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Magnus Dehli Vigeland
Magnus Dehli Vigeland
Senior scientist, Department of Forensic Sciences, Oslo University Hospital, Norway
Verified email at medisin.uio.no - Homepage
Title
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Cited by
Year
The Atlantic salmon genome provides insights into rediploidization
S Lien, BF Koop, SR Sandve, JR Miller, MP Kent, T Nome, TR Hvidsten, ...
Nature 533 (7602), 200-205, 2016
9992016
DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes
K Gervin, MD Vigeland, M Mattingsdal, M Hammerø, H Nygård, AO Olsen, ...
PLoS genetics 8 (1), e1002454, 2012
1842012
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein–Taybi syndrome
LA Menke, DDD study, T Gardeitchik, P Hammond, KR Heimdal, G Houge, ...
American Journal of Medical Genetics Part A 176 (4), 862-876, 2018
682018
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T‐cell dysfunction
HS Sorte, LT Osnes, B Fevang, P Aukrust, HC Erichsen, PH Backe, ...
Molecular Genetics & Genomic Medicine 4 (6), 604-616, 2016
672016
FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector
MD Vigeland, KS Gjøtterud, KK Selmer
Bioinformatics 32 (10), 1592-1594, 2016
602016
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features
KJ Low, M Ansari, R Abou Jamra, A Clarke, S El Chehadeh, ...
European Journal of Human Genetics 25 (5), 552-559, 2017
522017
Evidence for adaptive evolution of low‐temperature stress response genes in a Pooideae grass ancestor
MD Vigeland, M Spannagl, T Asp, C Paina, H Rudi, OA Rognli, ...
New Phytologist 199 (4), 1060-1068, 2013
482013
Novel UCHL1 mutations reveal new insights into ubiquitin processing
SL Rydning, PH Backe, MML Sousa, Z Iqbal, AM Øye, Y Sheng, M Yang, ...
Human molecular genetics 26 (6), 1031-1040, 2017
442017
The group law on a tropical elliptic curve
MD Vigeland
Mathematica scandinavica, 188-204, 2009
43*2009
Smooth tropical surfaces with infinitely many tropical lines
MD Vigeland
Arkiv för Matematik 48 (1), 177-206, 2010
412010
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport
MN Moen, R Fjær, EH Hamdani, JK Laerdahl, RJ Menchini, MD Vigeland, ...
Brain 139 (12), 3109-3120, 2016
392016
A general approach to power calculation for relationship testing
T Egeland, N Pinto, MD Vigeland
Forensic Science International: Genetics 9, 186-190, 2014
322014
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia
SL Rydning, A Dudesek, F Rimmele, C Funke, S Krüger, S Biskup, ...
European journal of neurology 25 (7), 943-e71, 2018
302018
Mitochondrial genome-wide association study of migraine–the HUNT Study
S Børte, JA Zwart, AH Skogholt, ME Gabrielsen, LF Thomas, LG Fritsche, ...
Cephalalgia 40 (6), 625-634, 2020
282020
Tropical lines on cubic surfaces
M Panizzut, MD Vigeland
arXiv preprint arXiv:0708.3847, 2007
28*2007
A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13
T Barøy, CRJ Pedurupillay, YT Bliksrud, M Rasmussen, A Holmgren, ...
European journal of medical genetics 59 (6-7), 342-346, 2016
272016
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7
L Castilla-Vallmanya, KK Selmer, C Dimartino, R Rabionet, ...
Genetics in Medicine 22 (7), 1215-1226, 2020
252020
Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis
TC Berger, MD Vigeland, HS Hjorthaug, L Etholm, CG Nome, E Taubøll, ...
PLoS One 14 (12), e0226575, 2019
252019
Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis
SL Rydning, J Koht, Y Sheng, P Sowa, HS Hjorthaug, IM Wedding, ...
Brain 142 (4), e12-e12, 2019
252019
Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2
R Fjaer, E Brodtkorb, AM Øye, Y Sheng, MD Vigeland, KA Kvistad, ...
European Journal of Medical Genetics 58 (11), 624-628, 2015
252015
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