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Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains.
Monk D, Morales J, den Dunnen JT, Russo S, Court F, Prawitt D, Eggermann T, Beygo J, Buiting K, Tümer Z; Nomenclature group of the European Network for Human Congenital Imprinting Disorders. Monk D, et al. Among authors: eggermann t. Epigenetics. 2018;13(2):117-121. doi: 10.1080/15592294.2016.1264561. Epub 2018 Jan 25. Epigenetics. 2018. PMID: 27911167 Free PMC article. Review.
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia.
Zeschnigk M, Albrecht B, Buiting K, Kanber D, Eggermann T, Binder G, Gromoll J, Prott EC, Seland S, Horsthemke B. Zeschnigk M, et al. Among authors: eggermann t. Eur J Hum Genet. 2008 Mar;16(3):328-34. doi: 10.1038/sj.ejhg.5201974. Epub 2008 Jan 9. Eur J Hum Genet. 2008. PMID: 18159214
Clinical utility gene card for: Silver-Russell syndrome.
Eggermann T, Buiting K, Temple IK. Eggermann T, et al. Eur J Hum Genet. 2011 Mar;19(3). doi: 10.1038/ejhg.2010.202. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150879 Free PMC article. No abstract available.
Frequency and characterization of DNA methylation defects in children born SGA.
Bens S, Haake A, Richter J, Leohold J, Kolarova J, Vater I, Riepe FG, Buiting K, Eggermann T, Gillessen-Kaesbach G, Platzer K, Prawitt D, Caliebe A, Siebert R. Bens S, et al. Among authors: eggermann t. Eur J Hum Genet. 2013 Aug;21(8):838-43. doi: 10.1038/ejhg.2012.262. Epub 2012 Dec 12. Eur J Hum Genet. 2013. PMID: 23232699 Free PMC article.
Clinical utility gene card for: Beckwith-Wiedemann Syndrome.
Eggermann T, Algar E, Lapunzina P, Mackay D, Maher ER, Mannens M, Netchine I, Prawitt D, Riccio A, Temple IK, Weksberg R. Eggermann T, et al. Eur J Hum Genet. 2014 Mar;22(3). doi: 10.1038/ejhg.2013.132. Epub 2013 Jul 3. Eur J Hum Genet. 2014. PMID: 23820480 Free PMC article. No abstract available.
345 results