International Journal of Immunogenetics

Papers
(The median citation count of International Journal of Immunogenetics is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-02-01 to 2025-02-01.)
ArticleCitations
Association of single‐nucleotide polymorphisms in tumour necrosis factor and human leukocyte antigens genes with type 1 diabetes64
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Association study of TAP and HLA‐I gene combination with chronic hepatitis C virus infection in a Han population in China31
ICOS gene polymorphisms in systemic lupus erythematosus: A case–control study21
Issue Information20
HLA‐A*02:06 allele may be susceptible to myelodysplastic syndrome in Zhejiang Han population, China19
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Nomenclature for factors of the HLA system, update October, November and December 202316
Nomenclature for factors of the HLA system, update July, August and September 202312
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Issue Information9
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Erythropoiesis signature and ubiquitin‐mediated proteolysis are enriched in systematic juvenile idiopathic arthritis7
Vitamin D receptor gene polymorphisms influence on clinical profile and bone mineral density at different skeletal sites in postmenopausal osteoporotic women6
Forming a new perspective: Post‐structural approaches to determination of donor compatibility and post‐transplant assessment of allograft health6
Nomenclature for factors of the HLA system, update July, August and September 20225
The correlation between soluble human leukocyte antigen (sHLA‐G) levels and +3010 polymorphism5
Issue Information5
Association analysis of B7‐H3 and B7‐H4 gene single nucleotide polymorphisms in susceptibility to ankylosing spondylitis in eastern Chinese Han population5
Issue Information5
Estimating HLA haplotype frequencies from homozygous individuals – A Technical Report5
Genetic associations with lymphomas in Polish patients: A pooled‐DNA genome‐wide association analysis5
HDAC3‐mediated lncRNA ZFAS1 inhibited IL‐13‐induced secretion of proinflammatory cytokines in nasal epithelial cells by regulating the miR‐7‐5p/SIRT1 pathway4
Familial Mediterranean fever and microRNAs4
Approaches for the characterization of clinically relevant pre‐transplant human leucocyte antigen (HLA) antibodies in solid organ transplant patients4
Identification of the novel HLA‐DPA1*01:03:43 allele resulting from an intralocus recombination involving the DPA1*04:01:01:03 and DPA1*01:03:01:27 alleles sequenced by Next Generation Sequencing (NGS4
Association between the interferon‐γ +874 T/A polymorphism and susceptibility to systemic lupus erythematosus and rheumatoid arthritis: A meta‐analysis3
Unrepresented human leucocyte antigen alleles in single‐antigen bead assays: A single‐centre cohort study3
BSHI/BTS guidance on crossmatching before deceased donor kidney transplantation3
Systematic review of associations between HLA and renal function3
Human leukocyte antigen epitope mismatch loads and the development of de novo donor‐specific antibodies in cardiothoracic organ transplantation3
Should results of HLA haplotype frequency estimations be normalized?3
Nomenclature for factors of the HLA system, update April, May and June 20222
Nomenclature for factors of the HLA system, update January, February and March 20212
Issue Information2
IKZF1 rs4132601 and rs11978267 gene polymorphisms and paediatric systemic lupus erythematosus; relation to lupus nephritis2
Nomenclature for factors of the HLA system, update April, May and June 20232
Nomenclature for factors of the HLA system, update April, May and June 20242
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Issue Information2
Issue Information2
High‐resolution HLA sequencing and hypocretin receptor 2 autoantibodies in narcolepsy type 1 and type 22
Redundancy and absurd names in immunology2
Forming a new perspective: Post‐structural approaches to determination of donor compatibility and post‐transplant assessment of allograft health1
Interleukin‐21 receptor gene polymorphism (rs2285452 A/G) is associated with susceptibility to Behçet's disease1
Author Index1
Issue Information1
Associations between interleukin 17A and 17F polymorphisms and asthma susceptibility: A meta‐analysis1
