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Showing results 1-50 of 60
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2024
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1. |
Bjørnstad, Pål Marius; aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette; Dalland, Marianne; Sjursen, Wenche; Carrizosa, Christian; Vigeland, Magnus Dehli; Sorte, Hanne Sørmo; Sheng, Ying; Ariansen, Sarah Louise; Grindedal, Eli Marie; Gilfillan, Gregor. Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01494-7). European Journal of Human Genetics 2024 p. - UiO OUS NTNU STO
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2023
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2. |
Bjørnstad, Pål Marius; Aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette; Dalland, Marianne; Sjursen, Wenche; Balmont, Christian Carrizosa; Vigeland, Magnus Dehli; Sorte, Hanne Sørmo; Sheng, Ying; Ariansen, Sarah Louise; Grindedal, Eli Marie; Gilfillan, Gregor. A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing. European Journal of Human Genetics 2023 ;Volume 00.(xx) p. - UiO OUS NTNU STO
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Fantinato, Chiara; Fonneløp, Ane Elida; Bleka, Øyvind; Vigeland, Magnus Dehli; Gill, Peter. The invisible witness: air and dust as DNA evidence of human occupancy in indoor premises. Scientific Reports 2023 ;Volume 13:19059.(1) p. 1-16 OUS UiO
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Vigeland, Magnus Dehli. Two-locus identity coefficients in pedigrees. G3: Genes, Genomes, Genetics 2023 ;Volume 13:jkac326.(2) p. 1-13 UiO OUS
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Vigeland, Maria Dehli; Flåm, Siri Tennebø; Vigeland, Magnus Dehli; Espeland, Ansgar; Zucknick, Manuela; Wigemyr, Monica; Bråten, Lars Christian Haugli; Gjefsen, Elisabeth; Zwart, John Anker Henrik; Storheim, Kjersti; Pedersen, Linda Margareth; Selmer, Kaja Kristine; Lie, Benedicte Alexandra; Gervin, Kristina. Long-Term Use of Amoxicillin Is Associated with Changes in Gene Expression and DNA Methylation in Patients with Low Back Pain and Modic Changes. Antibiotics 2023 ;Volume 12.(7) p. - UiO OUS UiB HAUKELAND OSLOMET
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Wiedmann, Markus; Jensen Steinsvåg, Ingunn; Dinh, Tovy; Vigeland, Magnus Dehli; Larsson, Pål Gunnar; Hjorthaug, Hanne Sagsveen; Sheng, Ying; Mero, Inger-Lise; Selmer, Kaja Kristine. Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study. Brain and Spine 2023 ;Volume 3. p. - OUS UiO
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2022
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7. |
Panizzut, Marta; Vigeland, Magnus Dehli. TROPICAL LINES on CUBIC SURFACES. SIAM Journal on Discrete Mathematics 2022 ;Volume 36.(1) p. 383-410 OUS UiO
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Rajan, Deepa S.; Kour, Sukhleen; Fortuna, Tyler R.; Cousin, Margot A.; Barnett, Sarah S.; Niu, Zhiyv; Babovic-Vuksanovic, Dusica; Klee, Eric W.; Kirmse, Brian; Innes, Micheil; Rydning, Siri Lynne; Selmer, Kaja Kristine; Vigeland, Magnus Dehli; ERICHSEN, ANNE KJERSTI; Nemeth, Andrea H.; Millan, Francisca; DeVile, Catherine; Fawcett, Katherine; Legendre, Adrien; Sims, David; Schnekenberg, Ricardo Parolin; Burglen, Lydie; Mercier, Sandra; Bakhtiari, Somayeh; Francisco-Velilla, Rosario; Embarc-Buh, Azman; Martinez-Salas, Encarnacion; Wigby, Kristen; Lenberg, Jerica; Friedman, Jennifer R.; Kruer, Michael C.; Pandey, Udai Bhan. Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5. Frontiers in Cell and Developmental Biology 2022 ;Volume 10:783762. p. 1-14 UiO OUS
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Ratajska, Aleksandra; Vigeland, Magnus Dehli; Wirgenes, Katrine Verena; Krohg-Sørensen, Kirsten; Paus, Benedicte. The use of segregation analysis in interpretation of sequence variants in SMAD3: A case report. Molecular Genetics & Genomic Medicine 2022 p. - OUS UiO
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Tønne, Elin; Due-Tønnessen, Bernt Johan; Vigeland, Magnus Dehli; Amundsen, Silja Svanstrøm; Ribarska, Teodora Plamenova; Åsten, Pamela; Sheng, Ying; Helseth, Eirik; Gilfillan, Gregor; Mero, Inger-Lise; Heimdal, Ketil Riddervold. Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways. American Journal of Medical Genetics. Part A 2022 ;Volume 188A.(5) p. 1464-1475 OUS UiO LDS
