Publications by authors named "Magnus D Vigeland"

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EFMex: Using EuroForMix to evaluate DNA mixtures with multiple persons of interest.
Øyvind Bleka, Magnus Dehli Vigeland, Peter Gill

Forensic Sci Int Genet· February 2026

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Using autosomal and X-chromosomal SNPs to identify a victim of the 1956 Marcinelle mining disaster.
Magnus D Vigeland, Stijn Desmyter, Pernilla Haage, Henrik Nordtorp, Femke Van Puymbrouck

Forensic Sci Int Genet· December 2025

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Kinship cases with partially specified hypotheses.
Thore Egeland, Magnus Dehli Vigeland

Forensic Sci Int Genet· June 2025

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Uncovering genetic signatures of the Walser migration in the Alps: Patterns of diversity and differentiation.
Peter Resutik, Joëlle Schneider, Simon Aeschbacher, Magnus Dehli Vigeland, Mario Gysi

Forensic Sci Int Genet· March 2025

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Heating up three cold cases in Norway using investigative genetic genealogy.
Håvard Aanes, Magnus D Vigeland, Bastiaan Star, Gregor D Gilfillan, Morten Mattingsdal

Forensic Sci Int Genet· March 2025

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Gene Expression Correlates with Disability and Pain Intensity in Patients with Chronic Low Back Pain and Modic Changes in a Sex-Specific Manner.
Maria Dehli Vigeland, Siri Tennebø Flåm, Magnus Dehli Vigeland, Manuela Zucknick, Monica Wigemyr

Int J Mol Sci· January 2025

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A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing.
Pål Marius Bjørnstad, Ragnhild Aaløkken, June Åsheim, Arvind Y M Sundaram, Caroline N Felde, Magnus D Vigeland

Eur J Hum Genet· May 2024

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Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.
Pål Marius Bjørnstad, Ragnhild Aaløkken, June Åsheim, Arvind Y M Sundaram, Caroline N Felde, Magnus D Vigeland

Eur J Hum Genet· May 2024

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shinyseg: a web application for flexible cosegregation and sensitivity analysis.
Christian Carrizosa, Dag E Undlien, Magnus D Vigeland

Bioinformatics· May 2024

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The invisible witness: air and dust as DNA evidence of human occupancy in indoor premises.
Chiara Fantinato, Ane Elida Fonneløp, Øyvind Bleka, Magnus Dehli Vigeland, Peter Gill

Sci Rep· November 2023

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Long-Term Use of Amoxicillin Is Associated with Changes in Gene Expression and DNA Methylation in Patients with Low Back Pain and Modic Changes.
Maria Dehli Vigeland, Siri Tennebø Flåm, Magnus Dehli Vigeland, Ansgar Espeland, Manuela Zucknick

Antibiotics (Basel)· July 2023

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Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study.
Markus K H Wiedmann, Ingunn V Steinsvåg, Tovy Dinh, Magnus D Vigeland, Pål G Larsson

Brain Spine· April 2023

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The use of segregation analysis in interpretation of sequence variants in SMAD3: A case report.
Aleksandra Ratajska, Magnus D Vigeland, Katrine Verena Wirgenes, Kirsten Krohg-Sørensen, Benedicte Paus

Mol Genet Genomic Med· February 2023

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Two-locus identity coefficients in pedigrees.
Magnus Dehli Vigeland

G3 (Bethesda)· February 2023

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QuickPed: an online tool for drawing pedigrees and analysing relatedness.
Magnus D Vigeland

BMC Bioinformatics· June 2022

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Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways.
Elin Tønne, Bernt Johan Due-Tønnessen, Magnus Dehli Vigeland, Silja Svanstrøm Amundsen, Teodora Ribarska

Am J Med Genet A· May 2022

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Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in .
Deepa S Rajan, Sukhleen Kour, Tyler R Fortuna, Margot A Cousin, Sarah S Barnett, Magnus Dehli Vigeland

Front Cell Dev Biol· February 2022

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Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement.
Maria Dehli Vigeland, Siri Tennebø Flåm, Magnus Dehli Vigeland, Ansgar Espeland, Per Martin Kristoffersen

Sci Rep· January 2022

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A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome.
Roar Fjær, Katarzyna Marciniak, Olav Sundnes, Hanne Hjorthaug, Ying Sheng, Magnus Dehli Vigeland

Hum Mol Genet· October 2021

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Making decisions in missing person identification cases with low statistical power.
Franco L Marsico, Magnus D Vigeland, Thore Egeland, Mariana Herrera Piñero

Forensic Sci Int Genet· September 2021

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Joint DNA-based disaster victim identification.
Magnus D Vigeland, Thore Egeland

Sci Rep· July 2021

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Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.
Elin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero, Ulrikke Straume Wiig, Mari Ann Kulseth, Magnus Dehli Vigeland

Eur J Hum Genet· June 2021

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Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio.
Hilde Kjelgaard Brustad, Magnus Dehli Vigeland, Thore Egeland

Int J Legal Med· January 2021

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Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5.
Sjur Prestsæter, Jeanette Koht, Foudil Lamari, Chantal M E Tallaksen, Stian Tobias Juel Hoven, Magnus Dehli Vigeland

J Neurol Sci· December 2020

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Differential Glial Activation in Early Epileptogenesis-Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus.
Toni C Berger, Magnus D Vigeland, Hanne S Hjorthaug, Cecilie G Nome, Erik Taubøll

Front Neurol· November 2020

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