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Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Awamleh Z, Choufani S, Wu W, Rots D, Dingemans AJM, Nadif Kasri N, Boronat S, Ibañez-Mico S, Cuesta Herraiz L, Ferrer I, Martínez Carrascal A, Pérez-Jurado LA, Aznar Lain G, Ortigoza-Escobar JD, de Vries BBA, Koolen DA, Weksberg R. Awamleh Z, et al. Among authors: weksberg r. Eur J Hum Genet. 2024 Mar;32(3):366. doi: 10.1038/s41431-024-01561-7. Eur J Hum Genet. 2024. PMID: 38355964 Free PMC article. No abstract available.
Growth regulation, imprinted genes, and chromosome 11p15.5.
Smith AC, Choufani S, Ferreira JC, Weksberg R. Smith AC, et al. Among authors: weksberg r. Pediatr Res. 2007 May;61(5 Pt 2):43R-47R. doi: 10.1203/pdr.0b013e3180457660. Pediatr Res. 2007. PMID: 17413842 Review.
Beckwith-Wiedemann syndrome.
Weksberg R, Shuman C, Beckwith JB. Weksberg R, et al. Eur J Hum Genet. 2010 Jan;18(1):8-14. doi: 10.1038/ejhg.2009.106. Eur J Hum Genet. 2010. PMID: 19550435 Free PMC article. Review.
Beckwith-Wiedemann syndrome.
Choufani S, Shuman C, Weksberg R. Choufani S, et al. Among authors: weksberg r. Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):343-54. doi: 10.1002/ajmg.c.30267. Am J Med Genet C Semin Med Genet. 2010. PMID: 20803657 Review.
Cell specific patterns of methylation in the human placenta.
Grigoriu A, Ferreira JC, Choufani S, Baczyk D, Kingdom J, Weksberg R. Grigoriu A, et al. Among authors: weksberg r. Epigenetics. 2011 Mar;6(3):368-79. doi: 10.4161/epi.6.3.14196. Epub 2011 Mar 1. Epigenetics. 2011. PMID: 21131778 Free PMC article.
293 results