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2019
1 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.
Coexistence of congenital adrenal hyperplasia and autoimmune Addison's disease. Frontiers in Endocrinology 2019 ;Volum 10:648. s. 1-5
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2 Aslaksen, Sigrid; Wolff, Anette Susanne Bøe; Vigeland, Magnus Dehli; Breivik, Lars Ertesvåg; Sheng, Ying; Oftedal, Bergithe Eikeland; Skinningsrud, Beate; Undlien, Dag Erik; Selmer, Kaja Kristine; Husebye, Eystein Sverre; Bratland, Eirik.
Identification and characterization of rare Toll-like receptor 3 variants in patients with autoimmune Addison’s disease. Journal of translational autoimmunity 2019
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3 Wikenius, Ellen; Myhre, Anne Margrethe; Page, Christian Magnus; Moe, Vibeke; Smith, Lars; Heiervang, Einar; Undlien, Dag Erik; LeBlanc, Marissa Erin.
Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study. Nordic Journal of Psychiatry 2019 ;Volum 73.(4-5) s. 257-263
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2018
4 Norum, Jan; Grindedal, Eli Marie; Heramb, Cecilie; Karsrud, Inga; Ariansen, Sarah Louise; Undlien, Dag Erik; Schlichting, Ellen; Mæhle, Lovise Olaug.
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.. ESMO Open 2018 ;Volum 3.(3) s. -
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2017
5 Grindedal, Eli Marie; Heramb, Cecilie; Karsrud, Inga; Ariansen, Sarah Louise; Mæhle, Lovise Olaug; Undlien, Dag Erik; Norum, Jan; Schlichting, Ellen.
Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers. BMC Cancer 2017 ;Volum 17:438. s. 1-13
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2016
6 Eike, Morten Christoph; Seljebotn, Svein Tore; Nafstad, Eidi; Håndstad, Tony; Fontenelle, Hugues; Honneffer, David Jacob; Severinsen, Erik; Grünfeld, Thomas B.; Undlien, Dag Erik.
Ella: decision support and structured data in clinical variant classification. American Society of Human Genetics annual meeting 2016; 2016-10-19 - 2016-10-22
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7 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.
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF. Human Mutation 2016 ;Volum 37.(4) s. 359-363
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8 Filges, Isabel; Bruder, Elisabeth; Brandal, Kristin; Meier, Stephanie; Undlien, Dag Erik; Waage, Trine Rygvold; Hösli, Irene; Schubach, Max; de Beer, Tjaart; Sheng, Ying; Höller, Sylvia; Schulzke, Sven; Røsby, Oddveig; Miny, Peter; Tercanli, Sevgi; Oppedal, Truls; Meyer, Peter; Selmer, Kaja Kristine; Strømme, Petter.
Erratum to: Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF. Human Mutation 2016 ;Volum 37.(7) s. 711-711
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9 Gervin, Kristina; Kulle, Bettina; Hjorthaug, Hanne Sagsveen; Carlsen, Karin C. Lødrup; Carlsen, Kai-Håkon; Undlien, Dag Erik; Lyle, Robert; Munthe-Kaas, Monica Cheng.
Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood. Clinical Epigenetics 2016 ;Volum 8:110. s. 1-12
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10 Moen, Marivi Nabong; Fjær, Roar; Hamdani, El Hassan; Lærdahl, Jon Kristen; Menchini, Robin Johansen; Vigeland, Magnus Dehli; Sheng, Ying; Undlien, Dag Erik; Hassel, Bjørnar; Salih, MA; Khashab, HY; Selmer, Kaja Kristine; Chaudhry, Farrukh Abbas.
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport. Brain 2016 ;Volum 139. s. 3109-3120
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11 Solberg, Berge; Undlien, Dag Erik.
Da genetikken traff Norge. I: Det norske samfunn, bind 3. Gyldendal Akademisk 2016 ISBN 9788205496927. s. 136-159
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2015
12 Krogvold, Lars; Edwin, Bjørn; Buanes, Trond; Frisk, Gun; Skog, Oskar; Anagandula, Mahesh; Korsgren, Olle; Undlien, Dag Erik; Eike, Morten Christoph; Richardson, Sarah J.; Leete, Pia; Morgan, Noel; Oikarinen, Sami; Oikarinen, Maarit; Laiho, Jutta E.; Hyöty, Heikki; Ludvigsson, Johnny; Hanssen, Kristian Folkvord; Dahl-Jørgensen, Knut.
