PubMed registered articles
Benedicte A. Lie
Publications by Benedicte A. Lie
100 publications found
Publications in press
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CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
Genes Immun (in press)
PubMed 22513452
Publications 2012
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Novel genetic association of the VTCN1 region with rheumatoid arthritis
Ann Rheum Dis, 71 (4), 567-71
PubMed 22323440 -
Importance of Human Leukocyte Antigen (HLA) Class I and II Alleles on the Risk of Multiple Sclerosis
PLoS One, 7 (5), e36779
PubMed 22586495 -
Late Onset Myasthenia Gravis Is Associated with HLA DRB1*15:01 in the Norwegian Population
PLoS One, 7 (5), e36603
PubMed 22590574 -
Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course
J Neuroimmunol, 244 (1-2), 107-10
PubMed 22341604 -
Interferon regulatory factor 5 gene polymorphism confers risk to several rheumatic diseases and correlates with expression of alternative thymic transcripts
Rheumatology (Oxford), 51 (4), 619-26
PubMed 22179739 -
An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration
Open Orthop J, 6, 164-71
PubMed 22550553 -
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
PubMed 22461888 -
HLA-DRB1, -DQA1 and -DQB1 alleles and haplotypes in first-generation Pakistani immigrants in Norway
Scand J Immunol, 75 (4), 426-30
PubMed 22171671 -
LYP inhibits T-cell activation when dissociated from CSK
Nat Chem Biol, 8 (5), 437-46
PubMed 22426112
Publications 2011
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A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
Ann Rheum Dis, 70 (4), 638-41
PubMed 21187296 -
No extreme genetic risk for type 1 diabetes among DR3/4-DQ8 siblings sharing both extended HLA haplotypes with their diabetic proband
Tissue Antigens, 77 (4), 338-40
PubMed 21388358 -
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
PLoS Genet, 7 (7), e1002178
PubMed 21779181 -
[New gene map for multiple sclerosis]
Tidsskr Nor Laegeforen, 131 (21), 2126-30
PubMed 22048209 -
Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis
Hepatology, 53 (6), 1967-76
PubMed 21413052 -
FCRL3 -169C/C genotype is associated with anti-citrullinated protein antibody-positive rheumatoid arthritis and with radiographic progression
J Rheumatol, 38 (11), 2329-35
PubMed 21885492 -
Evidence for PTPN22 R620W polymorphism as the sole common risk variant for rheumatoid arthritis in the 1p13.2 region
J Rheumatol, 38 (11), 2290-6
PubMed 21965649 -
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
PubMed 21179112 -
The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples
Arthritis Rheum, 63 (2), 365-72
PubMed 21279993 -
Multiple loci in the HLA complex are associated with Addison's disease
J Clin Endocrinol Metab, 96 (10), E1703-8
PubMed 21816777 -
Proteasome immunosubunits protect against the development of CD8 T cell-mediated autoimmune diseases
J Immunol, 187 (5), 2302-9
PubMed 21804012
Publications 2010
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Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
Genes Immun, 11 (1), 79-86
PubMed 19693089 -
Primary sclerosing cholangitis in genetically diverse populations listed for liver transplantation: unique clinical and human leukocyte antigen associations
Liver Transpl, 16 (11), 1324-30
PubMed 21031548 -
Norwegian Sami differs significantly from other Norwegians according to their HLA profile
Tissue Antigens, 75 (3), 207-17
PubMed 20047643 -
Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis
PLoS One, 5 (8), e12403
PubMed 20811628 -
Genome-wide association analysis in primary sclerosing cholangitis
Gastroenterology, 138 (3), 1102-11
PubMed 19944697 -
Two HLA class I genes independently associated with multiple sclerosis
J Neuroimmunol, 226 (1-2), 172-6
PubMed 20678810 -
Association to the Glypican-5 gene in multiple sclerosis
J Neuroimmunol, 226 (1-2), 194-7
PubMed 20692050 -
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
Eur J Hum Genet, 18 (4), 502-4
PubMed 19888296 -
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Nat Genet, 42 (5), 426-9
PubMed 20383147 -
Long-term muscular outcome and predisposing and prognostic factors in juvenile dermatomyositis: A case-control study
Arthritis Care Res (Hoboken), 62 (8), 1103-11
PubMed 20506141 -
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
PubMed 19734133 -
Prediction of radiographic progression in rheumatoid arthritis and the role of antibodies against mutated citrullinated vimentin: results from a 10-year prospective study
Ann Rheum Dis, 69 (2), 345-51
PubMed 19648126 -