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Vigeland, Magnus Dehli. QuickPed: an online tool for drawing pedigrees and analysing relatedness. BMC Bioinformatics 2022 ;Volume 23:220.(1) p. 1-8 UiO OUS
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Vigeland, Maria Dehli; Flåm, Siri Tennebø; Vigeland, Magnus Dehli; Espeland, Ansgar; Kristoffersen, Per Martin; Vetti, Nils; Wigemyr, Monica; Bråten, Lars Christian Haugli; Gjefsen, Elisabeth; Schistad, Ellina Iordanova; Haugen, Anne Julsrud; Froholdt, Anne; Skouen, Jan Sture; Zwart, John Anker Henrik; Storheim, Kjersti; Pedersen, Linda Margareth; Lie, Benedicte Alexandra. Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement. Scientific Reports 2022 ;Volume 12.(1) p. 1-12 UiO OUS HAUKELAND UiB OSTFSYK VV OSLOMET
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2021
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13. |
Fjær, Roar; Marciniak, Katarzyna; Sundnes, Olav; Hjorthaug, Hanne; Sheng, Ying; Hammarström, Clara Louise; Sitek, Jan Cezary; Vigeland, Magnus Dehli; Backe, Paul Hoff; Øye, Ane-Marte; Hol, Johanna; Stav-Noraas, Tor Espen; Uchiyama, Yuri; Matsumoto, Naomichi; Comi, Anne; Pevsner, Jonathan; Haraldsen, Guttorm; Selmer, Kaja Kristine. A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome. Human Molecular Genetics 2021 ;Volume 30.(21) p. 1919-1931 OUS STO UiO
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Marsico, Franco L.; Vigeland, Magnus Dehli; Egeland, Thore; Piñero, Mariana Herrera. Making decisions in missing person identification cases with low statistical power. Forensic Science International: Genetics 2021 ;Volume 54:102519. p. 1-8 UiO NMBU
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Vigeland, Magnus Dehli; Egeland, Thore. Joint DNA-based disaster victim identification. Scientific Reports 2021 ;Volume 11:13661.(1) p. 1-13 NMBU UiO
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2020
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16. |
Berger, Toni; Vigeland, Magnus Dehli; Hjorthaug, Hanne Sagsveen; Nome, Cecilie; Taubøll, Erik; Selmer, Kaja Kristine; Heuser, Kjell. Differential Glial Activation in Early Epileptogenesis—Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus. Frontiers in Neurology 2020 ;Volume 11. p. - OUS UiO
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17. |
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 ;Volume 135. p. 117-129 NMBU UiO
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18. |
Børte, Sigrid; Zwart, John-Anker; Skogholt, Anne Heidi; Gabrielsen, Maiken Elvestad; Thomas, Laurent; Fritsche, Lars; 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 STO OUS UiO NTNU AHUS
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19. |
Castilla-Vallmanya, Laura; Selmer, Kaja Kristine; Dimartino, Clémantine; Rabionet, Raquel; Blanco-Sanchez, Bernardo; Yang, Sandra; Reijnders, Margot R. F.; Essen, Antonie J. van; Oufadem, Myriam; Vigeland, Magnus Dehli; Stadheim, Barbro; Houge, Gunnar; Cox, Helen; Kingston, Helen; Clayton-Smith, Jill; Innis, Jeffrey W.; Iascone, Maria; Cereda, Anna; Gabbiadini, Sara; Chung, Wendy K.; Sanders, Victoria; Charrow, Joel; Bryant, Emily; Millichap, John J.; Vitobello, Antonio; Thauvin, Christelle; Tran Mau-Them, Frederic; Faivre, Laurence; Lesca, Gaetan; Labalme, Audrey; Rougeot, Christelle; Chatron, Nicolas; Sanlaville, Damien; Christensen, Katherine M.; Kirby, Amelia; Lewandowski, Raymond; Gannaway, Rachel; Aly, Maha; Lehman, Anna; Clarke, Lorne; Graul-Neumann, Luitgard; Zweier, Christiane; Lessel, Davor; Lozic, Bernarda; Aukrust, Ingvild; Peretz, Ryan; Stratton, Robert; Smol, Thomas; Dieux-Coeslier, Anne; Meira, Joanna. Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7. Genetics in Medicine 2020 ;Volume 22.(7) p. 1215-1226 OUS HAUKELAND UiO
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20. |
Prestsæter, Sjur; Koht, Jeanette; Lamari, Foudil; Tallaksen, Chantal; Hoven, Stian Tobias Juel; Vigeland, Magnus Dehli; Selmer, Kaja Kristine; Rydning, Siri Lynne. Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5. Journal of the Neurological Sciences 2020 ;Volume 419:117211. p. 1-4 UiO SI OUS VV
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21. |
Tønne, Elin; Due-Tønnessen, Bernt Johan; Mero, Inger-Lise; Wiig, Ulrikke Straume; Kulseth, Mari Ann; Vigeland, Magnus Dehli; Sheng, Ying; Lippe, Charlotte von der; Tveten, Kristian; Meling, Torstein Ragnar; Helseth, Eirik; Heimdal, Ketil Riddervold. Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis. European Journal of Human Genetics 2020 ;Volume 00.(0) p. 1-10 UiO OUS STHF
