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

Volltext

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes von Gervin, Kristina, Vigeland, Magnus D, Mattingsdal, Morten, Hammerø, Martin, Nygård, Heidi, Olsen, Anne O, Brandt, Ingunn, Harris, Jennifer R, Undlien, Dag E, Lyle, Robert

Volltext

Limitations and possibilities of low cell number ChIP-seq von Gilfillan, Gregor D, Hughes, Timothy, Sheng, Ying, Hjorthaug, Hanne S, Straub, Tobias, Gervin, Kristina, Harris, Jennifer R, Undlien, Dag E, Lyle, Robert

Volltext

Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry von Erichsen, Martina M., Løvås, Kristian, Skinningsrud, Beate, Wolff, Anette B., Undlien, Dag E., Svartberg, Johan, Fougner, Kristian J., Berg, Tore J., Bollerslev, Jens, Mella, Bjarne, Carlson, Joyce A., Erlich, Henry, Husebye, Eystein S.

Volltext

Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes von Molven, Anders, Ringdal, Monika, Nordbø, Anita M, Raeder, Helge, Støy, Julie, Lipkind, Gregory M, Steiner, Donald F, Philipson, Louis H, Bergmann, Ines, Aarskog, Dagfinn, Undlien, Dag E, Joner, Geir, Søvik, Oddmund, Bell, Graeme I, Njølstad, Pål R

Volltext

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

Volltext

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

Volltext

T Cell Responses to Steroid Cytochrome P450 21-Hydroxylase in Patients with Autoimmune Primary Adrenal Insufficiency von Bratland, Eirik, Skinningsrud, Beate, Undlien, Dag E., Mozes, Edna, Husebye, Eystein S.

Volltext

Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene von Nejentsev, Sergey, Godfrey, Lisa, Snook, Hywel, Rance, Helen, Nutland, Sarah, Walker, Neil M., Lam, Alex C., Guja, Cristian, Ionescu-Tirgoviste, Constantin, Undlien, Dag E., Rønningen, Kjersti S., Tuomilehto-Wolf, Eva, Tuomilehto, Jaakko, Newport, Melanie J., Clayton, David G., Todd, John A.

Volltext

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease von 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

Volltext

Multiple Loci in the HLA Complex Are Associated with Addison's Disease von Skinningsrud, Beate, Lie, Benedicte A, Lavant, Ewa, Carlson, Joyce A, Erlich, Henry, Akselsen, Hanne E, Gervin, Kristina, Wolff, Anette B, Erichsen, Martina M, Løvås, Kristian, Husebye, Eystein S, Undlien, Dag E

Volltext

Polymorphisms in CLEC16A and CIITA at 16p13 Are Associated with Primary Adrenal Insufficiency von Skinningsrud, Beate, Husebye, Eystein S., Pearce, Simon H., McDonald, David O., Brandal, Kristin, Wolff, Anette B., Løvås, Kristian, Egeland, Thore, Undlien, Dag E.

Volltext

Remapping the Insulin Gene/IDDM2 Locus in Type 1 Diabetes von BARRATT, Bryan J, PAYNE, Felicity, MCCORMACK, Rose, GUJA, Cristian, IONESCU-URGOVIGTE, Constantin, UNDLIEN, Dag E, RØNNINGEN, Kjersti S, GILLESPIE, Kathleen M, TUOMILEHTO-WOLF, Eva, TUOMILEHTO, Jaakko, BENNETT, Simon T, CLAYTON, David G, LOWE, Chris E, CORDELL, Heather J, TODD, John A, HERMANN, Robert, HEALY, Barry C, HAROLD, Denise, CONCANNON, Patrick, GHARANI, Neda, MCCARTHY, Mark I, OLAVESEN, Mark G

Volltext

Extensive variation and low heritability of DNA methylation identified in a twin study von Gervin, Kristina, Hammerø, Martin, Akselsen, Hanne E, Moe, Rune, Nygård, Heidi, Brandt, Ingunn, Gjessing, Håkon K, Harris, Jennifer R, Undlien, Dag E, Lyle, Robert

Volltext

Neonatal Diabetes Mellitus Due to Complete Glucokinase Deficiency von Njølstad, Pål R, Søvik, Oddmund, Cuesta-Muñoz, Antonio, Bjørkhaug, Lise, Massa, Ornella, Barbetti, Fabrizio, Undlien, Dag E, Shiota, Chiyo, Magnuson, Mark A, Molven, Anders, Matschinsky, Franz M, Bell, Graeme I

Volltext

Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility von Mitchell, Anna L., Cordell, Heather J., Soemedi, Rachel, Owen, Kate, Skinningsrud, Beate, Wolff, Anette Bøe, Ericksen, Martina, Undlien, Dag, Husebye, Eystein, Pearce, Simon H. S.

Volltext

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

Volltext

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

Volltext

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease von Skinningsrud, Beate, Husebye, Eystein S, Gervin, Kristina, Løvås, Kristian, Blomhoff, Anne, Wolff, Anette B, Kemp, E Helen, Egeland, Thore, Undlien, Dag E

Volltext

CD14 polymorphisms and serum CD14 levels through childhood: A role for gene methylation? von Munthe-Kaas, Monica Cheng, MD, PhD, Torjussen, Tale Mæhre, MD, Gervin, Kristina, MSc, Lødrup Carlsen, Karin C., MD, PhD, Carlsen, Kai Håkon, MD, PhD, Granum, Berit, MSc, PhD, Hjorthaug, Hanne Sagsveen, MS, Undlien, Dag, MD, PhD, Lyle, Robert, BSc, PhD

Volltext