Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Groves, C.J."'
Autor:
Groves, C.J. *, Carrell, J., Grady, R., Rajan, B., Morehouse, C.A., Halpin, R., Wang, J., Wu, J., Shrestha, Y., Rayanki, R., Kolbeck, R., Wang, Y., Herbst, R.
Publikováno v:
In Blood Advances 27 November 2018 2(22):3163-3176
To dissect the genetic architecture of blood pressure and assess effects on target organ damage, we analyzed 128,272 SNPs from targeted and genome-wide arrays in 201,529 individuals of European ancestry, and genotypes from an additional 140,886 indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::299f0c1d9dd002da0df74898ef79fc5f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085504
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085504
Autor:
Voight, B.F., Raychaudhuri, S., Purcell, S., McCarroll, S.A., Segrè, A.V., Ardlie, K., Burtt, N.P., Crawford, G., Elliott, A.L., Green, T., Guiducci, C., Saxena, R., Daly, M.J., Florez, J.C., Altshuler, D., Meigs, J.B., Scott, L.J., Welch, R.P., Willer, C.J., Ganser, M., Jackson, A.U., Stringham, H.M., Abecasis, G.R., Boehnke, M., Steinthorsdottir, V., Thorleifsson, G., Kong, A., Walters, G.B., Thorsteinsdottir, U., Stefansson, K., Dina, C., Proença, C., Cauchi, S., Froguel, P., Zeggini, E., Bumpstead, S., Payne, F., Smith, N., Barroso, I., Ferreira, T., Elliott, K.S., Lindgren, C.M., Prokopenko, I., Rayner, N.W., Robertson, N.R., Morris, A.P., McCarthy, M.I., Huth, C., Grallert, H., Gieger, C., Klopp, N., Meitinger, T., Petersen, A.-K., Thorand, B., Wichmann, H.-E., Illig, T., Aulchenko, Y.S., Amin, N., Witteman, J., Hofman, A., Van Duijn, C.M., McCulloch, L.J., Bennett, A.J., Groves, C.J., Hassanali, N., Owen, K.R., Gloyn, A.L., Wu, G., Stein, L.D., Langenberg, C., Griffin, S., Wareham, N.J., Hoffmann, O.M., Hide, W.A., Dupuis, J., Qi, L., Kraft, P., Sun, Q., Hunter, D., Hu, F.B., Cornelis, M., VanDam, R., Van Hoek, M., Van Herpt, T., Sijbrands, E., Uitterlinden, A., Navarro, P., Balkau, B., Benediktsson, R., Sigurdsson, G., Blagieva, R., Boehm, B.O., Boerwinkle, E., Bonnycastle, L.L., Chines, P.S., Erdos, M.R., Morken, M.A., Narisu, N., Swift, A.J., Boström, K.B., Bravenboer, B., Charpentier, G., Couper, D.J., Doney, A.S.F., Morris, A.D., Palmer, C.N.A., Fox, C.S., Franklin, C.S., Rudan, I., Grarup, N., Hadjadj, S., Thomas Sparsø, [No Value], Campbell, H., Wilson, J.F., Hansen, T., Pedersen, O., Herder, C., Roden, M., Isomaa, B., Tuomi, T., Johnson, P.R.V., Jørgensen, T., Kao, W.H.L., Kuusisto, J., Laakso, M., Lauritzen, T., Li, M., Lieverse, A., Lyssenko, V., Nilsson, P., Groop, L., Marre, M., Midthjell, K., Platou, C., Hveem, K., Perry, J.R.B., Shields, B.M., Weedon, M.N., Frayling, T.M., Hattersley, A.T., Rathmann, W., Strassburger, K., Rocheleau, G., Sladek, R., Sampson, M.J., Shrader, P., Tichet, J., Bergman, R.N., Collins, F.S., Gyllensten, U., Hitman, G.A., Mohlke, K.L., Pramstaller, P.P., Tuomilehto, J., Walker, M., Watanabe, R.M., Pankow, J.S.
