McFadden DE - Search Results

1

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders.

Bourque DK, Peñaherrera MS, Yuen RK, Van Allen MI, McFadden DE, Robinson WP. Bourque DK, et al. Among authors: mcfadden de. Clin Genet. 2011 Feb;79(2):169-75. doi: 10.1111/j.1399-0004.2010.01443.x. Clin Genet. 2011. PMID: 20507345

2

DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia.

Yuen RK, Peñaherrera MS, von Dadelszen P, McFadden DE, Robinson WP. Yuen RK, et al. Among authors: mcfadden de. Eur J Hum Genet. 2010 Sep;18(9):1006-12. doi: 10.1038/ejhg.2010.63. Epub 2010 May 5. Eur J Hum Genet. 2010. PMID: 20442742 Free PMC article.

3

DNA methylation profiling of placental villi from karyotypically normal miscarriage and recurrent miscarriage.

Hanna CW, McFadden DE, Robinson WP. Hanna CW, et al. Among authors: mcfadden de. Am J Pathol. 2013 Jun;182(6):2276-84. doi: 10.1016/j.ajpath.2013.02.021. Epub 2013 Apr 9. Am J Pathol. 2013. PMID: 23583422 Free article.

4

Pervasive polymorphic imprinted methylation in the human placenta.

Hanna CW, Peñaherrera MS, Saadeh H, Andrews S, McFadden DE, Kelsey G, Robinson WP. Hanna CW, et al. Among authors: mcfadden de. Genome Res. 2016 Jun;26(6):756-67. doi: 10.1101/gr.196139.115. Epub 2016 Jan 14. Genome Res. 2016. PMID: 26769960 Free PMC article.

5

Phenotype of triploid embryos.

McFadden DE, Robinson WP. McFadden DE, et al. J Med Genet. 2006 Jul;43(7):609-12. doi: 10.1136/jmg.2005.037747. Epub 2005 Oct 19. J Med Genet. 2006. PMID: 16236813 Free PMC article.

6

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5.

Robinson WP, Slee J, Smith N, Murch A, Watson SK, Lam WL, McFadden DE. Robinson WP, et al. Among authors: mcfadden de. Am J Med Genet A. 2007 Aug 1;143A(15):1752-9. doi: 10.1002/ajmg.a.31800. Am J Med Genet A. 2007. PMID: 17593542

7

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.

Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Robinson WP, et al. Among authors: mcfadden de. Prenat Diagn. 2002 Dec;22(12):1076-85. doi: 10.1002/pd.483. Prenat Diagn. 2002. PMID: 12454962

8

Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction.

Robinson WP, Peñaherrera MS, Jiang R, Avila L, Sloan J, McFadden DE, Langlois S, von Dadelszen P. Robinson WP, et al. Among authors: mcfadden de. Prenat Diagn. 2010 Jan;30(1):1-8. doi: 10.1002/pd.2409. Prenat Diagn. 2010. PMID: 19918961

9

Extensive epigenetic reprogramming in human somatic tissues between fetus and adult.

Yuen RK, Neumann SM, Fok AK, Peñaherrera MS, McFadden DE, Robinson WP, Kobor MS. Yuen RK, et al. Among authors: mcfadden de. Epigenetics Chromatin. 2011 May 5;4:7. doi: 10.1186/1756-8935-4-7. Epigenetics Chromatin. 2011. PMID: 21545704 Free PMC article.

10

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation.

Cotton AM, Lam L, Affleck JG, Wilson IM, Peñaherrera MS, McFadden DE, Kobor MS, Lam WL, Robinson WP, Brown CJ. Cotton AM, et al. Among authors: mcfadden de. Hum Genet. 2011 Aug;130(2):187-201. doi: 10.1007/s00439-011-1007-8. Epub 2011 May 20. Hum Genet. 2011. PMID: 21597963 Free PMC article.

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