BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Lange M, Begolli R, Giakountis A. Non-Coding Variants in Cancer: Mechanistic Insights and Clinical Potential for Personalized Medicine. Noncoding RNA 2021;7:47. [PMID: 34449663 DOI: 10.3390/ncrna7030047] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Shah H, Khan K, Badshah Y, Mahmood Ashraf N, Shabbir M, Trembley JH, Afsar T, Abusharha A, Razak S. Investigation of UTR Variants by Computational Approaches Reveal Their Functional Significance in PRKCI Gene Regulation. Genes 2023;14:247. [DOI: 10.3390/genes14020247] [Reference Citation Analysis]
2 Kin K, Bhogale S, Zhu L, Thomas D, Bertol J, Zheng WJ, Sinha S, Fakhouri WD. Sequence-to-expression approach to identify etiological non-coding DNA variations in P53 and cMYC-driven diseases.. [DOI: 10.1101/2022.12.05.519089] [Reference Citation Analysis]
3 Fachrul M, Karkey A, Shakya M, Judd L, Harshegyi T, Sim KS, Tonks S, Dongol S, Shrestha R, Salim A, Baker S, Pollard AJ, Khor CC, Dolecek C, Basnyat B, Dunstan SJ, Holt KE, Inouye M, STRATAA study group. Direct inference and control of genetic population structure from RNA sequencing data.. [DOI: 10.1101/2022.09.16.508259] [Reference Citation Analysis]
4 Vischioni C, Bove F, De Chiara M, Mandreoli F, Martoglia R, Pisi V, Liti G, Taccioli C. miRNAs Copy Number Variations Repertoire as Hallmark Indicator of Cancer Species Predisposition. Genes (Basel) 2022;13:1046. [PMID: 35741808 DOI: 10.3390/genes13061046] [Reference Citation Analysis]
5 Ramos L. WT1, NR0B1, NR5A1, LHX9, ZFP92, ZNF275, INSL3, and NRIP1 Genetic Variants in Patients with Premature Ovarian Insufficiency in a Mexican Cohort. Genes 2022;13:611. [DOI: 10.3390/genes13040611] [Reference Citation Analysis]