Magnus Dehli Vigeland

Bilde av Magnus Dehli Vigeland
English version of this page
Brukernavn
Besøksadresse Kirkeveien 166 Laboratoriebygget 0450 Oslo
Postadresse OUS HF Ullevål sykehus Postboks 4956 Nydalen 0424 Oslo

Publikasjoner

  • Brustad, Hilde Kjelgaard; Vigeland, Magnus Dehli & Egeland, Thore (2020). Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio. International journal of legal medicine (Print).  ISSN 0937-9827. . doi: 10.1007/s00414-020-02426-6
  • 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 Fulltekst i vitenarkiv.
  • Vigeland, Magnus Dehli; Marsico, Franco L.; Herrera Piñero, Mariana & Egeland, Thore (2020). Prioritising family members for genotyping in missing person cases: A general approach combining the statistical power of exclusion and inclusion. Forensic Science International: Genetics.  ISSN 1872-4973.  49:102376, s 1- 10 . doi: 10.1016/j.fsigen.2020.102376 Fulltekst i vitenarkiv.
  • 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 Fulltekst i vitenarkiv.
  • 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 Fulltekst i vitenarkiv.
  • 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 Fulltekst i vitenarkiv.
  • 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 Fulltekst i vitenarkiv.
  • 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 Vis sammendrag
  • 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 Fulltekst i vitenarkiv.
  • 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 Fulltekst i vitenarkiv.
  • 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 Vis sammendrag
  • 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 Fulltekst i vitenarkiv. Vis sammendrag
  • 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 Vis sammendrag
  • 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 Fulltekst i vitenarkiv.
  • 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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Publisert 16. mai 2018 13:16 - Sist endret 13. juni 2019 11:34