Detection of a low-grade enteroviral infection in the islets of langerhans of living patients newly diagnosed with type 1 diabetes. Diabetes 2015 ;Volum 64.(5) s. 1682-1687
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13 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.
CTLA-4 as a genetic determinant in autoimmune Addison's disease. Genes and Immunity 2015 ;Volum 16.(6) s. 430-436
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2014
14 Aanestad, Margunn; Eike, Morten Christoph; Grünfeld, Thomas B.; Undlien, Dag Erik.
Building an Infrastructure for Personalized Medicine: connecting the local knowing in practice to global 'circuits of knowledge'. International Conference on Organizational Learning, Knowledge and Capabilities; 2014-04-22 - 2014-04-24
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15 Brønstad, Ingeborg; Skinningsrud, Beate; Bratland, Eirik; Løvås, Kristian; Undlien, Dag Erik; Husebye, Eystein Sverre; Wolff, Anette Susanne Bøe.
CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles. European Journal of Endocrinology 2014 ;Volum 171.(6) s. 743-750
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16 Eike, Morten Christoph; Skorve, Espen; Håndstad, Tony; Fontenelle, Hugues; Børsting, Jorun; Aanestad, Margunn; Culén, Alma Leora; Grünfeld, Thomas; Undlien, Dag Erik.
GenAP workbench: aiding variant classification in clinical diagnostic settings. American Society of Human Genetics annual meeting 2014; 2014-10-18 - 2014-10-22
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17 Mitchell, Anna L.; Macarthur, Katie D.R.; Gan, Earn H.; Baggott, Lucy E.; Wolff, Anette Susanne Bøe; Skinningsrud, Beate; Platt, Hazel; Short, Andrea; Lobell, Anna; Kämpe, Olle; Bensing, Sophie; Betterle, Corrado; Kasperlik-Zaluska, Anna; Zurawek, Magdalena; Fichna, Marta; Kockum, Ingrid; Eriksson, Gabriel Nordling; Ekwall, Olov; Wahlberg, Jeanette; Dahlqvist, Per; Hulting, Anna-Lena; Penna-Martinez, Marissa; Meyer, Gesine; Kahles, Heinrich; Badenhoop, Klaus; Hahner, Stefanie; Quinkler, Marcus; Falorni, Alberto; Phipps-Green, Amanda; Merriman, Tony R.; Ollier, William; Cordell, Heather J.; Undlien, Dag Erik; Czarnocka, Barbara; Husebye, Eystein Sverre; Pearce, Simon H.S..
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European Cohorts. PLOS ONE 2014 ;Volum 9.(3:e88991)
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2013
18 Brønstad, Ingeborg; Skinningsrud, Beate; Wolff, Anette Susanne Bøe; Bratland, Eirik; Løvås, Kristian; Knappskog, Per; Undlien, Dag Erik; Husebye, Eystein Sverre.
Characterisation of the CYP21A2 Gene in Patients with Autoimmune Addison's Disease. Scandinavian Journal of Immunology 2013 ;Volum 77.(4) s. 310-310
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19 Eike, Morten Christoph; Håndstad, Tony; Nafstad, Eidi; Hughes, Timothy; Grünfeld, Thomas; Undlien, Dag Erik.
GenAP: automated analysis of genetic HTS data for clinical diagnostic use. American Society of Human Genetics annual meeting 2013; 2013-10-22 - 2013-10-26
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20 Irgens, Henrik Underthun; Molnes, Janne; Johansson, Bente Berg; Ringdal, Monika; Skrivarhaug, Torild; Undlien, Dag Erik; Søvik, Oddmund; Joner, Geir; Molven, Anders; Njølstad, Pål Rasmus.
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. Diabetologia 2013 ;Volum 56.(7) s. 1512-1519
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21 Torjussen, Tale Mæhre; Munthe-Kaas, Monica Cheng; Mowinckel, Petter; Carlsen, Kai-Håkon; Undlien, Dag Erik; Carlsen, Karin C. Lødrup.
