Search Results

A large Icelandic family with early osteoarthritis of the hip associated with a susceptibility locus on chromosome 16p.

by Ingvarsson, T, Stefánsson, SE, Gulcher, JR, Jónsson, HH, Jónsson, H, Frigge, ML, Pálsdóttir, E, Olafsdóttir, G, Jónsdóttir, T, Walters, GB, Lohmander, LS, Stefánsson, K
Published 2008

A common biological basis of obesity and nicotine addiction

by Thorgeirsson, TE, Gudbjartsson, DF, Sulem, P, Besenbacher, S, Styrkarsdottir, U, Thorleifsson, G, Walters, GB, Furberg, H, Sullivan, PF, Marchini, J, McCarthy, MI, Steinthorsdottir, V, Thorsteinsdottir, U, Stefansson, K
Published in Translational Psychiatry (2013)

Multiple genetic loci for bone mineral density and fractures

by Styrkarsdottir, U, Halldorsson, BV, Gretarsdottir, S, Gudbjartsson, DF, Walters, GB, Ingvarsson, T, Jonsdottir, T, Saemundsdottir, J, Center, JR, Nguyen, TV, Bagger, Y, Gulcher, JR, Eisman, JA, Christiansen, C, Sigurdsson, G, Kong, A, Thorsteinsdottir, U, Stefansson, K
Published 2008

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.

by Thorleifsson, G., Holm, H., Edvardsson, V., Walters, G.B., Styrkarsdottir, U., Gudbjartsson, D.F., Sulem, P., Halldorsson, B.V., Vegt, F. de, D'Ancona, F.C.H., Heijer, M. den, Franzson, L., Christiansen, C., Alexandersen, P., Rafnar, T., Kristjansson, K., Sigurdsson, G., Kiemeney, L.A.L.M., Bodvarsson, M., Indridason, O.S., Palsson, R., Kong, A., Thorsteinsdottir, U., Stefansson, K.
Published in Nature Genetics (2009)

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

by Styrkarsdottir, U, Thorleifsson, G, Sulem, P, Gudbjartsson, DF, Sigurdsson, A, Jonasdottir, A, Oddsson, A, Helgason, A, Magnusson, OT, Walters, GB, Frigge, ML, Helgadottir, HT, Johannsdottir, H, Bergsteinsdottir, K, Ogmundsdottir, MH, Center, JR, Nguyen, TV, Eisman, JA, Christiansen, C, Steingrimsson, E, Jonasson, JG, Tryggvadottir, L, Eyjolfsson, GI, Theodors, A, Jonsson, T, Ingvarsson, T, Olafsson, I, Rafnar, T, Kong, A, Sigurdsson, G, Masson, G, Thorsteinsdottir, U, Stefansson, K
Published 2013

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

by Sulem, P., Gudbjartsson, D.F., Geller, F., Prokopenko, I., Feenstra, B., Aben, K.K.H., Franke, B., Heijer, M. den, Kovacs, P., Stumvoll, M., Magi, R., Yanek, L.R., Becker, L.C., Boyd, H.A., Stacey, S.N., Walters, G.B., Jonasdottir, A., Thorleifsson, G., Holm, H., Gudjonsson, S.A., Rafnar, T., Bjornsdottir, G., Becker, D.M., Melbye, M., Kong, A., Tonjes, A., Thorgeirsson, T., Thorsteinsdottir, U., Kiemeney, L.A.L.M., Stefansson, K.
Published in Human Molecular Genetics (2011)

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

by Gudbjartsson, D.F., Holm, H., Gretarsdottir, S., Thorleifsson, G., Walters, G.B., Thorgeirsson, G., Gulcher, J., Mathiesen, E.B., Njølstad, I., Nyrnes, A., Wilsgaard, T., Hald, E.M., Hveem, K., Stoltenberg, C., Kucera, G., Stubblefield, T., Carter, S., Roden, D., Ng, M.C., Baum, L., So, W.Y., Wong, K.S., Chan, J.C., Gieger, C., Wichmann, H.-E., Gschwendtner, A., Dichgans, M., Kuhlenbäumer, G., Berger, K., Ringelstein, E.B., Bevan, S., Markus, H.S., Kostulas, K., Hillert, J., Sveinbjörnsdóttir, S., Valdimarsson, E.M., Løchen, M.L., Ma, R.C., Darbar, D., Kong, A., Arnar, D.O., Thorsteinsdottir, U., Stefansson, K.
Published in Nature Genetics (2009)

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

by Thorleifsson, G, Walters, GB, Hewitt, AW, Masson, G, Helgason, A, DeWan, A, Sigurdsson, A, Jonasdottir, A, Gudjonsson, SA, Magnusson, KP, Stefansson, H, Lam, DSC, Tam, POS, Gudmundsdottir, GJ, Southgate, L, Burdon, KP, Gottfredsdottir, MS, Aldred, MA, Mitchell, P, St Clair, D, Collier, DA, Tang, N, Sveinsson, O, Macgregor, S, Martin, NG, Cree, AJ, Gibson, J, MacLeod, A, Jacob, A, Ennis, S, Young, TL, Chan, JCN, Karwatowski, WSS, Hammond, CJ, Thordarson, K, Zhang, M, Wadelius, C, Lotery, AJ, Trembath, RC, Pang, CP, Hoh, J, Craig, JE, Kong, A, Mackey, DA, Jonasson, F, Thorsteinsdottir, U, Stefansson, K
Published in Nature Genetics (2010)

