Xiuli Zhao

948 citations

45 papers · 553 indexed · h-index 13

Co-authors: Xue Zhang Wilson H.Y. Lo Jung Keun Kim Yangjie Wu Yabo Li Mengmeng Huang Yang Luo Yixin Bian
Topics: Connective tissue disorders research (10 papers)Neurogenetic and Muscular Disorders Research (5 papers)Bone and Dental Protein Studies (5 papers)
Cited by: Developmental Biology Genetics Molecular Biology
Journals: Biomaterials The American Journal of Human Genetics Green Chemistry
Partner nations: China United States Australia

In The Last Decade

Xiuli Zhao

41 papers receiving 539 citations

Peers

Countries citing papers authored by Xiuli Zhao

Since Specialization

Citations

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

Fields of papers citing papers by Xiuli Zhao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiuli Zhao

This figure shows the co-authorship network connecting the top 25 collaborators of Xiuli Zhao. A scholar is included among the top collaborators of Xiuli Zhao 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 Xiuli Zhao. Xiuli Zhao 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	Investigation of the role and mechanism of dapagliflozin in mitigating renal injury in rats afflicted with diabetic kidney disease 2025 ·Biochemical Pharmacology ·Hao Wang,Xiuli Zhao,Xiao Wang,Yi Gong,(unknown),Yan-ting Gu,Bosai He,(unknown)	3
2	Tenuigenin targets Trim31 and NF-κB pathway to protect dopaminergic neurons in Parkinson’s disease mice 2025 ·Naunyn-Schmiedeberg s Archives of Pharmacology ·(unknown),Xu Chen,(unknown),(unknown),Shaohua Guo,(unknown),(unknown),Xiuli Zhao	0
3	The Spectra of Pathogenic Variants and Phenotypes in a Chinese Cohort of 298 Families with Osteogenesis Imperfecta 2025 ·Genes ·(unknown),Xiuzhi Ren,Yixuan Cao,(unknown),(unknown),Lulu Li,(unknown),Yuqian Ye,(unknown),B. Zhao,(unknown),Nan Wu,Zhen Li,Lingqian Wu,Xiuli Zhao	0
4	Advances in meniscus tissue engineering: Towards bridging the gaps from bench to bedside 2024 ·Biomaterials ·Yixin Bian,(unknown),(unknown),Zehui Lv,Yiming Xu,Yingjie Wang,Han Wang,Wei Zhu,(unknown),Xiuli Zhao,Bin Feng,Xisheng Weng	6
5	Advances in Mesenchymal Stem Cell Therapy for Osteoarthritis: From Preclinical and Clinical Perspectives 2023 ·Bioengineering ·Zehui Lv,(unknown),Yixin Bian,(unknown),(unknown),Xiuli Zhao,Xisheng Weng	27
6	Clinical and genetic analysis in Chinese families with synpolydactyly, and cellular localization of HOXD13 with different length of polyalanine tract 2023 ·Frontiers in Genetics ·(unknown),(unknown),Yiming Xu,Yixuan Cao,Shan Li,Xue Zhang,Xiuli Zhao	0
7	Identification of potential susceptibility genes in patients with primary Sjögren’s syndrome-associated pulmonary arterial hypertension through whole exome sequencing 2023 ·Arthritis Research & Therapy ·(unknown),Yue Shi,Jiuliang Zhao,Qian Wang,Mengtao Li,Xiuli Zhao	2
8	Identification of six novel variants from nine Chinese families with hypophosphatemic rickets 2022 ·BMC Medical Genomics ·Yixuan Cao,Yi You,Qiong Wang,Xiuzhi Ren,Shan Li,Lulu Li,Weibo Xia,Xin Guan,(unknown),Shiro Ikegawa,Zheng Wang,Xiuli Zhao	0
9	Identification of variants in ACAN and PAPSS2 leading to spondyloepi(meta)physeal dysplasias in four Chinese families 2022 ·Molecular Genetics & Genomic Medicine ·Yixuan Cao,Xin Guan,Shan Li,Nan Wu,Xiumin Chen,(unknown),Bo Yang,Xiuli Zhao	4
