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
Tom Rabinowitz, Noam Shomron
Computational and Structural Biotechnology Journal (2020) Vol. 18, pp. 2463-2470
Open Access | Times Cited: 32
Showing 26-50 of 32 citing articles:
Couple screening for recessively inherited disorders
Silvina Sisterna, A. Borrell
Journal of Medical Screening (2022) Vol. 30, Iss. 2, pp. 55-61
Closed Access | Times Cited: 1
Silvina Sisterna, A. Borrell
Journal of Medical Screening (2022) Vol. 30, Iss. 2, pp. 55-61
Closed Access | Times Cited: 1
Diagnóstico genético prenatal de enfermedades monogénicas
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. 40-51
Open Access
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. 40-51
Open Access
Prenatal Genome-Wide Sequencing for the Investigation of Fetal Structural Anomalies: Is There a Role for Noninvasive Prenatal Diagnosis?
Elizabeth Wall, Stephanie Allen, James Castleman, et al.
Springer eBooks (2023), pp. 357-377
Closed Access
Elizabeth Wall, Stephanie Allen, James Castleman, et al.
Springer eBooks (2023), pp. 357-377
Closed Access
Whole-genome sequencing as a method of prenatal genetic diagnosis: Ethical issues
Fermín J. González-Melado
Elsevier eBooks (2023), pp. 275-304
Closed Access
Fermín J. González-Melado
Elsevier eBooks (2023), pp. 275-304
Closed Access
Application of whole-exome sequencing technology in clarifying 269 cases of fetal skeletal system disorders
yijun ge, Huizhen Yuan, Baitao Zeng, et al.
Research Square (Research Square) (2023)
Open Access
yijun ge, Huizhen Yuan, Baitao Zeng, et al.
Research Square (Research Square) (2023)
Open Access
Effects of Maternal Factors on Fetal Aneuploidy and Reliability of Screening: A Cohort Study Based on 12,186 Karyotype Reports
Lun Wei, Jiakai Zhang, Ningxian Shi, et al.
Research Square (Research Square) (2022)
Open Access
Lun Wei, Jiakai Zhang, Ningxian Shi, et al.
Research Square (Research Square) (2022)
Open Access
Detection of foetal single gene mutations using only maternal blood samples
Junghyun Namkung
International Journal of Data Mining and Bioinformatics (2021) Vol. 25, Iss. 1/2, pp. 53-53
Open Access
Junghyun Namkung
International Journal of Data Mining and Bioinformatics (2021) Vol. 25, Iss. 1/2, pp. 53-53
Open Access
