Zobrazeno 1 - 10
of 714
pro vyhledávání: '"Hanson, Rl"'
Autor:
Piaggi, P, Masindova, I, Muller, Yl, Mercader, J, Wiessner, Gb, Chen, P, Sigma Type, 2 Diabetes Consortium, Kobes, S, Hsueh, Wc, Mongalo, M, Knowler, Wc, Krakoff, J, Hanson, Rl, Bogardus, C, Baier, Lj
Publikováno v:
Diabetes
Pima Indians living in Arizona have a high prevalence of obesity, and we have previously shown that a relatively lower energy expenditure (EE) predicts weight and fat mass gain in this population. EE is a familial trait (heritability = 0.52); therefo
Autor:
Zeggini, E, Rayner, W, Groves, CJ, Hanson, RL, Mitchell, BD, O'Connell, J, Vaxillaire, M, Froguel, P, Hunt, S, Cardon, L, Elbein, SC, Shuldiner, A, Deloukas, P, McCarthy, MI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2c06168dfda887123e3c93230e133e9
https://ora.ox.ac.uk/objects/uuid:e2ce62f7-cc22-414b-b7ec-d73f3b1c7af7
https://ora.ox.ac.uk/objects/uuid:e2ce62f7-cc22-414b-b7ec-d73f3b1c7af7
Autor:
Owen, KR, Groves, CJ, Hanson, RL, Knowler, WC, Shuldiner, AR, Elbein, SC, Mitchell, BD, Froguel, P, Ng, MC, Chan, JC, Jia, W, Deloukas, P, Hitman, GA, Walker, M, Frayling, TM, Hattersley, AT, Zeggini, E, McCarthy, MI
Mutations in the LMNA gene (encoding lamin A/C) underlie familial partial lipodystrophy, a syndrome of monogenic insulin resistance and diabetes. LMNA maps to the well-replicated diabetes-linkage region on chromosome 1q, and there are reported associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::91f486af56bf3be1b22e46802610ff95
https://doi.org/10.2337/db06-0930
https://doi.org/10.2337/db06-0930
Autor:
Williams, RC, Elston, RC, Kumar, P, Knowler, WC, Abboud, HE, Adler, S, Bowden, DW, Divers, J, Freedman, BI, Igo, RP, Ipp, E, Iyengar, SK, Kimmel, PL, Klag, MJ, Kohn, O, Langefeld, CD, Leehey, DJ, Nelson, RG, Nicholas, SB, Pahl, MV, Parekh, RS, Rotter, JI, Schelling, JR, Sedor, JR, Shah, VO, Smith, MW, Taylor, KD, Thameem, F, Thornley-Brown, D, Winkler, CA, Guo, X, Zager, P, Hanson, RL, FIND Research Group, S.K. Iyengar, Goddard, KAB, Olson, JM, Ialacci, S, Fondran, J, Horvath, A, Igo, R, Jun, G, Kramp, K, Molineros, J, Quade, SRE, Schelling, J, Pickens, A, Humbert, L, Getz-Fradley, L, Pahl, M, Seldin, MF, Snyder, S, Tayek, J, Hernandez, E, LaPage, J, Garcia, C, Gonzalez, J, Aguilar, M, Klag, M, Parekh, R, Kao, L, Meoni, L, Whitehead, T, Chester, J, Wolford, J, Jones, L, Juan, R, Lovelace, R, Luethe, C, Phillips, LM, Sewemaenewa, J, Sili, I, Waseta, B, Saad, MF, Chen, YDI, Rotter, J, Taylor, K, Budgett, M, Hariri, F, Shah, V, Scavini, M, Bobelu, A, Abboud, H, Arar, N, Duggirala, R, Kasinath, BS, Stern, M
Publikováno v:
Williams, RC; Elston, RC; Kumar, P; Knowler, WC; Abboud, HE; Adler, S; et al.(2016). Selecting SNPs informative for African, American Indian and European Ancestry: Application to the Family Investigation of Nephropathy and Diabetes (FIND). BMC Genomics, 17(1), 325. doi: 10.1186/s12864-016-2654-x. UCLA: Retrieved from: http://www.escholarship.org/uc/item/75f580zv
© 2016 Williams et al. Background: The presence of population structure in a sample may confound the search for important genetic loci associated with disease. Our four samples in the Family Investigation of Nephropathy and Diabetes (FIND), European
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::91cf6123a411ce24ad4e490acd6aadeb
http://www.escholarship.org/uc/item/75f580zv
http://www.escholarship.org/uc/item/75f580zv