FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector

Por Vigeland, Magnus D., Gjøtterud, Kristina S., Selmer, Kaja K.
Publicado no Bioinformatics (2016)

Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor

Por Vigeland, Magnus D, Spannagl, Manuel, Asp, Torben, Paina, Cristiana, Rudi, Heidi, Rognli, Odd-Arne, Fjellheim, Siri, Sandve, Simen R
Publicado em 2013

DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes

Por Gervin, Kristina, Vigeland, Magnus D., Mattingsdal, Morten, Hammerø, Martin, Nygård, Heidi, Olsen, Anne O., Brandt, Ingunn, Harris, Jennifer R., Undlien, Dag E., Lyle, Robert
Publicado em 2012

Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome

Por Lund, Caroline, Striano, Pasquale, Sorte, Hanne Sørmo, Parisi, Pasquale, Iacomino, Michele, Sheng, Ying, Vigeland, Magnus D., Øye, Anne-Marte, Møller, Rikke Steensbjerre, Selmer, Kaja K., Zara, Federico
Publicado no Mol Syndromol (2016)

A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T‐cell dysfunction

Por Sorte, Hanne S., Osnes, Liv T., Fevang, Børre, Aukrust, Pål, Erichsen, Hans C., Backe, Paul H., Abrahamsen, Tore G., Kittang, Ole B., Øverland, Torstein, Jhangiani, Shalini N., Muzny, Donna M., Vigeland, Magnus D., Samarakoon, Pubudu, Gambin, Tomasz, Akdemir, Zeynep H. C., Gibbs, Richard A., Rødningen, Olaug K., Lyle, Robert, Lupski, James R., Stray‐Pedersen, Asbjørg
Publicado no Mol Genet Genomic Med (2016)

PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features

Por Low, Karen J, Ansari, Morad, Abou Jamra, Rami, Clarke, Angus, El Chehadeh, Salima, FitzPatrick, David R, Greenslade, Mark, Henderson, Alex, Hurst, Jane, Keller, Kory, Kuentz, Paul, Prescott, Trine, Roessler, Franziska, Selmer, Kaja K, Schneider, Michael C, Stewart, Fiona, Tatton-Brown, Katrina, Thevenon, Julien, Vigeland, Magnus D, Vogt, Julie, Willems, Marjolaine, Zonana, Jonathan, Study, D D D, Smithson, Sarah F
Publicado no Eur J Hum Genet (2017)