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Cited by in F6Publishing
For: Abraham MB, Li D, Tang D, O'Connell SM, McKenzie F, Lim EM, Hakonarson H, Levine MA, Choong CS. Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene. Int J Pediatr Endocrinol 2017;2017:1. [PMID: 28138333 DOI: 10.1186/s13633-016-0041-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang Q, Zhang J, Jiang N, Xie J, Yang J, Zhao X. De novo nonsense variant in ASXL3 in a Chinese girl causing Bainbridge-Ropers syndrome: A case report and review of literature. Mol Genet Genomic Med 2022;10:e1924. [PMID: 35276034 DOI: 10.1002/mgg3.1924] [Reference Citation Analysis]
2 Ip WH, Wilkens B, Solomatina A, Martin J, Melling M, Hidalgo P, Bertzbach LD, Speiseder T, Dobner T. Differential Regulation of Cellular FAM111B by Human Adenovirus C Type 5 E1 Oncogenes. Viruses 2021;13:1015. [PMID: 34071532 DOI: 10.3390/v13061015] [Reference Citation Analysis]
3 Müller R, Steffensen T, Krstić N, Cain MA. Report of a novel variant in the FAM111A gene in a fetus with multiple anomalies including gracile bones, hypoplastic spleen, and hypomineralized skull. Am J Med Genet A 2021;185:1903-7. [PMID: 33750016 DOI: 10.1002/ajmg.a.62182] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Bilezikian JP. Hypoparathyroidism. J Clin Endocrinol Metab 2020;105:dgaa113. [PMID: 32322899 DOI: 10.1210/clinem/dgaa113] [Cited by in Crossref: 14] [Cited by in F6Publishing: 24] [Article Influence: 14.0] [Reference Citation Analysis]
5 Cheng SSW, Chan PKJ, Luk HM, Mok MT, Lo IFM. Adult Chinese twins with Kenny-Caffey syndrome type 2: A potential age-dependent phenotype and review of literature. Am J Med Genet A 2021;185:636-46. [PMID: 33263187 DOI: 10.1002/ajmg.a.61991] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Cavole TR, Perrone E, de Faria Soares MF, Dias da Silva MR, Maeda SS, Lazaretti-Castro M, Alvarez Perez AB. Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case report. Am J Med Genet A 2020;182:3029-34. [PMID: 33010201 DOI: 10.1002/ajmg.a.61896] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Hoffmann S, Pentakota S, Mund A, Haahr P, Coscia F, Gallo M, Mann M, Taylor NM, Mailand N. FAM111 protease activity undermines cellular fitness and is amplified by gain-of-function mutations in human disease. EMBO Rep 2020;21:e50662. [PMID: 32776417 DOI: 10.15252/embr.202050662] [Cited by in Crossref: 4] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
8 Yerawar C, Kabde A, Deokar P. Kenny–Caffey syndrome type 2. QJM: An International Journal of Medicine 2021;114:267-9. [DOI: 10.1093/qjmed/hcaa175] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Kojima Y, Machida Y, Palani S, Caulfield TR, Radisky ES, Kaufmann SH, Machida YJ. FAM111A protects replication forks from protein obstacles via its trypsin-like domain. Nat Commun 2020;11:1318. [PMID: 32165630 DOI: 10.1038/s41467-020-15170-7] [Cited by in Crossref: 19] [Cited by in F6Publishing: 28] [Article Influence: 9.5] [Reference Citation Analysis]
10 Deconte D, Kreusch TC, Salvaro BP, Perin WF, Ferreira MAT, Kopacek C, da Rosa EB, Heringer JI, Ligabue-Braun R, Zen PRG, Rosa RFM, Fiegenbaum M. Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2. J Pediatr Genet 2020;9:263-9. [PMID: 32765931 DOI: 10.1055/s-0039-3401831] [Reference Citation Analysis]