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Publications by Beate Skinningsrud

24 publications found

Original articles

Penna-Martinez M, Meyer G, Wolff AB, Skinningsrud B, Betterle C, Falorni A, Ollier W, Undlien D, Husebye E, Pearce S, Mitchell AL, Badenhoop K (2021)
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts
Eur J Endocrinol, 184 (3), 373-381
DOI 10.1530/EJE-20-0956, PubMed 33444227

Mizia E, Pekala PA, Skinningsrud B, Rutowicz B, Piekos P, Baginski A, Tomaszewski KA (2020)
The anatomical landmarks effective in the localisation of the median nerve during orthopaedic procedures
Folia Morphol (Warsz), 80 (2), 248-254
DOI 10.5603/FM.a2020.0049, PubMed 32394419

Aslaksen S, Methlie P, Vigeland MD, Jøssang DE, Wolff AB, Sheng Y, Oftedal BE, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease
Front Endocrinol (Lausanne), 10, 648
DOI 10.3389/fendo.2019.00648, PubMed 31611844

Aslaksen S, Wolff AB, Vigeland MD, Breivik L, Sheng Y, Oftedal BE, Artaza H, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease
J Transl Autoimmun, 1, 100005
DOI 10.1016/j.jtauto.2019.100005, PubMed 32743495

Wolff AS, Mitchell AL, Cordell HJ, Short A, Skinningsrud B, Ollier W, Badenhoop K, Meyer G, Falorni A, Kampe O, Undlien D, Pearce SH, Husebye ES (2015)
CTLA-4 as a genetic determinant in autoimmune Addison's disease
Genes Immun, 16 (6), 430-6
DOI 10.1038/gene.2015.27, PubMed 26204230

Brønstad I, Skinningsrud B, Bratland E, Løvås K, Undlien D, Sverre Husebye E, Wolff AS (2014)
CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
Eur J Endocrinol, 171 (6), 743-50
DOI 10.1530/EJE-14-0432, PubMed 25249698

Mitchell AL, Macarthur KD, Gan EH, Baggott LE, Wolff AS, Skinningsrud B, Platt H, Short A, Lobell A, Kämpe O, Bensing S, Betterle C, Kasperlik-Zaluska A, Zurawek M, Fichna M, Kockum I, Nordling Eriksson G, Ekwall O, Wahlberg J, Dahlqvist P, Hulting AL, Penna-Martinez M, Meyer G, Kahles H, Badenhoop K et al. (2014)
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts
PLoS One, 9 (3), e88991
DOI 10.1371/journal.pone.0088991, PubMed 24614117

Eike MC, Skinningsrud B, Ronninger M, Stormyr A, Kvien TK, Joner G, Njølstad PR, Førre O, Flatø B, Alfredsson L, Padyukov L, Undlien DE, Lie BA (2012)
CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
Genes Immun, 13 (5), 431-6
DOI 10.1038/gene.2012.11, PubMed 22513452

Ronninger M, Seddighzadeh M, Eike MC, Plant D, Daha NA, Skinningsrud B, Worthington J, Kvien TK, Toes RE, Lie BA, Alfredsson L, Padyukov L (2012)
Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis
PLoS One, 7 (3), e32861
DOI 10.1371/journal.pone.0032861, PubMed 22461888

Skinningsrud B, Lie BA, Lavant E, Carlson JA, Erlich H, Akselsen HE, Gervin K, Wolff AB, Erichsen MM, Løvås K, Husebye ES, Undlien DE (2011)
Multiple loci in the HLA complex are associated with Addison's disease
J Clin Endocrinol Metab, 96 (10), E1703-8
DOI 10.1210/jc.2011-0645, PubMed 21816777

Mero IL, Ban M, Lorentzen ÅR, Smestad C, Celius EG, Sæther H, Saeedi H, Viken MK, Skinningsrud B, Undlien DE, Aarseth J, Myhr KM, Granum S, Spurkland A, Sawcer S, Compston A, Lie BA, Harbo HF (2010)
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
Genes Immun, 12 (3), 191-8
DOI 10.1038/gene.2010.59, PubMed 21179112

