En‐Lin Dong

454 total citations
15 papers, 324 citations indexed

About

En‐Lin Dong is a scholar working on Genetics, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, En‐Lin Dong has authored 15 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Molecular Biology. Recurrent topics in En‐Lin Dong's work include Neurogenetic and Muscular Disorders Research (7 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (4 papers). En‐Lin Dong is often cited by papers focused on Neurogenetic and Muscular Disorders Research (7 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (4 papers). En‐Lin Dong collaborates with scholars based in China and United States. En‐Lin Dong's co-authors include Wan‐Jin Chen, Ning Wang, Miao Zhao, Xiang Lin, Hui‐Zhen Su, Ying‐Qian Lu, Xinxin Guo, Xiao-Hong Lin, Shuang Wu and J. He and has published in prestigious journals such as Neuron, Brain and Cell and Tissue Research.

In The Last Decade

En‐Lin Dong

15 papers receiving 323 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
En‐Lin Dong China	10	119	118	78	75	73	15	324
Ying‐Qian Lu China	7	69 0.6×	90 0.8×	47 0.6×	52 0.7×	78 1.1×	12	240
Hui‐Zhen Su China	8	79 0.7×	53 0.4×	57 0.7×	42 0.6×	95 1.3×	17	269
K Misu Japan	8	191 1.6×	213 1.8×	64 0.8×	25 0.3×	20 0.3×	10	465
Bianca M. de Graaf Netherlands	9	135 1.1×	301 2.6×	27 0.3×	12 0.2×	94 1.3×	15	458
Stayko Sarafov Bulgaria	9	29 0.2×	215 1.8×	17 0.2×	45 0.6×	40 0.5×	20	297
Ana L. Pelayo‐Negro Spain	13	304 2.6×	164 1.4×	99 1.3×	36 0.5×	14 0.2×	27	450
Caterina Marconi Italy	8	39 0.3×	86 0.7×	25 0.3×	38 0.5×	8 0.1×	18	243
Paola Rinchetti Italy	11	68 0.6×	234 2.0×	19 0.2×	167 2.2×	47 0.6×	16	339
Daigo Miyazaki Japan	10	41 0.3×	267 2.3×	8 0.1×	53 0.7×	59 0.8×	31	362
Yuta Ichinose Japan	10	119 1.0×	112 0.9×	73 0.9×	36 0.5×	18 0.2×	28	319

Countries citing papers authored by En‐Lin Dong

Since Specialization

Citations

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

Fields of papers citing papers by En‐Lin Dong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by En‐Lin Dong. 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 En‐Lin Dong. The network helps show where En‐Lin Dong may publish in the future.

Co-authorship network of co-authors of En‐Lin Dong

This figure shows the co-authorship network connecting the top 25 collaborators of En‐Lin Dong. A scholar is included among the top collaborators of En‐Lin Dong 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 En‐Lin Dong. En‐Lin Dong is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Chen, Yijun, Zaiqiang Zhang, Mengwen Wang, et al.. (2021). Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia. Frontiers in Neurology. 12. 627531–627531. 4 indexed citations

Wang, Mengwen, et al.. (2020). Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia. Annals of Clinical and Translational Neurology. 7(10). 1862–1869. 10 indexed citations

Chen, Yijun, Mengwen Wang, En‐Lin Dong, et al.. (2019). Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia. Parkinsonism & Related Disorders. 65. 256–260. 10 indexed citations

Zhao, Miao, Yijun Chen, Mengwen Wang, et al.. (2019). Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia. Molecular Diagnosis & Therapy. 23(6). 781–789. 22 indexed citations

Zou, Xiaohuan, Xinxin Guo, Hui‐Zhen Su, et al.. (2019). Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies. Journal of Molecular Neuroscience. 68(4). 640–646. 7 indexed citations

Lin, Xiang, Hui‐Zhen Su, En‐Lin Dong, et al.. (2019). Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia. Brain. 142(8). 2238–2252. 29 indexed citations

Yao, Xiang‐Ping, Xuewen Cheng, Chong Wang, et al.. (2018). Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification. Neuron. 98(6). 1116–1123.e5. 97 indexed citations

Lu, Ying‐Qian, En‐Lin Dong, Xiao-Hong Lin, et al.. (2018). Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76). Stem Cell Research. 34. 101354–101354. 4 indexed citations

Dong, En‐Lin, Chong Wang, Shuang Wu, et al.. (2018). Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China. Molecular Neurodegeneration. 13(1). 36–36. 55 indexed citations

10.

Wu, Shuang, Chong Wang, En‐Lin Dong, et al.. (2018). c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy. Journal of Molecular Neuroscience. 65(2). 196–202. 6 indexed citations

11.

Zhang, Qi‐Jie, Jin-Jing Li, Xiang Lin, et al.. (2017). Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons. Oncotarget. 8(7). 10945–10953. 21 indexed citations

12.

Yao, Xiang‐Ping, Xinxin Guo, Hui‐Zhen Su, et al.. (2017). Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families. Journal of Human Genetics. 62(7). 697–701. 12 indexed citations

13.

Zhang, Qi‐Jie, Xiang Lin, Jin-Jing Li, et al.. (2017). Application of urine cells in drug intervention for spinal muscular atrophy. Experimental and Therapeutic Medicine. 14(3). 1993–1998. 5 indexed citations

14.

Yao, Xiang‐Ping, Miao Zhao, Chong Wang, et al.. (2017). Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification. Cell and Tissue Research. 370(2). 267–273. 22 indexed citations

15.

Lin, Xiang, Jin-Jing Li, Qi‐Jie Zhang, et al.. (2017). Modeling the differential phenotypes of spinal muscular atrophy with high-yield generation of motor neurons from human induced pluripotent stem cells. Oncotarget. 8(26). 42030–42042. 20 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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