Huidan Wu

1.4k total citations
13 papers, 126 citations indexed

About

Huidan Wu is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Huidan Wu has authored 13 papers receiving a total of 126 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Cognitive Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Huidan Wu's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (5 papers) and Autism Spectrum Disorder Research (5 papers). Huidan Wu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (5 papers) and Autism Spectrum Disorder Research (5 papers). Huidan Wu collaborates with scholars based in China and United States. Huidan Wu's co-authors include Zhengmao Hu, Hui Guo, Jianjun Ou, Ting Bai, Kun Xia, Guanglei Xun, Xiangbin Jia, Lin Han, Qiumeng Zhang and Honghui Li and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Cellular and Molecular Medicine and Clinical Genetics.

In The Last Decade

Huidan Wu

13 papers receiving 125 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Huidan Wu China	8	68	65	28	11	8	13	126
M.P. Botella Spain	5	79 1.2×	80 1.2×	33 1.2×	7 0.6×	6 0.8×	7	135
Jessica Sebastian United States	6	92 1.4×	64 1.0×	13 0.5×	12 1.1×	5 0.6×	11	146
Taimoor I. Sheikh Canada	7	82 1.2×	77 1.2×	32 1.1×	12 1.1×	6 0.8×	11	135
Katrin Männik Estonia	7	163 2.4×	124 1.9×	41 1.5×	14 1.3×	5 0.6×	9	222
Craig Chinault United States	6	94 1.4×	98 1.5×	30 1.1×	10 0.9×	6 0.8×	6	189
Laura C. Murphy United Kingdom	8	64 0.9×	116 1.8×	44 1.6×	17 1.5×	11 1.4×	14	197
Lisa‐Marie Niestroj United States	6	136 2.0×	83 1.3×	24 0.9×	20 1.8×	3 0.4×	7	190
Jessica C. McAfee United States	6	146 2.1×	165 2.5×	42 1.5×	10 0.9×	9 1.1×	6	253
Carmen Esmer Mexico	5	157 2.3×	116 1.8×	46 1.6×	7 0.6×	6 0.8×	16	225
Engy A. Ashaat Egypt	7	53 0.8×	38 0.6×	40 1.4×	8 0.7×	16 2.0×	45	122

Countries citing papers authored by Huidan Wu

Since Specialization

Citations

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

Fields of papers citing papers by Huidan Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Huidan Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Huidan Wu. A scholar is included among the top collaborators of Huidan 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 Huidan Wu. Huidan 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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13 of 13 papers shown

Han, Lin, Xiangbin Jia, Huidan Wu, et al.. (2022). Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis. Journal of genetics and genomics. 49(9). 881–890. 10 indexed citations

Dong, Shanshan, Qi Tian, Tengfei Zhu, et al.. (2021). SLC39A5 dysfunction impairs extracellular matrix synthesis in high myopia pathogenesis. Journal of Cellular and Molecular Medicine. 25(17). 8432–8441. 9 indexed citations

Chen, Meilin, Guiqin Duan, Huidan Wu, et al.. (2021). Mutation pattern and genotype-phenotype correlations of SETD2 in neurodevelopmental disorders. European Journal of Medical Genetics. 64(5). 104200–104200. 11 indexed citations

Yu, Xiaohan & Huidan Wu. (2021). Research on Industrial Transformation and Upgrading and technological innovation of Cultural Manufacturing Industry ——Taking Deqing Piano Industry as Example. SHILAP Revista de lepidopterología. 235. 2062–2062. 1 indexed citations

Zhang, Qiumeng, Meilin Chen, Huidan Wu, et al.. (2020). Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders. Journal of Molecular Neuroscience. 70(12). 2085–2092. 8 indexed citations

Shah, Abid Ali, Ge Zhang, Kuokuo Li, et al.. (2020). Excess of RALGAPB de novo variants in neurodevelopmental disorders. European Journal of Medical Genetics. 63(11). 104041–104041. 1 indexed citations

Wu, Huidan, Honghui Li, Ting Bai, et al.. (2019). Phenotype‐to‐genotype approach reveals head‐circumference‐associated genes in an autism spectrum disorder cohort. Clinical Genetics. 97(2). 338–346. 27 indexed citations

Zhao, Wenjing, Jieqiong Tan, Tengfei Zhu, et al.. (2019). Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development. Journal of genetics and genomics. 46(5). 247–257. 16 indexed citations

Han, Lin, Meilin Chen, Yazhe Wang, et al.. (2019). Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders. Molecular Genetics & Genomic Medicine. 7(7). e00789–e00789. 7 indexed citations

10.

Zhao, Wenjing, Huidan Wu, Lin Han, et al.. (2019). POGZ de novo missense variants in neuropsychiatric disorders. Molecular Genetics & Genomic Medicine. 7(9). e900–e900. 9 indexed citations

11.

Wu, Huidan, et al.. (2018). Using triangles and latent factor cosine similarity prior to improve community detection in multi‐relational social networks. Concurrency and Computation Practice and Experience. 30(16). 2 indexed citations

12.

Li, Ying, Xiangbin Jia, Huidan Wu, et al.. (2018). Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders. American Journal of Medical Genetics Part A. 176(12). 2668–2676. 24 indexed citations

13.

Wu, Huidan, et al.. (2010). AN EFFECTIVE MAGNETIC SEPARATION TECHNIQUE FOR ANTIBODY BASED ON THIOPHILIC PARAMAGNETIC POLYMER BEADS. Acta Polymerica Sinica. 0(10). 1238–1244. 1 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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