Application and Interpretation of Transmission/Disequilibrium Tests: Transmission of HLA-DQ Haplotypes to Unaffected Siblings in 526 Families with Type 1 Diabetes

Autor Lie, Benedicte A., Rønningen, Kjersti S., Akselsen, Hanne E., Thorsby, Erik, Undlien, Dag E.
Vydáno 2000

Limitations and possibilities of low cell number ChIP-seq

Autor Gilfillan, Gregor D, Hughes, Timothy, Sheng, Ying, Hjorthaug, Hanne S, Straub, Tobias, Gervin, Kristina, Harris, Jennifer R, Undlien, Dag E, Lyle, Robert
Vydáno 2012

Extensive variation and low heritability of DNA methylation identified in a twin study

Autor Gervin, Kristina, Hammerø, Martin, Akselsen, Hanne E., Moe, Rune, Nygård, Heidi, Brandt, Ingunn, Gjessing, Håkon K., Harris, Jennifer R., Undlien, Dag E., Lyle, Robert
Vydáno 2011

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

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

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

Autor Skinningsrud, Beate, Lie, Benedicte A, Husebye, Eystein S, Kvien, Tore K, Førre, Øystein, Flatø, Berit, Stormyr, Alice, Joner, Geir, Njølstad, Pål R, Egeland, Thore, Undlien, Dag E
Vydáno 2010

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

Autor Aslaksen, Sigrid, Wolff, Anette B., Vigeland, Magnus D., Breivik, Lars, Sheng, Ying, Oftedal, Bergithe E., Artaza, Haydee, Skinningsrud, Beate, Undlien, Dag E., Selmer, Kaja K., Husebye, Eystein S., Bratland, Eirik
Vydáno v J Transl Autoimmun (2019)

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

Autor Aslaksen, Sigrid, Methlie, Paal, Vigeland, Magnus D., Jøssang, Dag E., Wolff, Anette B., Sheng, Ying, Oftedal, Bergithe E., Skinningsrud, Beate, Undlien, Dag E., Selmer, Kaja K., Husebye, Eystein S., Bratland, Eirik
Vydáno v Front Endocrinol (Lausanne) (2019)

A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions

Autor Selmer, Kaja K, Gilfillan, Gregor D, Strømme, Petter, Lyle, Robert, Hughes, Timothy, Hjorthaug, Hanne S, Brandal, Kristin, Nakken, Sigve, Misceo, Doriana, Egeland, Thore, Munthe, Ludvig A, Braekken, Sigrun K, Undlien, Dag E
Vydáno 2012

Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes

Autor Savage David A, Ionescu-Tîrgovişte Constantin, Guja Cristian, Rønningen Kjersti S, Undlien Dag E, Nutland Sarah, Walker Neil, Chamberlain Giselle, Hunter Kara M, Moule Carolyn, Fraser Heather, Smink Luc J, Hulme John, Lowe Christopher, Pask Rebecca, Cooper Jason D, Payne Felicity, Vella Adrian, Smyth Deborah J, Maier Lisa M, Strachan David P, Peterson Laurence B, Todd John A, Wicker Linda S, Twells Rebecca C
Vydáno 2005-02-01

Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes

Autor Maier, Lisa M, Smyth, Deborah J, Vella, Adrian, Payne, Felicity, Cooper, Jason D, Pask, Rebecca, Lowe, Christopher, Hulme, John, Smink, Luc J, Fraser, Heather, Moule, Carolyn, Hunter, Kara M, Chamberlain, Giselle, Walker, Neil, Nutland, Sarah, Undlien, Dag E, Rønningen, Kjersti S, Guja, Cristian, Ionescu-Tîrgovişte, Constantin, Savage, David A, Strachan, David P, Peterson, Laurence B, Todd, John A, Wicker, Linda S, Twells, Rebecca C
Vydáno 2005

SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

Autor Gilfillan, Gregor D., Selmer, Kaja K., Roxrud, Ingrid, Smith, Raffaella, Kyllerman, Mårten, Eiklid, Kristin, Kroken, Mette, Mattingsdal, Morten, Egeland, Thore, Stenmark, Harald, Sjøholm, Hans, Server, Andres, Samuelsson, Lena, Christianson, Arnold, Tarpey, Patrick, Whibley, Annabel, Stratton, Michael R., Futreal, P. Andrew, Teague, Jon, Edkins, Sarah, Gecz, Jozef, Turner, Gillian, Raymond, F. Lucy, Schwartz, Charles, Stevenson, Roger E., Undlien, Dag E., Strømme, Petter
Vydáno 2008

Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

Autor Farooqi, I. Sadaf, Wangensteen, Teresia, Collins, Stephan, Kimber, Wendy, Matarese, Giuseppe, Keogh, Julia M., Lank, Emma, Bottomley, Bill, Lopez-Fernandez, Judith, Ferraz-Amaro, Ivan, Dattani, Mehul T., Ercan, Oya, Myhre, Anne Grethe, Retterstol, Lars, Stanhope, Richard, Edge, Julie A., McKenzie, Sheila, Lessan, Nader, Ghodsi, Maryam, De Rosa, Veronica, Perna, Francesco, Fontana, Silvia, Barroso, Inês, Undlien, Dag E., O'Rahilly, Stephen
Vydáno 2007