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BeckwithWiedemann syndrome demonstrates a role for epigenetic control of normal development

Weksberg, Rosanna ; Smith, Adam C ; Squire, Jeremy ; Sadowski, Paul

Human Molecular Genetics, 2003, Vol.12(1), pp.R61-R68 [Rivista Peer Reviewed]

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DNA methylation and inflammation marker profiles associated with a history of depression

Crawford, Bethany ; Craig, Zoe ; Mansell, Georgina ; White, Isobel ; Smith, Adam ; Spaull, Steve ; Imm, Jennifer ; Hannon, Eilis ; Wood, Andrew ; Yaghootkar, Hanieh ; Ji, Yingjie ; Mullins, Niamh ; Lewis, Cathryn M ; Mill, Jonathan ; Murphy, Therese M

Human molecular genetics, 15 August 2018, Vol.27(16), pp.2840-2850 [Rivista Peer Reviewed]

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Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion

Martins - Taylor, Kristen ; Hsiao, Jack S ; Chen, Pin - Fang ; Glatt - Deeley, Heather ; De Smith, Adam J ; Blakemore, Alexandra I. F ; Lalande, Marc ; Chamberlain, Stormy J

Human Molecular Genetics, 2014, Vol. 23(9), pp.2364-2373 [Rivista Peer Reviewed]

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Novel association approach for variable number tandem repeats (VNTRs) identifies as a susceptibility gene for severe obesity

El - Sayed Moustafa, Julia S ; Eleftherohorinou, Hariklia ; De Smith, Adam J ; Andersson - Assarsson, Johanna C ; Couto Alves, Alexessander ; Hadjigeorgiou, Eleni ; Walters, Robin G ; Asher, Julian E ; Bottolo, Leonardo ; Buxton, Jessica L ; Sladek, Rob ; Meyre, David ; Dina, Christian ; Visvikis - Siest, Sophie ; Jacobson, Peter ; Sjöström, Lars ; Carlsson, Lena M. S ; Walley, Andrew ; Falchi, Mario ; Froguel, Philippe ; Blakemore, Alexandra I. F ; Coin, Lachlan J. M

Human Molecular Genetics, 2012, Vol. 21(16), pp.3727-3738 [Rivista Peer Reviewed]

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Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

Weksberg, Rosanna ; Smith, Adam C ; Squire, Jeremy ; Sadowski, Paul

Human molecular genetics, 01 April 2003, Vol.12 Spec No 1, pp.R61-8 [Rivista Peer Reviewed]

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for BeckwithWiedemann syndrome

Weksberg, Rosanna ; Shuman, Cheryl ; Caluseriu, Oana ; Smith, Adam C ; Fei, Yan - Ling ; Nishikawa, Joy ; Stockley, Tracy L ; Best, Lyle ; Chitayat, David ; Olney, Ann ; Ives, Elizabeth ; Schneider, Adele ; Bestor, Timothy H ; Li, Madeline ; Sadowski, Paul ; Squire, Jeremy

Human Molecular Genetics, 2002, Vol.11(11), pp.1317-1325 [Rivista Peer Reviewed]

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A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

De Smith, Adam J ; Purmann, Carolin ; Walters, Robin G ; Ellis, Richard J ; Holder, Susan E ; Van Haelst, Mieke M ; Brady, Angela F ; Fairbrother, Una L ; Dattani, Mehul ; Keogh, Julia M ; Henning, Elana ; Yeo, Giles S. H ; O'Rahilly, Stephen ; Froguel, Philippe ; Farooqi, I. Sadaf ; Blakemore, Alexandra I. F

Human Molecular Genetics, 2009, Vol. 18(17), pp.3257-3265 [Rivista Peer Reviewed]

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Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

De Smith, Adam J ; Tsalenko, Anya ; Sampas, Nick ; Scheffer, Alicia ; Yamada, N. Alice ; Tsang, Peter ; Ben - Dor, Amir ; Yakhini, Zohar ; Ellis, Richard J ; Bruhn, Laurakay ; Laderman, Stephen ; Froguel, Philippe ; Blakemore, Alexandra I. F

Human Molecular Genetics, 2007, Vol. 16(23), pp.2783-2794 [Rivista Peer Reviewed]

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Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

Warrington, Nicole M ; Shevroja, Enisa ; Hemani, Gibran ; Hysi, Pirro G ; Jiang, Yunxuan ; Auton, Adam ; Boer, Cindy G ; Mangino, Massimo ; Wang, Carol A ; Kemp, John P ; Mcmahon, George ; Medina - Gomez, Carolina ; Hickey, Martha ; Trajanoska, Katerina ; Wolke, Dieter ; Ikram, M Arfan ; Montgomery, Grant W ; Felix, Janine F ; Wright, Margaret J ; Mackey, David A ; Jaddoe, Vincent W ; Martin, Nicholas G ; Tung, Joyce Y ; Davey Smith, George ; Pennell, Craig E ; Spector, Tim D ; Van Meurs, Joyce ; Rivadeneira, Fernando ; Medland, Sarah E ; Evans, David M

Human Molecular Genetics, 2018, Vol. 27(11), pp.2025-2038 [Rivista Peer Reviewed]

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Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals

Nead, Kevin T ; Li, Aihua ; Wehner, Mackenzie R ; Neupane, Binod ; Gustafsson, Stefan ; Butterworth, Adam ; Engert, James C ; Davis, A. Darlene ; Hegele, Robert A ; Miller, Ruby ; Den Hoed, Marcel ; Khaw, Kay - Tee ; Kilpeläinen, Tuomas O ; Wareham, Nick ; Edwards, Todd L ; Hallmans, Göran ; Varga, Tibor V ; Kardia, Sharon L. R ; Smith, Jennifer A ; Zhao, Wei ; Faul, Jessica D ; Weir, David ; Mi, Jie ; Xi, Bo ; Quinteros, Samuel Canizales ; Cooper, Cyrus ; Sayer, Avan Aihie ; Jameson, Karen ; Grøntved, Anders ; Fornage, Myriam ; Sidney, Stephen ; Hanis, Craig L ; Highland, Heather M ; Häring, Hans - Ulrich ; Heni, Martin ; Lasky - Su, Jessica ; Weiss, Scott T ; Gerhard, Glenn S ; Still, Christopher ; Melka, Melkaey M ; Pausova, Zdenka ; Paus, Tomáš ; Grant, Struan F. A ; Hakonarson, Hakon ; Price, R. Arlen ; Wang, Kai ; Scherag, Andre ; Hebebrand, Johannes ; Hinney, Anke ; Franks, Paul W ; Frayling, Timothy M ; Mccarthy, Mark I ; Hirschhorn, Joel N ; Loos, Ruth J ; Ingelsson, Erik ; Gerstein, Hertzel C ; Yusuf, Salim ; Beyene, Joseph ; Anand, Sonia S ; Meyre, David

Human Molecular Genetics, 2015, Vol. 24(12), pp.3582-3594 [Rivista Peer Reviewed]

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di questo autore:

  1. Blakemore, Alexandra I F
  2. De Smith, Adam J
  3. Sadowski, Paul
  4. Squire, Jeremy
  5. Weksberg, Rosanna

su questo soggetto:

  1. Biology
  2. Medicine
  3. Humans
  4. Male
  5. Adult

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