Yanling Teng

455 total citations
33 papers, 195 citations indexed

About

Yanling Teng is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yanling Teng has authored 33 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yanling Teng's work include Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Yanling Teng is often cited by papers focused on Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Yanling Teng collaborates with scholars based in China, United States and Germany. Yanling Teng's co-authors include Lingqian Wu, Desheng Liang, Zhuo Li, Long Ma, H. Robert Horvitz, Yingdi Liu, Xiaoyang Gao, Huimin Zhu, Jing Liu and Aiping Mao and has published in prestigious journals such as Analytical Chemistry, Journal of Neurophysiology and International Journal of Molecular Sciences.

In The Last Decade

Yanling Teng

30 papers receiving 194 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yanling Teng China 9 130 69 31 22 16 33 195
Katalin Szakszon Hungary 10 178 1.4× 103 1.5× 16 0.5× 9 0.4× 11 0.7× 29 276
María J. Guillen Sacoto United States 10 118 0.9× 121 1.8× 16 0.5× 12 0.5× 12 0.8× 17 203
Yexing Xian China 9 184 1.4× 40 0.6× 48 1.5× 31 1.4× 5 0.3× 14 293
Stefano Petrocchi Italy 8 84 0.6× 129 1.9× 16 0.5× 15 0.7× 31 1.9× 15 236
Cara Skraban United States 10 106 0.8× 120 1.7× 45 1.5× 11 0.5× 43 2.7× 31 244
Dhanya Lakshmi Narayanan India 10 135 1.0× 88 1.3× 22 0.7× 17 0.8× 19 1.2× 42 261
Haruka Hamanoue Japan 10 118 0.9× 84 1.2× 33 1.1× 13 0.6× 12 0.8× 23 220
Benjamin Kamien Australia 9 124 1.0× 128 1.9× 42 1.4× 13 0.6× 20 1.3× 19 228
Hagar Mor‐Shaked Israel 10 154 1.2× 145 2.1× 27 0.9× 13 0.6× 10 0.6× 32 267
Malin Kvarnung Sweden 7 119 0.9× 90 1.3× 12 0.4× 9 0.4× 13 0.8× 16 233

Countries citing papers authored by Yanling Teng

Since Specialization
Citations

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

Fields of papers citing papers by Yanling Teng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yanling Teng

This figure shows the co-authorship network connecting the top 25 collaborators of Yanling Teng. A scholar is included among the top collaborators of Yanling Teng 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 Yanling Teng. Yanling Teng 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.
An, Jian, Han Li, Bojie Chen, et al.. (2025). Guanine-Quadruplex-Engineered crRNA Enables Light-Activated CRISPR/Cas12a System for Robust One-Pot Viral Assay. Analytical Chemistry. 97(48). 26580–26589. 1 indexed citations
2.
Deng, Jinhai, Xingxiang Pu, Tingting Yuan, et al.. (2025). PAM-Independent CRISPR-Cas12a System for Specific Assays of Single Nucleotide Variants. JACS Au. 5(3). 1392–1401. 9 indexed citations
3.
Zhang, Hongyun, Jun He, Yanling Teng, et al.. (2025). Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing. QJM. 118(5). 344–353. 1 indexed citations
4.
Teng, Yanling, Xinyan Wang, Lin Song, et al.. (2025). 3D printed polycaprolactone/poly (L-lactide-co-ϵ-caprolactone) composite ureteral stent with biodegradable and antibacterial properties. Biomedical Materials. 20(2). 25026–25026. 2 indexed citations
5.
Wang, Zhongjie, et al.. (2024). Application of whole exome sequencing in carrier screening for high-risk families without probands. Frontiers in Genetics. 15. 1415811–1415811.
6.
Zhou, Xiaowei, Yan Li, Fang Liu, et al.. (2024). PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation. Cell Death and Disease. 15(11). 808–808. 1 indexed citations
7.
8.
9.
Li, Yunlong, Yixuan Wang, Ranhui Duan, et al.. (2023). A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder. Cell Reports. 42(12). 113445–113445. 3 indexed citations
10.
Zhang, Hongyun, Siyuan Linpeng, Yanling Teng, et al.. (2023). A de novo heterozygous POU3F3 genotype for the p.(Q214*) variant in a fetus with transient isolated bilateral mild ventriculomegaly: a case report and review of the literature. Frontiers in Pediatrics. 11. 1177137–1177137. 1 indexed citations
11.
Teng, Yanling, Haoran Hu, Huimin Zhu, et al.. (2023). Two novel variants in CEP152 caused Seckel syndrome 5 in a Chinese family. Frontiers in Genetics. 13. 1052915–1052915. 1 indexed citations
12.
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
13.
Zhang, Hongyun, Xin Chen, Hu Tan, et al.. (2022). The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability. Clinica Chimica Acta. 538. 94–103. 1 indexed citations
14.
Zhou, Qimin, Yanling Teng, Yingdi Liu, et al.. (2022). Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemia. Clinica Chimica Acta. 531. 48–55. 3 indexed citations
15.
Liu, Yingdi, Yanling Teng, Zhuo Li, et al.. (2021). Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1–2 years after initial analysis. Clinica Chimica Acta. 523. 163–168. 9 indexed citations
16.
Chen, Xin, Yin Wu, Wenyu Zhang, et al.. (2021). Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis. Human Genetics. 140(5). 791–803. 11 indexed citations
17.
Teng, Yanling, et al.. (2020). Detection of Spinal Muscular Atrophy Using a Duplexed Real-Time PCR Approach With Locked Nucleic Acid-Modified Primers. Annals of Laboratory Medicine. 41(1). 101–107. 8 indexed citations
18.
Teng, Yanling, et al.. (2020). Six novel Mutation analysis of the androgen receptor gene in 17 Chinese patients with androgen insensitivity syndrome. Clinica Chimica Acta. 506. 180–186. 7 indexed citations
19.
Huang, Wen, et al.. (2019). [Prenatal diagnosis for 30 women carrying a FMR1 mutation].. PubMed. 36(9). 866–869. 1 indexed citations
20.
Ma, Long, Zhiping Tan, Yanling Teng, Sebastian Hoersch, & H. Robert Horvitz. (2011). In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans. RNA. 17(12). 2201–2211. 15 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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