Yanhui Liu

534 total citations
22 papers, 194 citations indexed

About

Yanhui Liu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yanhui Liu has authored 22 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yanhui Liu's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Yanhui Liu is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Yanhui Liu collaborates with scholars based in China and United States. Yanhui Liu's co-authors include Yi‐Xin Lin, Ross Ka‐Kit Leung, Qingming Wang, Yi He, Jiwu Lou, Jianxin Liu, Manna Sun, Guoquan Chen, Yiping Shen and Jianan Liu and has published in prestigious journals such as PLoS ONE, Clinica Chimica Acta and Frontiers in Genetics.

In The Last Decade

Yanhui Liu

21 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yanhui Liu China 8 69 61 50 35 26 22 194
Maha Tulbah Saudi Arabia 8 74 1.1× 67 1.1× 85 1.7× 24 0.7× 13 0.5× 24 236
Ioannis Papoulidis Greece 13 116 1.7× 251 4.1× 195 3.9× 12 0.3× 13 0.5× 52 388
Prochi F. Madon India 7 102 1.5× 190 3.1× 163 3.3× 12 0.3× 29 1.1× 25 320
Monika Mohenska Australia 5 253 3.7× 16 0.3× 36 0.7× 32 0.9× 31 1.2× 6 339
Denise Molina‐Gomes France 12 101 1.5× 162 2.7× 130 2.6× 39 1.1× 57 2.2× 32 406
Ellika Sahlin Sweden 9 72 1.0× 78 1.3× 82 1.6× 7 0.2× 6 0.2× 13 193
Anna R. Duncan United States 8 182 2.6× 52 0.9× 26 0.5× 56 1.6× 25 1.0× 9 287
Alison Lashwood United Kingdom 10 141 2.0× 168 2.8× 268 5.4× 9 0.3× 18 0.7× 20 439
Alok Javali Austria 5 304 4.4× 40 0.7× 43 0.9× 40 1.1× 54 2.1× 8 392
Jiexia Yang China 8 52 0.8× 104 1.7× 229 4.6× 22 0.6× 8 0.3× 21 280

Countries citing papers authored by Yanhui Liu

Since Specialization
Citations

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

Fields of papers citing papers by Yanhui Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yanhui Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Yanhui Liu. A scholar is included among the top collaborators of Yanhui Liu 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 Yanhui Liu. Yanhui Liu 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.
Wang, Li Ping, Weijun Zhong, Jing Cai, et al.. (2025). Single-Cell RNA Sequencing Reveals Peripheral Immune Cell Senescence and Inflammatory Phenotypes in Patients with Premature Ovarian Failure. Journal of Inflammation Research. Volume 18. 2699–2715. 2 indexed citations
2.
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Lou, Jiwu, Manna Sun, Aiping Mao, et al.. (2023). Molecular spectrum and prevalence of thalassemia investigated by third-generation sequencing in the Dongguan region of Guangdong Province, Southern China. Clinica Chimica Acta. 551. 117622–117622. 7 indexed citations
4.
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
5.
Wang, Qingming, et al.. (2022). Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8. Orphanet Journal of Rare Diseases. 17(1). 149–149. 4 indexed citations
6.
Wang, Qingming, et al.. (2022). Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review. Frontiers in Genetics. 13. 853183–853183. 3 indexed citations
7.
Lou, Jiwu, et al.. (2022). A stepwise haematological screening and whole‐exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A2 from a cohort of 47336 individuals. International Journal of Laboratory Hematology. 45(1). 90–95. 8 indexed citations
8.
Ji, Yanli, et al.. (2021). Case Report: Drug-Induced Immune Haemolytic Anaemia Caused by Cefoperazone-Tazobactam/ Sulbactam Combination Therapy. Frontiers in Medicine. 8. 697192–697192. 7 indexed citations
9.
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Wang, Qingming, et al.. (2020). A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with Atypical Rubinstein–Taybi Syndrome Phenotypes. Journal of Molecular Neuroscience. 71(3). 607–612. 3 indexed citations
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Wang, Qingming, et al.. (2020). Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1. BMC Medical Genomics. 13(1). 66–66. 6 indexed citations
13.
Leung, Ross Ka‐Kit, Yi‐Xin Lin, & Yanhui Liu. (2020). Recent Advances in Understandings Towards Pathogenesis and Treatment for Intrauterine Adhesion and Disruptive Insights from Single-Cell Analysis. Reproductive Sciences. 28(7). 1812–1826. 50 indexed citations
14.
Wang, Qingming, et al.. (2019). Microdeletion and microduplication of 1p36.11p35.3 involving AHDC1 contribute to neurodevelopmental disorder. European Journal of Medical Genetics. 63(1). 103611–103611. 13 indexed citations
15.
Sun, Manna, Jiwu Lou, Jianhong Chen, et al.. (2019). Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene. Taiwanese Journal of Obstetrics and Gynecology. 58(2). 292–295. 9 indexed citations
16.
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
17.
Wang, Qingming, Yanhui Liu, Wei Yang, et al.. (2018). A rare exonic NRXN3 deletion segregating with neurodevelopmental and neuropsychiatric conditions in a three‐generation Chinese family. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(6). 589–595. 24 indexed citations
18.
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Lou, Jiwu, Manna Sun, Ying Zhao, et al.. (2017). Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis. PLoS ONE. 12(2). e0171886–e0171886. 6 indexed citations
20.
Gao, Lan, Yanhui Liu, Manna Sun, et al.. (2015). Rapid detection of α-thalassaemia alleles of -- SEA /, -α 3.7 / and -α 4.2 / using a dual labelling, self-quenching hybridization probe/melting curve analysis. Molecular and Cellular Probes. 29(6). 438–441. 3 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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