Dong‐Zhi Li

3.4k total citations
270 papers, 1.9k citations indexed

About

Dong‐Zhi Li is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Hematology. According to data from OpenAlex, Dong‐Zhi Li has authored 270 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 138 papers in Pediatrics, Perinatology and Child Health, 124 papers in Genetics and 98 papers in Hematology. Recurrent topics in Dong‐Zhi Li's work include Prenatal Screening and Diagnostics (120 papers), Hemoglobinopathies and Related Disorders (118 papers) and Iron Metabolism and Disorders (66 papers). Dong‐Zhi Li is often cited by papers focused on Prenatal Screening and Diagnostics (120 papers), Hemoglobinopathies and Related Disorders (118 papers) and Iron Metabolism and Disorders (66 papers). Dong‐Zhi Li collaborates with scholars based in China, United States and United Kingdom. Dong‐Zhi Li's co-authors include Can Liao, Can Liao, Xing-Mei Xie, Min Pan, Jianying Zhou, Xin Yang, Jin Han, Yongling Zhang, Fang Fu and Can Liao and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Scientific Reports.

In The Last Decade

Dong‐Zhi Li

250 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dong‐Zhi Li China	21	910	753	613	496	427	270	1.9k
Can Liao China	16	676 0.7×	153 0.2×	124 0.2×	307 0.6×	270 0.6×	90	1.1k
Sean Maloney United States	14	675 0.7×	68 0.1×	394 0.6×	336 0.7×	340 0.8×	15	1.7k
Ariadni Mavrou Greece	24	575 0.6×	112 0.1×	120 0.2×	458 0.9×	626 1.5×	94	1.7k
Mariko Eguchi Japan	24	143 0.2×	249 0.3×	845 1.4×	170 0.3×	832 1.9×	123	2.1k
LoAnn Peterson United States	27	72 0.1×	1.1k 1.4×	804 1.3×	154 0.3×	483 1.1×	79	2.6k
Stephen J. Rosenfeld United States	14	134 0.1×	162 0.2×	845 1.4×	291 0.6×	153 0.4×	28	1.6k
Iván K. Chinn United States	20	46 0.1×	209 0.3×	269 0.4×	425 0.9×	498 1.2×	55	1.9k
Markus G. Seidel Austria	24	63 0.1×	160 0.2×	470 0.8×	373 0.8×	474 1.1×	74	2.2k
Terry D. Allen United States	22	222 0.2×	105 0.1×	194 0.3×	129 0.3×	1.5k 3.5×	53	2.5k
Michael R. Rossi United States	25	44 0.0×	322 0.4×	73 0.1×	216 0.4×	714 1.7×	76	1.7k

Countries citing papers authored by Dong‐Zhi Li

Since Specialization

Citations

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

Fields of papers citing papers by Dong‐Zhi Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dong‐Zhi Li

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

All Works

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20 of 20 papers shown

Jing, Xiangyi, et al.. (2025). Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder. Prenatal Diagnosis. 45(4). 551–558.

Wang, Zhibo, Shunli Liu, Dong‐Zhi Li, et al.. (2025). Development and validation of a CT-based radiomic nomogram for predicting surgical resection risk in patients with adhesive small bowel obstruction. BMC Medical Imaging. 25(1). 46–46. 1 indexed citations

Liu, Lei, Tingying Lei, Fei Guo, et al.. (2024). Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature. Frontiers in Genetics. 15. 1448341–1448341. 1 indexed citations

Jiang, Hua & Dong‐Zhi Li. (2024). Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report. Hemoglobin. 48(2). 118–120.

Yu, Qiuxia, et al.. (2024). Phenotypic and genotypic analysis of 11 fetal cases with Bardet–Biedl syndrome. Prenatal Diagnosis. 44(9). 1105–1110.

Liu, Yingdi, Dong‐Zhi Li, Guilan Chen, et al.. (2023). Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing. Thrombosis and Haemostasis. 123(12). 1151–1164. 15 indexed citations

Liu, Liyuan, Fang Fu, Ru Li, et al.. (2023). Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations. Genes. 14(10). 1872–1872. 2 indexed citations

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

Yu, Qiuxia, et al.. (2023). Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities. Prenatal Diagnosis. 43(13). 1662–1665. 2 indexed citations

10.

Fu, Fang, Ru Li, Qiuxia Yu, et al.. (2022). Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing. Frontiers in Genetics. 13. 951829–951829. 1 indexed citations

11.

Huang, Chao, Qiuming He, Zhe Wang, et al.. (2021). Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China. Prenatal Diagnosis. 41(6). 766–771. 4 indexed citations

12.

Wu, Lisha, et al.. (2021). Dominant β-Thalassemia Phenotype Caused by Hb Dieppe ( HBB : c.383A>G): Another Case Report. Hemoglobin. 45(5). 329–331. 2 indexed citations

13.

Li, Zhen, et al.. (2021). Fetal micrognathia in the first trimester: An ominous finding even after a normal array. European Journal of Obstetrics & Gynecology and Reproductive Biology. 263. 176–180. 9 indexed citations

14.

Li, Ru, Yongling Zhang, Xiangyi Jing, et al.. (2018). Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice. Prenatal Diagnosis. 38(11). 849–857. 25 indexed citations

15.

Yang, Xin, et al.. (2015). Relationship between absent or hypoplastic fetal nasal bone and chromosome abnormalities: analysis of 187 cases. Zhonghua weichan yixue zazhi. 18(5). 339–342. 1 indexed citations

16.

Fu, Fang, Ru Li, Jin Han, et al.. (2014). Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region. Gene. 546(2). 222–225. 13 indexed citations

17.

Liao, Can, et al.. (2013). Codon 62 (G T G>G C G, Val→Ala) ( α 1) ( HBA1 : c.188T>C) Causing Nondeletional α -Thalassemia in a Chinese Family. Hemoglobin. 37(2). 188–191. 1 indexed citations

18.

Liao, Can & Dong‐Zhi Li. (2012). α⁰-Thalassemia Trait with Normal Red Cell Indices: A Report of Two Cases. Hemoglobin. 36(6). 589–591. 2 indexed citations

19.

J, Li, Can Liao, Jianying Zhou, et al.. (2011). Phenotypic Variability in a Chinese Family with Nondeletional Hb H-Hb Quong Sze Disease. Hemoglobin. 35(4). 430–433. 5 indexed citations

20.

Li, Dong‐Zhi, et al.. (2006). Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.. PubMed. 91(5). 649–51. 21 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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