Publications by Magnus D. Vigeland

54 publications found

  1. Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2024)
    Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing
    Eur J Hum Genet (in press)
    DOI 10.1038/s41431-023-01519-1, PubMed 38172175
  2. Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2023)
    A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing
    Eur J Hum Genet (in press)
    DOI 10.1038/s41431-023-01494-7, PubMed 38030917
  3. Fantinato C, Fonneløp AE, Bleka Ø, Vigeland MD, Gill P (2023)
    The invisible witness: air and dust as DNA evidence of human occupancy in indoor premises
    Sci Rep, 13 (1), 19059
    DOI 10.1038/s41598-023-46151-7, PubMed 37925517
  4. Vigeland MD, Flåm ST, Vigeland MD, Espeland A, Zucknick M, Wigemyr M, Bråten LCH, Gjefsen E, Zwart JA, Storheim K, Pedersen LM, Selmer K, Lie BA, Gervin K, The Aim Study Group (2023)
    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 (Basel), 12 (7)
    DOI 10.3390/antibiotics12071217, PubMed 37508313
  5. Wiedmann MKH, Steinsvåg IV, Dinh T, Vigeland MD, Larsson PG, Hjorthaug H, Sheng Y, Mero IL, Selmer KK (2023)
    Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study
    Brain Spine, 3, 101745
    DOI 10.1016/j.bas.2023.101745, PubMed 37383439
  6. Gjefsen E, Gervin K, Bråten LCH, Goll GL, Aass HCD, Schistad EI, Wigemyr M, Pedersen LM, Skouen JS, Vigeland MD, Selmer KK, Storheim K, Zwart JA (2023)
    Longitudinal changes of serum cytokines in patients with chronic low back pain and Modic changes
    Osteoarthritis Cartilage, 31 (4), 543-547
    DOI 10.1016/j.joca.2023.01.001, PubMed 36640896
  7. Vigeland MD (2023)
    Two-locus identity coefficients in pedigrees
    G3 (Bethesda), 13 (2)
    DOI 10.1093/g3journal/jkac326, PubMed 36525359
  8. Ratajska A, Vigeland MD, Wirgenes KV, Krohg-Sørensen K, Paus B (2022)
    The use of segregation analysis in interpretation of sequence variants in SMAD3: A case report
    Mol Genet Genomic Med, 11 (2), e2107
    DOI 10.1002/mgg3.2107, PubMed 36495030
  9. Vigeland MD (2022)
    QuickPed: an online tool for drawing pedigrees and analysing relatedness
    BMC Bioinformatics, 23 (1), 220
    DOI 10.1186/s12859-022-04759-y, PubMed 35672681
  10. Rajan DS, Kour S, Fortuna TR, Cousin MA, Barnett SS, Niu Z, Babovic-Vuksanovic D, Klee EW, Kirmse B, Innes M, Rydning SL, Selmer KK, Vigeland MD, Erichsen AK, Nemeth AH, Millan F, DeVile C, Fawcett K, Legendre A, Sims D, Schnekenberg RP, Burglen L, Mercier S, Bakhtiari S, Francisco-Velilla R et al. (2022)
    Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5
    Front Cell Dev Biol, 10, 783762
    DOI 10.3389/fcell.2022.783762, PubMed 35295849
  11. Tønne E, Due-Tønnessen BJ, Vigeland MD, Amundsen SS, Ribarska T, Åsten PM, Sheng Y, Helseth E, Gilfillan GD, Mero IL, Heimdal KR (2022)
    Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways
    Am J Med Genet A, 188 (5), 1464-1475
    DOI 10.1002/ajmg.a.62663, PubMed 35080095
  12. Vigeland MD, Flåm ST, Vigeland MD, Espeland A, Kristoffersen PM, Vetti N, Wigemyr M, Bråten LCH, Gjefsen E, Schistad EI, Haugen AJ, Froholdt A, Skouen JS, Zwart JA, Storheim K, Pedersen LM, Lie BA, AIM Study Group (2022)
    Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement
    Sci Rep, 12 (1), 215
    DOI 10.1038/s41598-021-04189-5, PubMed 34997115
  13. Vigeland MD, Egeland T (2021)
    Joint DNA-based disaster victim identification
    Sci Rep, 11 (1), 13661
    DOI 10.1038/s41598-021-93071-5, PubMed 34211052
  14. Marsico FL, Vigeland MD, Egeland T, Piñero MH (2021)
    Making decisions in missing person identification cases with low statistical power
    Forensic Sci Int Genet, 54, 102519
