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For: Boniel S, Szymańska K, Śmigiel R, Szczałuba K. Kabuki Syndrome-Clinical Review with Molecular Aspects. Genes (Basel) 2021;12:468. [PMID: 33805950 DOI: 10.3390/genes12040468] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Montano C, Britton JF, Harris JR, Kerkhof J, Barnes BT, Lee JA, Sadikovic B, Sobreira N, Fahrner JA. Genome-wide DNA methylation profiling confirms a case of low-level mosaic Kabuki syndrome 1. Am J Med Genet A 2022. [PMID: 35384273 DOI: 10.1002/ajmg.a.62754] [Reference Citation Analysis]
2 Behbahanipour M, García-Pardo J, Ventura S. Decoding the role of coiled-coil motifs in human prion-like proteins. Prion 2021;15:143-54. [PMID: 34428113 DOI: 10.1080/19336896.2021.1961569] [Reference Citation Analysis]
3 Kirsten TB, Silva EP, Biondi TF, Rodrigues PS, Cardoso CV, Massironi SMG, Mori CMC, Bondan EF, Bernardi MM. Bate palmas mutant mice as a model of Kabuki syndrome: Higher susceptibility to infections and vocalization impairments? J Neurosci Res 2022. [PMID: 35362120 DOI: 10.1002/jnr.25050] [Reference Citation Analysis]
4 Lager TW, Zuo J, Alam MS, Calhoun B, Haldar K, Panopoulos AD. Generation of three induced pluripotent stem cell lines from a patient with Kabuki syndrome carrying the KMT2D p.R4198X mutation. Stem Cell Research 2022. [DOI: 10.1016/j.scr.2022.102799] [Reference Citation Analysis]
5 Barcellini W, Fattizzo B. Immune Phenomena in Myeloid Neoplasms: An "Egg or Chicken" Question. Front Immunol 2021;12:751630. [PMID: 34659257 DOI: 10.3389/fimmu.2021.751630] [Reference Citation Analysis]
6 Elling CL, Scholes MA, Streubel S, Larson ED, Wine TM, Bootpetch TC, Yoon PJ, Kofonow JM, Gubbels SP, Cass SP, Robertson CE, Jenkins HA, Prager JD, Frank DN, Chan KH, Friedman NR, Ryan AF, Santos-cortez RLP. The FUT2 Variant c.461G>A (p.Trp154*) Is Associated With Differentially Expressed Genes and Nasopharyngeal Microbiota Shifts in Patients With Otitis Media. Front Cell Infect Microbiol 2022;11:798246. [DOI: 10.3389/fcimb.2021.798246] [Reference Citation Analysis]
7 Panov J, Kaphzan H. Angelman Syndrome and Angelman-like Syndromes Share the Same Calcium-Related Gene Signatures. Int J Mol Sci 2021;22:9870. [PMID: 34576033 DOI: 10.3390/ijms22189870] [Reference Citation Analysis]
8 Guo L, Zhang M, Gao Y, Qin L, Xia H, Liu L, Wang H. A gonadal mosaicism novel KMT2D mutation identified by haplotype construction and clone sequencing strategy. Clin Chim Acta 2022:S0009-8981(22)00128-0. [PMID: 35421397 DOI: 10.1016/j.cca.2022.04.008] [Reference Citation Analysis]
9 Grisdela PT, Paschos N, Tanaka MJ. Fixed (Congenital) Patellar Dislocation. Clin Sports Med 2022;41:123-36. [PMID: 34782069 DOI: 10.1016/j.csm.2021.07.010] [Reference Citation Analysis]
10 Ma Q, Song C, Yin B, Shi Y, Ye L. The role of Trithorax family regulating osteogenic and Chondrogenic differentiation in mesenchymal stem cells. Cell Prolif 2022;:e13233. [PMID: 35481717 DOI: 10.1111/cpr.13233] [Reference Citation Analysis]