Childhood lung function and the association with beta 2-adrenergic receptor haplotypes. Acta Paediatrica 2013 ;Volum 102.(7) s. 727-731
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2012
22 Eike, Morten Christoph; Lærum, Hallvard; Hughes, Timothy; Bremer, Sara; Bergan, Stein; Thomassen, Gard O Sundby; Aanestad, Margunn; Grünfeld, Thomas; Undlien, Dag Erik.
A national platform for clinical genetic analysis of high-throughput sequencing data in Norway. American Society of Human Genetics annual meeting 2012; 2012-11-06 - 2012-11-10
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23 Eike, Morten Christoph; Lærum, Hallvard; Hughes, Timothy; Håndstad, Tony; Bremer, Sara; Bergan, Stein; Thomassen, Gard O Sundby; Aanestad, Margunn; Grünfeld, Thomas; Undlien, Dag Erik.
GenAP: a platform for clinical genetic analysis of high-throughput sequencing data. Fagmøte i Medisinsk Genetikk 2012 - Personalised medicine: Integrating genomics into general health care; 2012-11-28 - 2012-11-29
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24 Eike, Morten Christoph; Skinningsrud, Beate; Ronninger, Marcus; Stormyr, Alice; Kvien, Tore Kristian; Joner, Geir; Njølstad, Pål Rasmus; Førre, Øystein Thorleiv; Flatø, Berit; Alfredsson, Lars; Padyukov, Leonid; Undlien, Dag Erik; Lie, Benedicte Alexandra.
CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations. Genes and Immunity 2012 ;Volum 13.(5) s. 431-436
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25 Gervin, Kristina; Vigeland, Magnus Dehli; Mattingsdal, Morten; Hammerø, Martin; Nygård, Heidi; Olsen, Anne Olaug; Brandt, Ingunn; Harris, Jennifer; Undlien, Dag Erik; Lyle, Robert.
DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes. PLoS Genetics 2012 ;Volum 8.(1) s. -
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26 Gilfillan, Gregor Duncan; Hughes, Timothy; Sheng, Ying; Hjorthaug, Hanne Sagsveen; Straub, Tobias; Gervin, Kristina; Harris, Jennifer; Undlien, Dag Erik; Lyle, Robert.
Limitations and possibilities of low cell number ChIP-seq. BMC Genomics 2012 ;Volum 13. s. -
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27 Hekman, Katherine E.; Yu, Guo-Yun; Brown, C.; Zhu, Haipeng; Du, Xiaofei; Gervin, Kristina; Undlien, Dag Erik; Peterson, April; Stevanin, Giovanni; Clark, H. Brent; Pulst, Stefan; Bird, Thomas D.; White, Kevin P.; Gomez, Christopher.
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult. Human Molecular Genetics 2012 ;Volum 21.(26) s. 5472-5483
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28 ; Brandal, Kristin.
Strømme syndrom - Jakten på et gen. Trondheim: Norges teknisk naturvitenskapelige universitet 2012 91 s.
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29 Munthe-Kaas, Monica Cheng; Bertelsen, Randi Jacobsen; Torjussen, Tale Mæhre; Hjorthaug, Hanne Sagsveen; Undlien, Dag Erik; Lyle, Robert; Gervin, Kristina; Granum, Berit; Mowinckel, Petter; Carlsen, Kai-Håkon; Carlsen, Karin C. Lødrup.
Pet keeping and tobacco exposure influence CD14 methylation in childhood. Pediatric Allergy and Immunology 2012 ;Volum 23.(8) s. 746-753
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30 Selmer, Kaja Kristine; Gilfillan, Gregor Duncan; Strømme, Petter; Lyle, Robert; Hughes, Timothy; Hjorthaug, Hanne Sagsveen; Brandal, Kristin; Nakken, Sigve; Misceo, Doriana; Egeland, Thore; Munthe, Ludvig Andre; Brækken, Sigrun Kierulf; Undlien, Dag Erik.
