Magnus O Ulfarsson
Overview
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
21.
Sonderby I, van der Meer D, Moreau C, Kaufmann T, Walters G, Ellegaard M, et al.
Transl Psychiatry
. 2021 Mar;
11(1):182.
PMID: 33753722
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predisposed to multiple neurodevelopmental disorders, including schizophrenia, autism and intellectual disability. Human carriers display a high prevalence of...
22.
Sonderby I, Ching C, Thomopoulos S, van der Meer D, Sun D, Villalon-Reina J, et al.
Hum Brain Mapp
. 2021 Feb;
43(1):300-328.
PMID: 33615640
The Enhancing NeuroImaging Genetics through Meta-Analysis copy number variant (ENIGMA-CNV) and 22q11.2 Deletion Syndrome Working Groups (22q-ENIGMA WGs) were created to gain insight into the involvement of genetic factors in...
23.
Gisladottir R, Ivarsdottir E, Helgason A, Jonsson L, Hannesdottir N, Rutsdottir G, et al.
Curr Biol
. 2020 Oct;
30(23):4643-4653.e3.
PMID: 33035477
Olfactory receptor (OR) genes in humans form a special class characterized by unusually high DNA sequence diversity, which should give rise to differences in perception and behavior. In the largest...
24.
van der Meer D, Sonderby I, Kaufmann T, Walters G, Abdellaoui A, Ames D, et al.
JAMA Psychiatry
. 2019 Oct;
77(4):420-430.
PMID: 31665216
Importance: Recurrent microdeletions and duplications in the genomic region 15q11.2 between breakpoints 1 (BP1) and 2 (BP2) are associated with neurodevelopmental disorders. These structural variants are present in 0.5% to...
25.
Sonderby I, Gustafsson O, Doan N, Hibar D, Martin-Brevet S, Abdellaoui A, et al.
Mol Psychiatry
. 2019 Feb;
25(3):692-695.
PMID: 30705424
Prior to and following the publication of this article the authors noted that the complete list of authors was not included in the main article and was only present in...
26.
Silva A, Ulfarsson M, Stefansson H, Gustafsson O, Walters G, Linden D, et al.
Biol Psychiatry
. 2018 Dec;
85(7):563-572.
PMID: 30583851
Background: The 15q11.2 BP1-BP2 cytogenetic region has been associated with learning and motor delays, autism, and schizophrenia. This region includes a gene that codes for the cytoplasmic FMR1 interacting protein...
27.
Sonderby I, Gustafsson O, Doan N, Hibar D, Martin-Brevet S, Abdellaoui A, et al.
Mol Psychiatry
. 2018 Oct;
25(3):584-602.
PMID: 30283035
Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to e.g., autism spectrum disorder and schizophrenia. We...
28.
Walters G, Gustafsson O, Sveinbjornsson G, Eiriksdottir V, Agustsdottir A, Jonsdottir G, et al.
Nat Commun
. 2018 Aug;
9(1):3456.
PMID: 30150678
Discovery of coding variants in genes that confer risk of neurodevelopmental disorders is an important step towards understanding the pathophysiology of these disorders. Whole-genome sequencing of 31,463 Icelanders uncovers a...
29.
Hernandez-Garcia L, Ulfarsson M
Magn Reson Imaging
. 2011 Jan;
29(3):353-64.
PMID: 21232893
An iterative estimation algorithm for deconvolution of neuronal activity from Blood Oxygen Level Dependent (BOLD) time series data is presented. The algorithm requires knowledge of the hemodynamic impulse response function...