1. A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease. Issue 1 (December 2018) Authors: Arnadottir, Gudny; Norddahl, Gudmundur; Gudmundsdottir, Steinunn; Agustsdottir, Arna; Sigurdsson, Snaevar; Jensson, Brynjar; Bjarnadottir, Kristbjorg; Theodors, Fannar; Benonisdottir, Stefania; Ivarsdottir, Erna; Oddsson, Asmundur; Kristjansson, Ragnar; Sulem, Gerald; Alexandersson, Kristjan; Jul... Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. (24th March 2018) Authors: Bjornsson, Thorsteinn; Thorolfsdottir, Rosa B; Sveinbjornsson, Gardar; Sulem, Patrick; Norddahl, Gudmundur L; Helgadottir, Anna; Gretarsdottir, Solveig; Magnusdottir, Audur; Danielsen, Ragnar; Sigurdsson, Emil L; Adalsteinsdottir, Berglind; Gunnarsson, Sverrir I; Jonsdottir, Ingileif; Arnar, Davi... Journal: European heart journal Issue: Volume 39:Number 34(2018) Page Start: 3243 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin. (14th May 2018) Authors: Rafnar, Thorunn; Sigurjonsdottir, Gudbjorg R; Stacey, Simon N; Halldorsson, Gisli; Sulem, Patrick; Pardo, Luba M; Helgason, Hannes; Sigurdsson, Stefan T; Gudjonsson, Thorkell; Tryggvadottir, Laufey; Olafsdottir, Gudridur H; Jonasson, Jon G; Alexiusdottir, Kristin; Sigurdsson, Asgeir; Gudmundsson,... Journal: Journal of the National Cancer Institute Issue: Volume 110:Number 9(2018) Page Start: 967 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Author Correction: The rate of meiotic gene conversion varies by sex and age. (November 2018) Authors: Halldorsson, Bjarni; Hardarson, Marteinn; Kehr, Birte; Styrkarsdottir, Unnur; Gylfason, Arnaldur; Thorleifsson, Gudmar; Zink, Florian; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Sulem, Patrick; Masson, Gisli; Thorsteinsdottir, Unnur; Helgason, Agnar; Kong, Augustine; Gudbjartsson, Daniel; Stefa... Journal: Nature genetics Issue: Volume 50:Number 11(2018) Page Start: 1616 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic insight into sick sinus syndrome. (13th February 2021) Authors: Thorolfsdottir, Rosa B; Sveinbjornsson, Gardar; Aegisdottir, Hildur M; Benonisdottir, Stefania; Stefansdottir, Lilja; Ivarsdottir, Erna V; Halldorsson, Gisli H; Sigurdsson, Jon K; Torp-Pedersen, Christian; Weeke, Peter E; Brunak, Søren; Westergaard, David; Pedersen, Ole B; Sorensen, Erik; Nielsen... Journal: European heart journal Issue: Volume 42:Number 20(2021) Page Start: 1959 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease. (23rd July 2020) Authors: Helgadottir, Anna; Thorleifsson, Gudmar; Alexandersson, Kristjan F; Tragante, Vinicius; Thorsteinsdottir, Margret; Eiriksson, Finnur F; Gretarsdottir, Solveig; Björnsson, Eythór; Magnusson, Olafur; Sveinbjornsson, Gardar; Jonsdottir, Ingileif; Steinthorsdottir, Valgerdur; Ferkingstad, Egil; Jenss... Journal: European heart journal Issue: Volume 41:Number 28(2020) Page Start: 2618 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genome-wide association meta-analysis yields 20 loci associated with gallstone disease. Issue 1 (December 2018) Authors: Ferkingstad, Egil; Oddsson, Asmundur; Gretarsdottir, Solveig; Benonisdottir, Stefania; Thorleifsson, Gudmar; Deaton, Aimee; Jonsson, Stefan; Stefansson, Olafur; Norddahl, Gudmundur; Zink, Florian; Arnadottir, Gudny; Gunnarsson, Bjarni; Halldorsson, Gisli; Helgadottir, Anna; Jensson, Brynjar; Kris... Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Issue 1 (December 2018) Authors: Gudmundsson, Julius; Sigurdsson, Jon; Stefansdottir, Lilja; Agnarsson, Bjarni; Isaksson, Helgi; Stefansson, Olafur; Gudjonsson, Sigurjon; Gudbjartsson, Daniel; Masson, Gisli; Frigge, Michael; Stacey, Simon; Sulem, Patrick; Halldorsson, Gisli; Tragante, Vinicius; Holm, Hilma; Eyjolfsson, Gudmundur... Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. GWAS of Hematuria. Issue 5 (May 2022) Authors: Gagliano Taliun, Sarah A.; Sulem, Patrick; Sveinbjornsson, Gardar; Gudbjartsson, Daniel F.; Stefansson, Kari; Paterson, Andrew D.; Barua, Moumita Journal: Clinical journal of the American Society of Nephrology Issue: Volume 17:Issue 5(2022) Page Start: 672 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of Lynch syndrome risk variants in the Romanian population. Issue 12 (16th October 2018) Authors: Iordache, Paul D.; Mates, Dana; Gunnarsson, Bjarni; Eggertsson, Hannes P.; Sulem, Patrick; Benonisdottir, Stefania; Csiki, Irma Eva; Rascu, Stefan; Radavoi, Daniel; Ursu, Radu; Staicu, Catalin; Calota, Violeta; Voinoiu, Angelica; Jinga, Mariana; Rosoga, Gabriel; Danau, Razvan; Sima, Sorin Cristia... Journal: Journal of cellular and molecular medicine Issue: Volume 22:Issue 12(2018) Page Start: 6068 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