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For: Niceta M, Barresi S, Pantaleoni F, Capolino R, Dentici ML, Ciolfi A, Pizzi S, Bartuli A, Dallapiccola B, Tartaglia M, Digilio MC. TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations. Eur J Med Genet 2019;62:103534. [PMID: 30189253 DOI: 10.1016/j.ejmg.2018.09.001] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Daicheng H, Shiwen X, Jingxuan Z, Junbo H, Bo W. A Frameshift RBM10 Variant Associated With TARP Syndrome. Front Genet 2022;13:922048. [DOI: 10.3389/fgene.2022.922048] [Reference Citation Analysis]
2 Manotas H, Payán-Gómez C, Roa MF, Piñeros JG. TARP syndrome associated with renal malformation and optic nerve atrophy. BMJ Case Rep 2021;14:e240601. [PMID: 34031074 DOI: 10.1136/bcr-2020-240601] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
3 Gowans LJJ, Al Dhaheri N, Li M, Busch T, Obiri-Yeboah S, Oti AA, Sabbah DK, Arthur FKN, Awotoye WO, Alade AA, Twumasi P, Agbenorku P, Plange-Rhule G, Naicker T, Donkor P, Murray JC, Sobreira NLM, Butali A. Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes. Mol Genet Genomic Med 2021;9:e1655. [PMID: 33719213 DOI: 10.1002/mgg3.1655] [Reference Citation Analysis]
4 Kumps C, D'haenens E, Vergult S, Leus J, van Coster R, Jansen A, Devriendt K, Oostra A, Vanakker OM. Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clin Genet 2021;99:449-56. [PMID: 33340101 DOI: 10.1111/cge.13901] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Imagawa E, Konuma T, Cork EE, Diaz GA, Oishi K. A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features. Clin Genet 2020;98:606-12. [PMID: 32812661 DOI: 10.1111/cge.13835] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
6 Kunimoto H, Inoue A, Kojima H, Yang J, Zhao H, Tsuruta D, Nakajima K. RBM10 regulates centriole duplication in HepG2 cells by ectopically assembling PLK4‐STIL complexes in the nucleus. Genes Cells 2020;25:100-10. [DOI: 10.1111/gtc.12741] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]