Quanfei Huang

7.6k total citations
17 papers, 613 citations indexed

About

Quanfei Huang is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Quanfei Huang has authored 17 papers receiving a total of 613 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Quanfei Huang's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Quanfei Huang is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Quanfei Huang collaborates with scholars based in China, United States and Australia. Quanfei Huang's co-authors include Qi Zhou, Doris Bachtrog, Guojie Zhang, Erich D. Jarvis, M. Thomas P. Gilbert, Na An, Jilin Zhang, Xin Zhou, Xu Su and Yiyuan Li and has published in prestigious journals such as Science, American Journal of Obstetrics and Gynecology and BMC Genomics.

In The Last Decade

Quanfei Huang

15 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Quanfei Huang China 8 289 286 187 187 112 17 613
Daniel E. Cook United States 15 422 1.5× 417 1.5× 134 0.7× 214 1.1× 31 0.3× 35 1.1k
Élodie Gazave United States 19 383 1.3× 436 1.5× 80 0.4× 445 2.4× 36 0.3× 21 921
Pawan Pandoh Canada 11 396 1.4× 137 0.5× 117 0.6× 90 0.5× 59 0.5× 23 584
Ching-Hua Shih United States 6 151 0.5× 204 0.7× 70 0.4× 60 0.3× 63 0.6× 11 361
Yun Yu China 11 509 1.8× 336 1.2× 41 0.2× 124 0.7× 164 1.5× 22 727
Hasan Alhaddad Kuwait 14 181 0.6× 222 0.8× 58 0.3× 57 0.3× 62 0.6× 33 581
Toni I. Gossmann United Kingdom 18 595 2.1× 533 1.9× 71 0.4× 242 1.3× 144 1.3× 37 1.1k
C. A. Redi Italy 19 442 1.5× 420 1.5× 119 0.6× 351 1.9× 120 1.1× 45 934
Christopher J. Troll United States 6 367 1.3× 198 0.7× 71 0.4× 221 1.2× 49 0.4× 7 556
Halina Černohorská Czechia 17 333 1.2× 577 2.0× 85 0.5× 523 2.8× 40 0.4× 58 798

Countries citing papers authored by Quanfei Huang

Since Specialization
Citations

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

Fields of papers citing papers by Quanfei Huang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Quanfei Huang

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

All Works

17 of 17 papers shown
1.
Huang, Quanfei, Yuwei Liao, Lei Wei, et al.. (2023). A retrospective analysis of preemptive pharmacogenomic testing in 22,918 individuals from China. Journal of Clinical Laboratory Analysis. 37(5). e24855–e24855. 10 indexed citations
2.
Huang, Quanfei, Yanhui Liu, Lei Wei, et al.. (2022). Detecting mitochondrial mutations associated with aminoglycoside ototoxicity by noninvasive prenatal testing. Journal of Clinical Laboratory Analysis. 37(1). e24827–e24827. 2 indexed citations
3.
4.
Wu, Jie, Yu Su, Yang Wang, et al.. (2022). Molecular diagnose of a large hearing loss population from China by targeted genome sequencing. Journal of Human Genetics. 67(11). 643–649. 15 indexed citations
5.
Huang, Quanfei, et al.. (2022). Three-phase dynamic voltage restorer based on self-tuning fuzzy proportional resonance control. 1082–1086. 2 indexed citations
6.
Fang, Wenfeng, Jianwen Li, Delan Li, et al.. (2021). Impact of STAT1 polymorphisms on crizotinib-induced hepatotoxicity in ALK-positive non-small cell lung cancer patients. Journal of Cancer Research and Clinical Oncology. 147(3). 725–737. 12 indexed citations
7.
8.
Li, Dongshun, Quanfei Huang, Lihuan Guan, et al.. (2020). Targeted bile acids and gut microbiome profiles reveal the hepato-protective effect of WZ tablet (Schisandra sphenanthera extract) against LCA-induced cholestasis. Chinese Journal of Natural Medicines. 18(3). 211–218. 21 indexed citations
9.
Yang, Jiexia, Chunfang Peng, Yiming Qi, et al.. (2020). Noninvasive Prenatal Detection of Hemoglobin Bart Hydrops Fetalis Via Maternal Plasma Dispensed With Parental Haplotyping Using the Semiconductor Sequencing Platform. Obstetrical & Gynecological Survey. 75(7). 387–388.
10.
Yang, Jiexia, Chunfang Peng, Yiming Qi, et al.. (2019). Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform. American Journal of Obstetrics and Gynecology. 222(2). 185.e1–185.e17. 5 indexed citations
11.
Chen, Junkun, Ping Liu, Liqin Hu, et al.. (2018). A foetus with 18p11.32-q21.2 duplication and Xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(X;18)(q13;q21.3). Molecular Cytogenetics. 11(1). 37–37. 7 indexed citations
12.
Liu, Yanhui, Bo Yang, Xiaoyan Zhang, Quanfei Huang, & Hailiang Liu. (2018). The Gene Mutation Spectrum of Breast Cancer Analyzed by Semiconductor Sequencing Platform. Pathology & Oncology Research. 26(1). 491–497. 4 indexed citations
13.
Zhou, Qi, Jilin Zhang, Doris Bachtrog, et al.. (2014). Complex evolutionary trajectories of sex chromosomes across bird taxa. Science. 346(6215). 1246338–1246338. 221 indexed citations
14.
Zhou, Xin, Yiyuan Li, Shanlin Liu, et al.. (2013). Ultra-deep sequencing enables high-fidelity recovery of biodiversity for bulk arthropod samples without PCR amplification. GigaScience. 2(1). 4–4. 217 indexed citations
15.
Zhang, Jie, Quanfei Huang, Jie Jin, et al.. (2012). Stump-like mathematical model and computer simulation on dynamic separation of capillary zone electrophoresis with different sample injections. Talanta. 105. 278–286. 5 indexed citations
16.
Zhou, Qi, Hongmei Zhu, Quanfei Huang, et al.. (2012). Deciphering neo-sex and B chromosome evolution by the draft genome of Drosophila albomicans. BMC Genomics. 13(1). 109–109. 56 indexed citations
17.
Qin, Shuang, et al.. (2005). [Conventional cytogenetics and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in leukemia].. PubMed. 13(5). 798–803. 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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