Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease. by de Smith, A, Walters, R, Froguel, P, Blakemore, A

Childhood obesity is associated with shorter leukocyte telomere length. by Buxton, J, Walters, R, Visvikis-Siest, S, Meyre, D, Froguel, P, Blakemore, A

Does anxiety predict the use of urgent care by people with long term conditions? A systematic review with meta-analysis by Blakeley, C, Blakemore, A, Hunter, C, Guthrie, E, Tomenson, B, Dickens, C

Alu elements implicated in the generation of 9/20 CNV deletions investigated by breakpoint sequencing by de Smith, A, Walters, R, Coin, L, Steinfeld, I, Yakhini, Z, Sladek, R, Froguel, P, Blakemore, A

Small deletion variants have stable breakpoints commonly associated with alu elements by De Smith, A, Walters, R, Coin, L, Steinfeld, I, Yakhini, Z, Sladek, R, Froguel, P, Blakemore, A

Identification and validation of novel genomic CNVs associated with Type 2 diabetes by Buxton, J, Coin, L, Walters, R, Andersson, J, de Smith, A, Moustafa, J, Sladek, R, Froguel, P, Blakemore, A

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs. by Coin, L, Asher, J, Walters, R, Moustafa, J, de Smith, A, Sladek, R, Balding, D, Froguel, P, Blakemore, A

CNVs in Obesity: Uncovering a New Level of Genomic Variation by Moustafa, J, Coin, L, de Smith, A, Walters, R, Buxton, J, Asher, J, Meyre, D, Dina, C, Froguel, P, Blakemore, A

Genetic and environmental influences on leukocyte telomere length: studies in Northern Finns reveal gender differences by Buxton, J, Walters, R, Das, S, Lagou, V, Prokopenko, I, Poula, A, Hartikainen, A, Taanila, A, McCarthy, M, Jarvelin, MR, Blakemore, A

famCNV: copy number variant association for quantitative traits in families. by Eleftherohorinou, H, Andersson-Assarsson, J, Walters, R, El-Sayed Moustafa, J, Coin, L, Jacobson, P, Carlsson, L, Blakemore, A, Froguel, P, Walley, A, Falchi, M

Elucidating the aetiology of Prader-Willi syndrome: deletion of the HBII-85 class of snoRNA is associated with hyperphagia, obesity and hypogonadism by de Smith, A, Purmann, C, Walters, R, Ellis, R, Holder, SE, Haelst, v, Brady, A, Fairbrother, U, Dattani, M, Keogh, J, Henning, E, Yeo, G, O'Rahilly, S, Froguel, P, Farooqi, I, Blakemore, A

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism. by de Smith, A, Purmann, C, Walters, R, Ellis, R, Holder, SE, Haelst, V, Brady, A, Fairbrother, U, Dattani, M, Keogh, J, Henning, E, Yeo, G, O'Rahilly, S, Froguel, P, Farooqi, I, Blakemore, A

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. by Fanciulli, M, Norsworthy, P, Petretto, E, Dong, R, Harper, L, Kamesh, L, Heward, J, Gough, S, de Smith, A, Blakemore, A, Froguel, P, Owen, C, Pearce, S, Teixeira, L, Guillevin, L, Graham, D, Pusey, C, Cook, H, Vyse, T, Aitman, T

Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits. by Costelloe, S, El-Sayed Moustafa, J, Drenos, F, Palmen, J, Li, Q, Qiao, L, Whiting, S, Thomas, M, Kivimaki, M, Kumari, M, Hingorani, A, Tzoulaki, I, Järvelin, MR, Marjo-Riitta, J, Ruokonen, A, Aimo, R, Hartikainen, A, Pouta, A, Walters, R, Blakemore, A, Humphries, SE, Coin, L, Talmud, P

Technologies for global health. by Howitt, P, Darzi, A, Yang, G, Ashrafian, H, Atun, R, Barlow, J, Blakemore, A, Bull, A, Car, J, Conteh, L, Cooke, G, Ford, N, Gregson, SA, Kerr, K, King, D, Kulendran, M, Malkin, R, Majeed, A, Matlin, S, Merrifield, R, Penfold, H, Reid, S, Smith, P, Stevens, M, Templeton, MR

Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity. by El-Sayed Moustafa, J, Eleftherohorinou, H, de Smith, A, Andersson-Assarsson, J, Alves, A, Hadjigeorgiou, E, Walters, R, Asher, J, Bottolo, L, Buxton, J, Sladek, R, Meyre, D, Dina, C, Visvikis-Siest, S, Jacobson, P, Sjöström, L, Carlsson, L, Walley, A, Falchi, M, Froguel, P, Blakemore, A, Coin, L

Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity by Walters, R, Coin, L, Ruokonen, A, De Smith, A, El-Sayed Moustafa, J, Jacquemont, S, Elliott, P, Esko, T, Hartikainen, A, Laitinen, J, Männik, K, Martinet, D, Meyre, D, Nauck, M, Schurmann, C, Sladek, R, Thorleifsson, G, Thorsteinsdóttir, U, Valsesia, A, Waeber, G, Zufferey, F, Balkau, B, Pattou, F, Metspalu, A, Völzke, H, Vollenweider, P, Stefansson, K, Järvelin, MR, Beckmann, J, Froguel, P, Blakemore, A

A genome-wide association meta-analysis identifies new childhood obesity loci by Bradfield, J, Taal, H, Timpson, N, Scherag, A, Lecoeur, C, Warrington, N, Hypponen, E, Holst, C, Valcarcel, B, Thiering, E, Salem, R, Schumacher, F, Cousminer, D, Sleiman, P, Zhao, J, Berkowitz, R, Vimaleswaran, K, Jarick, I, Pennell, C, Evans, D, St Pourcain, B, Berry, D, Mook-Kanamori, DO, Hofman, A, Rivadeneira, F, Uitterlinden, A, van Duijn, C, van der Valk, R, de Jongste, J, Postma, D, Boomsma, D, Gauderman, W, Hassanein, M, Lindgren, C, Mägi, R, Boreham, C, Neville, C, Moreno, L, Elliott, P, Pouta, A, Hartikainen, A, Li, M, Raitakari, O, Lehtimäki, T, Eriksson, J, Palotie, A, Dallongeville, J, Das, S, Deloukas, P, McMahon, G, Ring, S, Kemp, J, Buxton, J, Blakemore, A, Bustamante, M, Guxens, M, Hirschhorn, J, Gillman, M, Kreiner-Møller, E, Bisgaard, H, Gilliland, F, Heinrich, J, Wheeler, E, Barroso, I, O'Rahilly, S, Meirhaeghe, A, Sørensen, T, Power, C, Palmer, L, Hinney, A, Widen, E, Farooqi, I, McCarthy, M, Froguel, P, Meyre, D, Hebebrand, J, Jarvelin, MR, Jaddoe, V, Smith, G, Hakonarson, H, Grant, S

Common variants at 12q15 and 12q24 are associated with infant head circumference. by Taal, H, St Pourcain, B, Thiering, E, Das, S, Mook-Kanamori, DO, Warrington, N, Kaakinen, M, Kreiner-Møller, E, Bradfield, J, Freathy, R, Geller, F, Guxens, M, Cousminer, D, Kerkhof, M, Timpson, N, Ikram, M, Beilin, L, Bønnelykke, K, Buxton, J, Charoen, P, Chawes, B, Eriksson, J, Evans, D, Hofman, A, Kemp, J, Kim, C, Klopp, N, Lahti, J, Lye, S, McMahon, G, Mentch, F, Müller-Nurasyid, M, O'Reilly, P, Prokopenko, I, Rivadeneira, F, Steegers, E, Sunyer, J, Tiesler, C, Yaghootkar, H, Breteler, M, Decarli, C, Breteler, M, Debette, S, Fornage, M, Gudnason, V, Launer, L, van der Lugt, A, Mosley, T, Seshadri, S, Smith, A, Vernooij, M, Blakemore, A, Chiavacci, R, Feenstra, B, Fernandez-Banet, J, Grant, S, Hartikainen, A, van der Heijden, A, Iñiguez, C, Lathrop, M, McArdle, W, Mølgaard, A, Newnham, J, Palmer, L, Palotie, A, Pouta, A, Ring, S, Sovio, U, Standl, M, Uitterlinden, A, Wichmann, H, Vissing, N, DeCarli, C, van Duijn, C, McCarthy, M, Koppelman, G, Estivill, X, Hattersley, A, Melbye, M, Bisgaard, H, Pennell, C, Widen, E, Hakonarson, H, Smith, G, Heinrich, J, Jarvelin, MR, Jaddoe, V