Genetic landscape of human platelet antigen variants in the Indian population analysed from 1029 whole genomes1
Correction to Abstracts from the 34th BSHI Annual Conference (2024), 24 September 2024, Manchester1
Influence of HLA‐B Leader (−21M/T) Dimorphism With Bw4/Bw6 Epitopes on Graft Versus Host Disease After Allogenic Haematopoietic Stem Cell Transplantation in North Indians1
Nomenclature for factors of the HLA system, update January, February and March 20241
Associations Between Interleukin‐10 Polymorphisms and Susceptibility to Sjögren's Syndrome: A Meta‐Analysis1
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Interleukin 17A and 17F polymorphisms and asthma susceptibility: Correspondence1
Frequencies of ABO and Rh (D) Blood Group Phenotypes in Pashtuns of North‐Western Pakistan: A population undergoing huge demographic changes1
Genetic epidemiology of human neutrophil antigen variants suggests significant global variability1
IL‐17A and IL‐17F polymorphisms and asthma risk: A meta‐analysis1
Reduced human leukocyte antigen mismatching is associated with more favourable outcomes after unrelated donor haematopoietic stem cell transplantation1
High plasma interleukin‐6 level, but not IL‐6 gene variants, as a predictive marker for the development of hepatocellular carcinoma in a Moroccan population1
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Author Index1
Immunological drivers of IgA nephropathy: Exploring the mucosa–kidney link1
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Research progress of B subfamily of leucocyte immunoglobulin‐like receptors in inflammation1
BSHI guideline: HLA matching and donor selection for haematopoietic progenitor cell transplantation1
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Association analysis of MALAT1 polymorphisms and risk of psoriasis among Iranian patients0
Nomenclature for factors of the HLA system, update January, February and March 20220
0
MALAT1 polymorphisms and psoriasis risk: Correspondence0
Investigation of the relationship between IL17A, IL17F and ILR1N polymorphisms and COVID‐19 severity: The predictive role of IL17A rs2275913 polymorphism in the clinical co0
Association between gene polymorphisms of IL‐12, IL‐12 receptor and IL‐27 and organ involvement in Iranian endometriosis patients0
Nomenclature for factors of the HLA system, update April, May and June 20210
Issue Information0
HLA‐G in Mayas from Yucatan: An evolutionary approach0
Issue Information0
Correlation analysis of IL‐37 gene polymorphisms and susceptibility to chronic HBV infection among Han people in Central China0
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Association between STAT4 gene polymorphism and susceptibility to pulmonary tuberculosis in the Moldavian population0
A susceptibility putative haplotype within NLRP3 inflammasome gene influences ischaemic stroke risk in the population of Punjab, India0
UK NEQAS and BSHI guideline: Laboratory testing and clinical interpretation of HLA genotyping results supporting the diagnosis of coeliac disease0
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Issue Information0
Nomenclature for factors of the HLA system, update July, August and September 20240
Issue Information0
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Issue Information0
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Possible impact of HLA class I and class II on malignancies driven by a single germ‐line BRCA1 mutation0
Homozygous HLA‐DQB1*06:02 combined with T‐cell receptor alpha polymorphism results in narcolepsy onset – A familial case report0
CCR5 promoter region polymorphisms in systemic lupus erythematosus0
Impact of VSIG4 gene polymorphisms on susceptibility and functional status of rheumatoid arthritis0
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Association of PADI4 Gene Polymorphisms With Susceptibility to Rheumatoid Arthritis: Evidence From 24 Case–Control Studies0
Gene polymorphisms of an interleukin‐23 receptor associated with susceptibility to rheumatoid arthritis in the Western Chinese Han population0
Association of C4 Null Alleles and Persistently Low C4 in Asian Indian Patients With Systemic Lupus Erythematosus0
HLA‐G 3′UTR haplotype analyses in HCV infection and HCV‐derived cirrhosis, hepatocellular carcinoma and fibrosis0