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22. |
Vigeland, Magnus Dehli. Relatedness coefficients in pedigrees with inbred founders. Journal of Mathematical Biology 2020 ;Volume 81.(1) p. 185-207 UiO
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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 UiO NMBU
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2019
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24. |
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 UiO HAUKELAND OUS UiB
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25. |
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. UiO OUS UiB
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26. |
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 UiO OUS
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27. |
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 UiO OUS VV
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28. |
Vigeland, Magnus Dehli; Egeland, Thore. Handling founder inbreeding in forensic kinship analysis. Forensic Science International: Genetics Supplement Series 2019 UiO NMBU
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2018
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29. |
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 OUS HAUKELAND UiB
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30. |
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 UiO OUS
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31. |
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 UiO NMBU
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2017
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32. |
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 NMBU OUS
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33. |
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 OUS
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34. |
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 OUS UiO
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35. |
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 UiO NTNU OUS
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36. |
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 OUS NTNU UiO
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2016
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37. |
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 UiO OUS
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38. |
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 NMBU OUS UiO FHI
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39. |
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 NMBU VETINST UiO OUS UiB NTNU NOFIMA
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40. |
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 OUS
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41. |
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 OUS UiO
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42. |
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. - OUS UiO
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43. |
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 OUS UiO VV
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44. |
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 UiO SSHF OUS
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45. |
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 KREFTREG UiO OUS
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2015
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46. |
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 OUS UiO
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47. |
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 OUS UiO NTNU STO
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2014
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48. |
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 OUS NMBU FHI
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49. |
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 FHI OUS NMBU
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2013
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50. |
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 UiO OUS NMBU
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