Shixiu Liao

464 total citations
37 papers, 162 citations indexed

About

Shixiu Liao is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Shixiu Liao has authored 37 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Shixiu Liao's work include Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (5 papers) and Prenatal Screening and Diagnostics (4 papers). Shixiu Liao is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (5 papers) and Prenatal Screening and Diagnostics (4 papers). Shixiu Liao collaborates with scholars based in China, United States and Hong Kong. Shixiu Liao's co-authors include Hongdan Wang, Dong Wu, Guiyu Lou, Hongwei Zhang, Qiang Fu, Tao Qin, Ning Su, Peng Xia, Pan Liu and Xu Zhang and has published in prestigious journals such as Scientific Reports, Gene and Clinica Chimica Acta.

In The Last Decade

Shixiu Liao

29 papers receiving 160 citations

Peers

Countries citing papers authored by Shixiu Liao

Since Specialization

Citations

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

Fields of papers citing papers by Shixiu Liao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shixiu Liao

This figure shows the co-authorship network connecting the top 25 collaborators of Shixiu Liao. A scholar is included among the top collaborators of Shixiu 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 Shixiu Liao. Shixiu Liao 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

#	Work	Indexed citations
1	Unraveling novel variants in the NF1 gene and investigating potential therapeutic strategies 2025 ·Scientific Reports ·Jianmei Huang, (unknown), Yaoping Wang, Xiang Ma, (unknown), Xiaodong Huo, Jie Bai, Hongjie Zhu, (unknown), Yibing Lv, Shixiu Liao	0
2	Integrative DNA methylome and transcriptome analysis identify potential genes on the influence of dilated cardiomyopathy-associated heart failure 2025 ·Clinical Epigenetics ·(unknown), Yunfei Liu, Zhiming Zhou, Jianchao Chen, Lin Guo, (unknown), (unknown), Bingtao Hao, Bin Yang, Shixiu Liao	2
3	Pregnancy outcomes of 4,200 fetuses with increased nuchal translucency in Henan, China 2025 ·Frontiers in Medicine ·(unknown), Wenke Yang, (unknown), Yuwei Zhang, Xin Wang, Jinming Wang, (unknown), Bingtao Hao, Shixiu Liao	0
4	Identification of novel biallelic mutations in CFAP53 associated with fetal situs inversus totalis and literature review 2025 ·Journal of Applied Genetics ·(unknown), Mengyao Tan, Hongjie Zhu, Guiyu Lou, (unknown), (unknown), Yibing Lv, Jianmei Huang, Ruili Wang, Bingtao Hao, Shixiu Liao	2
5	Prenatal finding of isolated ventricular septal defect: genetic association, outcomes and counseling 2024 ·Frontiers in Genetics ·Xin Chen, Qian Zhang, (unknown), Qiuxia Feng, (unknown), Shixiu Liao	0
6	HNRNPC mediated m6A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA 2023 ·Journal of Reproductive Immunology ·Mengting Zhang, Nana Huang, (unknown), (unknown), Bing Kang, Han Guo, (unknown), Shixiu Liao, Hongdan Wang	1
7	Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tarda 2023 ·Frontiers in Genetics ·Guiyu Lou, (unknown), (unknown), Yu-Wei Zhang, Bingtao Hao, (unknown), Hongyan Liu, Shixiu Liao	0
8	A comparison of algorithms for identifying copy number variants in family-based whole-exome sequencing data and its implications in inheritance pattern analysis 2023 ·Gene ·Bo Ye, (unknown), Shixiu Liao, Keyue Ding	0
9	<p>Emerging Roles Of hsa-circ-0046600 Targeting The miR-640/HIF-1α Signalling Pathway In The Progression Of HCC</p> 2019 ·OncoTargets and Therapy ·(unknown), Qiang Fu, (unknown), Xu Zhang, (unknown), Peng Xia, Pan Liu, Shixiu Liao, Tao Qin, Hongwei Zhang	34
10	Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population 2018 ·Scientific Reports ·(unknown), Guiyu Lou, (unknown), Yu-Wei Zhang, Hongdan Wang, (unknown), (unknown), Hongyan Liu, Xichuan Li, Shixiu Liao	2
11	Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome 2017 ·Clinica Chimica Acta ·(unknown), Xiaobo Li, (unknown), Hongdan Wang, Guiyu Lou, Tao Li, (unknown), Hongyan Liu, Xichuan Li, Shixiu Liao	4
12	Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report 2017 ·Molecular Medicine Reports ·Dong Wu, Hui Zhang, (unknown), Hongdan Wang, Tao Wang, Shixiu Liao	2
13	Evaluation of the genetic parameters and mutation analysis of 22 STR loci in the central Chinese Han population 2016 ·International Journal of Legal Medicine ·Hongdan Wang, Bing Kang, Ning Su, Miao He, Bo Zhang, Yuxin Guo, (unknown), Shixiu Liao, Zhaoshu Zeng	14
14	Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·(unknown), Dong Wu, (unknown), Shixiu Liao	5
15	A novel MIP mutation in familial congenital nuclear cataracts 2016 ·European Journal of Medical Genetics ·(unknown), (unknown), Hongdan Wang, Tao Li, Guiyu Lou, (unknown), (unknown), Hongyan Liu, Shixiu Liao, Zhe Liu	15
16	Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome 2016 ·Journal of Biomedical Science ·(unknown), (unknown), Hongdan Wang, Dong Wu, Hui Zhang, Haijun Xiao, (unknown), (unknown), Shixiu Liao	19
17	[Association of SPO11 and GST gene polymorphisms with idiopathic male infertility in ethnic Han Chinese]. 2015 ·PubMed ·(unknown), (unknown), (unknown), Shixiu Liao, (unknown), (unknown), Y. Liu, (unknown), Jiangtao Gao	6
18	Molecular diagnosis of X-linked hypohidrotic ectodermal dysplasia families 2015 ·Zhonghua shiyong erke linchuang zazhi ·(unknown), Shixiu Liao, Yu Wang, Lei Zhang, Tao Li	1
19	New compound heterozygous mutations of p. Thr101Ilefs2 and p. Thr306Ale in a child from a Chinese family with 17α-hydroxylase/17, 20-lyase deficiency 2015 ·Genetics and Molecular Research* ·Hong Xiao, (unknown), Tianxiao Li, Dong Wu, (unknown), Tianyun Wang, Bin Zhang, Shixiu Liao	0
20	DNA methylation study of fetus genome through a genome-wide analysis 2014 ·BMC Medical Genomics ·Hongdan Wang, (unknown), (unknown), Tao Li, Dong Wu, Xianping Zhang, (unknown), (unknown), (unknown), (unknown), Ke Yang, Shixiu Liao, Bofeng Zhu	9

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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