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Cited by in F6Publishing
For: Vado Y, Pereda A, Llano-Rivas I, Gorria-Redondo N, Díez I, Perez de Nanclares G. Novel Variant in PLAG1 in a Familial Case with Silver-Russell Syndrome Suspicion. Genes (Basel) 2020;11:E1461. [PMID: 33291420 DOI: 10.3390/genes11121461] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Jauss RT, Schließke S, Abou Jamra R. Routine Diagnostics Confirm Novel Neurodevelopmental Disorders. Genes (Basel) 2022;13. [PMID: 36553572 DOI: 10.3390/genes13122305] [Reference Citation Analysis]
2 Stenman G, Fehr A, Skálová A, Vander Poorten V, Hellquist H, Mikkelsen LH, Saba NF, Guntinas-Lichius O, Chiesa-Estomba CM, Andersson MK, Ferlito A. Chromosome Translocations, Gene Fusions, and Their Molecular Consequences in Pleomorphic Salivary Gland Adenomas. Biomedicines 2022;10. [PMID: 36009517 DOI: 10.3390/biomedicines10081970] [Reference Citation Analysis]
3 Baba N, Lengyel A, Pinti E, Yapici E, Schreyer I, Liehr T, Fekete G, Eggermann T. Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes. Mol Cytogenet 2022;15:19. [PMID: 35562807 DOI: 10.1186/s13039-022-00596-z] [Reference Citation Analysis]
4 Zaletaev DV, Nemtsova MV, Strelnikov VV. Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases. Mol Biol 2022;56:1-28. [DOI: 10.1134/s0026893321050149] [Reference Citation Analysis]
5 Brereton RE, Nickerson SL, Woodward KJ, Edwards T, Sivamoorthy S, Ramos Vasques Walters F, Chabros V, Marchin V, Grumball T, Kennedy D, Uzaraga J, Peverall J, Arscott G, Beilby J, Choong CS, Townshend S, Azmanov DN. Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement. Am J Med Genet A 2021. [PMID: 34223693 DOI: 10.1002/ajmg.a.62391] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
6 Netchine I, van der Steen M, López-Bermejo A, Koledova E, Maghnie M. New Horizons in Short Children Born Small for Gestational Age. Front Pediatr 2021;9:655931. [PMID: 34055692 DOI: 10.3389/fped.2021.655931] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
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