Protection against anti-citrullinated protein antibody-positive rheumatoid arthritis is predominantly associated with HLA-DRB1*1301: a meta-analysis of HLA-DRB1 associations with anti-citrullinated protein antibody-positive and anti-citrullinated protein antibody-negative rheumatoid arthritis in four European populations
Arthritis Rheum, 62 (5), 1236-45
PubMed 20131291
Publications 2009
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Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B
Genes Immun, 10 (1), 56-67
PubMed 18830248 -
Three microsatellites from the T1DGC MHC data set show highly significant association with type 1 diabetes, independent of the HLA-DRB1, -DQA1 and -DQB1 genes
Diabetes Obes Metab, 11 Suppl 1, 17-24
PubMed 19143811 -
Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families
Genes Immun, 10 (2), 141-50
PubMed 18987644 -
Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis
Ann Neurol, 65 (6), 658-66
PubMed 19630074 -
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
Genes Immun, 10 (2), 120-4
PubMed 18946481 -
Association analysis of the interleukin 17A gene in Caucasian rheumatoid arthritis patients from Norway and New Zealand
Rheumatology (Oxford), 48 (4), 367-70
PubMed 19208686 -
HLA-DRB1 and month of birth in multiple sclerosis
Neurology, 73 (24), 2107-11
PubMed 20018638 -
Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex
Genes Immun, 10 (4), 323-33
PubMed 19295542
Publications 2008
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Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families
Genes Immun, 9 (4), 364-7
PubMed 18418394 -
Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32
Tissue Antigens, 71 (1), 27-34
PubMed 17971050 -
The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases
Ann Rheum Dis, 67 (9), 1287-91
PubMed 18065500 -
The SH2D2A gene and susceptibility to multiple sclerosis
J Neuroimmunol, 197 (2), 152-8
PubMed 18554728 -
Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms
Hepatology, 47 (1), 90-6
PubMed 18023027
Publications 2007
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A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families
Eur J Hum Genet, 15 (9), 980-7
PubMed 17551518 -
Low frequency of the disease-associated DRB1*15-DQB1*06 haplotype may contribute to the low prevalence of multiple sclerosis in Sami
Tissue Antigens, 69 (4), 299-304
PubMed 17389012 -
Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis
J Hepatol, 46 (5), 899-906
PubMed 17383044 -
Different HLA class II associations in ulcerative colitis patients with and without primary sclerosing cholangitis
Genes Immun, 8 (3), 275-8
PubMed 17301827 -
Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis
Am J Gastroenterol, 102 (1), 115-21
PubMed 17100974 -
Molecular genetic studies of natives on Easter Island: evidence of an early European and Amerindian contribution to the Polynesian gene pool
Tissue Antigens, 69 (1), 10-8
PubMed 17212703 -
Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease
Hum Immunol, 68 (7), 592-8
PubMed 17584581 -
Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study
Ann Rheum Dis, 66 (12), 1604-9
PubMed 17472988 -
Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis
BMC Med Genet, 8, 33
PubMed 17565662 -
The impact of HLA-A and -DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients
Eur J Neurol, 14 (8), 835-40
PubMed 17662002 -
The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material
Tissue Antigens, 70 (3), 190-7
PubMed 17661906 -
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis
Hum Immunol, 68 (9), 748-55
PubMed 17869649 -
Primary sclerosing cholangitis is associated with extended HLA-DR3 and HLA-DR6 haplotypes
Tissue Antigens, 69 (2), 161-9
PubMed 17257319
Publications 2006
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Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort
Hum Immunol, 67 (4-5), 341-5
PubMed 16720215 -
Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort
Tissue Antigens, 68 (3), 249-52
PubMed 16948647 -
FOXP3 polymorphisms in type 1 diabetes and coeliac disease
J Autoimmun, 27 (2), 140-4
PubMed 16996248 -
Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes
Genes Immun, 7 (2), 130-40
PubMed 16395395 -
Analysis of MAdCAM-1 and ICAM-1 polymorphisms in 365 Scandinavian patients with primary sclerosing cholangitis
J Hepatol, 45 (5), 704-10
PubMed 16750586 -
Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis
Gastroenterology, 131 (3), 781-7
PubMed 16952547 -
The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients
Tissue Antigens, 68 (1), 78-81
PubMed 16774544
Publications 2005
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CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases
Pigment Cell Res, 18 (1), 55-8
PubMed 15649153 -
Several genes in the extended human MHC contribute to predisposition to autoimmune diseases
Curr Opin Immunol, 17 (5), 526-31
