Zhengmao Hu

5.2k total citations
127 papers, 1.9k citations indexed

About

Zhengmao Hu is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Zhengmao Hu has authored 127 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 43 papers in Genetics and 29 papers in Cellular and Molecular Neuroscience. Recurrent topics in Zhengmao Hu's work include Genetics and Neurodevelopmental Disorders (30 papers), Autism Spectrum Disorder Research (25 papers) and Hereditary Neurological Disorders (19 papers). Zhengmao Hu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (30 papers), Autism Spectrum Disorder Research (25 papers) and Hereditary Neurological Disorders (19 papers). Zhengmao Hu collaborates with scholars based in China, United States and France. Zhengmao Hu's co-authors include Kun Xia, Beisha Tang, Hui Guo, Qian Pan, Jingping Zhao, Jiahui Xia, Ruxu Zhang, Jia‐Da Li, Kai Li and Liping Zeng and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Zhengmao Hu

125 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhengmao Hu China 25 1000 535 430 295 226 127 1.9k
Vinodh Narayanan United States 25 1.2k 1.2× 749 1.4× 418 1.0× 398 1.3× 157 0.7× 67 2.3k
Christian Windpassinger Austria 26 1.3k 1.3× 500 0.9× 451 1.0× 207 0.7× 130 0.6× 72 2.3k
Arnold Munnich France 25 1.6k 1.6× 580 1.1× 341 0.8× 155 0.5× 100 0.4× 55 2.3k
Max A. Tischfield United States 17 812 0.8× 306 0.6× 454 1.1× 136 0.5× 120 0.5× 27 1.6k
Hossein Darvish Iran 18 609 0.6× 332 0.6× 270 0.6× 80 0.3× 259 1.1× 96 1.3k
G. Ralph United Kingdom 19 1.3k 1.3× 437 0.8× 831 1.9× 200 0.7× 585 2.6× 28 2.2k
Julie A. Siegenthaler United States 28 1.2k 1.2× 331 0.6× 515 1.2× 60 0.2× 173 0.8× 50 2.4k
Bert van der Zwaag Netherlands 23 1.2k 1.2× 704 1.3× 372 0.9× 200 0.7× 161 0.7× 44 2.2k
Pascale Saugier-Véber France 28 1.1k 1.1× 672 1.3× 437 1.0× 85 0.3× 257 1.1× 82 2.3k
R. Sean Hill United States 13 956 1.0× 624 1.2× 286 0.7× 93 0.3× 73 0.3× 17 1.7k

Countries citing papers authored by Zhengmao Hu

Since Specialization
Citations

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

Fields of papers citing papers by Zhengmao Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhengmao Hu

This figure shows the co-authorship network connecting the top 25 collaborators of Zhengmao Hu. A scholar is included among the top collaborators of Zhengmao Hu 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 Zhengmao Hu. Zhengmao Hu 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.
Zhang, Qiumeng, et al.. (2025). Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay. International Journal of Molecular Sciences. 26(16). 7820–7820.
2.
Peng, Yu, Qi Tian, Bei Feng, et al.. (2024). Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2. JCI Insight. 9(9). 1 indexed citations
3.
Luo, Tianyou, Jing Pan, Ying Zhu, et al.. (2023). Association between de novo variants of nuclear-encoded mitochondrial-related genes and undiagnosed developmental disorder and autism. QJM. 117(4). 269–276. 1 indexed citations
4.
Zheng, Yu, Guanghui Zhu, Weihua Zhao, et al.. (2022). Case series of congenital pseudarthrosis of the tibia unfulfilling neurofibromatosis type 1 diagnosis: 21% with somatic NF1 haploinsufficiency in the periosteum. Human Genetics. 141(8). 1371–1383. 2 indexed citations
5.
Wang, Meng, Rizwan Hasan Khan, Abid Ali Shah, et al.. (2021). A splice-site variant (c.3289-1G>T) in OTOF underlies profound hearing loss in a Pakistani kindred. BMC Medical Genomics. 14(1). 2–2. 3 indexed citations
6.
Gao, Fei, Wen Huang, Jie Huang, et al.. (2020). Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy. Molecular Genetics & Genomic Medicine. 8(6). e1236–e1236. 10 indexed citations
7.
Xie, Yongzhi, Zhiqiang Lin, Xiaobo Li, et al.. (2020). Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families. Frontiers in Neurology. 11. 603003–603003. 7 indexed citations
8.
Naeem, Muhammad Asif, et al.. (2020). A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds. Ophthalmic Genetics. 41(1). 7–12. 1 indexed citations
9.
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
10.
11.
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
12.
Liu, Lei, Xiaobo Li, Zhengmao Hu, et al.. (2016). IGHMBP2-related clinical and genetic features in a cohort of Chinese Charcot–Marie–Tooth disease type 2 patients. Neuromuscular Disorders. 27(2). 193–199. 20 indexed citations
13.
Li, Bin, et al.. (2015). Identification of a GJA3 Mutation in a Large Family with Bilateral Congenital Cataract. DNA and Cell Biology. 35(3). 135–139. 8 indexed citations
14.
Li, Xiaobo, Zhengmao Hu, Lei Liu, et al.. (2015). A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy. Neurology. 84(24). 2430–2437. 68 indexed citations
15.
Lu, Lina, Hui Guo, Peng Yu, et al.. (2014). Common and rare variants of the THBS1 gene associated with the risk for autism. Psychiatric Genetics. 24(6). 235–240. 13 indexed citations
16.
Xiong, Zhimin, Yanmei Lu, Xiaojuan Xu, et al.. (2013). Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports. Journal of Medical Case Reports. 7(1). 63–63. 6 indexed citations
17.
Tania, Mousumi, Zhimin Xiong, Lina Lu, et al.. (2013). Identification of a known GJB6 mutation in an autosomal dominant inherited Chinese family with hidrotic ectodermal dysplasia.. PubMed. 38(8). 761–5. 2 indexed citations
18.
Peng, Hao, Yuhui Zhang, Zhigao Long, et al.. (2012). A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family. Gene. 502(2). 168–171. 7 indexed citations
19.
Jiang, Lu, Yalan Liu, Yong Feng, et al.. (2011). Gene localization in a Chinese family with autosomal dominant non-syndromic deafness. Acta Oto-Laryngologica. 131(10). 1061–1068. 2 indexed citations
20.
Chen, Hongsheng, Lu Jiang, Zhiguo Xie, et al.. (2010). Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. Biochemical and Biophysical Research Communications. 397(1). 70–74. 57 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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