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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:

Genome-wide noninvasive prenatal diagnosis of monogenic disorders: Current and future trends
Tom Rabinowitz, Noam Shomron
Computational and Structural Biotechnology Journal (2020) Vol. 18, pp. 2463-2470
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Detecting monogenic disorders in utero non-invasively based on fetal nucleated red blood cells highly-purified by multi-functional magnetic nanoparticles
Lin Cheng, Chun Feng, Ke Wu, et al.
Analytica Chimica Acta (2025) Vol. 1343, pp. 343690-343690
Closed Access | Times Cited: 1
The path winds along isolation and analyses of fetal nucleated red blood cells in maternal peripheral blood: Past, present, and future toward non-invasive prenatal diagnosis
Chun Feng, Jing Tang, Ke Wu, et al.
Life Sciences (2025) Vol. 369, pp. 123530-123530
Closed Access
Cell-Free DNA in the Pathogenesis and Therapy of Non-Infectious Inflammations and Tumors
Györgyi Műzes, Bettina Bohusné Barta, Orsolya Szabó, et al.
Biomedicines (2022) Vol. 10, Iss. 11, pp. 2853-2853
Open Access | Times Cited: 16
Prenatal and postnatal genetic testing toward personalized care: The non-invasive perinatal testing
Lilla Botos, E Szatmári, G Nagy
Molecular and Cellular Probes (2023) Vol. 72, pp. 101942-101942
Open Access | Times Cited: 9
In Utero Gene Therapy and its Application in Genetic Hearing Loss
Chenyang Kong, Ge Yin, Xiaohui Wang, et al.
Advanced Biology (2024) Vol. 8, Iss. 10
Closed Access | Times Cited: 3
Droplet‑based digital PCR for non‑invasive prenatal genetic diagnosis of α and β‑thalassemia
Kritchakorn Sawakwongpra, Kulvadee Tangmansakulchai, Wasinee Ngonsawan, et al.
Biomedical Reports (2021) Vol. 15, Iss. 4
Open Access | Times Cited: 22
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: 8
Single-cell whole-genome sequencing, haplotype analysis in prenatal diagnosis of monogenic diseases
Liang Chang, Haining Jiao, Jiucheng Chen, et al.
Life Science Alliance (2023) Vol. 6, Iss. 5, pp. e202201761-e202201761
Open Access | Times Cited: 8
Machine learning‐enhanced noninvasive prenatal testing of monogenic disorders
Noa Liscovitch‐Brauer, Ravit Mesika, Tom Rabinowitz, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 9, pp. 1024-1032
Closed Access | Times Cited: 2
Clinical and genetic features of Fanconi anemia associated with a variant of FANCA gene: Case report and literature review
Lin Zhong, Wenhua Zhang, Kaihui Zhang, et al.
Medicine (2024) Vol. 103, Iss. 36, pp. e39358-e39358
Open Access | Times Cited: 2
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders
Wenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
Human Genomics (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 11
Association of maternal risk factors with fetal aneuploidy and the accuracy of prenatal aneuploidy screening: a correlation analysis based on 12,186 karyotype reports
Lun Wei, Jiakai Zhang, Ningxian Shi, et al.
BMC Pregnancy and Childbirth (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 5
Focus on the frontier issue: progress in noninvasive prenatal screening for fetal trisomy from clinical perspectives
Meng Tian, Lei Feng, Jinming Li, et al.
Critical Reviews in Clinical Laboratory Sciences (2023) Vol. 60, Iss. 4, pp. 248-269
Closed Access | Times Cited: 4
From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns
Lidiia Zhytnik, Maire Peters, Kadi Tilk, et al.
Human Reproduction Update (2021) Vol. 27, Iss. 6, pp. 1056-1085
Closed Access | Times Cited: 9
Non-invasive prenatal screening tests – update 2022
Elena Kypri, Marios Ioannides, Achilleas Achilleos, et al.
Journal of Laboratory Medicine (2022) Vol. 46, Iss. 4, pp. 311-320
Open Access | Times Cited: 6
Prenatal genetic diagnosis of monogenic diseases
Carmen Prior‐de Castro, Clara Gómez‐González, Raquel Rodríguez‐López, et al.
Advances in Laboratory Medicine / Avances en Medicina de Laboratorio (2023) Vol. 4, Iss. 1, pp. 28-39
Open Access | Times Cited: 2
Population monitoring of trisomy 21: problems and approaches
Karl Sperling, Hagen Scherb, Heidemarie Neitzel
Molecular Cytogenetics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?
Michaela Hýblová, Andrej Gnip, Marcel Kucharík, et al.
Diagnostics (2022) Vol. 12, Iss. 12, pp. 3056-3056
Open Access | Times Cited: 4
Estimation of cell-free fetal DNA fraction from maternal plasma based on linkage disequilibrium information
Jia Ju, Jia Li, Siyang Liu, et al.
npj Genomic Medicine (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 5
Should non-invasive prenatal testing be recommended for patients who achieve pregnancy with PGT?
Yunhao Liang, Meiyi Li, Jia Fei, et al.
BMC Pregnancy and Childbirth (2024) Vol. 24, Iss. 1
Open Access
Application of an Optimized Non-Invasive Prenatal Testing For Thalassemia Based on Change of Haplotype Doses
Fei Sun, Yao Zhou, Xing Zhao, et al.
(2024)
Closed Access
Sequencing: A Promising Path in the Detection of Fetal Health
Indu Sharma, Neha Negi, Subhas Chandra Saha
(2024), pp. 273-288
Closed Access
Noninvasive fetal genotyping using deep neural networks
Yvonne Schwammenthal, Tom Rabinowitz, Lina Basel‐Vanagaite, et al.
Briefings in Bioinformatics (2024) Vol. 26, Iss. 1
Open Access
Improved noninvasive fetal variant calling using standardized benchmarking approaches
Tom Rabinowitz, Shira Deri-Rozov, Noam Shomron
Computational and Structural Biotechnology Journal (2020) Vol. 19, pp. 509-517
Open Access | Times Cited: 3
First prenatal case of Noonan syndrome with SOS2 mutation: Implications of early diagnosis for genetic counseling
Mattia Gentile, Tiziana Fanelli, Francesca Romana Lepri, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 6, pp. 1897-1902
Closed Access | Times Cited: 2
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