Showing 1 - 20 results of 34 for search 'Grarup, N', query time: 0.09s
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1
The genetic history of Greenlandic-European contact by Waples, RK, Hauptmann, AL, Seiding, I, Jørsboe, E, Jørgensen, ME, Grarup, N, Andersen, MK, Larsen, CVL, Bjerregaard, P, Hellenthal, G, Hansen, T, Albrechtsen, A, Moltke, I
Published 2021Journal article -
2
Physical activity attenuates postprandial hyperglycaemia in homozygous TBC1D4 loss-of-function mutation carriers by Schnurr, TM, Jørsboe, E, Chadt, A, Dahl-Petersen, IK, Kristensen, JM, Wojtaszewski, JFP, Springer, C, Bjerregaard, P, Brage, S, Pedersen, O, Moltke, I, Grarup, N, Al-Hasani, H, Albrechtsen, A, Jørgensen, ME, Hansen, T
Published 2021Journal article -
3
An LDLR missense variant poses high risk of familial hypercholesterolemia in 30% of Greenlanders and offers potential of early cardiovascular disease intervention by Jørsboe, E, Andersen, MK, Skotte, L, Stæger, FF, Færgeman, NJ, Hanghøj, K, Santander, CG, Senftleber, NK, Diaz, LJ, Overvad, M, Waples, RK, Geller, F, Bjerregaard, P, Melbye, M, Larsen, CVL, Feenstra, B, Anders Koch, Jørgensen, ME, Grarup, N, Moltke, I, Albrechtsen, A, Hansen, T
Published 2022Journal article -
4
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. by Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T, Tian, G, Cao, H, Jiang, T, Kim, S, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A, Bolund, L, Charpentier, G, Chen, Y, Dekker, J
Published 2013Journal article -
5
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes by Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T, Tian, G, Cao, H, Jiang, T, Kim, S, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A, Bolund, L, Charpentier, G, Chen, Y, Dekker, J
Published 2012Journal article -
6
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes by Flannick, J, Thorleifsson, G, Beer, N, Jacobs, S, Grarup, N, Burtt, N, Mahajan, A, Fuchsberger, C, Atzmon, G, Benediktsson, R, Blangero, J, Bowden, D, Brandslund, I, Brosnan, J, Burslem, F, Chambers, J, Cho, Y, Christensen, C, Douglas, D, Duggirala, R, Dymek, Z, Farjoun, Y, Fennell, T, Fontanillas, P, Forsén, T
Published 2014Journal article -
7
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. by Flannick, J, Thorleifsson, G, Beer, N, Jacobs, S, Grarup, N, Burtt, N, Mahajan, A, Fuchsberger, C, Atzmon, G, Benediktsson, R, Blangero, J, Bowden, D, Brandslund, I, Brosnan, J, Burslem, F, Chambers, J, Cho, Y, Christensen, C, Douglas, D, Duggirala, R, Dymek, Z, Farjoun, Y, Fennell, T, Fontanillas, P, Forsén, T
Published 2014Journal article -
8
Underlying genetic models of inheritance in established type 2 diabetes associations. by Salanti, G, Southam, L, Altshuler, D, Ardlie, K, Barroso, I, Boehnke, M, Cornelis, M, Frayling, T, Grallert, H, Grarup, N, Groop, L, Hansen, T, Hattersley, A, Hu, F, Hveem, K, Illig, T, Kuusisto, J, Laakso, M, Langenberg, C, Lyssenko, V, McCarthy, M, Morris, A, Morris, A, Palmer, C, Payne, F
Published 2009Journal article -
9
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity. by Dimas, A, Lagou, V, Barker, A, Knowles, J, Mägi, R, Hivert, M, Benazzo, A, Rybin, D, Jackson, A, Stringham, H, Song, C, Fischer-Rosinsky, A, Boesgaard, T, Grarup, N, Abbasi, F, Assimes, T, Hao, K, Yang, X, Lecoeur, C, Barroso, I, Bonnycastle, L, Böttcher, Y, Bumpstead, S, Chines, P, Erdos, MR
Published 2014Journal article -
10
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. by Saxena, R, Hivert, M, Langenberg, C, Tanaka, T, Pankow, J, Vollenweider, P, Lyssenko, V, Bouatia-Naji, N, Dupuis, J, Jackson, A, Kao, W, Li, M, Glazer, N, Manning, A, Luan, J, Stringham, H, Prokopenko, I, Johnson, T, Grarup, N, Boesgaard, T, Lecoeur, C, Shrader, P, O'Connell, J, Ingelsson, E, Couper, D
