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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 | 109 | 2019 |
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 | 96 | 2018 |
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 | 85 | 2016 |
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 | 80 | 2017 |
Epigenetic and genetic components of height regulation S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ... Nature communications 7 (1), 13490, 2016 | 64 | 2016 |
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 | 59 | 2020 |
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 | 54 | 2018 |
Genetic insight into sick sinus syndrome RB Thorolfsdottir, G Sveinbjornsson, HM Aegisdottir, S Benonisdottir, ... European heart journal 42 (20), 1959-1971, 2021 | 43 | 2021 |
Migraine polygenic risk score associates with efficacy of migraine-specific drugs LJA Kogelman, AL Esserlind, A Francke Christensen, S Awasthi, S Ripke, ... Neurology: Genetics 5 (6), e364, 2019 | 39 | 2019 |
Sequence variants with large effects on cardiac electrophysiology and disease K Norland, G Sveinbjornsson, RB Thorolfsdottir, OB Davidsson, ... Nature communications 10 (1), 4803, 2019 | 39 | 2019 |
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 | 34 | 2020 |
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 | 30 | 2018 |
Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human Molecular Genetics 28 (7), 1199-1211, 2019 | 29 | 2019 |
Sequence variant at 4q25 near PITX2 associates with appendicitis RP Kristjansson, S Benonisdottir, A Oddsson, TE Galesloot, ... Scientific Reports 7 (1), 3119, 2017 | 17 | 2017 |
Sex differences in clinical characteristics of migraine and its burden: a population‐based study MA Chalmer, LJA Kogelman, I Callesen, CG Christensen, TR Techlo, ... European Journal of Neurology 30 (6), 1774-1784, 2023 | 13 | 2023 |
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 | 13 | 2020 |
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 | 13 | 2018 |
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 | 12 | 2021 |
A rare missense variant in NR1H4 associates with lower cholesterol levels AM Deaton, P Sulem, P Nioi, S Benonisdottir, LD Ward, OB Davidsson, ... Communications Biology 1 (1), 14, 2018 | 8 | 2018 |