| human | Q5 |
| P213 | ISNI | 0000000484311710 |
| P8980 | KANTO ID | 000054829 |
| P2798 | Loop ID | 178346 |
| P3835 | Mendeley person ID | jukka-partanen2 |
| P1207 | NUKAT ID | n2019209430 |
| P496 | ORCID iD | 0000-0001-6681-4734 |
| P3829 | Publons author ID | 2561746 |
| P1053 | ResearcherID | B-7207-2014 |
| P214 | VIAF ID | 5404163813724239110008 |
| P27 | country of citizenship | Finland | Q33 |
| P69 | educated at | University of Oxford | Q34433 |
| P734 | family name | Partanen | Q27890935 |
| Partanen | Q27890935 | ||
| Partanen | Q27890935 | ||
| P735 | given name | Jukka | Q920373 |
| Jukka | Q920373 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q73425949 | A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction |
| Q73012097 | A collaborative European search for non-DQA1*05-DQB1*02 celiac disease loci on HLA-DR3 haplotypes: analysis of transmission from homozygous parents |
| Q71127103 | A comparative study of HLA genes in HLA-B27 positive ankylosing spondylitis and HLA-B27 positive peripheral reactive arthritis |
| Q57232760 | A new locus for coeliac disease mapped to chromosome 15 in a population isolate |
| Q71742082 | A rare neutral polymorphism in 21-hydroxylase genes as HLA haplotype marker. Evidence for strong founder effect in the Finnish population |
| Q61960534 | AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype |
| Q47564718 | Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing Data. |
| Q73407609 | Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease |
| Q73149614 | Alloimmunization against platelet antigens in renal transplant patients with acute vascular rejection |
| Q54338064 | An approach to mapping haplotype-specific recombination sites in human MHC class III. |
| Q82383808 | Antibodies against deamidated gliadin peptides in early-stage celiac disease |
| Q51582170 | Antibodies to glutamic acid decarboxylase and insulin-dependent diabetes in patients with autoimmune polyendocrine syndrome type I. |
| Q60032037 | Association of HLA B27 with benign clinical course of nephropathia epidemica caused by Puumala hantavirus |
| Q33437907 | Association of IL-10 and IL-10Rbeta gene polymorphisms with graft-versus-host disease after haematopoietic stem cell transplantation from an HLA-identical sibling donor |
| Q40437812 | Association of chest radiography findings with host-related genetic factors in patients with nephropathia epidemica. |
| Q50619112 | Association of genetic variation in inducible costimulator gene with outcome of kidney transplantation. |
| Q63258457 | Association study ofFUT2(rs601338) with celiac disease and inflammatory bowel disease in the Finnish population |
| Q73486161 | Autoimmunity to glutamic acid decarboxylase in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) |
| Q52343795 | Blood donors' preferences for blood donation for biomedical research. |
| Q33676915 | C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes. |
| Q56907069 | CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study |
| Q74470500 | CD80 (B7-1) and CD86 (B7-2) genes and genetic susceptibility to coeliac disease |
| Q73834078 | Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families |
| Q48025167 | Candidate gene region 2q33 in European families with coeliac disease |
| Q78388977 | Celiac disease and HLA DQ in patients with IgA nephropathy |
| Q72999268 | Celiac disease and autoimmune endocrinologic disorders |
| Q77319023 | Celiac disease and markers of celiac disease latency in patients with primary Sjögren's syndrome |
| Q43557858 | Celiac disease in patients with severe liver disease: gluten-free diet may reverse hepatic failure |
| Q47902680 | Celiac disease risk in the USA: high prevalence of antiendomysium antibodies in healthy blood donors |
| Q73823200 | Celiac disease without villous atrophy: revision of criteria called for |
| Q44079933 | Celiac disease, thyrotoxicosis, and autoimmune hepatitis in a child |
| Q81913394 | Celiac disease: from inflammation to atrophy: a long-term follow-up study |
| Q73294514 | Celiac patients predominantly inherit HLA-DPB1*0101 positive haplotype from HLA-DQ2 homozygous parent |
| Q47614274 | Characterization a novel HLA-B40 allele with serological Bw4 motif, HLA-B*4047, in the Finnish population and confirmation of B*270503 allele. |
| Q52040030 | Circulating T lymphocyte subsets in coeliac disease (CoD) patients and healthy family members. |
| Q77635238 | Coeliac disease among healthy members of multiple case coeliac disease families |
| Q81634792 | Collection of autologous blood for bone marrow donation: how useful is it? |
| Q33560757 | Complement activation and HLA-B27 |
| Q73307474 | Concordance of dermatitis herpetiformis and celiac disease in monozygous twins |
| Q50249146 | Conflicting HLA assignment by three different typing methods due to the apparent loss of heterozygosity in the MHC region. |
| Q56968738 | Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations |
