Decreased Placental Methylation at the H19 / IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia von Bourque, D.K, Avila, L, Peñaherrera, M, von Dadelszen, P, Robinson, W.P

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Review: A high capacity of the human placenta for genetic and epigenetic variation: Implications for assessing pregnancy outcome von Yuen, R.K.C, Robinson, W.P

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Evaluating DNA methylation and gene expression variability in the human term placenta von Avila, L, Yuen, R.K, Diego-Alvarez, D, Peñaherrera, M.S, Jiang, R, Robinson, W.P

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Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia von Blair, J.D, Langlois, S, McFadden, D.E, Robinson, W.P

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IGF2/H19 DMR methylation in placentas conceived by IVF or ICSI von Chan Wong, E, Hatakeyama, C, Robinson, W.P, Ma, S

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Epigenetic alterations associated with premature ovarian failure von Ghahremani, M, Hanna, C.W, Bretherick, K.L, Penaherrera, M.S, Fluker, M.R, Robinson, W.P

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Activation of endocrine-related gene expression in placental choriocarcinoma cell lines following DNA methylation knock-down von Hogg, K, Robinson, W P, Beristain, A G

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Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss von Rajcan-Separovic, E., Diego-Alvarez, D., Robinson, W.P., Tyson, C., Qiao, Y., Harvard, C., Fawcett, C., Kalousek, D., Philipp, T., Somerville, M.J., Stephenson, M.D.

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Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants von Filges, I, Manokhina, I, Peñaherrera, M S, McFadden, D E, Louie, K, Nosova, E, Friedman, J M, Robinson, W P

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Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case–control study von Stephenson, M.D., Awartani, K.A., Robinson, W.P.

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Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation von Peñaherrera, M.S., Jiang, R., Avila, L., Yuen, R.K.C., Brown, C.J., Robinson, W.P.

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A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder von Matthews, A.M., Tarailo-Graovac, M., Price, E.M., Blydt-Hansen, I., Ghani, A., Drögemöller, B.I., Robinson, W.P., Ross, C.J., Wasserman, W.W., Siden, H., van Karnebeek, C.D.

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P-159 von Hatakeyama, C., Robinson, W.P., Ma, S.

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P-159: Epigenetic analysis of H19/IGF2 in placentas from low birth weight (LBW) pregnancies following intracytoplasmic sperm injection (ICSI) von Hatakeyama, C., Robinson, W.P., Ma, S.

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Skewed X-Chromosome Inactivation Is Associated with Trisomy in Women Ascertained on the Basis of Recurrent Spontaneous Abortion or Chromosomally Abnormal Pregnancies von Beever, C.L., Stephenson, M.D., Peñaherrera, M.S., Jiang, R.H., Kalousek, D.K., Hayden, M., Field, L., Brown, C.J., Robinson, W.P.

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The Origin of Abnormalities in Recurrent Aneuploidy/Polyploidy von Robinson, W.P., McFadden, D.E., Stephenson, M.D.

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Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism von Yong, P J, Barrett, I J, Kalousek, D K, Robinson, W P

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An association between sex chromosomal aneuploidy in sperm and an abortus with 45,X of paternal origin: possible transmission of chromosomal abnormalities through ICSI von Tang, S.S., Gao, H., Robinson, W.P., Ho Yuen, B., Ma, S.

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Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5 von Robinson, W.P., Slee, J., Smith, N., Murch, A., Watson, S. K., Lam, W.L., McFadden, D.E.

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Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriage von Hirschfeld, A.F., Jiang, R., Robinson, W.P., McFadden, D.E., Turvey, S.E.

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