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.

by Gretarsdottir, S, Baas, AF, Thorleifsson, G, Holm, H, den Heijer, M, de Vries, JP, Kranendonk, SE, Zeebregts, CJ, van Sterkenburg, SM, Geelkerken, RH, van Rij, AM, Williams, MJ, Boll, AP, Kostic, JP, Jonasdottir, A, Walters, GB, Masson, G, Sulem, P, Saemundsdottir, J, Mouy, M, Magnusson, KP, Tromp, G, Elmore, JR, Sakalihasan, N, Limet, R, Defraigne, JO, Ferrell, RE, Ronkainen, A, Ruigrok, YM, Wijmenga, C, Grobbee, DE, Shah, SH, Granger, CB, Quyyumi, AA, Vaccarino, V, Patel, RS, Zafari, AM, Levey, AI, Austin, H, Girelli, D, Pignatti, PF, Olivieri, O, Martinelli, N, Malerba, G, Trabetti, E, Becker, LC, Becker, DM, Reilly, MP, Rader, DJ, Mueller, T, Dieplinger, B, Haltmayer, M, Urbonavicius, S, Lindblad, B, Gottsäter, A, Gaetani, E, Pola, R, Wells, P, Rodger, M, Forgie, M, Langlois, N, Corral, J, Vicente, V, Fontcuberta, J, España, F, Grarup, N, Jørgensen, T, Witte, DR, Hansen, T, Pedersen, O, Aben, KK, de Graaf, J, Holewijn, S, Folkersen, L, Franco-Cereceda, A, Eriksson, P, Collier, DA, Stefansson, H, Steinthorsdottir, V, Rafnar, T, Valdimarsson, EM, Magnadottir, HB, Sveinbjornsdottir, S, Olafsson, I, Magnusson, MK, Palmason, R, Haraldsdottir, V, Andersen, K, Onundarson, PT, Thorgeirsson, G, Kiemeney, LA, Powell, JT, Carey, DJ, Kuivaniemi, H, Lindholt, JS, Jones, GT, Kong, A, Blankensteijn, JD, Matthiasson, SE, Thorsteinsdottir, U, Stefansson, K
Published 2010

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

by Gretarsdottir S, Baas AF, Thorleifsson G, Holm H, den Heijer M, de Vries JP, Kranendonk SE, Zeebregts CJ, van Sterkenburg SM, Geelkerken RH, van Rij AM, Williams MJ, Boll AP, Kostic JP, Jonasdottir A, Walters GB, Masson G, Sulem P, Saemundsdottir J, Mouy M, Magnusson KP, Tromp G, Elmore JR, Sakalihasan N, Limet R, Defraigne JO, Ferrell RE, Ronkainen A, Ruigrok YM, Wijmenga C, Grobbee DE, Shah SH, Granger CB, Quyyumi AA, Vaccarino V, Patel RS, Zafari AM, Levey AI, Austin H, Becker LC, Becker DM, Reilly MP, Rader DJ, Mueller T, Dieplinger B, Haltmayer M, Urbonavicius S, Lindblad B, Gottsäter A, Gaetani E, Pola R, Wells P, Rodger M, Forgie M, Langlois N, Corral J, Vicente V, Fontcuberta J, España F, Grarup N, Jørgensen T, Witte DR, Hansen T, Pedersen O, Aben KK, de Graaf J, Holewijn S, Folkersen L, Franco Cereceda A, Eriksson P, Collier DA, Stefansson H, Steinthorsdottir V, Rafnar T, Valdimarsson EM, Magnadottir HB, Sveinbjornsdottir S, Olafsson I, Magnusson MK, Palmason R, Haraldsdottir V, Andersen K, Onundarson PT, Thorgeirsson G, Kiemeney LA, Powell JT, Carey DJ, Kuivaniemi H, Lindholt JS, Jones GT, Kong A, Blankensteijn JD, Matthiasson SE, Thorsteinsdottir U, Stefansson K., GIRELLI, Domenico, PIGNATTI, Pierfranco, OLIVIERI, Oliviero, MARTINELLI, Nicola, MALERBA, Giovanni, TRABETTI, Elisabetta
Published in Nature Genetics (2010)

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

by van der Meer, D, Sonderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bulow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gustafsson, O, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jonsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Muhleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Burke Quinlan, E, Reinbold, CS, Marques, TR, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Uhlmann, A, Ulfarsson, MO, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefansson, H, Stefansson, K, Thompson, PM, Andreassen, OA
Published in JAMA Psychiatry (2020)

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

by van der Meer, D, Sonderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bulow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gustafsson, O, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jonsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Muhleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Burke Quinlan, E, Reinbold, CS, Marques, TR, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Uhlmann, A, Ulfarsson, MO, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefansson, H, Stefansson, K, Thompson, PM, Andreassen, OA
Published in JAMA Psychiatry (2020)

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

by Writing Committee for the ENIGMA-CNV Working Group, van der Meer, D, Sønderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bülow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gústafsson, Ó, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jönsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Mühleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Olde Loohuis, LM, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Quinlan, EB, Reinbold, CS, Reis Marques, T, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Schork, AJ, Schumann, G, Shin, J, Shumskaya, E, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutiérrez, D, Uhlmann, A, Úlfarsson, MÖ, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefánsson, H, Stefánsson, K, Thompson, PM, Andreassen, OA
Published 2019