Synthesis and reactivity of a strained silicon-bridged [1]ferrocenophanium ion. by Masson, G, Herbert, D, Whittell, G, Holland, J, Lough, A, Green, J, Manners, I

Relatedness disequilibrium regression estimates heritability without environmental bias by Young, A, Frigge, M, Gudbjartsson, D, Thorleifsson, G, Bjornsdottir, G, Sulem, P, Masson, G, Thorsteinsdottir, U, Stefansson, K, Kong, A

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31. by Styrkarsdottir, U, Thorleifsson, G, Helgadottir, H, Bomer, N, Metrustry, S, Bierma-Zeinstra, S, Strijbosch, A, Evangelou, E, Hart, D, Beekman, M, Jonasdottir, A, Sigurdsson, A, Eiriksson, F, Thorsteinsdottir, M, Frigge, M, Kong, A, Gudjonsson, SA, Magnusson, O, Masson, G, Hofman, A, Arden, N, Ingvarsson, T, Lohmander, S, Kloppenburg, M, Rivadeneira, F

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. by Kiemeney, L, Sulem, P, Besenbacher, S, Vermeulen, S, Sigurdsson, A, Thorleifsson, G, Gudbjartsson, D, Stacey, SN, Gudmundsson, J, Zanon, C, Kostic, J, Masson, G, Bjarnason, H, Palsson, S, Skarphedinsson, O, Gudjonsson, SA, Witjes, J, Grotenhuis, A, Verhaegh, G, Bishop, D, Sak, S, Choudhury, A, Elliott, F, Barrett, J, Hurst, C

Parental origin of sequence variants associated with complex diseases by Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K, Jonasdottir, A, Frigge, M, Gylfason, A, Olason, P, Gudjonsson, SA, Sverrisson, S, Stacey, SN, Sigurgeirsson, B, Benediktsdottir, K, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J, Johannsson, O, Hreidarsson, AB, Sigurdsson, G

A common inversion under selection in Europeans. by Stefansson, H, Helgason, A, Thorleifsson, G, Steinthorsdottir, V, Masson, G, Barnard, J, Baker, A, Jonasdottir, A, Ingason, A, Gudnadottir, V, Desnica, N, Hicks, A, Gylfason, A, Gudbjartsson, D, Jonsdottir, G, Sainz, J, Agnarsson, K, Birgisdottir, B, Ghosh, S, Olafsdottir, A, Cazier, J, Kristjansson, K, Frigge, M, Thorgeirsson, T, Gulcher, JR

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. by Gudmundsson, J, Sulem, P, Gudbjartsson, D, Masson, G, Agnarsson, B, Benediktsdottir, K, Sigurdsson, A, Magnusson, O, Gudjonsson, SA, Magnusdottir, D, Johannsdottir, H, Helgadottir, H, Stacey, SN, Jonasdottir, A, Olafsdottir, S, Thorleifsson, G, Jonasson, J, Tryggvadottir, L, Navarrete, S, Fuertes, F, Helfand, B, Hu, Q, Csiki, I, Mates, I, Jinga, V

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer by Gudmundsson, J, Sulem, P, Gudbjartsson, D, Masson, G, Agnarsson, B, Agnarsson, B, Benediktsdottir, K, Benediktsdottir, K, Sigurdsson, A, Magnusson, O, Gudjonsson, SA, Magnusdottir, D, Johannsdottir, H, Helgadottir, H, Stacey, SN, Jonasdottir, A, Olafsdottir, S, Thorleifsson, G, Jonasson, J, Jonasson, J, Jonasson, J, Tryggvadottir, L, Tryggvadottir, L, Navarrete, S, Fuertes, F

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility by Stacey, SN, Sulem, P, Jonasdottir, A, Masson, G, Gudmundsson, J, Gudbjartsson, D, Magnusson, O, Gudjonsson, SA, Sigurgeirsson, B, Thorisdottir, K, Ragnarsson, R, Benediktsdottir, K, Nexø, B, Tjønneland, A, Overvad, K, Rudnai, P, Gurzau, E, Koppova, K, Hemminki, K, Corredera, C, Fuentelsaz, V, Grasa, P, Navarrete, S, Fuertes, F, García-Prats, MD

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. by Stacey, SN, Sulem, P, Jonasdottir, A, Masson, G, Gudmundsson, J, Gudbjartsson, D, Magnusson, O, Gudjonsson, SA, Sigurgeirsson, B, Thorisdottir, K, Ragnarsson, R, Benediktsdottir, K, Nexø, B, Tjønneland, A, Overvad, K, Rudnai, P, Gurzau, E, Koppova, K, Hemminki, K, Corredera, C, Fuentelsaz, V, Grasa, P, Navarrete, S, Fuertes, F, García-Prats, MD

Parental origin of sequence variants associated with complex diseases. by Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K, Jonasdottir, A, Frigge, M, Gylfason, A, Olason, P, Gudjonsson, SA, Sverrisson, S, Stacey, SN, Sigurgeirsson, B, Benediktsdottir, K, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J, Johannsson, O, Hreidarsson, AB, Sigurdsson, G, Ferguson-Smith, A, Gudbjartsson, D, Thorsteinsdottir, U, Stefansson, K

Maternal sildenafil for severe fetal growth restriction (STRIDER): a multicentre, randomised, placebo-controlled, double-blind trial by Sharp, A, Cornforth, C, Jackson, R, Harrold, J, Turner, M, Kenny, L, Baker, P, Johnstone, E, Khalil, A, von Dadelszen, P, Papageorghiou, A, Alfirevic, Z, Agarwal, U, Willis, E, Mammarella, S, Masson, G, Aquilina, J, Greco, E, Higgins, S, Vinayagam, D, Shaw, L, Stephens, L, Howe, D, Rand, A, Patni, S, Mousa, T, Rabab, A, Russell, H, Hannon, T, Fenn, A, Kilby, M, Selman, T, David, A, Spencer, R, Cohen, K, Breeze, A, McKelvey, A, Impey, L, Loannou, C, Stock, S, Poon, L, Pasupathy, D, Webster, L, Bugg, G