Ólafur Birgir Davíðsson
Ólafur Birgir Davíðsson
Danish Headache Center, Region H
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Cited by
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Genetic predisposition to mosaic Y chromosome loss in blood
DJ Thompson, G Genovese, J Halvardson, JC Ulirsch, DJ Wright, C Terao, ...
Nature 575 (7784), 652-657, 2019
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
RP Kristjansson, A Oddsson, H Helgason, G Sveinbjornsson, ...
Nature communications 7 (1), 10572, 2016
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
T Rafnar, B Gunnarsson, OA Stefansson, P Sulem, A Ingason, ML Frigge, ...
Nature communications 9 (1), 3636, 2018
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ...
Nature genetics 51 (2), 267-276, 2019
A Missense Variant in PLEC Increases Risk of Atrial Fibrillation
RB Thorolfsdottir, G Sveinbjornsson, P Sulem, A Helgadottir, ...
Journal of the American College of Cardiology 70 (17), 2157-2168, 2017
Epigenetic and genetic components of height regulation
S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ...
Nature communications 7 (1), 13490, 2016
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation
RB Thorolfsdottir, G Sveinbjornsson, P Sulem, JB Nielsen, S Jonsson, ...
Communications biology 1 (1), 68, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death
G Sveinbjornsson, EF Olafsdottir, RB Thorolfsdottir, OB Davidsson, ...
Circulation: Genomic and Precision Medicine 11 (8), e002151, 2018
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
LJA Kogelman, AL Esserlind, AF Christensen, S Awasthi, S Ripke, ...
Neurology Genetics 5 (6), 2019
Genetic insight into sick sinus syndrome
RB Thorolfsdottir, G Sveinbjornsson, HM Aegisdottir, S Benonisdottir, ...
European heart journal 42 (20), 1959-1971, 2021
Fish skin grafts compared to human amnion/chorion membrane allografts: a double‐blind, prospective, randomized clinical trial of acute wound healing
RS Kirsner, DJ Margolis, BT Baldursson, K Petursdottir, OB Davidsson, ...
Wound Repair and Regeneration 28 (1), 75-80, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
GR Oskarsson, A Oddsson, MK Magnusson, RP Kristjansson, ...
Communications Biology 3 (1), 189, 2020
Sequence variants with large effects on cardiac electrophysiology and disease
K Norland, G Sveinbjornsson, RB Thorolfsdottir, OB Davidsson, ...
Nature communications 10 (1), 4803, 2019
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human Molecular Genetics 28 (7), 1199-1211, 2019
Sequence variant at 4q25 near PITX2 associates with appendicitis
RP Kristjansson, S Benonisdottir, A Oddsson, TE Galesloot, ...
Scientific Reports 7 (1), 3119, 2017
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
GR Oskarsson, RP Kristjansson, AL Lee, G Sveinbjornsson, ...
Communications Biology 1 (1), 49, 2018
Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers
DJ Thompson, G Genovese, J Halvardson, JC Ulirsch, DJ Wright, C Terao, ...
bioRxiv, 514026, 2019
Familial analysis reveals rare risk variants for migraine in regulatory regions
TR Techlo, AH Rasmussen, PL Møller, M Bøttcher, S Winther, ...
neurogenetics 21, 149-157, 2020
Twenty-five years of triptans–a nationwide population study
OB Davidsson, IA Olofsson, LJA Kogelman, MA Andersen, K Rostgaard, ...
Cephalalgia 41 (8), 894-904, 2021
Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) Consortium. Kidney Cancer GWAS Meta-Analysis Project. eQTLGen …
DJ Thompson, G Genovese, J Halvardson, JC Ulirsch, DJ Wright, C Terao, ...
Nature 575, 652-657, 2019
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