about
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasisA genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis.Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to susceptibility to psoriatic arthritis in German patientsSystematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgaris.Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6.Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterization.Association of β-defensin copy number and psoriasis in three cohorts of European origin.Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patientsMolecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arraysGenotyping microarray for CSNB-associated genes.Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1.Tumor necrosis factor receptor-associated periodic syndrome characterized by a mutation affecting the cleavage site of the receptor: implications for pathogenesis.Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1.Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition.Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis.Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohort.Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.Cytokine balance in infants undergoing cardiac operation.Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts.Mutations in IL36RN in patients with generalized pustular psoriasis.New mutations of EXT1 and EXT2 genes in German patients with Multiple Osteochondromas.Tumor necrosis factor polymorphisms in psoriatic arthritis: association with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele.Association between protein tyrosine phosphatase 22 variant R620W in conjunction with the HLA-DRB1 shared epitope and humoral autoimmunity to an immunodominant epitope of cartilage-specific type II collagen in early rheumatoid arthritis.Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis.Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis.The genetic basis for most patients with pustular skin disease remains elusive.Successful therapy with anakinra in a patient with generalized pustular psoriasis carrying IL36RN mutations.Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.Corrigendum: Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis.Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients.Severe skeletal dysplasia caused by undiagnosed hypothyroidism.Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in IL36RN in German patients.Mannan-induced Nos2 in macrophages enhances IL-17-driven psoriatic arthritis by innate lymphocytes.Variants inRUNX3Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground With Ankylosing SpondylitisReplication of LCE3C–LCE3B CNV as a Risk Factor for Psoriasis and Analysis of Interaction with Other Genetic Risk FactorsTNF polymorphisms in psoriasis: Association of psoriatic arthritis with the promoter polymorphismTNF*-857 independent of thePSORS1 risk allele
P50
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P50
description
hulumtuese
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wetenschapper
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հետազոտող
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
@nl
Ulrike Hüffmeier
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type
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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Ulrike Hüffmeier
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P1053
D-2806-2013
P106
P21
P31
P3829
P496
0000-0001-6448-4671