检索结果 - Thorsteinsdottir, U

Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b. 由 Kroon, E, Krosl, J, Thorsteinsdottir, U, Baban, S, Buchberg, A M, Sauvageau, G

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Deletions at the chromosome 3 common eliminated region 1 on 3p21.3 in human breast tumors 由 Petursdottir, ThE, Thorsteinsdottir, U, Jonasson, JG, Moller, PH, Huiping, C, Bjornsson, J, Egilsson, V, Imreh, S, Ingvarsson, S

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Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia. 由 Thorsteinsdottir, U, Sauvageau, G, Hough, M R, Dragowska, W, Lansdorp, P M, Lawrence, H J, Largman, C, Humphries, R K

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A common biological basis of obesity and nicotine addiction 由 Thorgeirsson, T E, Gudbjartsson, D F, Sulem, P, Besenbacher, S, Styrkarsdottir, U, Thorleifsson, G, Walters, G B, Furberg, H, Sullivan, P F, Marchini, J, McCarthy, M I, Steinthorsdottir, V, Thorsteinsdottir, U, Stefansson, K

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Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population 由 Helgadottir, A., Gretarsdottir, S., St. Clair, D., Manolescu, A., Cheung, J., Thorleifsson, G., Pasdar, A., Grant, S. F. A., Whalley, L. J., Hakonarson, H., Thorsteinsdottir, U., Kong, A., Gulcher, J., Stefansson, K., MacLeod, M. J.

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The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms 由 Oddsson, A, Kristinsson, S Y, Helgason, H, Gudbjartsson, D F, Masson, G, Sigurdsson, A, Jonasdottir, A, Jonasdottir, A, Steingrimsdottir, H, Vidarsson, B, Reykdal, S, Eyjolfsson, G I, Olafsson, I, Onundarson, P T, Runarsson, G, Sigurdardottir, O, Kong, A, Rafnar, T, Sulem, P, Thorsteinsdottir, U, Stefansson, K

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Association analysis of 29,956 individuals confirms that a low frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion 由 Yaghootkar, H, Stancáková, A, Freathy, RM, Vangipurapu, J, Weedon, MN, Xie, W, Wood, AR, Ferrannini, E, Mari, A, Ring, SM, Lawlor, DA, Davey, Smith G, Jørgensen, T, Hansen, T, Pedersen, O, Steinthorsdottir, V, Guðbjartsson, DF, Thorleifsson, G, Thorsteinsdottir, U, Stefansson, K, Hattersley, AT, Walker, M, Morris, AD, McCarthy, MI, Palmer, CNA, Laakso, M, Frayling, TM

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A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences 由 Thorgeirsson, T E, Steinberg, S, Reginsson, G W, Bjornsdottir, G, Rafnar, T, Jonsdottir, I, Helgadottir, A, Gretarsdottir, S, Helgadottir, H, Jonsson, S, Matthiasson, S E, Gislason, T, Tyrfingsson, T, Gudbjartsson, T, Isaksson, H J, Hardardottir, H, Sigvaldason, A, Kiemeney, L A, Haugen, A, Zienolddiny, S, Wolf, H J, Franklin, W A, Panadero, A, Mayordomo, J I, Hall, I P, Rönmark, E, Lundbäck, B, Dirksen, A, Ashraf, H, Pedersen, J H, Masson, G, Sulem, P, Thorsteinsdottir, U, Gudbjartsson, D F, Stefansson, K

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15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia 由 Ulfarsson, M O, Walters, G B, Gustafsson, O, Steinberg, S, Silva, A, Doyle, O M, Brammer, M, Gudbjartsson, D F, Arnarsdottir, S, Jonsdottir, G A, Gisladottir, R S, Bjornsdottir, G, Helgason, H, Ellingsen, L M, Halldorsson, J G, Saemundsen, E, Stefansdottir, B, Jonsson, L, Eiriksdottir, V K, Eiriksdottir, G R, Johannesdottir, G H, Unnsteinsdottir, U, Jonsdottir, B, Magnusdottir, B B, Sulem, P, Thorsteinsdottir, U, Sigurdsson, E, Brandeis, D, Meyer-Lindenberg, A, Stefansson, H, Stefansson, K

