Magnus O Ulfarsson
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Explore the profile of Magnus O Ulfarsson including associated specialties, affiliations and a list of published articles.
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29
Citations
970
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Recent Articles
11.
Magnusson M, Agnarsson B, Jonasson J, Tryggvason T, Aeffner F, le Roux L, et al.
Br J Cancer
. 2023 Aug;
129(7):1142-1151.
PMID: 37596405
Background: The TNM system is used to assess prognosis after colorectal cancer (CRC) diagnosis. Other prognostic factors reported include histopathological assessments of the tumour, tumour mutations and proteins in the...
12.
Holm H, Ivarsdottir E, Olafsdottir T, Thorolfsdottir R, Eythorsson E, Norland K, et al.
Commun Med (Lond)
. 2023 Jul;
3(1):94.
PMID: 37414856
Background: Persistent symptoms are common after SARS-CoV-2 infection but correlation with objective measures is unclear. Methods: We invited all 3098 adults who tested SARS-CoV-2 positive in Iceland before October 2020...
13.
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...
14.
Nawaz M, Einarsson G, Bustamante M, Gisladottir R, Walters G, Jonsdottir G, et al.
Brain Commun
. 2022 Nov;
4(6):fcac271.
PMID: 36415660
Intracranial volume, measured through magnetic resonance imaging and/or estimated from head circumference, is heritable and correlates with cognitive traits and several neurological disorders. We performed a genome-wide association study meta-analysis...
15.
Sveinbjornsson G, Ulfarsson M, Thorolfsdottir R, Jonsson B, Einarsson E, Gunnlaugsson G, et al.
Nat Genet
. 2022 Oct;
54(11):1652-1663.
PMID: 36280732
Nonalcoholic fatty liver (NAFL) and its sequelae are growing health problems. We performed a genome-wide association study of NAFL, cirrhosis and hepatocellular carcinoma, and integrated the findings with expression and...
16.
Halldorsson B, Eggertsson H, Moore K, Hauswedell H, Eiriksson O, Ulfarsson M, et al.
Nature
. 2022 Jul;
607(7920):732-740.
PMID: 35859178
Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the...
17.
Silva A, Ehrhart F, Ulfarsson M, Stefansson H, Stefansson K, Wilkinson L, et al.
Biol Psychiatry
. 2022 Jun;
92(5):341-361.
PMID: 35659384
Genomic copy number variants (CNVs) are associated with a high risk of neurodevelopmental disorders. A growing body of genetic studies suggests that these high-risk genetic variants converge in common molecular...
18.
Ferkingstad E, Sulem P, Atlason B, Sveinbjornsson G, Magnusson M, Styrmisdottir E, et al.
Nat Genet
. 2021 Dec;
53(12):1712-1721.
PMID: 34857953
The plasma proteome can help bridge the gap between the genome and diseases. Here we describe genome-wide association studies (GWASs) of plasma protein levels measured with 4,907 aptamers in 35,559...
19.
Eiriksdottir T, Ardal S, Jonsson B, Lund S, Ivarsdottir E, Norland K, et al.
Commun Biol
. 2021 Jun;
4(1):758.
PMID: 34145379
Predicting all-cause mortality risk is challenging and requires extensive medical data. Recently, large-scale proteomics datasets have proven useful for predicting health-related outcomes. Here, we use measurements of levels of 4,684...
20.
Silva A, Kirov G, Kendall K, Bracher-Smith M, Wilkinson L, Hall J, et al.
Biol Psychiatry
. 2021 May;
90(5):307-316.
PMID: 33931204
Background: Copy number variations at the 15q11.2 BP1-BP2 locus are present in 0.5%-1.0% of the population, and the deletion is associated with several neurodevelopmental disorders. Previously, we showed a reciprocal...