The importance of imprinting in the human placenta von Frost, Jennifer M, Moore, Gudrun E

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The role of imprinted genes in humans von Ishida, Miho, Moore, Gudrun E.

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

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Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS von Kinsler, Veronica A., Thomas, Anna C., Ishida, Miho, Bulstrode, Neil W., Loughlin, Sam, Hing, Sandra, Chalker, Jane, McKenzie, Kathryn, Abu-Amero, Sayeda, Slater, Olga, Chanudet, Estelle, Palmer, Rodger, Morrogh, Deborah, Stanier, Philip, Healy, Eugene, Sebire, Neil J., Moore, Gudrun E.

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Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects von Alvizi, Lucas, Ke, Xiayi, Brito, Luciano Abreu, Seselgyte, Rimante, Moore, Gudrun E., Stanier, Philip, Passos-Bueno, Maria Rita

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Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2 von Hiby, Susan E, Apps, Richard, Sharkey, Andrew M, Farrell, Lydia E, Gardner, Lucy, Mulder, Arend, Claas, Frans H, Walker, James J, Redman, Christopher W, Redman, Christopher C, Morgan, Linda, Tower, Clare, Regan, Lesley, Moore, Gudrun E, Carrington, Mary, Moffett, Ashley

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SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20 von Bryant, Dale, Liu, Yang, Datta, Sanchari, Hariri, Hanaa, Seda, Marian, Anderson, Glenn, Peskett, Emma, Demetriou, Charalambos, Sousa, Sergio, Jenkins, Dagan, Clayton, Peter, Bitner-Glindzicz, Maria, Moore, Gudrun E, Henne, W Mike, Stanier, Philip

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

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The role and interaction of imprinted genes in human fetal growth von Moore, Gudrun E., Ishida, Miho, Demetriou, Charalambos, Al-Olabi, Lara, Leon, Lydia J., Thomas, Anna C., Abu-Amero, Sayeda, Frost, Jennifer M., Stafford, Jaime L., Chaoqun, Yao, Duncan, Andrew J., Baigel, Rachel, Brimioulle, Marina, Iglesias-Platas, Isabel, Apostolidou, Sophia, Aggarwal, Reena, Whittaker, John C., Syngelaki, Argyro, Nicolaides, Kypros H., Regan, Lesley, Monk, David, Stanier, Philip

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Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate von Mangold, Elisabeth, Böhmer, Anne C., Ishorst, Nina, Hoebel, Ann-Kathrin, Gültepe, Pinar, Schuenke, Hannah, Klamt, Johanna, Hofmann, Andrea, Gölz, Lina, Raff, Ruth, Tessmann, Peter, Nowak, Stefanie, Reutter, Heiko, Hemprich, Alexander, Kreusch, Thomas, Kramer, Franz-Josef, Braumann, Bert, Reich, Rudolf, Schmidt, Gül, Jäger, Andreas, Reiter, Rudolf, Brosch, Sibylle, Stavusis, Janis, Ishida, Miho, Seselgyte, Rimante, Moore, Gudrun E., Nöthen, Markus M., Borck, Guntram, Aldhorae, Khalid A., Lace, Baiba, Stanier, Philip, Knapp, Michael, Ludwig, Kerstin U.

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The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta von Noguer-Dance, Marie, Abu-Amero, Sayeda, Al-Khtib, Mohamed, Lefèvre, Annick, Coullin, Philippe, Moore, Gudrun E., Cavaillé, Jérôme

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Imprinted Chromatin around DIRAS3 Regulates Alternative Splicing of GNG12-AS1, a Long Noncoding RNA von Niemczyk, Malwina, Ito, Yoko, Huddleston, Joanna, Git, Anna, Abu-Amero, Sayeda, Caldas, Carlos, Moore, Gudrun E., Stojic, Lovorka, Murrell, Adele

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Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans von Demetriou, Charalambos, Chanudet, Estelle, Joseph, Agnel, Topf, Maya, Thomas, Anna C, Bitner-Glindzicz, Maria, Regan, Lesley, Stanier, Philip, Moore, Gudrun E

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Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight von Demetriou, Charalambos, Abu-Amero, Sayeda, Thomas, Anna C, Ishida, Miho, Aggarwal, Reena, Al-Olabi, Lara, Leon, Lydia J, Stafford, Jaime L, Syngelaki, Argyro, Peebles, Donald, Nicolaides, Kypros H, Regan, Lesley, Stanier, Philip, Moore, Gudrun E

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The role of imprinted genes in humans von Moore, Gudrun E, Oakey, Rebecca

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Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome von Sousa, Sérgio B, Jenkins, Dagan, Chanudet, Estelle, Tasseva, Guergana, Ishida, Miho, Anderson, Glenn, Docker, James, Ryten, Mina, Sa, Joaquim, Saraiva, Jorge M, Barnicoat, Angela, Scott, Richard, Calder, Alistair, Wattanasirichaigoon, Duangrurdee, Chrzanowska, Krystyna, Simandlová, Martina, Van Maldergem, Lionel, Stanier, Philip, Beales, Philip L, Vance, Jean E, Moore, Gudrun E

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Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression von Monk, David, Arnaud, Philippe, Frost, Jennifer, Hills, Frank A., Stanier, Philip, Feil, Robert, Moore, Gudrun E.

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Fat dads must not be blamed for their children's health problems von Moore, Gudrun E, Stanier, Philip

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Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts von Stanier, Philip, Moore, Gudrun E.

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Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome von Suntharalingham, Jenifer P, Ishida, Miho, Del Valle, Ignacio, Stalman, Susanne E, Solanky, Nita, Wakeling, Emma, Moore, Gudrun E, Achermann, John C, Buonocore, Federica

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