Magnus Dehli Vigeland

Postdoctoral Fellow - Department of Medical Genetics
Image of Magnus Dehli Vigeland
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Visiting address Kirkeveien 166 Laboratoriebygget 0450 OSLO
Postal address Postboks 4956 Nydalen 0424 OSLO

Publications

  • Børte, Sigrid; Zwart, John-Anker; Skogholt, Anne Heidi; Gabrielsen, Maiken Elvestad; Thomas, Laurent; Fritsche, Lars G; Surakke, Ida; Nielsen, Jonas B.; Zhou, Wei; Wolford, Brooke; Vigeland, Magnus Dehli; Hagen, Knut; Kristoffersen, Espen Saxhaug; Nyholt, Dale R; Chasman, Daniel I; Brumpton, Ben Michael; Willer, Christen & Winsvold, Bendik K S (2020). Mitochondrial genome-wide association study of migraine – the HUNT Study. Cephalalgia.  ISSN 0333-1024.  40(6), s 625- 634 . doi: 10.1177/0333102420906835 Full text in Research Archive.
  • Aslaksen, Sigrid; Methlie, Paal; Vigeland, Magnus Dehli; Jøssang, Dag Eirik; Wolff, Anette Susanne Bøe; Sheng, Ying; Oftedal, Bergithe Eikeland; Skinningsrud, Beate; Undlien, Dag Erik; Selmer, Kaja Kristine; Husebye, Eystein Sverre & Bratland, Eirik (2019). Coexistence of congenital adrenal hyperplasia and autoimmune Addison's disease. Frontiers in Endocrinology.  ISSN 1664-2392.  10:648, s 1- 5 . doi: 10.3389/fendo.2019.00648 Full text in Research Archive.
  • Aslaksen, Sigrid; Wolff, Anette Susanne Bøe; Vigeland, Magnus Dehli; Breivik, Lars Ertesvåg; Sheng, Ying; Oftedal, Bergithe Eikeland; Skinningsrud, Beate; Undlien, Dag Erik; Selmer, Kaja Kristine; Husebye, Eystein Sverre & Bratland, Eirik (2019). Identification and characterization of rare Toll-like receptor 3 variants in patients with autoimmune Addison’s disease. Journal of translational autoimmunity.  ISSN 2589-9090.  1 . doi: 10.1016/j.jtauto.2019.100005 Full text in Research Archive.
  • Berger, Toni; Vigeland, Magnus Dehli; Hjorthaug, Hanne Sagsveen; Etholm, Lars; Nome, Cecilie; Taubøll, Erik; Heuser, Kjell & Selmer, Kaja Kristine (2019). Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis. PLOS ONE.  ISSN 1932-6203.  14:e0226575(12), s 1- 32 . doi: 10.1371/journal.pone.0226575 Full text in Research Archive.
  • Rydning, Siri Lynne; Koht, Jeanette; Sheng, Ying; Sowa, Piotr; Hjorthaug, Hanne Sagsveen; Wedding, Iselin Marie; ERICHSEN, ANNE KJERSTI; Hynås, Inger Anette; Backe, Paul Hoff; Tallaksen, Chantal; Vigeland, Magnus Dehli & Selmer, Kaja Kristine (2019). Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis. Brain.  ISSN 0006-8950.  142:e12(4), s 1- 5 . doi: 10.1093/brain/awz041 Full text in Research Archive.
