Monk D - Search Results

1

Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes.

Court F, Martin-Trujillo A, Romanelli V, Garin I, Iglesias-Platas I, Salafsky I, Guitart M, Perez de Nanclares G, Lapunzina P, Monk D. Court F, et al. Among authors: monk d. Hum Mutat. 2013 Apr;34(4):595-602. doi: 10.1002/humu.22276. Epub 2013 Feb 19. Hum Mutat. 2013. PMID: 23335487

2

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.

3

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

4

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes.

Monk D, Arnaud P, Frost JM, Wood AJ, Cowley M, Martin-Trujillo A, Guillaumet-Adkins A, Iglesias Platas I, Camprubi C, Bourc'his D, Feil R, Moore GE, Oakey RJ. Monk D, et al. Nucleic Acids Res. 2011 Jun;39(11):4577-86. doi: 10.1093/nar/gkq1230. Epub 2011 Feb 7. Nucleic Acids Res. 2011. PMID: 21300645 Free PMC article.

5

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.

Nakabayashi K, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K, Monk D. Nakabayashi K, et al. Among authors: monk d. Hum Mol Genet. 2011 Aug 15;20(16):3188-97. doi: 10.1093/hmg/ddr224. Epub 2011 May 18. Hum Mol Genet. 2011. PMID: 21593219

6

Does genomic imprinting play a role in autoimmunity?

Camprubí C, Monk D. Camprubí C, et al. Among authors: monk d. Adv Exp Med Biol. 2011;711:103-16. doi: 10.1007/978-1-4419-8216-2_8. Adv Exp Med Biol. 2011. PMID: 21627045 Review.

7

The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer.

Lapunzina P, Monk D. Lapunzina P, et al. Among authors: monk d. Biol Cell. 2011 Jul;103(7):303-17. doi: 10.1042/BC20110013. Biol Cell. 2011. PMID: 21651501 Review.

8

Genotype of an individual single nucleotide polymorphism regulates DNA methylation at the TRPC3 alternative promoter.

Martin-Trujillo A, Iglesias-Platas I, Coto E, Corral-Juan M, San Nicolás H, Corral J, Volpini V, Matilla-Dueñas A, Monk D. Martin-Trujillo A, et al. Among authors: monk d. Epigenetics. 2011 Oct 1;6(10):1236-41. doi: 10.4161/epi.6.10.17654. Epub 2011 Oct 1. Epigenetics. 2011. PMID: 21931279 Free article.

9

Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.

Iglesias-Platas I, Martin-Trujillo A, Cirillo D, Court F, Guillaumet-Adkins A, Camprubi C, Bourc'his D, Hata K, Feil R, Tartaglia G, Arnaud P, Monk D. Iglesias-Platas I, et al. Among authors: monk d. PLoS One. 2012;7(6):e38907. doi: 10.1371/journal.pone.0038907. Epub 2012 Jun 19. PLoS One. 2012. PMID: 22723905 Free PMC article.

10

Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop.

Iglesias-Platas I, Court F, Camprubi C, Sparago A, Guillaumet-Adkins A, Martin-Trujillo A, Riccio A, Moore GE, Monk D. Iglesias-Platas I, et al. Among authors: monk d. Nucleic Acids Res. 2013 Feb 1;41(4):2171-9. doi: 10.1093/nar/gks1355. Epub 2013 Jan 7. Nucleic Acids Res. 2013. PMID: 23295672 Free PMC article.

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