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Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans.
Sanchez-Delgado M, Riccio A, Eggermann T, Maher ER, Lapunzina P, Mackay D, Monk D. Sanchez-Delgado M, et al. Among authors: monk d. Trends Genet. 2016 Jul;32(7):444-455. doi: 10.1016/j.tig.2016.05.001. Epub 2016 May 24. Trends Genet. 2016. PMID: 27235113 Review.
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?
Mergenthaler S, Hitchins MP, Blagitko-Dorfs N, Monk D, Wollmann HA, Ranke MB, Ropers HH, Apostolidou S, Stanier P, Preece MA, Eggermann T, Kalscheuer VM, Moore GE. Mergenthaler S, et al. Among authors: monk d. Am J Hum Genet. 2001 Feb;68(2):543-5. doi: 10.1086/318192. Am J Hum Genet. 2001. PMID: 11170901 Free PMC article. No abstract available.
Transcript- and tissue-specific imprinting of a tumour suppressor gene.
Schulz R, McCole RB, Woodfine K, Wood AJ, Chahal M, Monk D, Moore GE, Oakey RJ. Schulz R, et al. Among authors: monk d. Hum Mol Genet. 2009 Jan 1;18(1):118-27. doi: 10.1093/hmg/ddn322. Epub 2008 Oct 4. Hum Mol Genet. 2009. PMID: 18836209 Free PMC article.
Deciphering the cancer imprintome.
Monk D. Monk D. Brief Funct Genomics. 2010 Jul;9(4):329-39. doi: 10.1093/bfgp/elq013. Epub 2010 Jun 15. Brief Funct Genomics. 2010. PMID: 20551091 Review.
Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism.
Romanelli V, Nevado J, Fraga M, Trujillo AM, Mori MÁ, Fernández L, Pérez de Nanclares G, Martínez-Glez V, Pita G, Meneses H, Gracia R, García-Miñaur S, García de Miguel P, Lecumberri B, Rodríguez JI, González Neira A, Monk D, Lapunzina P. Romanelli V, et al. Among authors: monk d. J Med Genet. 2011 Mar;48(3):212-6. doi: 10.1136/jmg.2010.081919. Epub 2010 Nov 19. J Med Genet. 2011. PMID: 21097775
202 results