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57 results for Moore,+Gudrun+E.

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The Importance of Imprinting in the Human Placenta
Author / Creator:Frost, Jennifer M. ; Moore, Gudrun E.
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2010-07, Vol.6 (7), p.e1001015-e1001015
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Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS
Author / Creator: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.
Publisher:United States: Elsevier Inc
Journal title:Journal of investigative dermatology, 2013-09, Vol.133 (9), p.2229-2236
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Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects
Author / Creator:Alvizi, Lucas ; Ke, Xiayi ; Brito, Luciano Abreu ; Seselgyte, Rimante ; Moore, Gudrun E. ; Stanier, Philip ; Passos-Bueno, Maria Rita
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-05, Vol.7 (1), p.2441-8, Article 2441
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Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2
Author / Creator:Hiby, Susan E. ; Apps, Richard ; Sharkey, Andrew M. ; Farrell, Lydia E. ; Gardner, Lucy ; Mulder, Arend ; Claas, Frans H. ; Walker, James J. ; Redman, Christopher C. ; Morgan, Linda ; Tower, Clare ; Regan, Lesley ; Moore, Gudrun E. ; Carrington, Mary ; Moffett, Ashley
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2010-11, Vol.120 (11), p.4102-4110
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The role and interaction of imprinted genes in human fetal growth
Author / Creator: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
Publisher:England: The Royal Society
Journal title:Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2015-03, Vol.370 (1663), p.20140074-20140074
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Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood
Author / Creator: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
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2020-10, Vol.57 (10), p.683-691
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Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome
Author / Creator: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
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2014-01, Vol.46 (1), p.70-76
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Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight
Author / Creator: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.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-01, Vol.9 (1), p.e85454-e85454
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The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development
Author / Creator:Suntharalingham, Jenifer P. ; del Valle, Ignacio ; Buonocore, Federica ; McGlacken-Byrne, Sinead M. ; Brooks, Tony ; Ogunbiyi, Olumide K. ; Liptrot, Danielle ; Dunton, Nathan ; Madhan, Gaganjit K. ; Metcalfe, Kate ; Nel, Lydia ; Marshall, Abigail R. ; Ishida, Miho ; Sebire, Neil J. ; Moore, Gudrun E. ; Crespo, Berta ; Solanky, Nita ; Conway, Gerard S. ; Achermann, John C.
Publisher:London: Nature Publishing Group UK
Journal title:Communications biology, 2025-02, Vol.8 (1), p.249-19
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ArticlesPeer ReviewedFull Text
Fat dads must not be blamed for their children's health problems
Author / Creator:Moore, Gudrun E ; Stanier, Philip
Publisher:England: BioMed Central Ltd
Journal title:BMC medicine, 2013-02, Vol.11 (1), p.30-30, Article 30
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A Screen for Retrotransposed Imprinted Genes Reveals an Association between X Chromosome Homology and Maternal Germ-Line Methylation
Author / Creator:Wood, Andrew J ; Roberts, Roland G ; Monk, David ; Moore, Gudrun E ; Schulz, Reiner ; Oakey, Rebecca J
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2007-02, Vol.3 (2), p.e20-e20
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Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved]
Author / Creator:Suntharalingham, Jenifer P ; Ishida, Miho ; Buonocore, Federica ; del Valle, Ignacio ; Solanky, Nita ; Demetriou, Charalambos ; Regan, Lesley ; Moore, Gudrun E ; Achermann, John C
Publisher:England: Faculty of 1000 Ltd
Journal title:F1000 research, 2019, Vol.8, p.90
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Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages [version 1; peer review: 2 approved]
Author / Creator:Seda, Marian ; Peskett, Emma ; Demetriou, Charalambos ; Bryant, Dale ; Moore, Gudrun E ; Stanier, Philip ; Jenkins, Dagan
Publisher:England: Faculty of 1000 Ltd
Journal title:F1000 research, 2019, Vol.8, p.273-273
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Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution
Author / Creator:Parker-Katiraee, Layla ; Carson, Andrew R ; Yamada, Takahiro ; Arnaud, Philippe ; Feil, Robert ; Abu-Amero, Sayeda N ; Moore, Gudrun E ; Kaneda, Masahiro ; Perry, George H ; Stone, Anne C ; Lee, Charles ; Meguro-Horike, Makiko ; Sasaki, Hiroyuki ; Kobayashi, Keiko ; Nakabayashi, Kazuhiko ; Scherer, Stephen W
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2007-05, Vol.3 (5), p.e65-e65
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Evaluation of Allelic Expression of Imprinted Genes in Adult Human Blood
Author / Creator:Frost, Jennifer M. ; Monk, Dave ; Stojilkovic-Mikic, Taita ; Woodfine, Kathryn ; Chitty, Lyn S. ; Murrell, Adele ; Stanier, Philip ; Moore, Gudrun E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-10, Vol.5 (10), p.e13556-e13556
