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

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. by Wallace, C, Newhouse, S, Braund, P, Zhang, F, Tobin, M, Falchi, M, Ahmadi, K, Dobson, R, Marçano, A, Hajat, C, Burton, P, Deloukas, P, Brown, M, Connell, J, Dominiczak, A, Lathrop, G, Webster, J, Farrall, M, Spector, T, Samani, N, Caulfield, M, Munroe, P

Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. by Marquez, M, Huyvaert, M, Perry, JR, Pearson, R, Falchi, M, Morris, A, Vivequin, S, Lobbens, S, Yengo, L, Gaget, S, Pattou, F, Poulain-Godefroy, O, Charpentier, G, Carlsson, L, Jacobson, P, Sjöström, L, Lantieri, O, Heude, B, Walley, A, Balkau, B, Marre, M, Froguel, P, Cauchi, S

Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease by Wallace, C, Newhouse, S, Braund, P, Zhang, F, Tobin, M, Falchi, M, Ahmadi, K, Dobson, R, Marcano, A, Hajat, C, Burton, P, Deloukas, P, Brown, M, Connell, J, Dominiczak, A, Lathrop, M, Webster, J, Farrall, M, Farrall, M, Spector, T, Samani, N, Caulfield, M, Munroe, P, Consor, W

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

Decreased STARD10 expression is associated with defective insulin secretion in humans and mice by Carrat, G, Hu, M, Nguyen-Tu, M, Chabosseau, P, Gaulton, K, van de Bunt, M, Siddiq, A, Falchi, M, Thurner, M, Canouil, M, Pattou, F, Leclerc, I, Pullen, T, Cane, M, Prabhala, P, Greenwald, W, Schulte, A, Marchetti, P, Ibberson, M, MacDonald, P, Manning Fox, J, Gloyn, A, Froguel, P, Solimena, M, McCarthy, M, Rutter, G

Decreased STARD10 expression is associated with defective insulin secretion in humans and mice. by Carrat, G, Hu, M, Nguyen-Tu, M, Chabosseau, P, Gaulton, K, van de Bunt, M, Siddiq, A, Falchi, M, Thurner, M, Canouil, M, Pattou, F, Leclerc, I, Pullen, T, Cane, M, Prabhala, P, Greenwald, W, Schulte, A, Marchetti, P, Ibberson, M, MacDonald, P, Manning Fox, J, Gloyn, A, Froguel, P, Solimena, M, McCarthy, M, Rutter, G

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways by Duffy, DL, Zhu, G, Li, X, Sanna, M, Iles, MM, Jacobs, LC, Evans, DM, Yazar, S, Beesley, J, Law, MH, Kraft, P, Visconti, A, Taylor, JC, Liu, F, Wright, MJ, Henders, AK, Bowdler, L, Glass, D, Ikram, MA, Uitterlinden, AG, Madden, PA, Heath, AC, Nelson, EC, Green, AC, Chanock, S, Barrett, JH, Brown, MA, Hayward, NK, Macgregor, S, Sturm, RA, Hewitt, AW, Kayser, M, Hunter, DJ, Newton Bishop, JA, Spector, TD, Montgomery, GW, Mackey, DA, Smith, GD, Nijsten, TE, Bishop, DT, Bataille, V, Falchi, M, Han, J, Martin, NG