Huamei Hu

575 total citations
13 papers, 457 citations indexed

About

Huamei Hu is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Huamei Hu has authored 13 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Huamei Hu's work include Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Huamei Hu is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Huamei Hu collaborates with scholars based in China, Hong Kong and United States. Huamei Hu's co-authors include Gang Xiong, Xingying Guan, Kang Yang, Xueqing Xu, Yun Bai, Kai Wang, Hong Guo, Zhiqing Liang, Hong Yao and Dongmei Wang and has published in prestigious journals such as International Journal of Cancer, Human Mutation and Frontiers in Genetics.

In The Last Decade

Huamei Hu

12 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Huamei Hu China 9 324 249 126 78 32 13 457
Sabina Benko France 5 273 0.8× 103 0.4× 146 1.2× 20 0.3× 22 0.7× 6 353
Thomas R. W. Oliver United Kingdom 5 119 0.4× 90 0.4× 70 0.6× 73 0.9× 11 0.3× 9 252
Javier del Rey Spain 10 103 0.3× 84 0.3× 96 0.8× 60 0.8× 42 1.3× 24 302
Nadja Kokalj-Vokač Slovenia 11 276 0.9× 55 0.2× 176 1.4× 51 0.7× 13 0.4× 19 406
Wilfredo Torres‐Martinez United States 8 143 0.4× 19 0.1× 144 1.1× 66 0.8× 57 1.8× 18 345
Skye C McIver United States 9 300 0.9× 148 0.6× 99 0.8× 13 0.2× 46 1.4× 10 548
Narendra Kumar Chunduri Germany 6 223 0.7× 143 0.6× 77 0.6× 27 0.3× 12 0.4× 6 409
Henrik Hornshøj Denmark 7 198 0.6× 125 0.5× 154 1.2× 7 0.1× 76 2.4× 8 343
M. Murer‐Orlando United Kingdom 11 200 0.6× 32 0.1× 118 0.9× 43 0.6× 14 0.4× 19 294
Elizabeth R Perdeaux United Kingdom 4 283 0.9× 117 0.5× 116 0.9× 46 0.6× 83 2.6× 4 403

Countries citing papers authored by Huamei Hu

Since Specialization
Citations

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

Fields of papers citing papers by Huamei Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Huamei Hu

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

All Works

13 of 13 papers shown
1.
Hu, Huamei, et al.. (2023). Xp22.31 copy number variations in 87 fetuses: refined genotype–phenotype correlations by prenatal and postnatal follow-up. BMC Medical Genomics. 16(1). 69–69. 3 indexed citations
2.
Hu, Huamei, et al.. (2021). Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees. Frontiers in Genetics. 12. 731815–731815. 2 indexed citations
3.
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5.
Zhang, Haiping, Peng Zeng, Fengxia Su, et al.. (2019). Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation. BMC Medical Genomics. 12(1). 151–151. 20 indexed citations
6.
Yao, Hong, Ya Gao, Jia Zhao, et al.. (2018). Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women. Science China Life Sciences. 62(2). 215–224. 8 indexed citations
7.
Yi, Yuting, Hong Yao, Huamei Hu, et al.. (2016). Targeted next-generation sequencing identification of mutations in patients with disorders of sex development. BMC Medical Genetics. 17(1). 23–23. 51 indexed citations
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Dong, Zirui, Lupin Jiang, Hua Hu, et al.. (2014). A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage Sequencing. Human Mutation. 35(5). 625–636. 65 indexed citations
10.
Chen, Xuedan, Huamei Hu, Xingying Guan, et al.. (2011). CpG island methylation status of miRNAs in esophageal squamous cell carcinoma. International Journal of Cancer. 130(7). 1607–1613. 110 indexed citations
11.
Wang, Kai, Hong Guo, Huamei Hu, et al.. (2010). A functional variation in pre-microRNA-196a is associated with susceptibility of esophageal squamous cell carcinoma risk in Chinese Han. Biomarkers. 15(7). 614–618. 49 indexed citations
12.
Xiong, Gang, Hong Guo, Kai Wang, et al.. (2010). Polymorphisms of decoy receptor 3 are associated with risk of esophageal squamous cell carcinoma in Chinese Han. Tumor Biology. 31(5). 443–449. 13 indexed citations
13.
Guo, Hong, Kai Wang, Gang Xiong, et al.. (2010). A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han. Familial Cancer. 9(4). 599–603. 95 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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Breakdown of academic impact, for papers by Sabina Benko Breakdown of academic impact, for papers by Thomas R. W. Oliver Breakdown of academic impact, for papers by Javier del Rey Breakdown of academic impact, for papers by Nadja Kokalj-Vokač Breakdown of academic impact, for papers by Wilfredo Torres‐Martinez Breakdown of academic impact, for papers by Skye C McIver Breakdown of academic impact, for papers by Narendra Kumar Chunduri Breakdown of academic impact, for papers by Henrik Hornshøj Breakdown of academic impact, for papers by M. Murer‐Orlando Breakdown of academic impact, for papers by Elizabeth R Perdeaux
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2026