  • Vigeland, Magnus Dehli & Egeland, Thore (2019). Handling founder inbreeding in forensic kinship analysis. Forensic Science International: Genetics Supplement Series.  ISSN 1875-1768. . doi: 10.1016/j.fsigss.2019.10.175
  • Menke, Leonie A.; Gardeitchik, Thatjana; Hammond, Peter; Heimdal, Ketil Riddervold; Houge, Gunnar; Hufnagel, Sophia B.; Ji, Jianling; Johansson, Stefan; Kant, Sarina G.; Kinning, Esther; Leon, Eyby L.; Newbury-Ecob, Ruth; Paolacci, Stefano; Pfundt, Rolph; Ragge, Nicola K.; Rinne, Tuula; Ruivenkamp, Claudia; Saitta, Sulagna C.; Sun, Yu; Tartaglia, Marco; Terhal, Paulien A.; van Essen, Anthony J.; Vigeland, Magnus Dehli; Xiao, Bing & Hennekam, Raoul C. (2018). Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome. American Journal of Medical Genetics. Part A.  ISSN 1552-4825.  176(4), s 862- 876 . doi: 10.1002/ajmg.a.38626 Show summary
  • Rydning, Siri Lynne; Dudesek, Ales; Rimmele, Florian; Funke, Claudia; Krüger, Stefanie; Biskup, Saskia; Vigeland, Magnus Dehli; Hjorthaug, Hanne Sagsveen; Sejersted, Yngve; Tallaksen, Chantal; Selmer, Kaja Kristine & Kamm, Christoph (2018). A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European Journal of Neurology.  ISSN 1351-5101.  25(7), s 943- 948 . doi: 10.1111/ene.13625
  • Kling, Daniel; Egeland, Thore; Pinero, Mariana Herrera & Vigeland, Magnus Dehli (2017). Evaluating the statistical power of DNA-based identification, exemplified by `The missing grandchildren of Argentina?. Forensic Science International: Genetics.  ISSN 1872-4973.  31, s 57- 66 . doi: 10.1016/j.fsigen.2017.08.006
  • Low, Karen J.; Ansari, M; Abou Jamra, Rami; Clarke, Angus; El Chehadeh, Salima; FitzPatrick, David R.; Greenslade, Mark; Henderson, Alex; Hurst, Jane; Keller, Kory; Kuentz, Paul; Prescott, Trine; Rössler, Franziska; Selmer, Kaja Kristine; Schneider, Michael C.; Stewart, Fiona; Tatton-Brown, Katrina; Thevenon, Julien; Vigeland, Magnus Dehli; Vogt, Julie; Willems, Marjolaine; Zonana, Jonathan & Smithson, Sarah (2017). PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features. European Journal of Human Genetics.  ISSN 1018-4813.  25(5), s 552- 559 . doi: 10.1038/ejhg.2017.27
  • Mero, Inger-Lise; Mørk, Hanne Håberg; Sheng, Ying; Blomhoff, Anne; Opheim, Gun Lisbeth; Erichsen, Aage; Vigeland, Magnus Dehli & Selmer, Kaja Kristine (2017). Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures. Human Molecular Genetics.  ISSN 0964-6906.  26(19), s 3792- 3796 . doi: 10.1093/hmg/ddx263
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying; Yang, Mingyi; Lin, Xiaolin; Slupphaug, Geir; Nordenmark, Tonje Haug; Vigeland, Magnus Dehli; Bjørås, Magnar; Tallaksen, Chantal & Selmer, Kaja Kristine (2017). Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics.  ISSN 0964-6906.  26(6), s 1031- 1040 . doi: 10.1093/hmg/ddw391 Full text in Research Archive.
  • Barøy, Tuva; Pedurupillay Jesuthasan, Christeen Ramane; Bliksrud, Yngve Thomas; Rasmussen, Magnhild; Holmgren, Asbjørn; Vigeland, Magnus Dehli; Hughes, Timothy; Brink, Maaike; Rodenburg, Richard J.; Nedregaard, Bård; Strømme, Petter; Frengen, Eirik & Misceo, Doriana (2016). A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. European Journal of Medical Genetics.  ISSN 1769-7212.  59(6-7), s 342- 346 . doi: 10.1016/j.ejmg.2016.05.005
  • Dørum, Guro; Kling, Daniel; Tillmar, Andreas; Vigeland, Magnus Dehli & Egeland, Thore (2016). Mixtures with relatives and linked markers. International journal of legal medicine (Print).  ISSN 0937-9827.  130(3), s 621- 634 . doi: 10.1007/s00414-015-1288-x
  • Lien, Sigbjørn; Koop, Ben F; Sandve, Simen Rød; Miller, Jason R.; Kent, Matthew Peter; Nome, Torfinn; Hvidsten, Torgeir Rhoden; Leong, Jong; Minkley, David R.; Zimin, Aleksey; Grammes, Fabian; Grove, Harald; Gjuvsland, Arne Bjørke; Walenz, Brian; Hermansen, Russell A.; von Schalburg, Kristian R.; Rondeau, Eric; Genova, Alex Di; Antony Samy, Jeevan Karloss; Vik, Jon Olav; Vigeland, Magnus Dehli; Caler, Lis; Grimholt, Unni; Jentoft, Sissel; Våge, Dag Inge; de Jong, Pieter J.; Moen, Thomas; Baranski, Matthew; Palti, Yniv; Smith, Douglas W.; Yorke, James A.; Nederbragt, Alexander J.; Tooming-Klunderud, Ave; Jakobsen, Kjetill Sigurd; Jiang, Xuanting; Fan, Dingding; Hu, Yan; Liberles, David A.; Vidal, Rodrigo; Iturra, Patricia; Jones, Steven J.M.; Jonassen, Inge; Maass, Alejandro; Omholt, Stig William & Davidson, William S (2016). The Atlantic salmon genome provides insights into rediploidization. Nature.  ISSN 0028-0836.  533(7602), s 200- 205 . doi: 10.1038/nature17164 Full text in Research Archive.