    DOI 10.1016/j.fsigen.2021.102519, PubMed 34139527
  15. Fjær R, Marciniak K, Sundnes O, Hjorthaug H, Sheng Y, Hammarström C, Sitek JC, Vigeland MD, Backe PH, Øye AM, Fosse JH, Stav-Noraas TE, Uchiyama Y, Matsumoto N, Comi A, Pevsner J, Haraldsen G, Selmer KK (2021)
    A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome
    Hum Mol Genet, 30 (21), 1919-1931
    DOI 10.1093/hmg/ddab144, PubMed 34124757
  16. Berger TC, Vigeland MD, Hjorthaug HS, Nome CG, Taubøll E, Selmer KK, Heuser K (2020)
    Differential Glial Activation in Early Epileptogenesis-Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus
    Front Neurol, 11, 573575
    DOI 10.3389/fneur.2020.573575, PubMed 33312155
  17. Tønne E, Due-Tønnessen BJ, Mero IL, Wiig US, Kulseth MA, Vigeland MD, Sheng Y, von der Lippe C, Tveten K, Meling TR, Helseth E, Heimdal KR (2020)
    Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis
    Eur J Hum Genet, 29 (6), 920-929
    DOI 10.1038/s41431-020-00788-4, PubMed 33288889
  18. Prestsæter S, Koht J, Lamari F, Tallaksen CME, Hoven STJ, Vigeland MD, Selmer KK, Rydning SL (2020)
    Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5
    J Neurol Sci, 419, 117211
    DOI 10.1016/j.jns.2020.117211, PubMed 33160247
  19. Brustad HK, Vigeland MD, Egeland T (2020)
    Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio
    Int J Legal Med, 135 (1), 117-129
    DOI 10.1007/s00414-020-02426-6, PubMed 32989564
  20. Vigeland MD, Marsico FL, Herrera Piñero M, Egeland T (2020)
    Prioritising family members for genotyping in missing person cases: A general approach combining the statistical power of exclusion and inclusion
    Forensic Sci Int Genet, 49, 102376
    DOI 10.1016/j.fsigen.2020.102376, PubMed 32979623
  21. Aslaksen S, Wolff AB, Vigeland MD, Breivik L, Sheng Y, Oftedal BE, Artaza H, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
    Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease
    J Transl Autoimmun, 1, 100005
    DOI 10.1016/j.jtauto.2019.100005, PubMed 32743495
  22. Vigeland MD (2020)
    Relatedness coefficients in pedigrees with inbred founders
    J Math Biol, 81 (1), 185-207
    DOI 10.1007/s00285-020-01505-x, PubMed 32514944
  23. Castilla-Vallmanya L, Selmer KK, Dimartino C, Rabionet R, Blanco-Sánchez B, Yang S, Reijnders MRF, van Essen AJ, Oufadem M, Vigeland MD, Stadheim B, Houge G, Cox H, Kingston H, Clayton-Smith J, Innis JW, Iascone M, Cereda A, Gabbiadini S, Chung WK, Sanders V, Charrow J, Bryant E, Millichap J, Vitobello A et al. (2020)
    Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7
    Genet Med, 22 (7), 1215-1226
    DOI 10.1038/s41436-020-0792-7, PubMed 32376980
  24. Børte S, Zwart JA, Skogholt AH, Gabrielsen ME, Thomas LF, Fritsche LG, Surakka I, Nielsen JB, Zhou W, Wolford BN, Vigeland MD, Hagen K, Kristoffersen ES, Nyholt DR, Chasman DI, Brumpton BM, Willer CJ, Winsvold BS (2020)
    Mitochondrial genome-wide association study of migraine - the HUNT Study
    Cephalalgia, 40 (6), 625-634
    DOI 10.1177/0333102420906835, PubMed 32056457
  25. Berger TC, Vigeland MD, Hjorthaug HS, Etholm L, Nome CG, Taubøll E, Heuser K, Selmer KK (2019)
    Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis
    PLoS One, 14 (12), e0226575
    DOI 10.1371/journal.pone.0226575, PubMed 31887157
  26. Aslaksen S, Methlie P, Vigeland MD, Jøssang DE, Wolff AB, Sheng Y, Oftedal BE, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
    Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease
    Front Endocrinol (Lausanne), 10, 648
    DOI 10.3389/fendo.2019.00648, PubMed 31611844
  27. Rydning SL, Koht J, Sheng Y, Sowa P, Hjorthaug HS, Wedding IM, Erichsen AK, Hovden IA, Backe PH, Tallaksen CME, Vigeland MD, Selmer KK (2019)
    Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis
    Brain, 142 (4), e12
    DOI 10.1093/brain/awz041, PubMed 30847471
  28. Rydning SL, Dudesek A, Rimmele F, Funke C, Krüger S, Biskup S, Vigeland MD, Hjorthaug HS, Sejersted Y, Tallaksen C, Selmer KK, Kamm C (2018)
    A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia
    Eur J Neurol, 25 (7), 943-e71
    DOI 10.1111/ene.13625, PubMed 29528531
  29. Menke LA, DDD study, Gardeitchik T, Hammond P, Heimdal KR, Houge G, Hufnagel SB, Ji J, Johansson S, Kant SG, Kinning E, Leon EL, Newbury-Ecob R, Paolacci S, Pfundt R, Ragge NK, Rinne T, Ruivenkamp C, Saitta SC, Sun Y, Tartaglia M, Terhal PA, van Essen AJ, Vigeland MD, Xiao B et al. (2018)
    Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome
    Am J Med Genet A, 176 (4), 862-876
    DOI 10.1002/ajmg.a.38626, PubMed 29460469
  30. Mero IL, Mørk HH, Sheng Y, Blomhoff A, Opheim GL, Erichsen A, Vigeland MD, Selmer KK (2017)
    Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures
    Hum Mol Genet, 26 (19), 3792-3796
    DOI 10.1093/hmg/ddx263, PubMed 28934391
  31. Kling D, Egeland T, Piñero MH, Vigeland MD (2017)
    Evaluating the statistical power of DNA-based identification, exemplified by 'The missing grandchildren of Argentina'
    Forensic Sci Int Genet, 31, 57-66
    DOI 10.1016/j.fsigen.2017.08.006, PubMed 28858673
  32. Rydning SL, Backe PH, Sousa MML, Iqbal Z, Øye AM, Sheng Y, Yang M, Lin X, Slupphaug G, Nordenmark TH, Vigeland MD, Bjørås M, Tallaksen CM, Selmer KK (2017)
    Novel UCHL1 mutations reveal new insights into ubiquitin processing
    Hum Mol Genet, 26 (6), 1217-1218
    DOI 10.1093/hmg/ddx072, PubMed 28334853
  33. Low KJ, Ansari M, Abou Jamra R, Clarke A, El Chehadeh S, FitzPatrick DR, Greenslade M, Henderson A, Hurst J, Keller K, Kuentz P, Prescott T, Roessler F, Selmer KK, Schneider MC, Stewart F, Tatton-Brown K, Thevenon J, Vigeland MD, Vogt J, Willems M, Zonana J, Study DD, Smithson SF (2017)
    PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features
    Eur J Hum Genet, 25 (5), 552-559
    DOI 10.1038/ejhg.2017.27, PubMed 28327570
  34. Rydning SL, Backe PH, Sousa MML, Iqbal Z, Øye AM, Sheng Y, Yang M, Lin X, Slupphaug G, Nordenmark TH, Vigeland MD, Bjørås M, Tallaksen CM, Selmer KK (2017)
    Novel UCHL1 mutations reveal new insights into ubiquitin processing
    Hum Mol Genet, 26 (6), 1031-1040
    DOI 10.1093/hmg/ddw391, PubMed 28007905
  35. Sorte HS, Osnes LT, Fevang B, Aukrust P, Erichsen HC, Backe PH, Abrahamsen TG, Kittang OB, Øverland T, Jhangiani SN, Muzny DM, Vigeland MD, Samarakoon P, Gambin T, Akdemir ZH, Gibbs RA, Rødningen OK, Lyle R, Lupski JR, Stray-Pedersen A (2016)
    A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction
    Mol Genet Genomic Med, 4 (6), 604-616
    DOI 10.1002/mgg3.237, PubMed 27896283
  36. Lund C, Striano P, Sorte HS, Parisi P, Iacomino M, Sheng Y, Vigeland MD, Øye AM, Møller RS, Selmer KK, Zara F (2016)
    Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome
    Mol Syndromol, 7 (4), 234-238
    DOI 10.1159/000448367, PubMed 27781033
  37. Moen MN, Fjær R, Hamdani EH, Laerdahl JK, Menchini RJ, Vigeland MD, Sheng Y, Undlien DE, Hassel B, Salih MA, El Khashab HY, Selmer KK, Chaudhry FA (2016)
    Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport
    Brain, 139 (Pt 12), 3109-3120
    DOI 10.1093/brain/aww244, PubMed 27742667
  38. Pedurupillay CR, Landsend EC, Vigeland MD, Ansar M, Frengen E, Misceo D, Strømme P (2016)
    Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
    Genes (Basel), 7 (8)
    DOI 10.3390/genes7080041, PubMed 27472364
  39. Barøy T, Pedurupillay CR, Bliksrud YT, Rasmussen M, Holmgren A, Vigeland MD, Hughes T, Brink M, Rodenburg R, Nedregaard B, Strømme P, Frengen E, Misceo D (2016)
