Fat dads must not be blamed for their children's health problems

por Moore, Gudrun E, Stanier, Philip
Publicado 2013

The Importance of Imprinting in the Human Placenta

por Frost, Jennifer M., Moore, Gudrun E.
Publicado 2010

Telomeric NAP1L4 and OSBPL5 of the KCNQ1 Cluster, and the DECORIN Gene Are Not Imprinted in Human Trophoblast Stem Cells

por Frost, Jennifer M., Udayashankar, Ramya, Moore, Harry D., Moore, Gudrun E.
Publicado 2010

Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages

por Seda, Marian, Peskett, Emma, Demetriou, Charalambos, Bryant, Dale, Moore, Gudrun E., Stanier, Philip, Jenkins, Dagan
Publicado 2019

A Screen for Retrotransposed Imprinted Genes Reveals an Association between X Chromosome Homology and Maternal Germ-Line Methylation

por Wood, Andrew J, Roberts, Roland G, Monk, David, Moore, Gudrun E, Schulz, Reiner, Oakey, Rebecca J
Publicado 2007

Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

por Alvizi, Lucas, Ke, Xiayi, Brito, Luciano Abreu, Seselgyte, Rimante, Moore, Gudrun E., Stanier, Philip, Passos-Bueno, Maria Rita
Publicado 2017

Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the Unite...

por Leon, Lydia J., Doyle, Ronan, Diez-Benavente, Ernest, Clark, Taane G., Klein, Nigel, Stanier, Philip, Moore, Gudrun E.
Publicado 2018

Evaluation of Allelic Expression of Imprinted Genes in Adult Human Blood

por Frost, Jennifer M., Monk, Dave, Stojilkovic-Mikic, Taita, Woodfine, Kathryn, Chitty, Lyn S., Murrell, Adele, Stanier, Philip, Moore, Gudrun E.
Publicado 2010

A new biological and clinical resource for research into pregnancy complications: The Baby Bio Bank

por Leon, Lydia J., Solanky, Nita, Stalman, Susanne E., Demetriou, Charalambos, Abu-Amero, Sayeda, Stanier, Philip, Regan, Lesley, Moore, Gudrun E.
Publicado 2016

Transcript- and tissue-specific imprinting of a tumour suppressor gene

por Schulz, Reiner, McCole, Ruth B., Woodfine, Kathryn, Wood, Andrew J., Chahal, Mandeep, Monk, David, Moore, Gudrun E., Oakey, Rebecca J.
Publicado 2009

Tbx22(null) mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

por Pauws, Erwin, Hoshino, Aya, Bentley, Lucy, Prajapati, Suresh, Keller, Charles, Hammond, Peter, Martinez-Barbera, Juan-Pedro, Moore, Gudrun E., Stanier, Philip
Publicado 2009

The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight

por Padidela, Raja, Bryan, Sinead M, Abu-Amero, Sayeda, Hudson-Davies, Rebecca E, Achermann, John C, Moore, Gudrun E, Hindmarsh, Peter C
Publicado 2012

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

por Iglesias-Platas, Isabel, Court, Franck, Camprubi, Cristina, Sparago, Angela, Guillaumet-Adkins, Amy, Martin-Trujillo, Alex, Riccio, Andrea, Moore, Gudrun E., Monk, David
Publicado 2013

Analysis of CDKN1C in fetal growth restriction and pregnancy loss

por Suntharalingham, Jenifer P., Ishida, Miho, Buonocore, Federica, del Valle, Ignacio, Solanky, Nita, Demetriou, Charalambos, Regan, Lesley, Moore, Gudrun E., Achermann, John C.
Publicado 2020

Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome

por Suntharalingham, Jenifer P., Ishida, Miho, Del Valle, Ignacio, Stalman, Susanne E., Solanky, Nita, Wakeling, Emma, Moore, Gudrun E., Achermann, John C., Buonocore, Federica
Publicado 2022

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo

por Derakhshan, Maria, Kessler, Noah J, Ishida, Miho, Demetriou, Charalambos, Brucato, Nicolas, Moore, Gudrun E, Fall, Caroline H D, Chandak, Giriraj R, Ricaut, Francois-Xavier, Prentice, Andrew M, Hellenthal, Garrett, Silver, Matt J
Publicado 2022

Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood

por Lokulo-Sodipe, Oluwakemi, Ballard, Lisa, Child, Jenny, Inskip, Hazel M, Byrne, Christopher D, Ishida, Miho, Moore, Gudrun E, Wakeling, Emma L, Fenwick, Angela, Mackay, Deborah J G, Davies, Justin Huw, Temple, I Karen
Publicado 2020

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

por Monk, David, Arnaud, Philippe, Frost, Jennifer M., Wood, Andrew J., Cowley, Michael, Martin-Trujillo, Alejandro, Guillaumet-Adkins, Amy, Iglesias Platas, Isabel, Camprubi, Cristina, Bourc’his, Deborah, Feil, Robert, Moore, Gudrun E., Oakey, Rebecca J.
Publicado 2011

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta

por Daelemans, Caroline, Ritchie, Matthew E, Smits, Guillaume, Abu-Amero, Sayeda, Sudbery, Ian M, Forrest, Matthew S, Campino, Susana, Clark, Taane G, Stanier, Philip, Kwiatkowski, Dominic, Deloukas, Panos, Dermitzakis, Emmanouil T, Tavaré, Simon, Moore, Gudrun E, Dunham, Ian
Publicado 2010

Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

por Kinsler, Veronica A, Abu-Amero, Sayeda, Budd, Peter, Jackson, Ian J, Ring, Susan M, Northstone, Kate, Atherton, David J, Bulstrode, Neil W, Stanier, Philip, Hennekam, Raoul C, Sebire, Neil J, Moore, Gudrun E, Healy, Eugene
Publicado 2012