Bratland E, Skinningsrud B, Undlien DE, Mozes E, Husebye ES (2009)
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency
J Clin Endocrinol Metab, 94 (12), 5117-24
DOI 10.1210/jc.2009-1115, PubMed 19890026

Erichsen MM, Løvås K, Skinningsrud B, Wolff AB, Undlien DE, Svartberg J, Fougner KJ, Berg TJ, Bollerslev J, Mella B, Carlson JA, Erlich H, Husebye ES (2009)
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry
J Clin Endocrinol Metab, 94 (12), 4882-90
DOI 10.1210/jc.2009-1368, PubMed 19858318

Mitchell AL, Cordell HJ, Soemedi R, Owen K, Skinningsrud B, Wolff AB, Ericksen M, Undlien D, Husebye E, Pearce SH (2009)
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility
J Clin Endocrinol Metab, 94 (12), 5139-45
DOI 10.1210/jc.2009-1404, PubMed 19850680

Skinningsrud B, Husebye ES, Gilfillan GD, Frengen E, Erichsen A, Gervin K, Ormerod E, Egeland T, Undlien DE (2009)
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene
J Clin Endocrinol Metab, 94 (10), 4086-93
DOI 10.1210/jc.2009-0923, PubMed 19773398

Skinningsrud B, Lie BA, Husebye ES, Kvien TK, Førre Ø, Flatø B, Stormyr A, Joner G, Njølstad PR, Egeland T, Undlien DE (2009)
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis
Ann Rheum Dis, 69 (8), 1471-4
DOI 10.1136/ard.2009.114934, PubMed 19734133

Magitta NF, Bøe Wolff AS, Johansson S, Skinningsrud B, Lie BA, Myhr KM, Undlien DE, Joner G, Njølstad PR, Kvien TK, Førre Ø, Knappskog PM, Husebye ES (2008)
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
Genes Immun, 10 (2), 120-4
DOI 10.1038/gene.2008.85, PubMed 18946481

Skinningsrud B, Husebye ES, Pearce SH, McDonald DO, Brandal K, Wolff AB, Løvås K, Egeland T, Undlien DE (2008)
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
J Clin Endocrinol Metab, 93 (9), 3310-7
DOI 10.1210/jc.2008-0821, PubMed 18593762

Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE (2008)
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
Eur J Hum Genet, 16 (8), 977-82
DOI 10.1038/ejhg.2008.33, PubMed 18301444

Munthe-Kaas MC, Gerritsen J, Carlsen KH, Undlien D, Egeland T, Skinningsrud B, Tørres T, Carlsen KL (2007)
Eosinophil cationic protein (ECP) polymorphisms and association with asthma, s-ECP levels and related phenotypes
Allergy, 62 (4), 429-36
DOI 10.1111/j.1398-9995.2007.01327.x, PubMed 17362255

Bjørnvold M, Amundsen SS, Stene LC, Joner G, Dahl-Jørgensen K, Njølstad PR, Ek J, Ascher H, Gudjònsdòttir AH, Lie BA, Skinningsrud B, Akselsen HE, Rønningen KS, Sollid LM, Undlien DE (2006)
FOXP3 polymorphisms in type 1 diabetes and coeliac disease
J Autoimmun, 27 (2), 140-4
DOI 10.1016/j.jaut.2006.06.007, PubMed 16996248

Munthe-Kaas MC, Lødrup Carlsen KC, Carlsen KH, Skinningsrud B, Håland G, Devulapalli CS, Pettersen M, Eiklid K (2006)
CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study
Respir Med, 100 (12), 2121-8
DOI 10.1016/j.rmed.2006.03.026, PubMed 16678395

Munthe-Kaas MC, Carlsen KH, Helms PJ, Gerritsen J, Whyte M, Feijen M, Skinningsrud B, Main M, Kwong GN, Lie BA, Lødrup Carlsen KC, Undlien DE (2004)
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm
J Allergy Clin Immunol, 114 (2), 280-7
DOI 10.1016/j.jaci.2004.03.050, PubMed 15316504

Theses

Skinningsrud B (2005)
Molekylærgenetisk undersøkelse av familie med Addisons sykdom og hypogonadotrop hypogonadisme
B. Skinningsrud, Trondheim, 107 s.
BIBSYS 06084471x