Published 2010Journal article -
11
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. by Helgadottir, A, Gretarsdottir, S, Thorleifsson, G, Holm, H, Patel, R, Gudnason, T, Jones, G, van Rij, A, Eapen, D, Baas, A, Tregouet, D, Morange, P, Emmerich, J, Lindblad, B, Gottsäter, A, Kiemeny, L, Lindholt, J, Sakalihasan, N, Ferrell, R, Carey, D, Elmore, JR, Tsao, P, Grarup, N, Jørgensen, T, Witte, DR
Published 2012Journal article -
12
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels. by Scott, R, Chu, A, Grarup, N, Manning, A, Hivert, M, Shungin, D, Tönjes, A, Yesupriya, A, Barnes, D, Bouatia-Naji, N, Glazer, N, Jackson, A, Kutalik, Z, Lagou, V, Marek, D, Rasmussen-Torvik, L, Stringham, H, Tanaka, T, Aadahl, M, Arking, D, Bergmann, S, Boerwinkle, E, Bonnycastle, L, Bornstein, SR, Brunner, E
Published 2012Journal article -
13
A common allele in FGF21 associated with sugar intake is associated with body shape, lower total body-fat percentage, and higher blood pressure by Frayling, TM, Beaumont, RN, Jones, SE, Yaghootkar, H, Tuke, MA, Ruth, KS, Casanova, F, West, B, Locke, J, Sharp, S, Ji, Y, Thompson, W, Harrison, J, Etheridge, AS, Gallins, PJ, Jima, D, Wright, F, Zhou, Y, Innocenti, F, Lindgren, CM, Grarup, N, Murray, A, Freathy, RM, Weedon, MN, Tyrrell, J, Wood, AR
Published 2018Journal article -
14
Loss of sucrase-isomaltase function increases acetate levels and improves metabolic health in Greenlandic cohorts by Andersen, MK, Skotte, L, Jørsboe, E, Polito, R, Stæger, FF, Aldiss, P, Hanghøj, K, Waples, RK, Santander, CG, Grarup, N, Dahl-Petersen, IK, Diaz, LJ, Overvad, M, Senftleber, NK, Søborg, B, Larsen, CVL, Lemoine, C, Pedersen, O, Feenstra, B, Bjerregaard, P, Melbye, M, Jørgensen, ME, Færgeman, NJ, Koch, A, Moritz, T, Gillum, MP, Moltke, I, Hansen, T, Albrechtsen, A
Published 2021Journal article -
15
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria by Ahluwalia, T, Schulz, C, Waage, J, Skaaby, T, Sandholm, N, Van Zuydam, N, Charmet, R, Bork-Jensen, J, Almgren, P, Thuesen, B, Bedin, M, Brandslund, I, Christensen, C, Linneberg, A, Ahlqvist, E, Groop, P, Hadjadj, S, Tregouet, D, Jørgensen, M, Grarup, N, Pedersen, O, Simons, M, Groop, L, Orho-Melander, M, McCarthy, M, Melander, O, Rossing, P, Kilpeläinen, T, Hansen, T
Published 2018Journal article -
16
A genome-wide association study of IVGTT-based measures of first phase insulin secretion refines the underlying physiology of Type 2 Diabetes variants. by Wood, A, Jonsson, A, Jackson, A, Wang, N, van Leewen, N, Palmer, N, Kobes, S, Deelen, J, Boquete-Vilarino, L, Paananen, J, Stančáková, A, Boomsma, D, de Geus, E, Eekhoff, E, Fritsche, A, Kramer, M, Nijpels, G, Simonis-Bik, A, van Haeften, T, Mahajan, A, Boehnke, M, Bergman, R, Tuomilehto, J, Collins, F, Mohlke, K, Banasik, K, Groves, C, McCarthy, M, Pearson, E, Natali, A, Mari, A, Buchanan, T, Taylor, K, Xiang, A, Gjesing, A, Grarup, N, Eiberg, H, Pedersen, O, Chen, Y, Laakso, M, Norris, J, Smith, U, Wagenknecht, L, Baier, L, Bowden, D, Hansen, T, Walker, M, Watanabe, R, 't Hart, L, Hanson, R, Frayling, T
Published 2017Journal article -
17
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity by Yaghootkar, H, Zhang, Y, Spracklen, CN, Karaderi, T, Huang, LO, Bradfield, J, Schurmann, C, Fine, RS, Preuss, MH, Kutalik, Z, Wittemans, LB, Lu, Y, Metz, S, Willems, SM, Li-Gao, R, Grarup, N, Wang, S, Molnos, S, Sandoval-Zárate, AA, Nalls, MA, Lange, LA, Haesser, J, Guo, X, Lyytikäinen, L-P, Feitosa, MF, Sitlani, CM, Venturini, C, Mahajan, A, Kacprowski, T, Wang, CA, Chasman, DI, Amin, N, Broer, L, Robertson, N, Young, KL, Allison, M, Auer, PL, Blüher, M, Borja, JB, Bork-Jensen, J, Carrasquilla, GD, Christofidou, P, Demirkan, A, Doege, CA, Garcia, ME, Graff, M, Guo, K, Hakonarson, H, Hong, J, Ida Chen, Y-D, van Duijn, CM, Et al.