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Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes 由 Loviglio, M N, Leleu, M, Männik, K, Passeggeri, M, Giannuzzi, G, van der Werf, I, Waszak, S M, Zazhytska, M, Roberts-Caldeira, I, Gheldof, N, Migliavacca, E, Alfaiz, A A, Hippolyte, L, Maillard, A M, Van Dijck, A, Kooy, R F, Sanlaville, D, Rosenfeld, J A, Shaffer, L G, Andrieux, J, Marshall, C, Scherer, S W, Shen, Y, Gusella, J F, Thorsteinsdottir, U, Thorleifsson, G, Dermitzakis, E T, Deplancke, B, Beckmann, J S, Rougemont, J, Jacquemont, S, Reymond, A

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Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM 由 Amin, N, Byrne, E, Johnson, J, Chenevix-Trench, G, Walter, S, Nolte, I M, Vink, J M, Rawal, R, Mangino, M, Teumer, A, Keers, J C, Verwoert, G, Baumeister, S, Biffar, R, Petersmann, A, Dahmen, N, Doering, A, Isaacs, A, Broer, L, Wray, N R, Montgomery, G W, Levy, D, Psaty, B M, Gudnason, V, Chakravarti, A, Sulem, P, Gudbjartsson, D F, Kiemeney, L A, Thorsteinsdottir, U, Stefansson, K, van Rooij, F J A, Aulchenko, Y S, Hottenga, J J, Rivadeneira, F R, Hofman, A, Uitterlinden, A G, Hammond, C J, Shin, S-Y, Ikram, A, Witteman, J C M, Janssens, A C J W, Snieder, H, Tiemeier, H, Wolfenbuttel, B H R, Oostra, B A, Heath, A C, Wichmann, E, Spector, T D, Grabe, H J, Boomsma, D I, Martin, N G, van Duijn, C M

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Expanding the range of ZNF804A variants conferring risk of psychosis 由 Steinberg, S, Mors, O, Børglum, AD, Gustafsson, O, Werge, T, Mortensen, PB, Andreassen, OA, Sigurdsson, E, Thorgeirsson, TE, Böttcher, Y, Olason, P, Ophoff, RA, Cichon, S, Gudjonsdottir, IH, Pietiläinen, OPH, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Athanasiu, L, Suvisaari, J, Lonnqvist, J, Paunio, T, Hartmann, A, Jürgens, G, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Breuer, R, Möller, H-J, Giegling, I, Glenthøj, B, Rasmussen, HB, Mattheisen, M, Bitter, I, Réthelyi, JM, Sigmundsson, T, Fossdal, R, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Strengman, E, Kiemeney, LA, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Walshe, M, Bramon, E, Vassos, E, Li, T, Fraser, G, Walker, N, Toulopoulou, T, Yoon, J, Freimer, NB, Cantor, RM, Murray, R, Kong, A, Golimbet, V, Jönsson, EG, Terenius, L, Agartz, I, Petursson, H, Nöthen, MM, Rietschel, M, Peltonen, L, Rujescu, D, Collier, DA, Stefansson, H, St Clair, D, Stefansson, K

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Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study 由 Panoutsopoulou, K, Southam, L, Elliott, K S, Wrayner, N, Zhai, G, Beazley, C, Thorleifsson, G, Arden, N K, Carr, A, Chapman, K, Deloukas, P, Doherty, M, McCaskie, A, Ollier, W E R, Ralston, S H, Spector, T D, Valdes, A M, Wallis, G A, Wilkinson, J M, Arden, E, Battley, K, Blackburn, H, Blanco, F J, Bumpstead, S, Cupples, L A, Day-Williams, A G, Dixon, K, Doherty, S A, Esko, T, Evangelou, E, Felson, D, Gomez-Reino, J J, Gonzalez, A, Gordon, A, Gwilliam, R, Halldorsson, B V, Hauksson, V B, Hofman, A, Hunt, S E, Ioannidis, J P A, Ingvarsson, T, Jonsdottir, I, Jonsson, H, Keen, R, Kerkhof, H J M, Kloppenburg, M G, Koller, N, Lakenberg, N, Lane, N E, Lee, A T, Metspalu, A, Meulenbelt, I, Nevitt, M C, O'Neill, F, Parimi, N, Potter, S C, Rego-Perez, I, Riancho, J A, Sherburn, K, Slagboom, P E, Stefansson, K, Styrkarsdottir, U, Sumillera, M, Swift, D, Thorsteinsdottir, U, Tsezou, A, Uitterlinden, A G, van Meurs, J B J, Watkins, B, Wheeler, M, Mitchell, S, Zhu, Y, Zmuda, J M, Zeggini, E, Loughlin, J

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