Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b.

Por Kroon, E, Krosl, J, Thorsteinsdottir, U, Baban, S, Buchberg, A M, Sauvageau, G
Publicado em 1998

Deletions at the chromosome 3 common eliminated region 1 on 3p21.3 in human breast tumors

Por Petursdottir, ThE, Thorsteinsdottir, U, Jonasson, JG, Moller, PH, Huiping, C, Bjornsson, J, Egilsson, V, Imreh, S, Ingvarsson, S
Publicado no Breast Cancer Res (2005)

Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia.

Por Thorsteinsdottir, U, Sauvageau, G, Hough, M R, Dragowska, W, Lansdorp, P M, Lawrence, H J, Largman, C, Humphries, R K
Publicado em 1997

A common biological basis of obesity and nicotine addiction

Por 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
Publicado em 2013

Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population

Por 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.
Publicado em 2005

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

Por 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
Publicado em 2014

Genetically Determined Height and Coronary Artery Disease

Por Nelson, C.P., Hamby, S.E., Saleheen, D., Hopewell, J.C., Zeng, L., Assimes, T.L., Kanoni, S., Willenborg, C., Burgess, S., Amouyel, P., Anand, S., Blankenberg, S., Boehm, B.O., Clarke, R.J., Collins, R., Dedoussis, G., Farrall, M., Franks, P.W., Groop, L., Hall, A.S., Hamsten, A., Hengstenberg, C., Hovingh, G. Kees, Ingelsson, E., Kathiresan, S., Kee, F., König, I.R., Kooner, J., Lehtimäki, T., März, W., McPherson, R., Metspalu, A., Nieminen, M.S., O’Donnell, C.J., Palmer, C.N.A., Peters, A., Perola, M., Reilly, M.P., Ripatti, S., Roberts, R., Salomaa, V., Shah, S.H., Schreiber, S., Siegbahn, A., Thorsteinsdottir, U., Veronesi, G., Wareham, N., Willer, C.J., Zalloua, P.A., Erdmann, J., Deloukas, P., Watkins, H., Schunkert, H., Danesh, J., Thompson, J.R., Samani, N.J.
Publicado no N Engl J Med (2015)

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

Por 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
Publicado em 2012

Expanding the range of ZNF804A variants conferring risk of psychosis

Por 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
Publicado em 2010

Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

Por 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
Publicado em 2010