Counterfactual Desirability

por Bradley, Richard, Stefánsson, H. Orri
Publicado 2017

Against the De Minimis Principle

por Lundgren, Björn, Stefánsson, H. Orri
Publicado 2020

EHMTI-0377. The influence of genetic constitution on migraine drug responses

por Christensen, AF, Esserlind, AL, Werge, T, Stefansson, H, Olesen, J
Publicado 2014

Dissociation of accumulated genetic risk and disease severity in patients with schizophrenia

por Papiol, S, Malzahn, D, Kästner, A, Sperling, S, Begemann, M, Stefansson, H, Bickeböller, H, Nave, K-A, Ehrenreich, H
Publicado 2011

Brain age prediction using deep learning uncovers associated sequence variants

por Jonsson, B. A., Bjornsdottir, G., Thorgeirsson, T. E., Ellingsen, L. M., Walters, G. Bragi, Gudbjartsson, D. F., Stefansson, H., Stefansson, K., Ulfarsson, M. O.
Publicado 2019

EHMTI-0380. The association of migraine susceptibility loci with severe migraine characteristics in a clinic-based migraine sample

por Esserlind, A, Christensen, AF, Steinberg, S, Grarup, N, Pedersen, O, Hansen, T, Werge, T, Folkmann-Hansen, T, Husemoen, LL, Linneberg, A, Budtz-Jorgensen, E, Westergaard, M Lurenda, Stefansson, H, Olesen, J
Publicado 2014

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

por Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, van de Lagemaat, L N, Bayés, À, Fernandez, E, Olason, P I, Böttcher, Y, Komiyama, N H, Collins, M O, Choudhary, J, Stefansson, K, Stefansson, H, Grant, S G N, Purcell, S, Sklar, P, O'Donovan, M C, Owen, M J
Publicado 2012

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Publicado 2017

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

por 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
Publicado 2017

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Publicado 2016

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Publicado 2017