Xinghua Luan

1.2k total citations
48 papers, 456 citations indexed

About

Xinghua Luan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Xinghua Luan has authored 48 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Xinghua Luan's work include Genetic Neurodegenerative Diseases (12 papers), Hereditary Neurological Disorders (10 papers) and Mitochondrial Function and Pathology (6 papers). Xinghua Luan is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Hereditary Neurological Disorders (10 papers) and Mitochondrial Function and Pathology (6 papers). Xinghua Luan collaborates with scholars based in China, United States and Japan. Xinghua Luan's co-authors include Li Cao, Yun Yuan, Daojun Hong, Wotu Tian, Xiaojun Huang, Haiyan Zhou, Zhaoxia Wang, Wei Zhang, Bin Chen and Ahmet Höke and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Xinghua Luan

45 papers receiving 450 citations

Peers

Xinghua Luan
Alessandro Malandrini Italy
Andrea Legati Italy
Lauren Brady Canada
Carola Hedberg‐Oldfors Sweden
David S. Lynch United Kingdom
Annabelle Chaussenot France
Maria Piane Italy
Karlla W. Brigatti United States
Cristina Domínguez‐González Spain
Carmen Paradas Spain
Alessandro Malandrini Italy
Xinghua Luan
Citations per year, relative to Xinghua Luan Xinghua Luan (= 1×) peers Alessandro Malandrini

Countries citing papers authored by Xinghua Luan

Since Specialization
Citations

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

Fields of papers citing papers by Xinghua Luan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xinghua Luan

This figure shows the co-authorship network connecting the top 25 collaborators of Xinghua Luan. A scholar is included among the top collaborators of Xinghua Luan 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 Xinghua Luan. Xinghua Luan 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.
2.
Chen, Qian, Xinghua Luan, Ping Sun, et al.. (2024). Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series. Frontiers in Medicine. 11. 1188193–1188193.
3.
Zhu, Xiaowei, Xinghua Luan, Kaili Jiang, et al.. (2023). Case report: Muscular tuberculosis with lower-extremity muscular masses as the initial presentation: Clinicopathological analysis of two cases and review of the literature. Frontiers in Medicine. 10. 1106412–1106412. 2 indexed citations
4.
Zhang, Jiawei, Wotu Tian, Qingqing Jiang, et al.. (2022). Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series. Biomolecules. 12(10). 1382–1382.
5.
Cao, Yuwen, et al.. (2022). Generation of an induced pluripotent stem cell JTUi005-A from a patient with neuronal intranuclear inclusion disease. Stem Cell Research. 65. 102938–102938. 1 indexed citations
6.
Luan, Xinghua, Xiaohong Liu, Xiangning Wang, et al.. (2021). Characteristics of ocular findings of patients with neuronal intranuclear inclusion disease. Neurological Sciences. 43(5). 3231–3237. 8 indexed citations
7.
Cao, Yuwen, Chao Zhang, Ping Zhong, et al.. (2021). Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease. Acta Neurologica Belgica. 122(3). 647–658. 16 indexed citations
8.
Qian, Xiaohang, Xiaoying Liu, Zeyu Zhu, et al.. (2021). Variants in LAMC3 Causes Occipital Cortical Malformation. Frontiers in Genetics. 12. 616761–616761. 6 indexed citations
9.
Liu, Xiaoli, Taotao Liu, Yuwen Cao, et al.. (2021). Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome. Metabolic Brain Disease. 37(2). 311–317. 3 indexed citations
10.
11.
Tian, Wotu, Xinghua Luan, Haiyan Zhou, et al.. (2019). Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. Neuromuscular Disorders. 29(4). 282–289. 8 indexed citations
12.
Tian, Wotu, Xiaoli Liu, Xiaojun Huang, et al.. (2018). Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review. Seizure. 57. 80–86. 11 indexed citations
13.
Tian, Wotu, Xiaoli Liu, Tian Wang, et al.. (2016). Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18. Chinese Medical Journal. 129(22). 2759–2761. 13 indexed citations
14.
Luan, Xinghua, Xiaojun Huang, Xiaoli Liu, et al.. (2016). Infantile spinal muscular atrophy with respiratory distress type I presenting without respiratory involvement: Novel mutations and review of the literature. Brain and Development. 38(7). 685–689. 10 indexed citations
15.
Luan, Xinghua, Wotu Tian, & Li Cao. (2016). Limb-girdle congenital myasthenic syndrome in a Chinese family with novel mutations in MUSK gene and literature review. Clinical Neurology and Neurosurgery. 150. 41–45. 15 indexed citations
16.
Liu, Xiaoli, Tian Wang, Xiaojun Huang, et al.. (2015). Novel ATM mutations with ataxia-telangiectasia. Neuroscience Letters. 611. 112–115. 8 indexed citations
17.
Luan, Xinghua, et al.. (2012). Pathologic and genetic features in 6 Chinese X-linked Charcot-Marie-Tooth disease type 1 families. Chin J Neurol. 45(1). 6–10. 1 indexed citations
18.
Hong, Daojun, Xinghua Luan, Wei Zhang, et al.. (2009). A novel mutation of SI2F in desmin causing desminopathy: a family report. Chin J Neurol. 42(10). 682–685. 1 indexed citations
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20.
Chen, Bin, et al.. (2009). Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2. Neuropathology. 29(5). 543–547. 10 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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