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

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

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

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

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. by Walters, R, Jacquemont, S, Valsesia, A, de Smith, A, Martinet, D, Andersson, J, Falchi, M, Chen, F, Andrieux, J, Lobbens, S, Delobel, B, Stutzmann, F, El-Sayed Moustafa, J, Chèvre, J, Lecoeur, C, Vatin, V, Bouquillon, S, Buxton, J, Boute, O, Holder-Espinasse, M, Cuisset, J, Lemaitre, M, Ambresin, A, Brioschi, A, Gaillard, M

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