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For: Schmit M, Bielinsky AK. Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms. Int J Mol Sci 2021;22:E911. [PMID: 33477564 DOI: 10.3390/ijms22020911] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
Number Citing Articles
1 Grange LJ, Reynolds JJ, Ullah F, Isidor B, Shearer RF, Latypova X, Baxley RM, Oliver AW, Ganesh A, Cooke SL, Jhujh SS, Mcnee GS, Hollingworth R, Higgs MR, Natsume T, Khan T, Martos-moreno GÁ, Chupp S, Mathew CG, Parry D, Simpson MA, Nahavandi N, Yüksel Z, Drasdo M, Kron A, Vogt P, Jonasson A, Seth SA, Gonzaga-jauregui C, Brigatti KW, Stegmann APA, Kanemaki M, Josifova D, Uchiyama Y, Oh Y, Morimoto A, Osaka H, Ammous Z, Argente J, Matsumoto N, Stumpel CT, Taylor AMR, Jackson AP, Bielinsky A, Mailand N, Le Caignec C, Davis EE, Stewart GS. Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy. Nat Commun 2022;13:6664. [DOI: 10.1038/s41467-022-34349-8] [Reference Citation Analysis]
2 Begemann A, Oneda B, Baumer A, Guldimann M, Tutschek B, Rauch A. A Xp22.11-p21.3 microdeletion in a three-generation family supports male lethality of POLA1 nullisomy resulting in reduced fertility of female carriers. Eur J Med Genet 2022;:104628. [PMID: 36182037 DOI: 10.1016/j.ejmg.2022.104628] [Reference Citation Analysis]
3 Nazarenko MS, Viakhireva IV, Skoblov MY, Soloveva EV, Sleptcov AA, Nazarenko LP. Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test. IJMS 2022;23:9234. [DOI: 10.3390/ijms23169234] [Reference Citation Analysis]
4 Rubio-ferrera I, Baladrón-de-juan P, Clarembaux-badell L, Truchado-garcia M, Jordán-álvarez S, Thor S, Benito-sipos J, Monedero Cobeta I. Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation. PLoS Genet 2022;18:e1010255. [DOI: 10.1371/journal.pgen.1010255] [Reference Citation Analysis]
5 Dmowski M, Jedrychowska M, Makiela-dzbenska K, Denkiewicz-kruk M, Sharma S, Chabes A, Araki H, Fijalkowska IJ. Increased contribution of DNA polymerase delta to the leading strand replication in yeast with an impaired CMG helicase complex. DNA Repair 2022;110:103272. [DOI: 10.1016/j.dnarep.2022.103272] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Demerdjieva Z, Trifunova BK, Damevska S. A Pediatric Case Presenting with Poikiloderma. Clinical Cases in Pediatric Skin Cancers 2022. [DOI: 10.1007/978-3-030-93666-2_14] [Reference Citation Analysis]
7 Si N, Zhang Z, Huang X, Wang C, Guo P, Pan B, Jiang H. De novo 22q11.2 deletions and auricular findings in two Chinese patients with microtia. Mol Genet Genomic Med 2021;:e1862. [PMID: 34971493 DOI: 10.1002/mgg3.1862] [Reference Citation Analysis]
8 Caballero M, Ge T, Rebelo AR, Seo S, Kim S, Brooks K, Zuccaro M, Kanagaraj R, Vershkov D, Kim D, Smogorzewska A, Smolka M, Benvenisty N, West SC, Egli D, Mace EM, Koren A. Comprehensive analysis of DNA replication timing in genetic diseases and gene knockouts identifies MCM10 as a novel regulator of the replication program.. [DOI: 10.1101/2021.09.08.459433] [Reference Citation Analysis]
9 Chang YC, Oram MK, Bielinsky AK. SUMO-Targeted Ubiquitin Ligases and Their Functions in Maintaining Genome Stability. Int J Mol Sci 2021;22:5391. [PMID: 34065507 DOI: 10.3390/ijms22105391] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]