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Cited by in F6Publishing
For: Binder G, Ziegler J, Schweizer R, Habhab W, Haack TB, Heinrich T, Eggermann T. Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome. Clin Epigenetics 2020;12:152. [PMID: 33076988 DOI: 10.1186/s13148-020-00945-y] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Lozano-Ureña A, Lázaro-Carot L, Jiménez-Villalba E, Montalbán-Loro R, Mateos-White I, Duart-Abadía P, Martínez-Gurrea I, Nakayama KI, Fariñas I, Kirstein M, Gil-Sanz C, Ferrón SR. IGF2 interacts with the imprinted gene Cdkn1c to promote terminal differentiation of neural stem cells. Development 2023;150. [PMID: 36633189 DOI: 10.1242/dev.200563] [Reference Citation Analysis]
2 Hara-Isono K, Yamazawa K, Tanaka S, Nishi E, Fukami M, Kagami M. CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR. J Med Genet 2022;59:1241-6. [PMID: 35906012 DOI: 10.1136/jmg-2022-108700] [Reference Citation Analysis]
3 Li J, He H, Chen L. CDKN1C gene mutation causing familial Silver–Russell syndrome, with family pedigree.. [DOI: 10.21203/rs.3.rs-2314166/v1] [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 Sparago A, Cerrato F, Pignata L, Cammarata-Scalisi F, Garavelli L, Piscopo C, Vancini A, Riccio A. Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C. Genes (Basel) 2021;12:706. [PMID: 34065128 DOI: 10.3390/genes12050706] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Grünert SC, Matysiak U, Hodde F, Ruzaike G, Lausch E, Schumann A, van der Werf-Grohmann N, Spiekerkoetter U, Schmidts M. Isolated Hypomethylation of IGF2 Associated with Severe Hypoglycemia Responsive to Growth Hormone Treatment. Diagnostics (Basel) 2021;11:749. [PMID: 33922271 DOI: 10.3390/diagnostics11050749] [Reference Citation Analysis]
7 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]
8 Berland S, Haukanes BI, Juliusson PB, Houge G. Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay. J Med Genet 2020:jmedgenet-2020-107401. [PMID: 33443097 DOI: 10.1136/jmedgenet-2020-107401] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]