Hanbing Xie

743 total citations
32 papers, 544 citations indexed

About

Hanbing Xie is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hanbing Xie has authored 32 papers receiving a total of 544 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hanbing Xie's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Lung Cancer Diagnosis and Treatment (3 papers). Hanbing Xie is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Lung Cancer Diagnosis and Treatment (3 papers). Hanbing Xie collaborates with scholars based in China, Netherlands and United States. Hanbing Xie's co-authors include Qin He, Man Li, Zhirong Zhang, Yingke Liu, Qianwen Yu, Xian Tang, Jianping Li, Kebai Ren, Yiliang Yang and Mengmeng Li and has published in prestigious journals such as Scientific Reports, Journal of Controlled Release and American Journal of Obstetrics and Gynecology.

In The Last Decade

Hanbing Xie

28 papers receiving 535 citations

Peers

Countries citing papers authored by Hanbing Xie

Since Specialization

Citations

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

Fields of papers citing papers by Hanbing Xie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanbing Xie

This figure shows the co-authorship network connecting the top 25 collaborators of Hanbing Xie. A scholar is included among the top collaborators of Hanbing Xie 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 Hanbing Xie. Hanbing Xie 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	Identifying a novel SRCAP variant in floating-harbor syndrome and prenatal genetic diagnosis in this Chinese family: A case report 2025 ·World Journal of Clinical Cases ·Xiao Xiao, Ping Wang, He Wang, Hanbing Xie, Shanling Liu	0
2	Functional characterization of SOX5 variant causing Lamb–Shaffer syndrome and literature review of variants in the SOX5 gene 2025 ·Orphanet Journal of Rare Diseases ·Ping Wang, Hanbing Xie, Xiao Xiao, (unknown), Yan Wang, Shanling Liu	0
3	An Integrated Nomogram Combining Deep Learning and Radiomics for Predicting Malignancy of Pulmonary Nodules Using CT ‐Derived Nodules and Adipose Tissue: A Multicenter Study 2024 ·Cancer Medicine ·(unknown), (unknown), Hanbing Xie, Yuyang Jiang, Meng Sun, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ruitao Wang	1
4	RCAN family member 3 deficiency contributes to noncompaction of the ventricular myocardium 2024 ·Journal of genetics and genomics ·Ting Hu, Lan Liu, He Wang, Mei Yang, Bocheng Xu, Hanbing Xie, Ziyuan Lin, Xiaolei Jin, Ping Wang, Yanyan Liu, Huaqin Sun, Shanling Liu	1
5	Case Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family 2023 ·Frontiers in Genetics ·Qinqin Xiang, Jing Chen, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, (unknown), Shanling Liu	1
6	Synthesis of Carbon Dots with Hemostatic Effects Using Traditional Chinese Medicine as a Biomass Carbon Source 2023 ·ACS Omega ·(unknown), (unknown), Hanbing Xie, (unknown), Dan Zhao, (unknown), Xiaohong Chen, Jun Li	20
7	Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family 2022 ·BMC Medical Genomics ·Jing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, Shanling Liu	5
8	NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism 2022 ·BMC Genomics ·Yuanyuan Xiao, (unknown), Hanbing Xie, Shuang Huang, Jing Wang, Shanling Liu	3
9	A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis 2022 ·Molecular Genetics & Genomic Medicine ·Qianying Zhao, Qinqin Xiang, (unknown), Xiao Xiao, Hanbing Xie, He Wang, Mei Yang, Shanling Liu	1
10	L1 Syndrome Prenatal Diagnosis Supplemented by Functional Analysis of One L1CAM Gene Missense Variant 2021 ·Reproductive Sciences ·Ping Wang, Hong Liao, (unknown), Hanbing Xie, (unknown), Mei Yang, Shanling Liu	4
11	Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability 2021 ·Epilepsy Research ·Mei Yang, Bocheng Xu, Jiamin Wang, Zhu Zhang, Hanbing Xie, He Wang, Ting Hu, Shanling Liu	6
12	A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report 2021 ·BMC Medical Genomics ·(unknown), Yuanyuan Xiao, Hanbing Xie, Shanling Liu, Jing Wang	2
13	Rapid pH-responsive self-disintegrating nanoassemblies balance tumor accumulation and penetration for enhanced anti-breast cancer therapy 2021 ·Acta Biomaterialia ·Jianping Li, Yashi Wang, Chaoqun Xu, Qianwen Yu, Xuhui Wang, Hanbing Xie, Lifeng Tian, Yue Qiu, Rong Guo, Zhengze Lu, Man Li, Qin He	37
14	Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family 2021 ·Frontiers in Genetics ·(unknown), Yuanyuan Xiao, Hanbing Xie, Jing Wang, Shanling Liu	1
15	Ultrasound-guided transmuscular quadratus lumborum block reduced postoperative opioids consumptions in patients after laparoscopic hepatectomy: a three-arm randomized controlled trial 2021 ·BMC Anesthesiology ·(unknown), Guoliang Sun, Weifeng Yao, Shaoli Zhou, Ning Shen, (unknown), Hanbing Xie, (unknown), Mian Ge	20
16	Remodeling tumor immune microenvironment via targeted blockade of PI3K-γ and CSF-1/CSF-1R pathways in tumor associated macrophages for pancreatic cancer therapy 2020 ·Journal of Controlled Release ·Man Li, Mengmeng Li, Yiliang Yang, Yingke Liu, Hanbing Xie, Qianwen Yu, Lifeng Tian, Xian Tang, Kebai Ren, Jianping Li, Zhirong Zhang, Qin He	174
17	Knockdown of hypoxia-inducible factor-1 alpha by tumor targeted delivery of CRISPR/Cas9 system suppressed the metastasis of pancreatic cancer 2019 ·Journal of Controlled Release ·Man Li, Hanbing Xie, Yingke Liu, Chunyu Xia, Xingli Cun, Yang Long, Xiaoxiao Chen, Miao Deng, Rong Guo, Zhirong Zhang, Qin He	103
18	Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing 2018 ·Scientific Reports ·(unknown), Lin Chen, (unknown), Li Wang, Hanbing Xie, Yuanyuan Xiao, (unknown), Yang Zeng, (unknown), (unknown), Hongmei Zhu, Xinlian Chen, Qian Zhu, Zhiying Liu, Hongqian Liu	23
19	Determination of three exogenous plant hormone residues in bean sprout by high performance liquid chromatography-quadrupole-time of flight mass spectrometry 2014 ·Chinese Journal of Chromatography ·Hanbing Xie, (unknown), Haifeng Zhao, Yigang Wang, (unknown), Shan Zhao	2
20	Association of mtDNA D-Loop Polymorphisms with Risk of Gastric Cancer in Chinese Population 2011 ·Pathology & Oncology Research ·Wei Li, (unknown), Tiankang Guo, Peiqiang Li, Hua Wu, Hanbing Xie, (unknown), Feng Gao, Xiaodong Xie	8

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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