Publikováno v:
Voight, B F, Raychaudhuri, S, Purcell, S, McCarroll, S A, Segrè, A V, Ardlie, K, Burtt, N P, Crawford, G, Elliott, A L, Green, T, Guiducci, C, Saxena, R, Daly, M J, Florez, J C, Altshuler, D, Meigs, J B, Scott, L J, Welch, R P, Willer, C J, Ganser, M, Jackson, A U, Stringham, H M, Abecasis, G R, Boehnke, M, Steinthorsdottir, V, Thorleifsson, G, Kong, A, Walters, G B, Thorsteinsdottir, U, Stefansson, K, Dina, C, Proença, C, Cauchi, S, Froguel, P, Zeggini, E, Bumpstead, S, Payne, F, Smith, N, Barroso, I, Ferreira, T, Elliott, K S, Lindgren, C M, Prokopenko, I, Rayner, N W, Robertson, N R, Morris, A P, McCarthy, M I, Huth, C, Grallert, H, Gieger, C, Klopp, N, Meitinger, T, Petersen, A-K, Thorand, B, Wichmann, H-E, Illig, T, Aulchenko, Y S, Amin, N, Witteman, J, Hofman, A, Van Duijn, C M, McCulloch, L J, Bennett, A J, Groves, C J, Hassanali, N, Owen, K R, Gloyn, A L, Wu, G, Stein, L D, Langenberg, C, Griffin, S, Wareham, N J, Hoffmann, O M, Hide, W A, Dupuis, J, Qi, L, Kraft, P, Sun, Q, Hunter, D, Hu, F B, Cornelis, M, VanDam, R, Van Hoek, M, Van Herpt, T, Sijbrands, E, Uitterlinden, A, Navarro, P, Balkau, B, Benediktsson, R, Sigurdsson, G, Blagieva, R, Boehm, B O, Boerwinkle, E, Bonnycastle, L L, Chines, P S, Erdos, M R, Morken, M A, Narisu, N, Swift, A J, Boström, K B, Bravenboer, B, Charpentier, G, Couper, D J, Doney, A S F, Morris, A D, Palmer, C N A, Fox, C S, Franklin, C S, Rudan, I, Grarup, N, Hadjadj, S, Thomas Sparsø, N V, Campbell, H, Wilson, J F, Hansen, T, Pedersen, O, Herder, C, Roden, M, Isomaa, B, Tuomi, T, Johnson, P R V, Jørgensen, T, Kao, W H L, Kuusisto, J, Laakso, M, Lauritzen, T, Li, M, Lieverse, A, Lyssenko, V, Nilsson, P, Groop, L, Marre, M, Midthjell, K, Platou, C, Hveem, K, Perry, J R B, Shields, B M, Weedon, M N, Frayling, T M, Hattersley, A T, Rathmann, W, Strassburger, K, Rocheleau, G, Sladek, R, Sampson, M J, Shrader, P, Tichet, J, Bergman, R N, Collins, F S, Gyllensten, U, Hitman, G A, Mohlke, K L, Pramstaller, P P, Tuomilehto, J, Walker, M, Watanabe, R M & Pankow, J S 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-874 . https://doi.org/10.1038/nature08625
Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K T, Jonasdottir, A, Frigge, M L, Gylfason, A, Olason, P I, Gudjonsson, S A, Sverrisson, S, Stacey, S N, Sigurgeirsson, B, Benediktsdottir, K R, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J H, Johannsson, O T, Hreidarsson, A B, Sigurdsson, G, Ferguson-Smith, A C, Gudbjartsson, D F, Thorsteinsdottir, U, Stefansson, K, DIAGRAM Consortium & Lauritzen, T 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-74 . https://doi.org/10.1038/nature08625
Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K T, Jonasdottir, A, Frigge, M L, Gylfason, A, Olason, P I, Gudjonsson, S A, Sverrisson, S, Stacey, S N, Sigurgeirsson, B, Benediktsdottir, K R, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J H, Johannsson, O T, Hreidarsson, A B, Sigurdsson, G, Ferguson-Smith, A C, Gudbjartsson, D F, Thorsteinsdottir, U, Stefansson, K, DIAGRAM Consortium & Lauritzen, T 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-74 . https://doi.org/10.1038/nature08625
To access publisher full text version of this article. Please click on the hyperlink in Additional Links field Effects of susceptibility variants may depend on from which parent they are inherited. Although many associations between sequence variants
Autor:
