Liwen Wu

603 total citations
14 papers, 420 citations indexed

About

Liwen Wu is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Liwen Wu has authored 14 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Clinical Biochemistry. Recurrent topics in Liwen Wu's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Liwen Wu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Liwen Wu collaborates with scholars based in China, United States and Albania. Liwen Wu's co-authors include Fang He, Fei Yin, Chen Chen, Jing Peng, Nan Pang, Lifen Yang, Shiqi Guang, Xiaolu Deng, Lei Qiao and Ying Liu and has published in prestigious journals such as Medicine, Journal of Medical Genetics and Molecular Neurobiology.

In The Last Decade

Liwen Wu

14 papers receiving 417 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liwen Wu China	7	227	179	113	94	77	14	420
Ayako Nunokawa Japan	14	199 0.9×	147 0.8×	112 1.0×	70 0.7×	92 1.2×	34	455
Yanyan Ruan China	13	179 0.8×	179 1.0×	119 1.1×	45 0.5×	53 0.7×	23	387
Naoshi Kaneko Japan	14	204 0.9×	203 1.1×	93 0.8×	76 0.8×	86 1.1×	33	513
Atsushi Shimohata Japan	10	181 0.8×	246 1.4×	71 0.6×	52 0.6×	117 1.5×	15	519
Haim Belinson Israel	12	184 0.8×	288 1.6×	121 1.1×	39 0.4×	140 1.8×	17	580
Robert G. Wither Canada	12	172 0.8×	139 0.8×	162 1.4×	56 0.6×	65 0.8×	20	385
C. Nicole Sunnen United States	7	127 0.6×	272 1.5×	36 0.3×	76 0.8×	112 1.5×	7	430
Guohe Tan China	9	331 1.5×	270 1.5×	72 0.6×	188 2.0×	140 1.8×	22	659
Daniel W. Meechan United States	13	277 1.2×	550 3.1×	122 1.1×	34 0.4×	138 1.8×	17	761
Kyungdeok Kim South Korea	14	163 0.7×	166 0.9×	139 1.2×	26 0.3×	187 2.4×	24	493

Countries citing papers authored by Liwen Wu

Since Specialization

Citations

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

Fields of papers citing papers by Liwen Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liwen Wu

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

All Works

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14 of 14 papers shown

Zhou, Chao, Xingzhi Chang, Liwen Wu, et al.. (2024). Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation. Journal of Medical Genetics. 61(7). 626–632. 4 indexed citations

Hu, Wenjing, Peng Yu, Li Li, et al.. (2022). Nabais Sa‐de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report. Molecular Genetics & Genomic Medicine. 10(12). e2075–e2075. 2 indexed citations

Xiao, Ting, et al.. (2022). ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration. Molecular Genetics & Genomic Medicine. 10(7). e1967–e1967. 7 indexed citations

Yang, Liming, et al.. (2021). CNKSR2 gene mutation leads to Houge type of X-linked syndromic mental retardation. Medicine. 100(23). e26093–e26093. 4 indexed citations

Yang, Liming, et al.. (2021). Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation. Frontiers in Pediatrics. 9. 801719–801719. 2 indexed citations

Wu, Liwen, et al.. (2021). Krabbe Disease Associated With Mitochondrial Dysfunction in a Chinese Family. Frontiers in Neurology. 12. 750095–750095. 5 indexed citations

Wu, Liwen, et al.. (2021). Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutation. Neurogenetics. 22(4). 323–332. 10 indexed citations

Guang, Shiqi, Nan Pang, Xiaolu Deng, et al.. (2018). Synaptopathology Involved in Autism Spectrum Disorder. Frontiers in Cellular Neuroscience. 12. 470–470. 197 indexed citations

Peng, Jing, Ying Wang, Fang He, et al.. (2018). Novel West syndrome candidate genes in a Chinese cohort. CNS Neuroscience & Therapeutics. 24(12). 1196–1206. 60 indexed citations

10.

Chen, Chao, Yibin Wang, Liwen Wu, et al.. (2016). Analysis copy number variation of Chinese children in early‐onset epileptic encephalopathies with unknown cause. Clinical Genetics. 90(5). 428–436. 11 indexed citations

11.

Peng, Jing, et al.. (2014). [Clinical features and genome-wide copy number variation analysis in 60 children with early-onset epileptic encephalopathies of unknown cause].. PubMed. 16(11). 1100–4. 1 indexed citations

12.

Sha, Longze, Xiaofeng Wu, Yuan Yao, et al.. (2013). Notch Signaling Activation Promotes Seizure Activity in Temporal Lobe Epilepsy. Molecular Neurobiology. 49(2). 633–644. 40 indexed citations

13.

Liu, Qing, Xinhua Wan, Jingyun Li, et al.. (2011). Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression. Journal of Medical Genetics. 49(2). 79–82. 73 indexed citations

14.

Zhao, Yi, et al.. (2007). SPINK5 gene mutation and decreased LEKTI activity in three Chinese patients with Netherton's syndrome. Clinical and Experimental Dermatology. 32(5). 564–567. 4 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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