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:
Precision medicine via the integration of phenotype-genotype information in neonatal genome project
Xinran Dong, Tiantian Xiao, Bin Chen, et al.
Fundamental Research (2022) Vol. 2, Iss. 6, pp. 873-884
Open Access | Times Cited: 6
Xinran Dong, Tiantian Xiao, Bin Chen, et al.
Fundamental Research (2022) Vol. 2, Iss. 6, pp. 873-884
Open Access | Times Cited: 6
Showing 6 citing articles:
An Analysis of Ethics-Based Foundation and Regulatory Issues for Genomic Data Privacy
Yesodhai Balagurunathan, Raja Rajeswari Sethuraman
Journal of The Institution of Engineers (India) Series B (2024) Vol. 105, Iss. 4, pp. 1097-1107
Closed Access | Times Cited: 4
Yesodhai Balagurunathan, Raja Rajeswari Sethuraman
Journal of The Institution of Engineers (India) Series B (2024) Vol. 105, Iss. 4, pp. 1097-1107
Closed Access | Times Cited: 4
Advancements in pharmacological interventions for atopic dermatitis current strategies and future directions
Yan Zhang, Shaoying Yuan, Yixing Wu, et al.
Inflammopharmacology (2025)
Closed Access
Yan Zhang, Shaoying Yuan, Yixing Wu, et al.
Inflammopharmacology (2025)
Closed Access
Review of Precision Medicine and Diagnosis of Neonatal Illness
Safaa ELMeneza, Naglaa Agaba, Rasha Abd El Samad Fawaz, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 478-478
Open Access
Safaa ELMeneza, Naglaa Agaba, Rasha Abd El Samad Fawaz, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 478-478
Open Access
Fructose-1,6-bisphosphatase deficiency: estimation of prevalence in the Chinese population and analysis of genotype-phenotype association
Qi Ni, Meiling Tang, Xiang Chen, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Qi Ni, Meiling Tang, Xiang Chen, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Diagnostic Utility of Whole Genome Sequencing After Negative Karyotyping/Chromosomal Microarray in Infants Born With Multiple Congenital Anomalies
Misun Yang, Jee Ah Kim, Heui Seung Jo, et al.
Journal of Korean Medical Science (2024) Vol. 39, Iss. 36
Open Access | Times Cited: 2
Misun Yang, Jee Ah Kim, Heui Seung Jo, et al.
Journal of Korean Medical Science (2024) Vol. 39, Iss. 36
Open Access | Times Cited: 2
Primary carnitine deficiency: Estimation of prevalence in Chinese population and insights into newborn screening
Xiaoshan Ji, Y Ge, Qi Ni, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
Xiaoshan Ji, Y Ge, Qi Ni, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