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension by Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J, Manning, A, Grarup, N, Sim, X, Barnes, D, Witkowska, K, Staley, J, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A, Nielsen, S, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L, Jackson, A, Narisu, N, Swift, A, Southam, L, Marten, J, Huyghe, J, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K, Bork-Jensen, J, Gjesing, A, Kontto, J, Perola, M, Shaw-Hawkins, S, Havulinna, A, Zhang, H, Donnelly, L, Groves, C, Rayner, N, Neville, M, Robertson, N, Yiorkas, A, Herzig, K, Kajantie, E, Zhang, W, Willems, S, Lannfelt, L, Malerba, G, Soranzo, N, Trabetti, E, Verweij, N, Evangelou, E, Moayyeri, A, Vergnaud, A, Nelson, C, Poveda, A, Varga, T, Caslake, M, de Craen, A, Trompet, S, Luan, J, Scott, R, Harris, S, Liewald, D, Marioni, R, Menni, C, Farmaki, A, Hallmans, G, Renström, F, Huffman, J, Hassinen, M, Burgess, S, Vasan, R, Felix, J, Uria-Nickelsen, M, Malarstig, A, Reilly, D, Hoek, M, Vogt, T, Lin, H, Lieb, W, Traylor, M, Markus, H, Highland, H, Justice, A, Marouli, E, Lindström, J, Uusitupa, M, Komulainen, P, Lakka, T, Rauramaa, R, Polasek, O, Rudan, I, Rolandsson, O, Franks, P, Dedoussis, G, Spector, T, Jousilahti, P, Männistö, S, Deary, I, Starr, J, Langenberg, C, Wareham, N, Brown, M, Dominiczak, A, Connell, J, Jukema, J, Sattar, N, Ford, I, Packard, C, Esko, T, Mägi, R, Metspalu, A, de Boer, R, van der Meer, P, van der Harst, P, Gambaro, G, Ingelsson, E, Lind, L, de Bakker, P, Numans, M, Brandslund, I, Christensen, C, Petersen, E, Korpi-Hyövälti, E, Oksa, H, Chambers, J, Kooner, J, Blakemore, A, Franks, S, Jarvelin, M, Husemoen, L, Linneberg, A, Skaaby, T, Thuesen, B, Karpe, F, Tuomilehto, J, Doney, A, Morris, A, Palmer, C, Holmen, O, Hveem, K, Willer, C, Tuomi, T, Groop, L, Käräjämäki, A, Palotie, A, Ripatti, S, Salomaa, V, Alam, D, Majumder, A, Di Angelantonio, E, Chowdhury, R, McCarthy, M, Poulter, N, Stanton, A, Sever, P, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, Deloukas, P, Elliott, P, Zeggini, E, Kathiresan, S, Melander, O, Kuusisto, J, Laakso, M, Padmanabhan, S, Porteous, D, Hayward, C, Scotland, G, Collins, F, Mohlke, K, Hansen, T, Pedersen, O, Boehnke, M, Stringham, H, Frossard, P, Newton-Cheh, C, Tobin, M, Nordestgaard, B, Caulfield, M, Mahajan, A, Morris, A, Tomaszewski, M, Samani, N, Saleheen, D, Asselbergs, F, Lindgren, C, Danesh, J, Wain, L, Butterworth, A, Howson, J, Munroe, P