Search Results

Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes.

by Buckley, Matthew T, Racimo, Fernando, Allentoft, Morten E, Jensen, Majken K, Jonsson, Anna, Huang, Hongyan, Hormozdiari, Farhad, Sikora, Martin, Marnetto, Davide, Eskin, Eleazar, Jørgensen, Marit E, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Kraft, Peter, Willerslev, Eske, Nielsen, Rasmus
Published 2017

Archaic Adaptive Introgression in TBX15/WARS2.

by Racimo, Fernando, Gokhman, David, Fumagalli, Matteo, Ko, Amy, Hansen, Torben, Moltke, Ida, Albrechtsen, Anders, Carmel, Liran, Huerta-Sánchez, Emilia, Nielsen, Rasmus
Published 2017

Allelic variation in a willow warbler genomic region is associated with climate clines

by KW Larson, M Liedvogel, Brianne Addison, O Kleven, T Laskemoen, JT Lifjeld, M Lundberg, S Äkesson, S Bensch
Published 2014

CDKN2A mutations and melanoma risk in the Icelandic population.

by Goldstein, A M, Stacey, S N, Olafsson, J H, Jonsson, G F, Helgason, A, Sulem, P, Sigurgeirsson, B, Benediktsdottir, K R, Thorisdottir, K, Ragnarsson, R, Kjartansson, J, Kostic, J, Masson, G, Kristjansson, K, Gulcher, J R, Kong, A, Thorsteinsdottir, U, Rafnar, T, Tucker, M A, Stefansson, K
Published in Journal of Medical Genetics (2008)

Tests of linkage, allelic and genotypic association between schizophrenia and the gene for the D3 dopamine receptor, DRD3.

by Kalsi, G, Curtis, D, Brynjolfsson, J, Sigmundsson, T, Petursson, H, Butler, R, Read, T, Murphy, P, Gurling, HM
Published 1998

Tests of linkage, allelic and genotypic association between schizophrenia and the gene for the D3 dopamine receptor, DRD3

by Kalsi, G, Curtis, D, Brynjolfsson, J, Sigmundsson, T, Petursson, H, Butler, R, Read, T, Murphy, P, Gurling, H M
Published 2010

A study of the association of HLA DR, DQ, and complement C4 alleles with systemic lupus erythematosus in Iceland

by Steinsson, K, Jonsdottir, S, Arason, G J, Kristjansdottir, H, Fossdal, R, Skaftadottir, I, Arnason, A
Published in Annals of the Rheumatic Diseases (2009)

Evidence for a complex role of HLA class II genotypes in susceptibility to multiple sclerosis in Iceland

by Haegert, D G, Swift, F V, Benedikz, J
Published 2011

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

by Gretarsdottir, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J, Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Urbonavicius, Sigitas, Lindblad, Bengt, Gottsäter, Anders, Gaetani, Eleonora, Pola, Roberto, Wells, Philip, Rodger, Marc, Forgie, Melissa, Langlois, Nicole, Corral, Javier, Vicente, Vicente, Fontcuberta, Jordi, España, Francisco, Grarup, Niels, Jørgensen, Torben, Witte, Daniel R, Hansen, Torben, Pedersen, Oluf, Aben, Katja K, de Graaf, Jacqueline, Holewijn, Suzanne, Folkersen, Lasse, Franco-Cereceda, Anders, Eriksson, Per, Collier, David A, Stefansson, Hreinn, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, Valdimarsson, Einar M, Magnadottir, Hulda B, Sveinbjornsdottir, Sigurlaug, Olafsson, Isleifur, Magnusson, Magnus Karl, Palmason, Robert, Haraldsdottir, Vilhelmina, Andersen, Karl, Onundarson, Pall T, Thorgeirsson, Gudmundur, Kiemeney, Lambertus A, Powell, Janet T, Carey, David J, Kuivaniemi, Helena, Lindholt, Jes S., Jones, Gregory T, Kong, Augustine, Blankensteijn, Jan D, Matthiasson, Stefan E, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Localization of a gene for migraine without aura to chromosome 4q21.

by Bjornsson, Asgeir, Gudmundsson, Gretar, Gudfinnsson, Einar, Hrafnsdottir, María, Benedikz, John, Skuladottir, Svanhildur, Kristjansson, Kristleifur, Frigge, Michael L, Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R
Published 2008

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

by Ferreira, Ricardo C, Pan-Hammarström, Qiang, Graham, Robert R, Gateva, Vesela, Fontán, Gumersindo, Lee, Annette T, Ortmann, Ward, Urcelay, Elena, Fernández-Arquero, Miguel, Núñez, Concepción, Jorgensen, Gudmundur, Ludviksson, Bjorn R, Koskinen, Sinikka, Haimila, Katri, Clark, Hilary F, Klareskog, Lars, Gregersen, Peter K, Behrens, Timothy W, Hammarström, Lennart
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, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J
Published in Nature Genetics (2011)

Genetic variability in a temperate intertidal phoronid, Phoronopsis viridis.

by Ayala, FJ, Valentine, JW, Barr, LG, Zumwalt, GS
Published 1974

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignanc...

by Karppinen, S-M, Barkardottir, R B, Backenhorn, K, Sydenham, T, Syrjäkoski, K, Schleutker, J, Ikonen, T, Pylkäs, K, Rapakko, K, Erkko, H, Johannesdottir, G, Gerdes, A-M, Thomassen, M, Agnarsson, B A, Grip, M, Kallioniemi, A, Kere, J, Aaltonen, L A, Arason, A, Møller, P, Kruse, T A, Borg, A, Winqvist, R
Published in Journal of Medical Genetics (2009)

Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome.

by Katsanis, N, Beales, PL, Woods, MO, Lewis, RA, Green, JS, Parfrey, PS, Ansley, SJ, Davidson, WS, Lupski, JR
Published 2000

Association of BsmI vitamin-D receptor gene polymorphism with combined bone mass in spine and proximal femur in Icelandic women

by Sigurdsson, G, Magnusdottir, D N, Kristinsson, J O, Kristjansson, K, Olafsson, I
Published in Journal of Internal Medicine (2010)

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)

by Fossdal, Ragnheidur, Jonasson, Fridbert, Kristjansdottir, Gudlaug T, Kong, Augustine, Stefansson, Hreinn, Gosh, Shyamali, Gulcher, Jeffrey R, Stefansson, Kari
Published in Human Molecular Genetics (2004)

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

Linkage analysis of manic depression (bipolar affective disorder) in Icelandic and British kindreds using markers on the short arm of chromosome 18.

by Kalsi, G, Smyth, C, Brynjolfsson, J, Sherrington, RS, O'Neill, J, Curtis, D, Rifkin, L, Murphy, P, Petursson, H, Gurling, HM
Published 1997

A major susceptibility gene for asthma maps to chromosome 14q24

by Hakonarson, Hakon, Bjornsdottir, Unnur S, Halapi, Eva, Palsson, Snaebjorn, Adalsteinsdottir, Elva, Gislason, David, Finnbogason, Gudmundur, Gislason, Thorarinn, Kristjansson, Kristleifur, Arnason, Thor, Birkisson, Illugi, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefansson, Kari
Published in The American Journal of Human Genetics (2008)