Lu Meng

1.4k total citations
7 papers, 257 citations indexed

About

Lu Meng is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Lu Meng has authored 7 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Lu Meng's work include Prenatal Screening and Diagnostics (3 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Congenital Heart Disease Studies (2 papers). Lu Meng is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Congenital Heart Disease Studies (2 papers). Lu Meng collaborates with scholars based in China, United States and Denmark. Lu Meng's co-authors include Ping Hu, Zhengfeng Xu, Wei Wang, Meiyan Zhang, Fang Chen, Yun Li, Qi Tian, Jinjin Xu, Shanshan Yu and Jiansheng Xie and has published in prestigious journals such as Cell Reports, Ultrasound in Obstetrics and Gynecology and Genetics in Medicine.

In The Last Decade

Lu Meng

7 papers receiving 232 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lu Meng China 6 153 139 81 48 31 7 257
Yongyi Ma China 10 102 0.7× 95 0.7× 112 1.4× 17 0.4× 13 0.4× 20 263
Fatao Li China 10 157 1.0× 185 1.3× 120 1.5× 60 1.3× 4 0.1× 20 326
Núria Clusellas Spain 9 195 1.3× 189 1.4× 100 1.2× 30 0.6× 59 1.9× 14 319
Mary Goetsch United States 9 76 0.5× 63 0.5× 228 2.8× 124 2.6× 16 0.5× 16 345
Pascale Kleinfinger France 12 153 1.0× 244 1.8× 93 1.1× 5 0.1× 41 1.3× 27 334
Jenn-Jhy Tseng Taiwan 8 43 0.3× 164 1.2× 21 0.3× 42 0.9× 5 0.2× 20 277
Lotte Hatt Denmark 12 99 0.6× 289 2.1× 146 1.8× 9 0.2× 6 0.2× 24 405
Thanh Tung Truong United States 5 83 0.5× 16 0.1× 385 4.8× 12 0.3× 27 0.9× 8 467

Countries citing papers authored by Lu Meng

Since Specialization
Citations

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

Fields of papers citing papers by Lu Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lu Meng

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

All Works

7 of 7 papers shown
1.
Xu, Xiaomei, Lu Meng, Emmanuel Talla, et al.. (2025). Functional dissection of the CRP-family transcription factor DevH and its interplay with NtcA in a cyanobacterium. Cell Reports. 44(10). 116435–116435. 1 indexed citations
2.
Qiao, Fengchang, Yishuang Wang, Renping Zhou, et al.. (2020). Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect. Ultrasound in Obstetrics and Gynecology. 58(3). 377–387. 38 indexed citations
3.
Meng, Lu, et al.. (2019). Automatic display of fetal brain planes and automatic measurements of fetal brain parameters by transabdominal three‐dimensional ultrasound. Journal of Clinical Ultrasound. 48(2). 82–88. 11 indexed citations
4.
Hu, Ping, Fengchang Qiao, Yishuang Wang, et al.. (2018). Clinical application of targeted next‐generation sequencing in fetuses with congenital heart defect. Ultrasound in Obstetrics and Gynecology. 52(2). 205–211. 35 indexed citations
5.
Cai, Ailu, et al.. (2018). Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China. Molecular Genetics & Genomic Medicine. 6(6). 1015–1020. 5 indexed citations
6.
Dong, Zirui, Jun Zhang, Ping Hu, et al.. (2016). Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach. Genetics in Medicine. 18(9). 940–948. 130 indexed citations
7.
Wang, Yang, Hao Hu, J. Zhang, et al.. (2016). Clinical application of whole‐genome low‐coverage next‐generation sequencing to detect and characterize balanced chromosomal translocations. Clinical Genetics. 91(4). 605–610. 37 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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