10	Meniscus repair: up-to-date advances in stem cell-based therapy 2022 ·Stem Cell Research & Therapy ·Yixin Bian,Han Wang,Xiuli Zhao,Xisheng Weng	23
11	CRISPR/Cas9 correction of a dominant cis-double-variant in COL1A1 isolated from a patient with osteogenesis imperfecta increases the osteogenic capacity of induced pluripotent stem cells 2020 ·Journal of Bone and Mineral Research ·Yixuan Cao,Lulu Li,Xiuzhi Ren,Bin Mao,Yujiao Yang,(unknown),Yun Guan,Shan Li,(unknown),Xin Guan,(unknown),Xiuli Zhao	4
12	Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta 2020 ·Frontiers in Genetics ·Shan Li,Yixuan Cao,Han Wang,Lulu Li,Xiuzhi Ren,(unknown),Yanzhou Wang,Yun Guan,(unknown),Bin Mao,(unknown),Yi You,Xin Guan,Yujiao Yang,Xue Zhang,Xiuli Zhao	24
13	Autologous correction in patient induced pluripotent stem cell‐endothelial cells to identify a novel pathogenic mutation of hereditary hemorrhagic telangiectasia 2019 ·Pulmonary Circulation ·Fang Zhou,Xiuli Zhao,Xiu Liu,Yanyan Liu,Feng Ma,Bao Liu,Jun Yang	3
14	Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing 2019 ·BMC Medical Genetics ·Shan Li,Jianfei Zhang,Yixuan Cao,Yi You,Xiuli Zhao	12
15	Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia 2018 ·Genetic Testing and Molecular Biomarkers ·Yanshan Liu,(unknown),Rui Hua,Xiuli Zhao,Wei Yang,Yaping Liu,Xue Zhang	6
16	Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1 2018 ·BMC Medical Genetics ·Bin Mao,Siyu Chen,Xin Chen,Xiumei Yu,(unknown),(unknown),Lulu Li,Zheng Wang,Xiuli Zhao,Xue Zhang	12
17	Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families 2018 ·BMC Medical Genetics ·Shan Li,Yi You,Jinsong Gao,Bin Mao,Yixuan Cao,Xiuli Zhao,Xue Zhang	13
18	[Identification of a novel mutation of DSPP gene in a Chinese family affected with dentinogenesis imperfecta shields type II]. 2016 ·PubMed ·Yanshan Liu,(unknown),Jinsong Gao,Shan Li,Xiuli Zhao,Xue Zhang	6
19	A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family 2009 ·Journal of Human Genetics ·Dan Lv,Yang Luo,Wei Yang,Lihua Cao,Yaran Wen,Xiuli Zhao,Miao Sun,Wilson H.Y. Lo,Xue Zhang	9
20	A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression 2006 ·Human Genetics ·Miao Jiang,Xiuli Zhao,(unknown),(unknown),Xuefu Li,(unknown),(unknown),Yun-Qing Li,(unknown),(unknown),Wilson H.Y. Lo,Xue Zhang,Jianxin Li	26

About Xiuli Zhao

Xiuli Zhao is a scholar working on Developmental Biology, Genetics and Rheumatology, having authored 45 papers that have together received 553 indexed citations. Recurring topics across this work include Connective tissue disorders research (10 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Bone and Dental Protein Studies (5 papers). The work is most often cited by research in Developmental Biology (57 citations), Genetics (56 citations) and Molecular Biology (299 citations). Xiuli Zhao has collaborated with scholars based in China, United States and Australia. Frequent co-authors include Xue Zhang, Wilson H.Y. Lo, Jung Keun Kim, Yangjie Wu, Yabo Li, Mengmeng Huang, Yang Luo, Yixin Bian, Xisheng Weng and Bin Mao. Their work appears in journals such as Biomaterials, The American Journal of Human Genetics and Green Chemistry.

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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