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Cited by in F6Publishing
For: Powis Z, Hart A, Cherny S, Petrik I, Palmaer E, Tang S, Jones C. Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration. BMC Med Genet 2017;18:60. [PMID: 28577551 DOI: 10.1186/s12881-017-0426-3] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Kaeppler KE, Stetson RC, Lanpher BC, Collura CA. Infant male with TARP syndrome: Review of clinical features, prognosis, and commonalities with previously reported patients. Am J Med Genet 2018;176:2911-4. [DOI: 10.1002/ajmg.a.40645] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [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] [Reference Citation Analysis]
3 Cao Y, Di X, Zhang Q, Li R, Wang K. RBM10 Regulates Tumor Apoptosis, Proliferation, and Metastasis. Front Oncol 2021;11:603932. [PMID: 33718153 DOI: 10.3389/fonc.2021.603932] [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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 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: 4] [Article Influence: 1.5] [Reference Citation Analysis]
6 Varadarajan S, Balaji TM, Raj AT, Gupta AA, Patil S, Alhazmi TH, Alaqi HAA, Al Omar NEM, Almutaher SABA, Jafer AA, Hedad IA. Genetic Mutations Associated with Pierre Robin Syndrome/Sequence: A Systematic Review. Mol Syndromol 2021;12:69-86. [PMID: 34012376 DOI: 10.1159/000513217] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Smith HS, Swint JM, Lalani SR, Yamal JM, de Oliveira Otto MC, Castellanos S, Taylor A, Lee BH, Russell HV. Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature. Genet Med 2019;21:3-16. [PMID: 29760485 DOI: 10.1038/s41436-018-0024-6] [Cited by in Crossref: 41] [Cited by in F6Publishing: 38] [Article Influence: 10.3] [Reference Citation Analysis]
8 Clark MM, Hildreth A, Batalov S, Ding Y, Chowdhury S, Watkins K, Ellsworth K, Camp B, Kint CI, Yacoubian C, Farnaes L, Bainbridge MN, Beebe C, Braun JJA, Bray M, Carroll J, Cakici JA, Caylor SA, Clarke C, Creed MP, Friedman J, Frith A, Gain R, Gaughran M, George S, Gilmer S, Gleeson J, Gore J, Grunenwald H, Hovey RL, Janes ML, Lin K, McDonagh PD, McBride K, Mulrooney P, Nahas S, Oh D, Oriol A, Puckett L, Rady Z, Reese MG, Ryu J, Salz L, Sanford E, Stewart L, Sweeney N, Tokita M, Van Der Kraan L, White S, Wigby K, Williams B, Wong T, Wright MS, Yamada C, Schols P, Reynders J, Hall K, Dimmock D, Veeraraghavan N, Defay T, Kingsmore SF. Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation. Sci Transl Med 2019;11:eaat6177. [PMID: 31019026 DOI: 10.1126/scitranslmed.aat6177] [Cited by in Crossref: 83] [Cited by in F6Publishing: 71] [Article Influence: 41.5] [Reference Citation Analysis]
9 Højland AT, Lolas I, Okkels H, Lautrup CK, Diness BR, Petersen MB, Nielsen IK. First reported adult patient with TARP syndrome: A case report. Am J Med Genet A 2018;176:2915-8. [PMID: 30462380 DOI: 10.1002/ajmg.a.40638] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
10 Inoue A. RBM10: Structure, functions, and associated diseases. Gene 2021;783:145463. [PMID: 33515724 DOI: 10.1016/j.gene.2021.145463] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
11 Pang S, Sun Z, Lu W, Si-ma H, Lin Z, Shi Y, Yang Y, Zhao X, Yang G, Jin G, Yang N. Integrated Bioinformatics Analysis and Validation of the Prognostic Value of RBM10 Expression in Hepatocellular Carcinoma. CMAR 2022;Volume 14:969-80. [DOI: 10.2147/cmar.s349884] [Reference Citation Analysis]
12 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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Loiselle JJ, Sutherland LC. RBM10: Harmful or helpful-many factors to consider. J Cell Biochem 2018;119:3809-18. [PMID: 29274279 DOI: 10.1002/jcb.26644] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]