| Q50777586 | Cytokine gene polymorphisms and genetic association with coeliac disease in the Finnish population. |
| Q50779412 | Cytokine gene polymorphisms and risks of acute rejection and delayed graft function after kidney transplantation. |
| Q69916661 | DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia |
| Q57232823 | Determination of deletion sizes in the MHC-linked complement C4 and steroid 21-hydroxylase genes by pulsed-field gel electrophoresis |
| Q83102309 | Diagnosing mild enteropathy celiac disease: a randomized, controlled clinical study |
| Q50699689 | Diagnosis of acute renal allograft rejection by analyzing whole blood mRNA expression of lymphocyte marker molecules. |
| Q79293034 | Diagnostic significance of HLA-DQ typing in patients with previous coeliac disease diagnosis based on histology alone |
| Q71620558 | Distinct immunologic features of Finnish Sjögren's syndrome patients with HLA alleles DRB1*0301, DQA1*0501, and DQB1*0201. Alterations in circulating T cell receptor gamma/delta subsets |
| Q39998188 | Domestic and foreign donor candidates result in differential probability of matching minor histocompatibility antigens--relevance of selection for hematopoietic stem cell transplantation. |
| Q41829086 | Donor Haplotype B of NK KIR Receptor Reduces the Relapse Risk in HLA-Identical Sibling Hematopoietic Stem Cell Transplantation of AML Patients |
| Q33583414 | Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease |
| Q22306528 | Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency |
| Q35988487 | Endomysial antibodies predict celiac disease irrespective of the titers or clinical presentation |
| Q24679813 | Endomysial antibody-negative coeliac disease: clinical characteristics and intestinal autoantibody deposits |
| Q73461527 | Expression of HSP-65 in jejunal epithelial cells in patients clinically suspected of coeliac disease |
| Q68017763 | Extended HLA haplotypes in families with insulin-dependent diabetes mellitus in northern Finland |
| Q90965123 | FinDonor 10 000 study: a cohort to identify iron depletion and factors affecting it in Finnish blood donors |
| Q33498523 | Full likelihood analysis of genetic risk with variable age at onset disease--combining population-based registry data and demographic information |
| Q40007698 | Functional network reconstruction reveals somatic stemness genetic maps and dedifferentiation-like transcriptome reprogramming induced by GATA2. |
| Q98196756 | Gamete-level immunogenetic incompatibility in humans-towards deeper understanding of fertilization and infertility? |
| Q56903521 | Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33 |
| Q44608172 | Genetic background of type I protein C deficiency in Finland |
| Q78672918 | Genetic dissection between coeliac disease and dermatitis herpetiformis in sib pairs |
| Q73141719 | Genetic dissection between silent and clinically diagnosed symptomatic forms of coeliac disease in multiplex families |
| Q46267696 | Genetic diversity of KIR natural killer cell markers in populations from France, Guadeloupe, Finland, Senegal and Réunion |
| Q33503779 | Genetic polymorphism H131R of Fcgamma receptor type IIA (FcgammaRIIA) in a healthy Finnish population and in patients with or without platelet-associated IgG. |
| Q33504147 | Genetic polymorphism in human platelet glycoprotein GP Ib/IX/V complex is enriched in GP V (CD42d). |
| Q28208298 | Genetic polymorphism of the human ICOS gene |
| Q45853292 | Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease. |
| Q67577291 | Genetic structure of the novel low-frequency haplotype HLA-B49, SC01, DR4 and its contribution to insulin-dependent diabetes susceptibility |
| Q77813431 | Genetic susceptibility to gluten sensitive enteropathy in Irish setter dogs is not linked to the major histocompatibility complex |
| Q40675093 | Genetic susceptibility to severe course of nephropathia epidemica caused by Puumala hantavirus. |
| Q72991342 | Genetic susceptibility to variant Creutzfeldt-Jakob disease |
| Q50720441 | Genetic variation in ICOS regulates mRNA levels of ICOS and splicing isoforms of CTLA4. |
| Q34145715 | Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q. |
| Q40751383 | Genomewide linkage analysis of celiac disease in Finnish families |
| Q90841517 | Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation |
| Q36975020 | Geographic distribution of cervical cancer-associated human leucocyte antigens and cervical cancer incidence in Finland |
| Q43812144 | Gliadin antibodies in older population and neurological and psychiatric disorders. |
| Q50752717 | Global gene expression profile of human cord blood-derived CD133+ cells. |
| Q82286254 | Gluten-dependent small bowel mucosal transglutaminase 2-specific IgA deposits in overt and mild enteropathy coeliac disease |
| Q83898810 | Gluten-sensitive hypertransaminasemia in celiac disease: an infrequent and often subclinical finding |