Published 2020Journal article -
18
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits by Van Setten, J, Verweij, N, Mbarek, H, Niemeijer, MN, Trompet, S, Arking, DE, Brody, JA, Gandin, I, Grarup, N, Hall, LM, Hemerich, D, Lyytikäinen, L-P, Mei, H, Müller-Nurasyid, M, Prins, BP, Robino, A, Smith, AV, Warren, HR, Asselbergs, FW, Boomsma, DI, Caulfield, MJ, Eijgelsheim, M, Ford, I, Hansen, T, Harris, TB, Heckbert, SR, Hottenga, J-J, Iorio, A, Kors, JA, Linneberg, A, Macfarlane, PW, Meitinger, T, Nelson, CP, Raitakari, OT, Aldana, CT, Sinagra, G, Sinner, M, Soliman, EZ, Stoll, M, Uitterlinden, A, Van Duijn, CM, Waldenberger, M, Alonso, A, Gasparini, P, Gudnason, V, Jamshidi, Y, Kääb, S, Kanters, JK, Lehtimäki, T, Munroe, PB, Peters, A, Samani, NJ, Sotoodehnia, N, Ulivi, S, Wilson, JG, De Geus, EJC, Jukema, JW, Stricker, B, Van Der Harst, P, De Bakker, PIW, Isaacs, A
Published 2019Journal article -
19
A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes by van Zuydam, NR, Ahlqvist, E, Sandholm, N, Deshmukh, H, Rayner, NW, Abdalla, M, Ladenvall, C, Ziemek, D, Fauman, E, Robertson, NR, McKeigue, PM, Valo, E, Forsblom, C, Harjutsalo, V, Perna, A, Rurali, E, Marcovecchio, ML, Igo, RP, Salem, RM, Perico, N, Lajer, M, Käräjämäki, A, Imamura, M, Kubo, M, Takahashi, A, Sim, X, Liu, J, van Dam, RM, Jiang, G, Tam, CHT, Luk, AOY, Lee, HM, Lim, CKP, Szeto, CC, So, WY, Chan, JCN, Ang, SF, Dorajoo, R, Wang, L, Clara, TS, McKnight, A-J, Duffy, S, Pezzolesi, MG, Consortium, G, Marre, M, Gyorgy, B, Hadjadj, S, Hiraki, LT, Ahluwalia, TS, Almgren, P, Schulz, C-A, Orho-Melander, M, Linneberg, A, Christensen, C, Witte, DR, Grarup, N, Brandslund, I, Melander, O, Paterson, AD, Tregouet, D, Maxwell, AP, Lim, SC, Ma, RCW, Tai, ES, Maeda, S, Lyssenko, V, Tuomi, T, Krolewski, AS, Rich, SS, Hirschhorn, JN, Florez, JC, Dunger, D, Pedersen, O, Hansen, T, Rossing, P, Remuzzi, G, Brosnan, MJ, Palmer, CNA, Groop, P-H, Colhoun, HM, Groop, LC, McCarthy, MI
Published 2018Journal article -
20
Genomewide meta‐analysis identifies loci associated with IGF‐I and IGFBP‐3 levels with impact on age‐related traits by Teumer, A, Qi, Q, Nethander, M, Aschard, H, Bandinelli, S, Beekman, M, Berndt, SI, Bidlingmaier, M, Broer, L, Charge Longevity Working Group, Cappola, A, Ceda, GP, Chanock, S, Chen, M-H, Chen, TC, Chen, Y-DI, Chung, J, Del Greco Miglianico, F, Eriksson, J, Ferrucci, L, Friedrich, N, Gnewuch, C, Goodarzi, MO, Grarup, N, Guo, T, Hammer, E, Hayes, RB, Hicks, AA, Hofman, A, Houwing-Duistermaat, JJ, Hu, F, Hunter, DJ, Husemoen, LL, Isaacs, A, Jacobs, KB, Janssen, JAMJL, Jansson, J-O, Jehmlich, N, Johnson, S, Juul, A, Karlsson, M, Kilpelainen, TO, Kovacs, P, Kraft, P, Li, C, Linneberg, A, Liu, Y, Loos, RJF, Body Composition Genetics Consortium, Lorentzon, M, Lu, Y, Maggio, M, Magi, R, Meigs, J, Mellström, D, Nauck, M, Newman, AB, Pollak, MN, Pramstaller, PP, Prokopenko, I, Psaty, BM, Reincke, M, Rimm, EB, Rotter, JI, Pierre, A, Schurmann, C, Seshadri, S, Sjögren, K, Slagboom, PE, Strickler, HD, Stumvoll, M, Suh, Y, Sun, Q, Zhang, C, Svensson, J, Tanaka, T, Tare, A, Tönjes, A, Uh, H-W, Van Duijn, CM, Van Heemst, D, Vandenput, L, Vasan, RS, Völker, U, Willems, SM, Ohlsson, C, Wallaschofski, H, Kaplan, RC
Published 2016Journal article