  • Lund, Caroline; Striano, Pasquale; Sorte, Hanne Sørmo; Parisi, Pasquale; Iacomino, Michele; Sheng, Ying; Vigeland, Magnus Dehli; Øye, Ane-Marte; Steensbjerre Møller, Rikke; Selmer, Kaja Kristine & Zara, Federico (2016). Exome sequencing fails to identify the genetic cause of Aicardi syndrome. Molecular Syndromology.  ISSN 1661-8769.  7(4), s 234- 238 . doi: 10.1159/000448367
  • Moen, Marivi Nabong; Fjær, Roar; Hamdani, El Hassan; Lærdahl, Jon Kristen; Menchini, Robin Johansen; Vigeland, Magnus Dehli; Sheng, Ying; Undlien, Dag Erik; Hassel, Bjørnar; Salih, MA; Khashab, HY; Selmer, Kaja Kristine & Chaudhry, Farrukh Abbas (2016). Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport. Brain.  ISSN 0006-8950.  139, s 3109- 3120 . doi: 10.1093/brain/aww244
  • Pedurupillay Jesuthasan, Christeen Ramane; Landsend, Erlend Christoffer Sommer; Vigeland, Magnus Dehli; Ansar, Muhammad; Frengen, Eirik; Misceo, Doriana & Strømme, Petter (2016). Segregation of incomplete achromatopsia and alopecia due to PDE6H and LPAR6 variants in a consanguineous family from Pakistan. Genes.  ISSN 2073-4425.  7(8) . doi: 10.3390/genes7080041 Show summary
  • Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Chawla, Maninder Singh; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Selmer, Kaja Kristine & Tallaksen, Chantal (2016). A founder mutation p.H701P identified as a major cause of SPG7 in Norway. European Journal of Neurology.  ISSN 1351-5101.  23(4), s 763- 771 . doi: 10.1111/ene.12937 Full text in Research Archive. Show summary
  • Sorte, Hanne Sørmo; Osnes, Liv T. N.; Fevang, Børre; Aukrust, Pål; Erichsen, Hans Christian; Backe, Paul Hoff; Abrahamsen, Tore G; Kittang, Ole Bjørn; Øverland, Torstein; Jhangiani, Shalini N.; Muzny, Donna M.; Vigeland, Magnus Dehli; Samarakoon, Pubudu Saneth; Gambin, Tomasz; Akdemir, Zeynep H.C.; Gibbs, Richard A.; Rødningen, Olaug Kristin; Lyle, Robert; Lupski, James R. & Stray-Pedersen, Asbjørg (2016). A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction. Molecular Genetics & Genomic Medicine.  ISSN 2324-9269.  4(6), s 604- 616 . doi: 10.1002/mgg3.237
  • Vigeland, Magnus Dehli; Stormo, Kristina & Selmer, Kaja Kristine (2016). FILTUS: A desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector. Bioinformatics.  ISSN 1367-4803.  32(10), s 1592- 1594 . doi: 10.1093/bioinformatics/btw046
  • Christeen Ramane, Pedurupillay Jesuthasan; Barøy, Tuva; Holmgren, Asbjørn; Blomhoff, Anne; Vigeland, Magnus Dehli; Sheng, Ying; Frengen, Eirik; Strømme, Petter & Misceo, Doriana (2015). Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B. American Journal of Medical Genetics. Part A.  ISSN 1552-4825.  167(3), s 657- 663 . doi: 10.1002/ajmg.a.36944
  • Fjær, Roar; Brodtkorb, Eylert; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Kvistad, Kjell Arne; Backe, Paul Hoff & Selmer, Kaja Kristine (2015). Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2. European Journal of Medical Genetics.  ISSN 1769-7212.  58(11), s 624- 628 . doi: 10.1016/j.ejmg.2015.10.005 Show summary
  • Egeland, Thore; Dørum, Guro; Vigeland, Magnus Dehli & Sheehan, Nuala (2014). Mixtures with relatives: A pedigree perspective. Forensic Science International: Genetics.  ISSN 1872-4973.  10, s 49- 54 . doi: 10.1016/j.fsigen.2014.01.007
  • Egeland, Thore; Pinto, Nádia & Vigeland, Magnus Dehli (2014). A general approach to power calculation for relationship testing. Forensic Science International: Genetics.  ISSN 1872-4973.  9, s 186- 190 . doi: 10.1016/j.fsigen.2013.05.001
  • Vigeland, Magnus Dehli; Spannagl, Manuel; Asp, Torben; Paina, Cristiana; Rudi, Heidi; Rognli, Odd Arne; Fjellheim, Siri & Sandve, Simen Rød (2013). Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor. New Phytologist.  ISSN 0028-646X.  199(4), s 1060- 1068 . doi: 10.1111/nph.12337 Full text in Research Archive.