    A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13
    Eur J Med Genet, 59 (6-7), 342-6
    DOI 10.1016/j.ejmg.2016.05.005, PubMed 27182039
  40. Lien S, Koop BF, Sandve SR, Miller JR, Kent MP, Nome T, Hvidsten TR, Leong JS, Minkley DR, Zimin A, Grammes F, Grove H, Gjuvsland A, Walenz B, Hermansen RA, von Schalburg K, Rondeau EB, Di Genova A, Samy JK, Olav Vik J, Vigeland MD, Caler L, Grimholt U, Jentoft S, Våge DI et al. (2016)
    The Atlantic salmon genome provides insights into rediploidization
    Nature, 533 (7602), 200-5
    DOI 10.1038/nature17164, PubMed 27088604
  41. Vigeland MD, Gjøtterud KS, Selmer KK (2016)
    FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector
    Bioinformatics, 32 (10), 1592-4
    DOI 10.1093/bioinformatics/btw046, PubMed 26819469
  42. Rydning SL, Wedding IM, Koht J, Chawla M, Øye AM, Sheng Y, Vigeland MD, Selmer KK, Tallaksen CM (2016)
    A founder mutation p.H701P identified as a major cause of SPG7 in Norway
    Eur J Neurol, 23 (4), 763-71
    DOI 10.1111/ene.12937, PubMed 26756429
  43. Dørum G, Kling D, Tillmar A, Vigeland MD, Egeland T (2015)
    Mixtures with relatives and linked markers
    Int J Legal Med, 130 (3), 621-34
    DOI 10.1007/s00414-015-1288-x, PubMed 26614310
  44. Fjaer R, Brodtkorb E, Øye AM, Sheng Y, Vigeland MD, Kvistad KA, Backe PH, Selmer KK (2015)
    Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2
    Eur J Med Genet, 58 (11), 624-8
    DOI 10.1016/j.ejmg.2015.10.005, PubMed 26475232
  45. Pedurupillay CR, Barøy T, Holmgren A, Blomhoff A, Vigeland MD, Sheng Y, Frengen E, Strømme P, Misceo D (2015)
    Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B
    Am J Med Genet A, 167A (3), 657-63
    DOI 10.1002/ajmg.a.36944, PubMed 25691420
  46. Egeland T, Dørum G, Vigeland MD, Sheehan NA (2014)
    Mixtures with relatives: a pedigree perspective
    Forensic Sci Int Genet, 10, 49-54
    DOI 10.1016/j.fsigen.2014.01.007, PubMed 24572837
  47. Egeland T, Pinto N, Vigeland MD (2013)
    A general approach to power calculation for relationship testing
    Forensic Sci Int Genet, 9, 186-90
    DOI 10.1016/j.fsigen.2013.05.001, PubMed 23810238
  48. Vigeland MD, Spannagl M, Asp T, Paina C, Rudi H, Rognli OA, Fjellheim S, Sandve SR (2013)
    Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor
    New Phytol, 199 (4), 1060-1068
    DOI 10.1111/nph.12337, PubMed 23701123
  49. Gervin K, Vigeland MD, Mattingsdal M, Hammerø M, Nygård H, Olsen AO, Brandt I, Harris JR, Undlien DE, Lyle R (2012)
    DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes
    PLoS Genet, 8 (1), e1002454
    DOI 10.1371/journal.pgen.1002454, PubMed 22291603
  50. Sandve SR, Rudi H, Dorum G, Vigeland MD, Berg PR, Rognli OA (2010)
    Genotyping Unknown Genomic Terrain in Complex Plant Genomes
    SUSTAINABLE USE OF GENETIC DIVERSITY IN FORAGE AND TURF BREEDING, 455-+
    DOI 10.1007/978-90-481-8706-5_67
  51. Colman JE, Lilleeng MS, Tsegaye D, Vigeland MD, Reimers E (2012)
    Responses of wild reindeer (Rangifer tarandus tarandus) when provoked by a snow-kiter or skier: A model approach
    Appl. Anim. Behav. Sci., 142 (1-2), 82-89
    DOI 10.1016/j.applanim.2012.08.009
  52. Vigeland MD (2009)
    THE GROUP LAW ON A TROPICAL ELLIPTIC CURVE
    Math. Scand., 104 (2), 188-204
  53. Vigeland MD, Egeland T (2019)
    Handling founder inbreeding in forensic kinship analysis
    Forensic Sci. Int. Genet. Suppl. Ser., 7 (1), 780-781
    DOI 10.1016/j.fsigss.2019.10.175
  54. Vigeland MD (2010)
    Smooth tropical surfaces with infinitely many tropical lines
    Ark. Mat., 48 (1), 177-206
    DOI 10.1007/s11512-009-0116-2

 
Page visits: 1145