Weigang Lv

731 total citations
24 papers, 469 citations indexed

About

Weigang Lv is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Weigang Lv has authored 24 papers receiving a total of 469 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Genetics. Recurrent topics in Weigang Lv's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Parvovirus B19 Infection Studies (3 papers). Weigang Lv is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Parvovirus B19 Infection Studies (3 papers). Weigang Lv collaborates with scholars based in China, United Kingdom and France. Weigang Lv's co-authors include Lingqian Wu, Desheng Liang, Haoxian Li, Liangpu Xu, David S. Cram, Liang Hu, Jing Liu, Hua Wang, Jianguang Zhang and Ying Peng and has published in prestigious journals such as Clinical Chemistry, Gene and Medicine.

In The Last Decade

Weigang Lv

22 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Weigang Lv China	10	264	191	118	87	79	24	469
Varsha Shridhar United States	8	80 0.3×	92 0.5×	200 1.7×	125 1.4×	35 0.4×	17	445
Y-M.D. Lo United Kingdom	7	202 0.8×	130 0.7×	167 1.4×	33 0.4×	90 1.1×	9	480
Yongyi Ma China	10	95 0.4×	102 0.5×	112 0.9×	23 0.3×	24 0.3×	20	263
Kohzo Aisaka Japan	8	108 0.4×	195 1.0×	272 2.3×	29 0.3×	18 0.2×	16	416
Dong Zhen United States	9	199 0.8×	31 0.2×	111 0.9×	38 0.4×	102 1.3×	13	329
Eunhee Han South Korea	11	33 0.1×	70 0.4×	119 1.0×	48 0.6×	26 0.3×	44	387
Orapan Sripichai Thailand	16	140 0.5×	86 0.5×	215 1.8×	30 0.3×	28 0.4×	29	894
Katarzyna Guz Poland	12	96 0.4×	115 0.6×	50 0.4×	15 0.2×	69 0.9×	49	417
Rebecca Darlay United Kingdom	9	52 0.2×	51 0.3×	117 1.0×	35 0.4×	68 0.9×	19	305

Countries citing papers authored by Weigang Lv

Since Specialization

Citations

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

Fields of papers citing papers by Weigang Lv

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Weigang Lv

This figure shows the co-authorship network connecting the top 25 collaborators of Weigang Lv. A scholar is included among the top collaborators of Weigang Lv 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 Weigang Lv. Weigang Lv 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

Lv, Weigang, et al.. (2025). A retrospective analysis of 38,652 amniotic fluid karyotype. Frontiers in Genetics. 16. 1655290–1655290.

Zhao, Xingping, et al.. (2024). DNA methylation detection is a significant biomarker for screening endometrial cancer in premenopausal women with abnormal uterine bleeding. International Journal of Gynecological Cancer. 34(8). 1165–1171. 1 indexed citations

Lv, Weigang, et al.. (2024). Detection of walnut internal quality via improved YOLOv5 and x‐ray imaging. Journal of Food Process Engineering. 47(10).

Liu, Huiping, et al.. (2023). The predictive value of uterine artery Doppler in the success rate of pregnancy from the first frozen embryo transfer during the implantation window. BMC Pregnancy and Childbirth. 23(1). 825–825. 1 indexed citations

Zhang, Yan, et al.. (2023). Efficacy and safety of macrolides in the treatment of children with bronchiectasis: a meta-analysis. Pediatric Research. 94(5). 1600–1608. 1 indexed citations

Zhai, Panpan, Weigang Lv, Xiaoqing Yang, et al.. (2022). Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene. Pediatric and Developmental Pathology. 25(4). 397–403. 1 indexed citations

Lv, Weigang, Lili Liang, Zhuo Li, et al.. (2022). Noninvasive Prenatal Testing of Methylmalonic Acidemia cblC Type Using the cSMART Assay for MMACHC Gene Mutations. Frontiers in Genetics. 12. 750719–750719. 6 indexed citations

Wan, Zhengqing, Xiaoqing Peng, Lu Ma, et al.. (2020). Targeted Sequencing of Genomic Repeat Regions Detects Circulating Cell-free Echinococcus DNA. PLoS neglected tropical diseases. 14(3). e0008147–e0008147. 16 indexed citations

Lv, Weigang, et al.. (2019). Development and validation of a haplotype‐free technique for non‐invasive prenatal diagnosis of spinal muscular atrophy. Journal of Clinical Laboratory Analysis. 34(2). e23046–e23046. 10 indexed citations

10.

Lv, Weigang, Zhuo Li, Haiyan Zhu, et al.. (2019). Noninvasive fetal genotyping in pregnancies at risk for PKU using a comprehensive quantitative cSMART assay for PAH gene mutations: a clinical feasibility study. BJOG An International Journal of Obstetrics & Gynaecology. 126(12). 1466–1474. 10 indexed citations

11.

Zhang, Yan, et al.. (2019). Chrysophanol attenuates airway inflammation and remodeling through nuclear factor‐kappa B signaling pathway in asthma. Phytotherapy Research. 33(10). 2702–2713. 34 indexed citations

12.

Tan, Hu, Xin Chen, Weigang Lv, et al.. (2018). Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review. Journal of Human Genetics. 63(7). 851–855. 10 indexed citations

13.

Huang, Yanru, Hu Tan, Zhuo Li, et al.. (2018). Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis. Eye. 32(8). 1359–1364. 7 indexed citations

14.

Lv, Weigang, et al.. (2017). Comparative efficacy and safety of contact force-sensing catheter and second-generation cryoballoon ablation for atrial fibrillation: a meta-analysis. Brazilian Journal of Medical and Biological Research. 50(9). e6409–e6409. 6 indexed citations

15.

Huang, Yanru, Weigang Lv, Haoxian Li, et al.. (2016). Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIII. Clinica Chimica Acta. 464. 170–175. 4 indexed citations

16.

Zhang, Shujie, Weigang Lv, Shiyu Luo, et al.. (2015). Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis. Gene. 577(2). 187–192. 9 indexed citations

17.

Liang, Desheng, Ying Peng, Weigang Lv, et al.. (2014). Copy Number Variation Sequencing for Comprehensive Diagnosis of Chromosome Disease Syndromes. Journal of Molecular Diagnostics. 16(5). 519–526. 105 indexed citations

18.

Lv, Weigang, Ruolan Guo, Qin Liu, et al.. (2014). Noninvasive Prenatal Testing for Wilson Disease by Use of Circulating Single-Molecule Amplification and Resequencing Technology (cSMART). Clinical Chemistry. 61(1). 172–181. 74 indexed citations

19.

Li, Zhuo, Jing Liu, Haoxian Li, et al.. (2013). Phenotypic expansion of the interstitial 16p13.3 duplication: A case report and review of the literature. Gene. 531(2). 502–505. 24 indexed citations

20.

Wu, Lingqian, Jing Liu, Weigang Lv, et al.. (2013). An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother. Birth Defects Research Part A Clinical and Molecular Teratology. 97(7). 467–470. 14 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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