Mahajan, A., Sim, X., Ng, H.J., Manning, A., Rivas, M.A., Highland, H.M., Locke, A.E., Grarup, N., Im, H.K., Cingolani, P., Flannick, J., Fontanillas, P., Fuchsberger, C., Gaulton, K.J., Teslovich, T.M., Rayner, N.W., Robertson, N.R., Beer, N.L., Rundle, J.K., Bork-Jensen, J., Ladenvall, C., Blancher, C., Buck, D., Buck, G., Burtt, N.P., Gabriel, S., Gjesing, A.P., Groves, C.J., Hollensted, M., Huyghe, J.R., Jackson, A.U., Jun, G., Justesen, J.M., Mangino, M., Murphy, J., Neville, M., Onofrio, R., Small, K.S., Stringham, H.M., Syvanen, A.C., Trakalo, J., Abecasis, G., Bell, G.I., Blangero, J., Cox, N.J., Duggirala, R., Hanis, C.L., Seielstad, M., Wilson, J.G., Christensen, C., Brandslund, I., Rauramaa, R., Surdulescu, G.L., Doney, A.S., Lannfelt, L., Linneberg, A., Isomaa, B., Tuomi, T., Jørgensen, M.E., Jørgensen, T., Kuusisto, J., Uusitupa, M., Salomaa, V., Spector, T.D., Morris, A.D., Palmer, C.N., Collins, F.S., Mohlke, K.L., Bergman, R.N., Ingelsson, E., Lind, L., Tuomilehto, J., Hansen, T., Watanabe, R.M., Prokopenko, I., Dupuis, J., Karpe, F., Groop, L., Laakso, M., Pedersen, O., Florez, J.C, Morris, A.P., Altshuler, D., Meigs, J.B., Boehnke, M., McCarthy, M.I., Lindgren, C.M., Gloyn, A.L., T2D-GENES Consortium (), GoT2D Consortium (Hrabě de Angelis, M., Gieger, C., Grallert, H., Huth, C., Kriebel, J., Meisinger, C., Meitinger, T., Müller-Nurasyid, M., Peters, A., Ried, J.S., Strauch, K., Strom, T.M.)
Publikováno v:
PLoS Genet. 11:e1004876 (2015)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS Genetics; 11(1), no e1004876 (2015)
PLoS Genetics
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS Genetics; 11(1), no e1004876 (2015)
PLoS Genetics
Genome wide association studies (GWAS) for fasting glucose (FG) and insulin (FI) have identified common variant signals which explain 4.8% and 1.2% of trait variance, respectively. It is hypothesized that low-frequency and rare variants could contrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d5f33ccf3f315e91b395a158989e23c0
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-242802
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-242802
Autor:
Nettleton, J.A., McKeown, N.M., Kanoni, S., Lemaitre, R.N., Hivert, M.F., Ngwa, J., van Rooij, F.J., Sonestedt, E., Wojczynski, M.K., Ye, Z., Tanaka, T., Garcia, M., Anderson, J.S., Follis, J.L., Djousse, L., Mukamal, K., Papoutsakis, C., Mozaffarian, D., Zillikens, M.C., Bandinelli, S., Bennett, A.J., Borecki, I.B., Feitosa, M.F., Ferrucci, L., Forouhi, N.G., Groves, C.J., Hallmans, G., Harris, T., Hofman, A., Houston, D.K., Hu, F.B., Johansson, I., Kritchevsky, S.B., Langenberg, C., Launer, L., Liu, Y., Loos, R.J., Nalls, M., Orho-Melander, M., Renstrom, F., Rice, K., Riserus, U., Rolandsson, O., Rotter, J.I., Saylor, G., Sijbrands, E.J., Sjogren, P., Smith, A., Steingrímsdóttir, L., Uitterlinden, A.G., Wareham, N.J., Prokopenko, I., Pankow, J.S., van Duijn, C.M., Florez, J.C., Witteman, J.C., Dupuis, J., Dedoussis, G.V., Ordovas, J.M., Ingelsson, E., Cupples, L., Siscovick, D.S., Franks, P.W., Meigs, J.B.
Publikováno v:
Diabetes Care
Diabetes care, vol. 33, no. 12, pp. 2684-2691
Diabetes care, vol. 33, no. 12, pp. 2684-2691
OBJECTIVE Whole-grain foods are touted for multiple health benefits, including enhancing insulin sensitivity and reducing type 2 diabetes risk. Recent genome-wide association studies (GWAS) have identified several single nucleotide polymorphisms (SNP
OBJECTIVE - Proinsulin is a precursor of mature insulin and C-peptide. Higher circulating proinsulin levels are associated with impaired b-cell function, raised glucose levels, insulin resistance, and type 2 diabetes (T2D). Studies of the insulin pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::cfada5530e266d02cec5db3682a5f7bb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111423
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111423
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Kniha
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.