  • Colman, Jonathan Edward; Lilleeng, Marte Synnøve; Tsegaye, Diress; Vigeland, Magnus Dehli & Reimers, Eigil (2012). Responses of wild reindeer (Rangifer tarandus tarandus) when provoked by a snow-kiter or skier: A model approach. Applied Animal Behaviour Science.  ISSN 0168-1591.  142(1-2), s 82- 89 . doi: 10.1016/j.applanim.2012.08.009
  • Gervin, Kristina; Vigeland, Magnus Dehli; Mattingsdal, Morten; Hammerø, Martin; Nygård, Heidi; Olsen, Anne Olaug; Brandt, Ingunn; Harris, Jennifer; Undlien, Dag Erik & Lyle, Robert (2012). DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes. PLoS Genetics.  ISSN 1553-7390.  8(1) . doi: 10.1371/journal.pgen.1002454
  • Stavik, Benedicte; Skretting, Grethe; Olstad, Ole Kristoffer; Sletten, Marit; Vigeland, Magnus Dehli; Sandset, Per Morten & Iversen, Nina (2012). TFPI Alpha and Beta Regulate mRNAs and microRNAs Involved in Cancer Biology and in the Immune System in Breast Cancer Cells. PLOS ONE.  ISSN 1932-6203.  7(10) . doi: 10.1371/journal.pone.0047184
  • Vigeland, Magnus Dehli; Selmer, Kaja Kristine & Egeland, Thore (2012). Statistical methods in genetics, In Marit Bragelien Veierød; Stian Lydersen & Petter Laake (ed.),  Medical statistics in clinical and epidemiological research.  Gyldendal Akademisk.  ISBN 9788205399594.  Kap 18.
  • Sandve, Simen Rød; Rudi, Heidi; Dørum, Guro; Vigeland, Magnus Dehli; Berg, Paul Ragnar & Rognli, Odd Arne (2010). Genotyping Unknown Genomic Terrain in Complex Plant Genomes, In Christian Huyghe (ed.),  Sustainable use of Genetic Diversity in Forage and Turf Breeding.  Springer Science+Business Media B.V..  ISBN 9789048187058.  Kapittel 67.  s 455 - 459
  • Vigeland, Magnus Dehli (2010). Smooth tropical surfaces with infinitely many tropical lines. Arkiv för matematik.  ISSN 0004-2080.  48(1), s 177- 206 . doi: 10.1007/s11512-009-0116-2
  • Vigeland, Magnus Dehli (2009). THE GROUP LAW ON A TROPICAL ELLIPTIC CURVE. Mathematica Scandinavica.  ISSN 0025-5521.  104(2), s 188- 204 . doi: http://www.mscand.dk/article.php?id=3141

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  • Storvik, Geir Olve; Vigeland, Magnus Dehli; Caliebe, Amke & Egeland, Thore (2018). Specification of mutation probabilities through Metropolis-Hastings steps.
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying; Yang, Mingyi; Lin, Xiaolin; Slupphaug, Geir; Nordenmark, Tonje Haug; Vigeland, Magnus Dehli; Bjørås, Magnar; Tallaksen, Chantal & Selmer, Kaja Kristine (2017). Corrigendum: Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics.  ISSN 0964-6906.  26(6), s 1217- 1218 . doi: 10.1093/hmg/ddx072
  • Fjellheim, Siri; Li, Chuan; Vigeland, Magnus Dehli; Rognli, Odd Arne & Sandve, Simen Rød (2012). Molecular Evolution of Pooideae Adaptation to Cool Climates.
  • Vigeland, Magnus Dehli (2004). Sjongleringsmatematikk og håndståendefysikk.
  • Vigeland, Magnus Dehli (2004). Sjongleringsmatematikk og håndståendefysikk.

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Published May 16, 2018 1:19 PM - Last modified June 13, 2019 11:35 AM