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions. European Journal of Human Genetics 2012 ;Volum 20.(1) s. 58-63
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31 Stray-Pedersen, Asbjørg; Sorte, Hanne Sørmo; Rødningen, Olaug Kristin; Lyle, Robert; Gonzaga-Jauregui, C G; Hanson, C I; Noroski, L M; Nicholas, S.; Erichsen, Hans Christian; Abrahamsen, Tore G; Flatø, Berit; Osnes, Liv T. N.; Heimdal, Ketil Riddervold; Undlien, Dag Erik; Lupski, J.R; Shearer, W T.
THE UTILITY OF EXOME SEQUENCING IN PRIMARY IMMUNODEFICIENCY DISEASES AND IMMUNODYSREGULATIVE DISORDERS. Journal of Clinical Immunology 2012 ;Volum 32.(Supp. 1) s. 184-185
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32 Torjussen, Tale Mæhre; Carlsen, Karin C. Lødrup; Munthe-Kaas, Monica Cheng; Mowinckel, Petter; Carlsen, Kai-Håkon; Helms, Peter J; Gerritsen, Jorrit; Whyte, Moira K.; Lenney, Warren; Undlien, Dag Erik; Shianna, Kevin V.; Zhu, Guohua H; Pillai, Sreekumar G.
Alpha-nicotinic acetylcholine receptor and tobacco smoke exposure: Effects on bronchial hyperresponsiveness in children. Pediatric Allergy and Immunology 2012 ;Volum 23.(1) s. 40-49
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33 Undlien, Dag Erik.
Individuell genomsekvensering. Tidsskrift for Den norske legeforening 2012 ;Volum 3.
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2011
34 Eike, Morten Christoph; Skinningsrud, Beate; Lie, Benedicte Alexandra; Husebye, Eystein Sverre; Undlien, Dag Erik.
No association with RFX, CCR5 or CD226 polymorphisms in Norwegian Addison’s disease patients. International Congress of Human Genetics/American Society of Human Genetics Annual Meeting 2011; 2011-10-11 - 2011-10-15
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35 Gervin, Kristina; Hammerø, Martin; Akselsen, Hanne Elisabeth; Moe, Rune; Nygård, Heidi; Brandt, Ingunn; Gjessing, Håkon; Harris, Jennifer; Undlien, Dag Erik; Lyle, Robert.
Extensive variation and low heritability of DNA methylation identified in a twin study. Genome Research 2011 ;Volum 21.(11) s. 1813-1821
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36 Mero, Inger-Lise; Ban, Maria; Lorentzen, Åslaug Rudjord; SMESTAD, CATHRINE; Celius, Elisabeth Gulowsen; Sæther, Hanne Skarpodde; Saeedi, Haleh; Viken, Marte K; Skinningsrud, Beate; Undlien, Dag Erik; Aarseth, Jan Harald; Myhr, Kjell-Morten; Granum, Stine; Spurkland, Anne; Sawcer, Stephen; Compston, Alastair; Lie, Benedicte Alexandra; Harbo, Hanne Flinstad.
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus. Genes and Immunity 2011 ;Volum 12.(3) s. 191-198
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37 Skinningsrud, Beate; Lie, Benedicte Alexandra; Lavant, Ewa; Carlson, Joyce A.; Erlich, Henry; Akselsen, Hanne Elisabeth; Gervin, Kristina; Wolff, Anette Susanne Bøe; Erichsen, Eva Martina Moter; Løvås, Kristian; Husebye, Eystein Sverre; Undlien, Dag Erik.
Multiple loci in the HLA complex are associated with Addison's Disease. Journal of Clinical Endocrinology and Metabolism 2011 ;Volum 96.(10) s. E1703-E1708
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38 Stene, Lars Christian; Rønningen, Kjersti Skjold; Undlien, Dag Erik; Joner, Geir.
Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section?. Pediatric Diabetes 2011 ;Volum 12.(2) s. 91-94
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39 Wangensteen, Urd Teresia; Akselsen, Hanne Elisabeth; Holmen, Jostein; Undlien, Dag Erik; Retterstøl, Lars.
A Common Haplotype in NAPEPLD Is Associated With Severe Obesity in a Norwegian Population-Based Cohort (the HUNT Study). Obesity 2011 ;Volum 19.(3) s. 612-617
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2010
40 Eike, Morten Christoph; Skinningsrud, Beate; Kvien, Tore Kristian; Stormyr, Alice; Undlien, Dag Erik; Lie, Benedicte Alexandra.