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Telomeric NAP1L4 and OSBPL5 of the KCNQ1 Cluster, and the DECORIN Gene Are Not Imprinted in Human Trophoblast Stem Cells
Author / Creator:Frost, Jennifer M. ; Udayashankar, Ramya ; Moore, Harry D. ; Moore, Gudrun E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-07, Vol.5 (7), p.e11595-e11595
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Diagnosis and management of Silver–Russell syndrome: first international consensus statement
Author / Creator:Wakeling, Emma L. ; Brioude, Frédéric ; Lokulo-Sodipe, Oluwakemi ; O'Connell, Susan M. ; Salem, Jennifer ; Bliek, Jet ; Canton, Ana P. M. ; Chrzanowska, Krystyna H. ; Davies, Justin H. ; Dias, Renuka P. ; Dubern, Béatrice ; Elbracht, Miriam ; Giabicani, Eloise ; Grimberg, Adda ; Grønskov, Karen ; Hokken-Koelega, Anita C. S. ; Jorge, Alexander A. ; Kagami, Masayo ; Linglart, Agnes ; Maghnie, Mohamad ; Mohnike, Klaus ; Monk, David ; Moore, Gudrun E. ; Murray, Philip G. ; Ogata, Tsutomu ; Petit, Isabelle Oliver ; Russo, Silvia ; Said, Edith ; Toumba, Meropi ; Tümer, Zeynep ; Binder, Gerhard ; Eggermann, Thomas ; Harbison, Madeleine D. ; Temple, I. Karen ; Mackay, Deborah J. G. ; Netchine, Irène
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Endocrinology, 2017-02, Vol.13 (2), p.105-124
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Genetic Analyses in Small-for-Gestational-Age Newborns
Author / Creator:Stalman, Susanne E ; Solanky, Nita ; Ishida, Miho ; Alemán-Charlet, Cristina ; Abu-Amero, Sayeda ; Alders, Marielle ; Alvizi, Lucas ; Baird, William ; Demetriou, Charalambos ; Henneman, Peter ; James, Chela ; Knegt, Lia C ; Leon, Lydia J ; Mannens, Marcel M A M ; Mul, Adi N ; Nibbering, Nicole A ; Peskett, Emma ; Rezwan, Faisal I ; Ris-Stalpers, Carrie ; van der Post, Joris A M ; Kamp, Gerdine A ; Plötz, Frans B ; Wit, Jan M ; Stanier, Philip ; Moore, Gudrun E ; Hennekam, Raoul C
Publisher:United States: Copyright Oxford University Press
Journal title:The journal of clinical endocrinology and metabolism, 2018-03, Vol.103 (3), p.917-925
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Evidence That Insulin is Imprinted in the Human Yolk Sac
Author / Creator:Moore, G. E. ; Abu-Amero, S. N. ; Bell, G. ; Wakeling, E. L. ; Kingsnorth, A. ; Stanier, P. ; Jauniaux, E. ; Bennett, S. T.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001-01, Vol.50 (1), p.199-203
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Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling
Author / Creator:Eggermann, Thomas ; Brioude, Frédéric ; Russo, Silvia ; Lombardi, Maria P ; Bliek, Jet ; Maher, Eamonn R ; Larizza, Lidia ; Prawitt, Dirk ; Netchine, Irène ; Gonzales, Marie ; Grønskov, Karen ; Tümer, Zeynep ; Monk, David ; Mannens, Marcel ; Chrzanowska, Krystyna ; Walasek, Malgorzata K ; Begemann, Matthias ; Soellner, Lukas ; Eggermann, Katja ; Tenorio, Jair ; Nevado, Julián ; Moore, Gudrun E ; Mackay, Deborah JG ; Temple, Karen ; Gillessen-Kaesbach, Gabriele ; Ogata, Tsutomu ; Weksberg, Rosanna ; Algar, Elizabeth ; Lapunzina, Pablo
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.784-793
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Showing 1 to 20 of 57 results

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The Importance of Imprinting in the Human Placenta

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Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

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

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Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2

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The role and interaction of imprinted genes in human fetal growth

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Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood

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Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome

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Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

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The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development

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

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

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Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved]

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Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages [version 1; peer review: 2 approved]

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Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution

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Evaluation of Allelic Expression of Imprinted Genes in Adult Human Blood

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

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Diagnosis and management of Silver–Russell syndrome: first international consensus statement

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Genetic Analyses in Small-for-Gestational-Age Newborns

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Evidence That Insulin is Imprinted in the Human Yolk Sac

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Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling

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