OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The role of non-invasive prenatal testing and ultrasound in prenatal screening of fetal chromosomal abnormalities in singleton: a retrospective study
Xiying Yuan, Wenjing Yong, Lei Dai, et al.
Annals of Translational Medicine (2023) Vol. 11, Iss. 2, pp. 111-111
Open Access | Times Cited: 9

Showing 9 citing articles:

Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies
Ziye Zeng, Lan Zhang, Yuqin Zhou, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access

The value of increasing sequencing depth for noninvasive prenatal screening for whole chromosomal aneuploidy
Dongmei Wang, Fangfang Guo, Yaping Hou, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access

Retrospective study on NIPT or NIPT plus combined with ultrasound in screening fetal chromosomal abnormalities
Meilin Chen, Peisong Chen, Si‐yang Yu, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access

Clinical Potential of Expanded Noninvasive Prenatal Testing for Detection of Aneuploidies and Microdeletion/Microduplication Syndromes
Chunyan Li, Menghua Xiong, Ying Zhan, et al.
Molecular Diagnosis & Therapy (2023) Vol. 27, Iss. 6, pp. 769-779
Closed Access | Times Cited: 10

Clinical value of screening prenatal ultrasound combined with chromosomal microarrays in prenatal diagnosis of chromosomal abnormalities
Hongru Jiang, Xiangtian Kong, Wenjun Bian, et al.
The Journal of Maternal-Fetal & Neonatal Medicine (2024) Vol. 37, Iss. 1
Open Access | Times Cited: 2

Ultrasound signs of fetal chromosomal abnormalities at 11–14 weeks of pregnancy and its value in the era of modern genetic testing
M. M. Bulanova, Daria S. Bokieva, О.Б. Панина
Ultrasound & Functional Diagnostics (2024), Iss. 3, pp. 67-95
Closed Access

Evaluation of the clinical utility of NIPT-plus and analysis of adverse pregnancy outcomes
Le Zhang, Brandon L. Chang, Lixia Wang, et al.
Archives of Gynecology and Obstetrics (2024)
Closed Access

NIPT/NIPT plus combined with ultrasound in screening fetal chromosomal abnormalities:a retrospective study
Meilin Chen, Jinghai Yan, Si‐yang Yu, et al.
Research Square (Research Square) (2024)
Closed Access

Application of Genetic Origin Analysis of Copy Number Variations in Non‐Invasive Prenatal Testing
Jing Wang, Qingwen Zhu, Aiming Cui, et al.
Prenatal Diagnosis (2024)
Closed Access

Page 1

Scroll to top