PubMed 16054351 -
Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients
J Neuroimmunol, 166 (1-2), 197-201
PubMed 16005527 -
Systemic lupus erythematosus and the extended major histocompatibility complex--evidence for several predisposing loci
Rheumatology (Oxford), 44 (11), 1368-73
PubMed 16174649 -
Celiac disease genetics: current concepts and practical applications
Clin Gastroenterol Hepatol, 3 (9), 843-51
PubMed 16234020 -
HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms
Transpl Immunol, 14 (3-4), 175-82
PubMed 15982560 -
Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases
Genes Immun, 6 (3), 271-3
PubMed 15759012
Publications 2004
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Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease
Tissue Antigens, 64 (5), 593-9
PubMed 15496203 -
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
J Clin Endocrinol Metab, 89 (7), 3474-6
PubMed 15240634 -
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
Tissue Antigens, 63 (3), 237-47
PubMed 14989713 -
Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease
Genes Immun, 5 (5), 381-8
PubMed 15164102 -
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm
J Allergy Clin Immunol, 114 (2), 280-7
PubMed 15316504
Publications 2003
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Discussion of the role of hemochromatosis susceptibility gene mutation in protecting against iron deficiency in celiac disease
Gastroenterology, 124 (5), 1562-3; author reply 1564
PubMed 12744238 -
Physical separation of HLA-A alleles by denaturing high-performance liquid chromatography
Tissue Antigens, 61 (6), 443-50
PubMed 12823768 -
No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex
Hum Immunol, 64 (10), 951-9
PubMed 14522092 -
HLA associations in type 1 diabetes: DPB1 alleles may act as markers of other HLA-complex susceptibility genes
Tissue Antigens, 61 (5), 344-51
PubMed 12753653 -
Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and -DRB1
Genes Immun, 4 (1), 46-53
PubMed 12595901 -
Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles
Immunogenetics, 55 (5), 339-43
PubMed 12845502 -
An additional susceptibility gene for juvenile idiopathic arthritis in the HLA class I region on several DR-DQ haplotypes
Tissue Antigens, 61 (1), 80-4
PubMed 12622778 -
Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene
Genome Res, 13 (5), 845-55
PubMed 12727905
Publications 2002
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Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases
Genes Immun, 3 (5), 306-12
PubMed 12140752 -
HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried
Tissue Antigens, 60 (2), 147-54
PubMed 12392509 -
A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis
Arthritis Rheum, 46 (6), 1614-9
PubMed 12115193
Publications 2001
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The polymorphism in the 3' untranslated region of IL12B has a negligible effect on the susceptibility to develop type 1 diabetes in Norway
Immunogenetics, 53 (7), 603-5
PubMed 11685474 -
HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?
Trends Genet, 17 (2), 93-100
PubMed 11173119
Publications 2000
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Application and interpretation of transmission/disequilibrium tests: transmission of HLA-DQ haplotypes to unaffected siblings in 526 families with type 1 diabetes
Am J Hum Genet, 66 (2), 740-3
PubMed 10677335 -
DR- and DQ-associated protection from type 1A diabetes: comparison of DRB1*1401 and DQA1*0102-DQB1*0602*
J Clin Endocrinol Metab, 85 (10), 3793-7
PubMed 11061540
Publications 1999
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A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease
Tissue Antigens, 54 (2), 162-8
PubMed 10488743 -
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene
Am J Hum Genet, 64 (3), 793-800
PubMed 10053014 -
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
Tissue Antigens, 54 (6), 543-51
PubMed 10674967
Publications 1997
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HLA associations in insulin-dependent diabetes mellitus: no independent association to particular DP genes
Hum Immunol, 55 (2), 170-5
PubMed 9361969
Publications 1996
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Detection of psoriasis-associated antigen pso p27 in sarcoidosis bronchoalveolar lavage fluid using monoclonal antibodies
Clin Immunol Immunopathol, 81 (1), 82-7
PubMed 8808646
Publications 1995
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The psoriasis-associated antigen, pso p27, is expressed by tryptase-positive cells in psoriatic lesions
Arch Dermatol Res, 287 (5), 503-5
PubMed 7625863




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