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Showing results 1-40 of 40

2020
1 Brustad, Hilde Kjelgaard; Vigeland, Magnus Dehli; Egeland, Thore.
Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio. International journal of legal medicine (Print) 2020 p. -
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2 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.
Mitochondrial genome-wide association study of migraine – the HUNT Study. Cephalalgia 2020 ;Volume 40.(6) p. 625-634
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3 Vigeland, Magnus Dehli; Marsico, Franco L.; Herrera Piñero, Mariana; Egeland, Thore.
Prioritising family members for genotyping in missing person cases: A general approach combining the statistical power of exclusion and inclusion. Forensic Science International: Genetics 2020 ;Volume 49:102376. p. 1-10
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2019
4 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.
Coexistence of congenital adrenal hyperplasia and autoimmune Addison's disease. Frontiers in Endocrinology 2019 ;Volume 10:648. p. 1-5
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5 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.
Identification and characterization of rare Toll-like receptor 3 variants in patients with autoimmune Addison’s disease. Journal of translational autoimmunity 2019 ;Volume 1.
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6 Berger, Toni; Vigeland, Magnus Dehli; Hjorthaug, Hanne Sagsveen; Etholm, Lars; Nome, Cecilie; Taubøll, Erik; Heuser, Kjell; Selmer, Kaja Kristine.
Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis. PLOS ONE 2019 ;Volume 14:e0226575.(12) p. 1-32
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7 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.
Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis. Brain 2019 ;Volume 142:e12.(4) p. 1-5
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8 Vigeland, Magnus Dehli; Egeland, Thore.
Handling founder inbreeding in forensic kinship analysis. Forensic Science International: Genetics Supplement Series 2019
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2018
9 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..
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome. American Journal of Medical Genetics. Part A 2018 ;Volume 176.(4) p. 862-876
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10 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.
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European Journal of Neurology 2018 ;Volume 25.(7) p. 943-948
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11 Storvik, Geir Olve; Vigeland, Magnus Dehli; Caliebe, Amke; Egeland, Thore.
Specification of mutation probabilities through Metropolis-Hastings steps. Advanced Statistical and Stochastic Methods in Forensic Genetics; 2018-08-27 - 2018-08-31
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2017
12 Kling, Daniel; Egeland, Thore; Pinero, Mariana Herrera; Vigeland, Magnus Dehli.
Evaluating the statistical power of DNA-based identification, exemplified by `The missing grandchildren of Argentina?. Forensic Science International: Genetics 2017 ;Volume 31. p. 57-66
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13 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.
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features. European Journal of Human Genetics 2017 ;Volume 25.(5) p. 552-559
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14 Mero, Inger-Lise; Mørk, Hanne Håberg; Sheng, Ying; Blomhoff, Anne; Opheim, Gun Lisbeth; Erichsen, Aage; Vigeland, Magnus Dehli; Selmer, Kaja Kristine.
Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures. Human Molecular Genetics 2017 ;Volume 26.(19) p. 3792-3796
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15 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.
Corrigendum: Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics 2017 ;Volume 26.(6) p. 1217-1218
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16 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.
Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics 2017 ;Volume 26.(6) p. 1031-1040
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2016
17 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.
A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. European Journal of Medical Genetics 2016 ;Volume 59.(6-7) p. 342-346
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18 Dørum, Guro; Kling, Daniel; Tillmar, Andreas; Vigeland, Magnus Dehli; Egeland, Thore.
Mixtures with relatives and linked markers. International journal of legal medicine (Print) 2016 ;Volume 130.(3) p. 621-634
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19 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.
The Atlantic salmon genome provides insights into rediploidization. Nature 2016 ;Volume 533.(7602) p. 200-205
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20 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.
Exome sequencing fails to identify the genetic cause of Aicardi syndrome. Molecular Syndromology 2016 ;Volume 7.(4) p. 234-238
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21 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.
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport. Brain 2016 ;Volume 139. p. 3109-3120
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22 Pedurupillay Jesuthasan, Christeen Ramane; Landsend, Erlend Christoffer Sommer; Vigeland, Magnus Dehli; Ansar, Muhammad; Frengen, Eirik; Misceo, Doriana; Strømme, Petter.
Segregation of incomplete achromatopsia and alopecia due to PDE6H and LPAR6 variants in a consanguineous family from Pakistan. Genes 2016 ;Volume 7.(8) p. -
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23 Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Chawla, Maninder Singh; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Selmer, Kaja Kristine; Tallaksen, Chantal.
A founder mutation p.H701P identified as a major cause of SPG7 in Norway. European Journal of Neurology 2016 ;Volume 23.(4) p. 763-771
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24 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.