Immune and inflammation‐related gene polymorphisms and susceptibility to tuberculosis in Southern Xinjiang population: A case‐control analysis0
High soluble HLA‐DQB2 levels in posttransplant serum are associated with kidney graft dysfunction0
0
Nomenclature for factors of the HLA system, update January, February and March 20230
Association between interleukin‐1 receptor antagonist (IL‐1ra) VNTR, gene polymorphism and breast cancer susceptibility in Iranian population: Experimental and web‐based analysis0
Nomenclature for factors of the HLA system, update October, November and December 20220
Allelic and haplotypic data of MHC class II Alu insertions in Ngazidja (Comoros archipelago) and insight on its historical biology0
Role of C–C chemokine receptor type 5 in pathogenesis of malaria and its severe forms0
Issue Information0
Differential distribution of vitamin D receptor (VDR) gene variants and its expression in systemic lupus erythematosus0
Genetic polymorphisms of TLR1, TLR2, TLR3 and TLR4 in patients with recurrent or severe infections0
A comment on estimating HLA haplotype frequencies from homozygous individuals0
Killer cell immunoglobulin‐like receptor three domains long cytoplasmic tail 1 gene *007 may modulate disease progression of human immunodeficiency virus‐1 infection in the Japanese population0
Issue Information0
An early evaluation of the HISTO SPOT® AB ID Class I & II test in cardiothoracic transplant patients0
Analysis of null deletion polymorphism of glutathione S‐transferase theta (GSTT‐1), associated with anti‐GSTT‐1 antibodies development in transplantation0
Issue Information0
Polymorphisms of HLA genes and hypersensitivity to penicillin among patients in a Taiwanese population0
Genetic polymorphisms of IL6 gene –174G > C and –597G > A are associated with the risk of COVID‐19 severity0
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Extended loci histocompatibility matching in HSCT—Going beyond classical HLA0
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VDR gene polymorphisms are associated with the increased susceptibility to COVID‐19 among iranian population: A case‐control study0
Oral Abstract0
Vitamin D receptor gene polymorphisms role in COVID‐19 severity: Results of a Mexican patients’ cohort0
Does HLA‐DQA1*05 carriage have a greater impact on the outcome of infliximab therapy for isolated small‐bowel Crohn's disease?0
The role of monocyte/macrophage chemokines in pathogenesis of osteoarthritis: A review0
A comparison of immune receptor recombination databases sourced from tumour exome or RNAseq files: Verifications of immunological distinctions between primary and metastatic melanoma0
Correlation of TBX21 gene polymorphisms with ankylosing spondylitis in a Chinese population0
TCR gene segment usage and HLA alleles that are associated with cancer survival rates also represent racial disparities0
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Issue Information0
Association of class II HLA alleles with susceptibility to develop immune‐mediated diseases in Paraguayan patients0
Leukocyte immunoglobulin‐like receptor A3 gene deletion in five Chinese populations and protective association with nasopharyngeal carcinoma0
NK cells in antibody‐mediated rejection – Key effector cells in microvascular graft damage0
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VDR gene polymorphisms and susceptibility to COVID‐19: Correspondence0
Nomenclature for factors of the HLA System, update October, November and December 20210
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The importance of establishing genetic phase in clinical medicine0
CIITA gene polymorphism (rs3087456) in systemic lupus erythematosus and rheumatoid arthritis: A population‐based cohort study0
The polymorphism of HLA‐A, ‐C, ‐B, ‐DRB3/4/5, ‐DRB1, ‐DQB1 loci in Zhejiang Han population, China using NGS technology0
Issue Information0
Association between a single‐nucleotide polymorphism of the angiotensin‐converting enzyme gene and susceptibility to systemic lupus erythematosus in the Hainanese population of China0
Issue Information0
ELISpot assay and prediction of organ transplant rejection0
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Frequency and distribution of HLA‐DQB1 alleles from 2076 cord blood samples of the Vietnamese cohort0