| Q33431066 | Glycosylation pattern of anti-platelet IgG is stable during pregnancy and predicts clinical outcome in alloimmune thrombocytopenia |
| Q42106581 | Graft Immune Cell Composition Associates with Clinical Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with AML |
| Q71523153 | HLA DQ and DP in Finnish families with celiac disease |
| Q68729114 | HLA antigens and complotypes in insulin-dependent diabetes mellitus |
| Q77451320 | HLA class II associated risk and protection against multiple sclerosis-a Finnish family study |
| Q28185658 | HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease |
| Q43704311 | HLA-DQ alleles and human papillomavirus DNA in adult-onset laryngeal papillomatosis |
| Q77845009 | HLA-DQ typing in the diagnosis of celiac disease |
| Q34746827 | HLA-DQ2-negative celiac disease in Finland and Spain. |
| Q83013117 | HLA-DRB1, -DQB1 alleles in head and neck carcinoma patients |
| Q50200953 | Haematopoietic stem cell transplantation induces severe dysbiosis in intestinal microbiota of paediatric ALL patients. |
| Q50688236 | Heme oxygenase 1 gene polymorphisms and outcome of renal transplantation. |
| Q52620753 | Hidden genomic MHC disparity between HLA-matched sibling pairs in hematopoietic stem cell transplantation. |
| Q47426417 | High birth weight is associated with human leukocyte antigen (HLA) DRB1*13 in full-term infants |
| Q45750945 | High-producer allele of tumour necrosis factor-alpha is part of the susceptibility MHC haplotype in severe puumala virus-induced nephropathia epidemica |
| Q40576039 | Human leukocyte antigen-B8-DR3 is a more important risk factor for severe Puumala hantavirus infection than the tumor necrosis factor-alpha(-308) G/A polymorphism. |
| Q40519033 | Human leukocyte antigens B8-DRB1*03 in pediatric patients with nephropathia epidemica caused by Puumala hantavirus |
| Q34174670 | IgA-class autoantibodies against neuronal transglutaminase, TG6 in celiac disease: no evidence for gluten dependency |
| Q33596525 | Immunogenetic characteristics of patients with autoimmune gastritis |
| Q64966964 | Immunoglobulin A autoantibodies against transglutaminase 2 in the small intestinal mucosa predict forthcoming coeliac disease. |
| Q52667946 | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety. |
| Q50241795 | In vitro Treg expansion favors the full-length splicing isoform of CTLA4. |
| Q90793317 | Increased MHC Matching by C4 Gene Compatibility in Unrelated Donor Hematopoietic Stem Cell Transplantation |
| Q78086086 | Increased density of jejunal gammadelta+ T cells in patients having normal mucosa--marker of operative autoimmune mechanisms? |
| Q37288390 | Interaction with intestinal epithelial cells promotes an immunosuppressive phenotype in Lactobacillus casei |
| Q48072150 | Interspliced transcription chimeras: neglected pathological mechanism infiltrating gene accession queries? |
| Q84088589 | Intestinal transglutaminase 2 specific antibody deposits in non-responsive coeliac disease |
| Q55034358 | Intolerance to cereals is not specific for coeliac disease. |
| Q54494218 | Killer-cell immunoglobulin-like receptor gene profile predicts good molecular response to dasatinib therapy in chronic myeloid leukemia. |
| Q50690561 | Killer-cell immunoglobulin-like receptor ligand compatibility in the outcome of Finnish unrelated donor hematopoietic stem cell transplantation. |
| Q50682631 | Lack of association between thrombosis-associated and cytokine candidate gene polymorphisms and acute rejection or vascular complications after kidney transplantation. |
| Q83653484 | Low-medium resolution HLA-DQ2/DQ8 typing for coeliac disease predisposition analysis by colorimetric assay |
| Q74221903 | Major histocompatibility complex (MHC)-linked microsatellite markers in a founder population |
| Q72555873 | Major histocompatibility complex class II and III in Addison's disease. MHC alleles do not predict autoantibody specificity and 21-hydroxylase gene polymorphism has no independent role in disease susceptibility |
| Q87450554 | Medium-high resolution electrochemical genotyping of HLA-DQ2/DQ8 for detection of predisposition to coeliac disease |
| Q50493937 | Minor histocompatibility antigens as determinants for graft-versus-host disease after allogeneic haematopoietic stem cell transplantation. |
| Q47724661 | Molecular characterization of two mutations in platelet glycoprotein (GP) Ib alpha in two Finnish Bernard-Soulier syndrome families |
| Q46507269 | Multicenter analyses demonstrate significant clinical effects of minor histocompatibility antigens on GvHD and GvL after HLA-matched related and unrelated hematopoietic stem cell transplantation |
| Q41172371 | Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation. |
| Q47797169 | Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles |
| Q56968827 | Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association |
| Q38299604 | N-glycan structures and associated gene expression reflect the characteristic N-glycosylation pattern of human hematopoietic stem and progenitor cells. |