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction. Molecular Genetics & Genomic Medicine 2016 ;Volume 4.(6) p. 604-616
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25 Vigeland, Magnus Dehli; Stormo, Kristina; Selmer, Kaja Kristine.
FILTUS: A desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector. Bioinformatics 2016 ;Volume 32.(10) p. 1592-1594
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2015
26 Christeen Ramane, Pedurupillay Jesuthasan; Barøy, Tuva; Holmgren, Asbjørn; Blomhoff, Anne; Vigeland, Magnus Dehli; Sheng, Ying; Frengen, Eirik; Strømme, Petter; Misceo, Doriana.
Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B. American Journal of Medical Genetics. Part A 2015 ;Volume 167.(3) p. 657-663
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27 Fjær, Roar; Brodtkorb, Eylert; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Kvistad, Kjell Arne; Backe, Paul Hoff; Selmer, Kaja Kristine.
Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2. European Journal of Medical Genetics 2015 ;Volume 58.(11) p. 624-628
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2014
28 Egeland, Thore; Dørum, Guro; Vigeland, Magnus Dehli; Sheehan, Nuala.
Mixtures with relatives: A pedigree perspective. Forensic Science International: Genetics 2014 ;Volume 10. p. 49-54
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29 Egeland, Thore; Pinto, Nádia; Vigeland, Magnus Dehli.
A general approach to power calculation for relationship testing. Forensic Science International: Genetics 2014 ;Volume 9. p. 186-190
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2013
30 Vigeland, Magnus Dehli; Spannagl, Manuel; Asp, Torben; Paina, Cristiana; Rudi, Heidi; Rognli, Odd Arne; Fjellheim, Siri; Sandve, Simen Rød.
Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor. New Phytologist 2013 ;Volume 199.(4) p. 1060-1068
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2012
31 Colman, Jonathan Edward; Lilleeng, Marte Synnøve; Tsegaye, Diress; Vigeland, Magnus Dehli; Reimers, Eigil.
Responses of wild reindeer (Rangifer tarandus tarandus) when provoked by a snow-kiter or skier: A model approach. Applied Animal Behaviour Science 2012 ;Volume 142.(1-2) p. 82-89
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32 Fjellheim, Siri; Li, Chuan; Vigeland, Magnus Dehli; Rognli, Odd Arne; Sandve, Simen Rød.
Molecular Evolution of Pooideae Adaptation to Cool Climates. VIPCA I 2012 Molecular Ecology; 2012-02-01 - 2012-02-07
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33 Gervin, Kristina; Vigeland, Magnus Dehli; Mattingsdal, Morten; Hammerø, Martin; Nygård, Heidi; Olsen, Anne Olaug; Brandt, Ingunn; Harris, Jennifer; Undlien, Dag Erik; Lyle, Robert.
DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes. PLoS Genetics 2012 ;Volume 8.(1) p. -
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34 Stavik, Benedicte; Skretting, Grethe; Olstad, Ole Kristoffer; Sletten, Marit; Vigeland, Magnus Dehli; Sandset, Per Morten; Iversen, Nina.
TFPI Alpha and Beta Regulate mRNAs and microRNAs Involved in Cancer Biology and in the Immune System in Breast Cancer Cells. PLOS ONE 2012 ;Volume 7.(10) p. -
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35 Vigeland, Magnus Dehli; Selmer, Kaja Kristine; Egeland, Thore.
Statistical methods in genetics. I: Medical statistics in clinical and epidemiological research. Gyldendal Akademisk 2012 ISBN 9788205399594.
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2010
36 Sandve, Simen Rød; Rudi, Heidi; Dørum, Guro; Vigeland, Magnus Dehli; Berg, Paul Ragnar; Rognli, Odd Arne.
Genotyping Unknown Genomic Terrain in Complex Plant Genomes. I: Sustainable use of Genetic Diversity in Forage and Turf Breeding. Springer Science+Business Media B.V. 2010 ISBN 9789048187058. p. 455-459
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37 Vigeland, Magnus Dehli.
Smooth tropical surfaces with infinitely many tropical lines. Arkiv för matematik 2010 ;Volume 48.(1) p. 177-206
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2009
38 Vigeland, Magnus Dehli.
THE GROUP LAW ON A TROPICAL ELLIPTIC CURVE. Mathematica Scandinavica 2009 ;Volume 104.(2) p. 188-204
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2004
39 Vigeland, Magnus Dehli.
Sjongleringsmatematikk og håndståendefysikk. Fagdag i matematikk; 2004-03-10
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40 Vigeland, Magnus Dehli.
Sjongleringsmatematikk og håndståendefysikk. Skolebesøk; 2004-03-17
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