Search Results

Private–public collaboration in Iceland: battling COVID-19 with deCODE genetics

by Olaf Sigurjonsson, Throstur, Johannsdottir, Lara, Gudmundsdottir, Svala
Published in European Political Science (2022)

Health care and privacy: An interview with Kári Stefánsson, founder and CEO of deCODE Genetics in Reykjavik, Iceland

Published in EMBO reports (2001)

Beating the odds with systematic individualized care Nationwide prospective follow‐up of all patients with COVID‐19 in Iceland

by Helgason, D, Eythorsson, E, Olafsdottir, LB, Agustsson, T, Ingvarsdottir, S, Sverrisdottir, S, Ragnarsdottir, ED, Gottfredsson, M, Gudlaugsson, O, Palsson, R, Ingvarsson, RF
Published in Journal of Internal Medicine (2020)

A genetic signature including apolipoprotein Eε4 potentiates the risk of herpes simplex–associated Alzheimer's disease

by Lopatko Lindman, Karin, Weidung, Bodil, Olsson, Jan, Josefsson, Maria, Kok, Eloise, Johansson, Anders, Eriksson, Sture, Hallmans, Göran, Elgh, Fredrik, Lövheim, Hugo
Published in Alzheimer's & Dementia: Translational Research & Clinical Interventions (2019)

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

by Stefansdottir, Vigdis, Thorolfsdottir, Eirny, Hognason, Hakon B., Patch, Christine, van El, Carla, Hentze, Sabine, Cordier, Christophe, Mendes, Álvaro, Jonsson, Jon J.
Published in European Journal of Human Genetics (2020)

A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome

by Klemenzdottir, Elin Ola, Arnadottir, Gudny Anna, Jensson, Brynjar Orn, Jonasdottir, Adalbjorg, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Gudjonsson, Sigurjon Axel, Jonsson, Jon Johannes, Stefansdottir, Vigdis, Danielsen, Ragnar, Palsdottir, Astridur, Jonsson, Hakon, Helgason, Agnar, Magnusson, Olafur Thor, Thorsteinsdottir, Unnur, Bjornsson, Hans Tomas, Stefansson, Kari, Sulem, Patrick
Published in European Journal of Human Genetics (2023)

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency

by Runolfsdottir, Hrafnhildur L., Sayer, John A., Indridason, Olafur S., Edvardsson, Vidar O., Jensson, Brynjar O., Arnadottir, Gudny A., Gudjonsson, Sigurjon A., Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur
Published in European Journal of Human Genetics (2021)