Li Du

1.4k total citations
56 papers, 903 citations indexed

About

Li Du is a scholar working on Genetics, Molecular Biology and Sensory Systems. According to data from OpenAlex, Li Du has authored 56 papers receiving a total of 903 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 21 papers in Molecular Biology and 18 papers in Sensory Systems. Recurrent topics in Li Du's work include Hemoglobinopathies and Related Disorders (22 papers), Hearing, Cochlea, Tinnitus, Genetics (18 papers) and Prenatal Screening and Diagnostics (8 papers). Li Du is often cited by papers focused on Hemoglobinopathies and Related Disorders (22 papers), Hearing, Cochlea, Tinnitus, Genetics (18 papers) and Prenatal Screening and Diagnostics (8 papers). Li Du collaborates with scholars based in China, United States and United Kingdom. Li Du's co-authors include Denise Yan, Xiao Mei Ouyang, Xue Zhong Liu, Simón I. Angeli, Xiaomei Ouyang, Xue-Zhong Liu, Walter E. Nance, Pu Dai, Kenneth R. Johnson and Heping Yu and has published in prestigious journals such as PLoS ONE, Journal of Molecular Biology and Scientific Reports.

In The Last Decade

Li Du

48 papers receiving 880 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Li Du China 16 548 506 212 113 112 56 903
Dongyang Kang China 19 710 1.3× 582 1.2× 328 1.5× 239 2.1× 105 0.9× 75 1.0k
Manuela Villamar Spain 14 650 1.2× 693 1.4× 195 0.9× 104 0.9× 129 1.2× 30 1.0k
Barbara Vona Germany 15 450 0.8× 349 0.7× 193 0.9× 129 1.1× 110 1.0× 64 751
Isabelle Schatteman Belgium 15 651 1.2× 365 0.7× 257 1.2× 252 2.2× 304 2.7× 28 1.1k
Matthew R. Avenarius United States 15 494 0.9× 499 1.0× 176 0.8× 54 0.5× 116 1.0× 35 1.1k
Ibis Menéndez United States 11 590 1.1× 487 1.0× 173 0.8× 106 0.9× 131 1.2× 20 776
Taha A. Jan United States 15 607 1.1× 540 1.1× 67 0.3× 62 0.5× 184 1.6× 37 1.1k
Nabiha Salem Lebanon 19 664 1.2× 1.1k 2.1× 208 1.0× 72 0.6× 187 1.7× 36 1.6k
Tomoko Makishima United States 22 700 1.3× 614 1.2× 260 1.2× 73 0.6× 168 1.5× 37 1.3k
Regina Célia Mingroni‐Netto Brazil 20 369 0.7× 506 1.0× 104 0.5× 61 0.5× 207 1.8× 80 1.2k

Countries citing papers authored by Li Du

Since Specialization
Citations

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

Fields of papers citing papers by Li Du

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Li Du

This figure shows the co-authorship network connecting the top 25 collaborators of Li Du. A scholar is included among the top collaborators of Li Du 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 Li Du. Li Du 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.
Ding, Liang, et al.. (2025). Association Between Dietary Patterns and All-Cause Mortality in Individuals with Hypertension and Osteoporosis: A Retrospective Cohort Study. Journal of Multidisciplinary Healthcare. Volume 18. 3781–3791.
2.
Wang, Jicheng, Jing Chen, Cuize Yao, et al.. (2023). Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families. Human Genomics. 17(1). 111–111.
3.
Lin, Jing, Fei Liu, Fei Gao, et al.. (2022). Vesicular stomatitis virus sensitizes immunologically cold tumors to checkpoint blockade by inducing pyroptosis. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1868(12). 166538–166538. 11 indexed citations
4.
Liu, Chang, Yanlin Huang, Yan Zhang, et al.. (2022). Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice. International Journal of Pediatric Otorhinolaryngology. 161. 111258–111258. 2 indexed citations
5.
Hu, Siqi, Jicheng Wang, Weiping Zhou, et al.. (2020). Establishment and application of a novel method based on single nucleotide polymorphism analysis for detecting β-globin gene cluster deletions. Scientific Reports. 10(1). 18298–18298. 3 indexed citations
6.
Liu, Chang, Yanlin Huang, Jing Wu, et al.. (2019). Development of a community-based hearing loss prevention and control service model in Guangdong, China. BMC Public Health. 19(1). 1601–1601. 3 indexed citations
7.
Du, Li, Jicheng Wang, Lihua Yu, et al.. (2019). Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese Gγ+(Aγδβ)0-thalassemia deletion in a Chinese family. Clinical Biochemistry. 76. 11–16. 1 indexed citations
8.
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
9.
Hua, Jing, Li Zhu, Li Du, et al.. (2018). Effects of midwife-led maternity services on postpartum wellbeing and clinical outcomes in primiparous women under China’s one-child policy. BMC Pregnancy and Childbirth. 18(1). 329–329. 16 indexed citations
10.
Zhang, Haihua, Na Chen, Lili Zang, et al.. (2015). Fifteen Novel EIF2B1-5 Mutations Identified in Chinese Children with Leukoencephalopathy with Vanishing White Matter and a Long Term Follow-Up. PLoS ONE. 10(3). e0118001–e0118001. 15 indexed citations
11.
Angeli, Simón I., Anthony Bared, Xiaomei Ouyang, et al.. (2012). Audioprofiles and antioxidant enzyme genotypes in presbycusis. The Laryngoscope. 122(11). 2539–2542. 12 indexed citations
12.
Ouyang, Xiao Mei, et al.. (2011). Mutation Screening of the GJA7 (Cx45) Gene in a Large International Series of Probands with Nonsyndromic Hearing Impairment. Genetic Testing and Molecular Biomarkers. 15(5). 333–336. 2 indexed citations
13.
Ouyang, Xiaomei, Li Du, Denise Yan, et al.. (2011). Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population. International Journal of Pediatric Otorhinolaryngology. 75(5). 611–617. 44 indexed citations
14.
Ouyang, Xiaomei, et al.. (2011). Clinical comparison of hearing‐impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations. The Laryngoscope. 121(4). 811–814. 12 indexed citations
15.
Wu, Ye, Li Du, Jingmin Wang, et al.. (2009). Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease. Journal of Human Genetics. 54(2). 74–77. 22 indexed citations
16.
Ouyang, Xiao Mei, et al.. (2009). The genetic bases for non-syndromic hearing loss among Chinese. Journal of Human Genetics. 54(3). 131–140. 47 indexed citations
17.
Yan, Denise, Xiaomei Ouyang, Danielle Patterson, et al.. (2009). Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II. Journal of Human Genetics. 54(12). 732–738. 31 indexed citations
18.
Liu, Xue-Zhong, Yongyi Yuan, Denise Yan, et al.. (2008). Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31. Human Genetics. 125(1). 53–62. 89 indexed citations
19.
Yan, Denise, et al.. (2007). Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss. American Journal of Medical Genetics Part A. 143A(4). 385–386. 22 indexed citations
20.
Zheng, Qing Yin, Denise Yan, Xiao Mei Ouyang, et al.. (2004). Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans. Human Molecular Genetics. 14(1). 103–111. 115 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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