Support for involvement of CIITA gene variants in rheumatoid arthritis. American Society of Human Genetics Annual Meeting 2010; 2010-11-03 - 2010-11-06
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41 Munthe-Kaas, Monica Cheng; Torjussen, Tale Mæhre; Gervin, Kristina; Carlsen, Karin C. Lødrup; Carlsen, Kai-Håkon; Granum, Berit; Hjorthaug, Hanne Sagsveen; Undlien, Dag; Lyle, Robert.
CD14 polymorphisms and serum CD14 levels through childhood: A role for gene methylation?. Journal of Allergy and Clinical Immunology 2010 ;Volum 125.(6) s. 1361-1368
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42 Selmer, Kaja Kristine; Grønddahl, Jan Robert; Riise, Ruth; Brandal, Kristin; Braaten, Øivind; Bragadottir, Ragnheidur; Undlien, Dag Erik.
Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene. Acta Ophthalmologica 2010 ;Volum 88.(3) s. 323-328
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43 Skinningsrud, Beate; Lie, Benedicte; Husebye, Eystein S; Kvien, Tore K; Førre, Øystein; Flatø, Berit; Stormyr, Alice; Joner, Geir; Njølstad, Pål R; Egeland, Thore; Undlien, Dag E..
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis. Annals of the Rheumatic Diseases 2010 ;Volum 69.(8) s. 1471-1474
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44 Stene, Lars Christian; Rønningen, Kjersti Skjold; Bjørnvold, Marit; Undlien, Dag E; Joner, Geir.
An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms. Pediatric Diabetes 2010 ;Volum 11.(6) s. 386-393
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45 Wangensteen, Urd Teresia; Egeland, Thore; Akselsen, Hanne Elisabeth; Holmen, Jostein; Undlien, Dag Erik; Retterstøl, Lars.
FTO Genotype and Weight Gain in Obese and Normal Weight Adults From a Norwegian Population Based Cohort (the HUNT Study). Experimental and clinical endocrinology & diabetes 2010 ;Volum 118.(9) s. 649-652
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2009
46 Skinningsrud, Beate; Lie, Benedicte Alexandra; Husebye, Eystein; Kvien, TK; Førre, Øystein Thorleiv; Flatø, Berit; Stormyr, Alice; Joner, Geir; Njølstad, Pål R.; Egeland, Thore; Undlien, Dag Erik.
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-CCP negative rheumatoid arthritis. Annals of the Rheumatic Diseases 2009
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47 Bjørnvold, Marit; Munthe-Kaas, Monica Cheng; Egeland, Thore; Joner, Geir; Dahl-Jørgensen, Knut; Njølstad, Pål Rasmus; Akselsen, Hanne Elisabeth; Gervin, Kristina; Carlsen, Karin Cecilie Lødrup; Carlsen, Kai-Håkon; Undlien, Dag Erik.
A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma. Genes and Immunity 2009 ;Volum 10.(2) s. 181-187
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48 Bratland, Eirik; Skinningsrud, B; Undlien, Dag Erik; Mozes, Edna; Husebye, Eystein Sverre.
T Cell Responses to Steroid Cytochrome P450 21-Hydroxylase in Patients with Autoimmune Primary Adrenal Insufficiency. Journal of Clinical Endocrinology and Metabolism 2009 ;Volum 94.(12) s. 5117-5124
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49 Eike, MC; Olsson, M; Undlien, DE; Dahl-Jørgensen, Knut; Joner, Geir; Rønningen, Kjersti Skjold; Thorsby, E; Lie, BA.
Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families. Genes and Immunity 2009 ;Volum 10.(2) s. 141-150
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50 Erichsen, Martina Moter; Erichsen, Martina M; Løvås, Kristian; Skinningsrud, Beate; Wolff, Anette; Undlien, Dag E; Svartberg, Johan; Fougner, Kristian J; Berg, Tore J.; Bollerslev, Jens; Mella, Bjarne; Mella, Bjarne; Carlson, Joyce A; Erlich, Henry; Ehrlich, H; Husebye, Eystein S.
Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry. Journal of Clinical Endocrinology and Metabolism 2009 ;Volum 94.(12) s. 4882-4890
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