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| A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo AT Skuladottir, G Bjornsdottir, MS Nawaz, H Petersen, S Rognvaldsson, ... Communications biology 4 (1), 1148, 2021 | 22 | 2021 |
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| A homozygous loss-of-function mutation in C17orf62 causes chronic granulomatous disease GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 835-836, 2019 | | 2019 |
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| 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 | 79 | 2017 |
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| A novel missense variant in the gene PLEC increases risk of atrial fibrillation RB Thorolfsdottir, G Sveinbjornsson, P Sulem, DO Arnar, H Holm, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 260-260, 2018 | | 2018 |
| A novel sequence variant on chromosome 16p22 associates with atrial fibrillation H Holm, D Gudbjartsson, DO Arnar, S Gretarsdottir, G Thorgeirsson, ... CARDIOLOGY 113, 39-39, 2009 | | 2009 |
| A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy G Bjornsdottir, EV Ivarsdottir, K Bjarnadottir, S Benonisdottir, ... Nature communications 10 (1), 1777, 2019 | 10 | 2019 |
| A Rare Deletion in the 3‘ Untranslated Region of LDLR Causes Very Low Levels of LDL Cholesterol E Björnsson, Á Sigurðsson, G Norðdahl, H Jónsson, S Roskosch, ... Circulation 138 (Suppl_1), A12962-A12962, 2018 | | 2018 |
| A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta T Bjornsson, RB Thorolfsdottir, G Sveinbjornsson, P Sulem, GL Norddahl, ... European heart journal 39 (34), 3243-3249, 2018 | 73 | 2018 |
| A rare missense mutation in MYH6 confers high risk of coarctation of the aorta T Bjornsson, RB Thorolfsdottir, G Sveinbjornsson, P Sulem, GL Norddahl, ... bioRxiv, 180794, 2017 | 3 | 2017 |
| 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 |
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| A rare variant in MYH6 is associated with high risk of sick sinus syndrome H Holm, DF Gudbjartsson, P Sulem, G Masson, HT Helgadottir, C Zanon, ... Nature genetics 43 (4), 316-320, 2011 | 357 | 2011 |