| Q77635201 | Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families |
| Q77359468 | Novel mutations in the human CYP21 gene |
| Q73218536 | Novel nonsense mutation (W302X) in the steroid 21-hydroxylase gene of a Finnish patient with the salt-wasting form of congenital adrenal hyperplasia |
| Q70348805 | Patients with rheumatoid arthritis and gold-induced pneumonitis express two high-risk major histocompatibility complex patterns |
| Q50671264 | Performance of a new rapid whole blood coeliac test in adult patients with low prevalence of endomysial antibodies. |
| Q80199326 | Persistent small bowel mucosal villous atrophy without symptoms in coeliac disease |
| Q61834994 | Persistently positive gliadin antibodies without transglutaminase antibodies in the elderly: Gluten intolerance beyond coeliac disease |
| Q70982965 | Platelet alloantigens HPA-1, -2, -3, -5 and -6b in Finns |
| Q73784944 | Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population |
| Q82256294 | Protein S gene polymorphisms Pro626 and nt2698--no correlation to free protein S levels or protein S activities |
| Q72178300 | Reappraisal of HLA in multiple sclerosis: close linkage in multiplex families |
| Q69376861 | Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles |
| Q81244446 | Resurrection of gliadin antibodies in coeliac disease. Deamidated gliadin peptide antibody test provides additional diagnostic benefit |
| Q89776985 | Retrospective analysis of capillary hemoglobin recovery in nearly 1 200 000 blood donor returns |
| Q33321946 | Secretion of celiac disease autoantibodies after in vitro gliadin challenge is dependent on small-bowel mucosal transglutaminase 2-specific IgA deposits |
| Q33916431 | Secretor genotype (FUT2 gene) is strongly associated with the composition of Bifidobacteria in the human intestine |
| Q83559355 | Serodiagnostic assays for celiac disease based on the open or closed conformation of the autoantigen, transglutaminase 2 |
| Q73043926 | Single founder mutation (W380G) in type II protein C deficiency in Finland |
| Q34435922 | Small-bowel mucosal transglutaminase 2-specific IgA deposits in coeliac disease without villous atrophy: a prospective and randomized clinical study. |
| Q71543842 | Steroid 21-hydroxylase gene polymorphism in Addison's disease patients |
| Q33431446 | Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia |
| Q33495977 | Systematic screening for genetic polymorphism in human platelet glycoprotein Ibalpha |
| Q60420151 | T cell epitope-containing peptides of the major dog allergen Can f 1 as candidates for allergen immunotherapy |
| Q44097382 | T cell regeneration in pediatric allogeneic stem cell transplantation. |
| Q71437269 | TAP1 and TAP2 polymorphism in HLA-B27-positive subpopulations: no allelic differences in ankylosing spondylitis and reactive arthritis |
| Q47809673 | TNF microsatellite alleles a2 and b3 are not primarily associated with celiac disease in the Finnish population |
| Q56904979 | Technical note: linkage disequilibrium and disease-associated CTLA4 gene polymorphisms |
| Q40406647 | The DR4-DQ8 haplotype and a specific T cell receptor Vbeta T cell subset are associated with absence of allergy to Can f 1. |
| Q73639261 | The HLA-DRB4 gene does not explain genetic susceptibility in HLA-DQ2-negative celiac disease |
| Q75196773 | The association between mannan-binding lectin gene alleles and celiac disease |
| Q34616316 | The duodenal microbiota composition of adult celiac disease patients is associated with the clinical manifestation of the disease |
| Q50713209 | The impact of donor cytokine gene polymorphisms on the incidence of cytomegalovirus infection after kidney transplantation. |
| Q42678139 | The natural history of an HLA haplotype and its recombinants. |
| Q80910697 | The prevalence of celiac disease among family members of celiac disease patients |
| Q60031833 | The severity of acute Puumala hantavirus infection does not predict the long-term outcome of patients |
| Q42603709 | The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency. |
| Q43477328 | Toll-like receptor gene polymorphisms confer susceptibility to graft-versus-host disease in allogenic hematopoietic stem cell transplantation. |
| Q33858239 | Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland |
| Q50707670 | Transcriptional profiling reflects shared and unique characters for CD34+ and CD133+ cells. |
| Q34043694 | Use of closely related affected individuals for the genetic study of complex diseases in founder populations. |
| Q33328670 | Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated Finnish families. |
| Q80165540 | Villous tip intraepithelial lymphocytes as markers of early-stage coeliac disease |
| Q73336619 | ss-cell autoantibodies, human leukocyte antigen II alleles, and type 1 diabetes in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy |
Search more.