Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers von Grindedal, Eli Marie, Heramb, Cecilie, Karsrud, Inga, Ariansen, Sarah Louise, Mæhle, Lovise, Undlien, Dag Erik, Norum, Jan, Schlichting, Ellen

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

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Erik Thorsby (1938–2021) von Lie, Benedicte A., Viken, Marte K., Egeland, Torstein, Undlien, Dag Erik, Vaage, John Torgils

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Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport von Moen, Marivi Nabong, Fjær, Roar, Hamdani, El Hassan, Laerdahl, Jon K, Menchini, Robin Johansen, Vigeland, Magnus Dehli, Sheng, Ying, Undlien, Dag Erik, Hassel, Bjørnar, Salih, Mustafa A, El Khashab, Heba Y, Selmer, Kaja Kristine, Chaudhry, Farrukh Abbas

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A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult von HEKMAN, Katherine E, YU, Guo-Yun, PULST, Stefan M, BIRD, Thomas D, WHITE, Kevin P, GOMEZ, Christopher M, BROWN, Christopher D, HAIPENG ZHU, XIAOFEI DU, GERVIN, Kristina, UNDLIEN, Dag Erik, PETERSON, April, STEVANIN, Giovanni, CLARK, H. Brent

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Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers von Grindedal, Eli Marie, Heramb, Cecilie, Karsrud, Inga, Ariansen, Sarah Louise, Mæhle, Lovise Olaug, Undlien, Dag Erik, Norum, Jan, Schlichting, Ellen

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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

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Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF von Filges, Isabel, Bruder, Elisabeth, Brandal, Kristin, Meier, Stephanie, Undlien, Dag Erik, Waage, Trine Rygvold, Hoesli, Irene, Schubach, Max, de Beer, Tjaart, Sheng, Ying, Hoeller, Sylvia, Schulzke, Sven, Røsby, Oddveig, Miny, Peter, Tercanli, Sevgi, Oppedal, Truls, Meyer, Peter, Selmer, Kaja Kristine, Strømme, Petter

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Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study von Wikenius, Ellen, Myhre, Anne Margrethe, Page, Christian Magnus, Moe, Vibeke, Smith, Lars, Heiervang, Einar, Undlien, Dag Erik, LeBlanc, Marissa Erin

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BRCA mutation carrier detection. A model-based cost-effectiveness analysis comparing the traditional family history approach and the testing of all patients with breast cancer von Norum, Jan, Grindedal, Eli Marie, Heramb, Cecilie, Karsrud, Inga, Ariansen, Sarah Louise, Undlien, Dag Erik, Schlichting, Ellen, Mæhle, Lovise

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Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts von Mitchell, Anna L, Macarthur, Katie D R, Gan, Earn H, Baggott, Lucy E, Wolff, Anette S B, Skinningsrud, Beate, Platt, Hazel, Short, Andrea, Lobell, Anna, Kämpe, Olle, Bensing, Sophie, Betterle, Corrado, Kasperlik-Zaluska, Anna, Zurawek, Magdalena, Fichna, Marta, Kockum, Ingrid, Nordling Eriksson, Gabriel, Ekwall, Olov, Wahlberg, Jeanette, Dahlqvist, Per, Hulting, Anna-Lena, Penna-Martinez, Marissa, Meyer, Gesine, Kahles, Heinrich, Badenhoop, Klaus, Hahner, Stephanie, Quinkler, Marcus, Falorni, Alberto, Phipps-Green, Amanda, Merriman, Tony R, Ollier, William, Cordell, Heather J, Undlien, Dag, Czarnocka, Barbara, Husebye, Eystein, Pearce, Simon H S

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Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease von Aslaksen, Sigrid, Methlie, Paal, Vigeland, Magnus Dehli, Jøssang, Dag Eirik, Wolff, Anette Susanne Bøe, Sheng, Ying, Oftedal, Bergithe Eikeland, Skinningsrud, Beate, Undlien, Dag Erik, Selmer, Kaja Kristine, Husebye, Eystein Sverre, Bratland, Eirik

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Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF von Filges, Isabel, Bruder, Elisabeth, Brandal, Kristin, Meier, Stephanie, Undlien, Dag Erik, Waage, Trine Rygvold, Hoesli, Irene, Schubach, Max, de Beer, Tjaart, Sheng, Ying, Hoeller, Sylvia, Schulzke, Sven, Røsby, Oddveig, Miny, Peter, Tercanli, Sevgi, Oppedal, Truls, Meyer, Peter, Selmer, Kaja Kristine, Strømme, Petter

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Stroemme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF von Filges, Isabel, Bruder, Elisabeth, Brandal, Kristin, Meier, Stephanie, Undlien, Dag Erik, Waage, Trine Rygvold, Hoesli, Irene, Schubach, Max, Beer, Tjaart, Sheng, Ying, Hoeller, Sylvia, Schulzke, Sven, Roesby, Oddveig, Miny, Peter, Tercanli, Sevgi, Oppedal, Truls, Meyer, Peter, Selmer, Kaja Kristine, Stroemme, Petter

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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

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SCN1A mutation screening in adult patients with Lennox–Gastaut syndrome features von Selmer, Kaja Kristine, Lund, Caroline, Brandal, Kristin, Undlien, Dag Erik, Brodtkorb, Eylert

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Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood von Gervin, Kristina, Andreassen, Bettina Kulle, Hjorthaug, Hanne Sagsveen, Carlsen, Karin C Lødrup, Carlsen, Kai-Håkon, Undlien, Dag Erik, Lyle, Robert, Munthe-Kaas, Monica Cheng

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CTLA-4 as a genetic determinant in autoimmune Addison's disease von Wolff, Anette Susanne Bøe, Mitchell, Anna L, Cordell, Heather J, Short, Andrea, Skinningsrud, Beate, Ollier, William, Badenhoop, Klaus, Meyer, Gesine, Falorni, Alberto, Kämpe, Olle, Undlien, Dag Erik, Pearce, Simon H.S, Husebye, Eystein Sverre

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Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene von Selmer, Kaja Kristine, Grøndahl, Jan, Riise, Ruth, Brandal, Kristin, Braaten, Øivind, Bragadottir, Ragnheidur, Undlien, Dag Erik

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CTLA-4 as a genetic determinant in autoimmune Addison’s disease von Wolff, A S B, Mitchell, A L, Cordell, H J, Short, A, Skinningsrud, B, Ollier, W, Badenhoop, K, Meyer, G, Falorni, A, Kampe, O, Undlien, D, Pearce, S H S, Husebye, E S

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