Lilja Stefansdottir
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Explore the profile of Lilja Stefansdottir including associated specialties, affiliations and a list of published articles.
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55
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1237
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Recent Articles
11.
Styrkarsdottir U, Tragante V, Stefansdottir L, Thorleifsson G, Oddsson A, Sorensen E, et al.
J Clin Endocrinol Metab
. 2023 Dec;
109(8):e1608-e1615.
PMID: 38118020
Context: It is not clear if antagonizing the GIP (glucose-dependent insulinotropic polypeptide) receptor (GIPR) for treatment of obesity is likely to increase the risk of fractures, or to lower bone...
12.
Stacey S, Zink F, Halldorsson G, Stefansdottir L, Gudjonsson S, Einarsson G, et al.
Nat Genet
. 2023 Nov;
55(12):2149-2159.
PMID: 37932435
Clonal hematopoiesis (CH) arises when a substantial proportion of mature blood cells is derived from a single hematopoietic stem cell lineage. Using whole-genome sequencing of 45,510 Icelandic and 130,709 UK...
13.
Bjornsdottir G, Chalmer M, Stefansdottir L, Skuladottir A, Einarsson G, Andresdottir M, et al.
Nat Genet
. 2023 Oct;
55(11):1843-1853.
PMID: 37884687
Migraine is a complex neurovascular disease with a range of severity and symptoms, yet mostly studied as one phenotype in genome-wide association studies (GWAS). Here we combine large GWAS datasets...
14.
Westergaard D, Steinthorsdottir V, Stefansdottir L, Rohde P, Wu X, Geller F, et al.
medRxiv
. 2023 Aug;
PMID: 37645979
Bleeding in early pregnancy and postpartum hemorrhage (PPH) bear substantial risks, with the former closely associated with pregnancy loss and the latter being the foremost cause of maternal death, underscoring...
15.
Kristjansson R, Oskarsson G, Skuladottir A, Oddsson A, Rognvaldsson S, Sveinbjornsson G, et al.
Commun Biol
. 2023 Jul;
6(1):703.
PMID: 37430141
Urticaria is a skin disorder characterized by outbreaks of raised pruritic wheals. In order to identify sequence variants associated with urticaria, we performed a meta-analysis of genome-wide association studies for...
16.
Gisladottir R, Helgason A, Halldorsson B, Helgason H, Borsky M, Chien Y, et al.
Sci Adv
. 2023 Jun;
9(23):eabq2969.
PMID: 37294764
The genetic basis of the human vocal system is largely unknown, as are the sequence variants that give rise to individual differences in voice and speech. Here, we couple data...
17.
Styrkarsdottir U, Stefansdottir L, Thorleifsson G, Stefansson O, Saevarsdottir S, Lund S, et al.
Ann Rheum Dis
. 2023 Mar;
82(6):873-880.
PMID: 36931692
Objectives: Erosive hand osteoarthritis (EHOA) is a severe subset of hand osteoarthritis (OA). It is unclear if EHOA is genetically different from other forms of OA. Sequence variants at ten...
18.
Rahmioglu N, Mortlock S, Ghiasi M, Moller P, Stefansdottir L, Galarneau G, et al.
Nat Genet
. 2023 Mar;
55(3):423-436.
PMID: 36914876
Endometriosis is a common condition associated with debilitating pelvic pain and infertility. A genome-wide association study meta-analysis, including 60,674 cases and 701,926 controls of European and East Asian descent, identified...
19.
Aegisdottir H, Thorolfsdottir R, Sveinbjornsson G, Stefansson O, Gunnarsson B, Tragante V, et al.
Eur Heart J
. 2023 Feb;
44(12):1070-1080.
PMID: 36747475
Aims: Syncope is a common and clinically challenging condition. In this study, the genetics of syncope were investigated to seek knowledge about its pathophysiology and prognostic implications. Methods And Results:...
20.
Henkel C, Styrkarsdottir U, Thorleifsson G, Stefansdottir L, Bjornsdottir G, Banasik K, et al.
Ann Rheum Dis
. 2022 Nov;
82(3):384-392.
PMID: 36376028
Objectives: Osteoarthritis is a common and severe, multifactorial disease with a well-established genetic component. However, little is known about how genetics affect disease progression, and thereby the need for joint...