosomal abnormalities (22 papers) and Congenital heart defects research (11 papers). Can Liao collaborates with scholars based in China, United States and Hong Kong. Can Liao's co-authors include Dong‐Zhi Li, Fang Fu, Min Pan, Ru Li, Xin Yang, Guie Xie, Tingying Lei, Junjie Li, Yongling Zhang and Fang Fu and has published in prestigious journals such as Gene, Molecular Therapy and Neuropharmacology.

In The Last Decade

Can Liao

76 papers receiving 907 citations

Peers

Can Liao
Karen Chong Canada
Gail Coghlan Canada
Jorge Román Corona‐Rivera Mexico
Emin Karaca Türkiye
Giuliana Giardino Italy
Zhenyu Diao China
Ja‐Hyun Jang South Korea
Stamatia Papoutsopoulou Greece
C. Mirella Spalluto United Kingdom
L.C. Giudice United States
Karen Chong Canada
Can Liao
Citations per year, relative to Can Liao Can Liao (= 1×) peers Karen Chong

Countries citing papers authored by Can Liao

Since Specialization
Citations

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

Fields of papers citing papers by Can Liao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Can Liao

This figure shows the co-authorship network connecting the top 25 collaborators of Can Liao. A scholar is included among the top collaborators of Can Liao 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 Can Liao. Can Liao 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.
Lu, Jiaming, Fang Fu, Hang Zhou, et al.. (2025). Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine‐year retrospective study from China. Acta Obstetricia Et Gynecologica Scandinavica. 105(2). 268–279.
2.
3.
Fu, Fang, Xin Yang, Ru Li, et al.. (2024). Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma. BMC Medical Genomics. 17(1). 96–96. 1 indexed citations
4.
Liu, Liyuan, Fang Fu, Ru Li, et al.. (2023). Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations. Genes. 14(10). 1872–1872. 2 indexed citations
5.
Fu, Fang, Ru Li, Jin Han, et al.. (2023). ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2. Biochemistry and Biophysics Reports. 35. 101505–101505. 2 indexed citations
6.
Yan, Shujuan, Fang Fu, Ru Li, et al.. (2023). Exome sequencing improves genetic diagnosis of congenital orofacial clefts. Frontiers in Genetics. 14. 1252823–1252823. 4 indexed citations
7.
8.
Fu, Fang, Tingying Lei, Zhen Li, et al.. (2023). Genetic diagnosis of fetal microcephaly at a single tertiary center in China. Frontiers in Genetics. 14. 1112153–1112153. 5 indexed citations
9.
Fu, Fang, Ru Li, Qiuxia Yu, et al.. (2022). Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing. Frontiers in Genetics. 13. 951829–951829. 1 indexed citations
10.
Huang, Yuxin, et al.. (2022). Distribution of Vaginal and Gut Microbiome in Advanced Maternal Age. Frontiers in Cellular and Infection Microbiology. 12. 819802–819802. 6 indexed citations
11.
Zhou, Hang, Fang Fu, Ru Li, et al.. (2022). The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study. Frontiers in Genetics. 13. 856522–856522. 9 indexed citations
12.
Zhang, Zhao, Bin Yan, Fei Gao, et al.. (2020). PSCs Reveal PUFA-Provoked Mitochondrial Stress as a Central Node Potentiating RPE Degeneration in Bietti’s Crystalline Dystrophy. Molecular Therapy. 28(12). 2642–2661. 31 indexed citations
13.
Jiang, Dan, Feng Hong, Zhao Zhang, et al.. (2019). Donation of mitochondria by iPSC-derived mesenchymal stem cells protects retinal ganglion cells against mitochondrial complex I defect-induced degeneration. Theranostics. 9(8). 2395–2410. 103 indexed citations
14.
Wang, Rongyue, Tingying Lei, Fang Fu, et al.. (2018). Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China. Pediatrics & Neonatology. 60(1). 35–42. 22 indexed citations
15.
Lei, Tingying, Hongtao Wang, Fan Li, et al.. (2016). Application of high resolution SNP arrays in patients with congenital oral clefts in south China. Journal of Genetics. 95(4). 801–809. 6 indexed citations
16.
Xie, Guie, Hongping Tang, Shaoqing Wu, et al.. (2014). The cyclin-dependent kinase inhibitor SNS-032 induces apoptosis in breast cancer cells via depletion of Mcl-1 and X-linked inhibitor of apoptosis protein and displays antitumor activity in vivo. International Journal of Oncology. 45(2). 804–812. 29 indexed citations
17.
Liao, Can, et al.. (2013). Codon 62 (G T G>G C G, Val→Ala) ( α 1) ( HBA1 : c.188T>C) Causing Nondeletional α -Thalassemia in a Chinese Family. Hemoglobin. 37(2). 188–191. 1 indexed citations
18.
Liao, Can, Fang Fu, Ru Li, et al.. (2013). Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation. European Journal of Medical Genetics. 56(9). 484–489. 27 indexed citations
19.
Li, Dong‐Zhi & Can Liao. (2008). Incidental Discovery of Nonpaternity during Prenatal Testing of Genetic Disease. Fetal Diagnosis and Therapy. 24(1). 39–41. 5 indexed citations
20.
Xu, Xiangmin, et al.. (1995). A novel amber mutation in a β°‐thalassaemia gene (β37TGG→TAG), with direct detection by mapping the restriction fragments in amplified genomic DNA. British Journal of Haematology. 90(4). 960–962. 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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