Commentary on review: Forming new perspective approaches to determination of donor compatibility0
Saliva direct PCR protocol for HLA‐DQB1*02 genotyping0
Impact of IRGM gene promoter polymorphisms on susceptibility to chronic HBV infection0
Association between the interleukin‐1B polymorphism at rs16944 T>C and diabetic retinopathy0
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Prevalence of Rh and K phenotypes among blood donors from different ethnicities in Samtah (Southwestern Region) Saudi Arabia0
Oral Abstracts0
Human leukocyte antigen‐G in gynaecological tumours0
Angiotensin‐converting enzyme 2 rs2285666 polymorphism and clinical parameters as the determinants of COVID‐19 severity in Iranian population0
Molecular investigation of vitamin D receptor (VDR) genetic variants and their impact on VDR mRNA and serum vitamin D levels in allergic rhinitis in an Indian population: A case–control study0
Author Index0
Issue Information0
Predicting flow cytometry crossmatch results from single‐antigen bead testing0
BSHI and BTS UK guideline on the detection of alloantibodies in solid organ (and islet) transplantation0
CCR5 promoter polymorphisms associated with nonsmall cell lung cancer0
Study of HLA class II loci reveals DQB1*03:03:02 as a risk factor for asthma in a Pakistani population0
MiR‐467b alleviates lipopolysaccharide‐induced inflammation through targeting STAT1 in chondrogenic ATDC5 cells0
Issue Information0
Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20‐year single centre experience0
Epigenome‐wide methylation haplotype association analysis identified HLA‐DRB1, HLA‐DRB5 and HLA‐DQB1 as risk factors for rheumatoid arthritis0
Polymorphisms in MHC class I molecules influence their interactions with components of the antigen processing and presentation pathway0
Exploring the immunological relevance of pre‐transplant donor‐specific antibody in intestinal transplantation, with special consideration to the liver0
Are the cut‐offs of the rheumatoid factor and anti‐cyclic citrullinated peptide antibody different to distinguish rheumatoid arthritis from their primary differential diagnoses?0
Correlation of CTLA‐4 polymorphism and the risk of gastric cancer in a Chinese Bai population0
Replication Study and Meta‐Analysis of the Contribution of Seven Genetic Polymorphisms in Immune‐Related Genes to the Risk of Gastric and Colorectal Cancers0
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Solute carrier family 11 member 1 genetic polymorphisms rs17235409 and rs3731865 associate with susceptibility to extremity post‐traumatic osteomyelitis in a Chinese Han population0
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Abstracts0
Investigation of cytokine polymorphisms on viral infections after renal transplantation exhibit association between IFN‐γ +874 A > T and CMV manifestations0
High‐resolution HLA class II sequencing of Swedish multiple sclerosis patients0
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Rheumatoid arthritis‐associated antibodies in healthy first‐degree relatives of RA patients0
Frequency distribution of HLA class I and II alleles in Greek population and their significance in orchestrating the National Donor Registry Program0
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Poster Abstract0
Issue Information0
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Nomenclature for Factors of the HLA System, Update October, November and December 20240
Response to MALAT1 polymorphisms and psoriasis risk: Correspondence0
HLA‐DQ7.5 and coeliac disease0
Evaluation of Hardy–Weinberg equilibrium in genetic association studies0
Issue Information0
LncRNA MALAT1 potentiates inflammation disorder in Parkinson's disease0
Nomenclature for factors of the HLA system, update July, August and September 20210
Non‐invasive molecular biomarkers for monitoring solid organ transplantation: A comprehensive overview0
Correlation of single nucleotide polymorphisms in the AGT gene with susceptibility to systemic lupus erythematosus in Northeast China0
0
Issue Information0
Nomenclature for factors of the HLA system, update October, November and December 20200
Association between PTPN22 C1858T polymorphism and juvenile idiopathic arthritis: A meta‐analysis update with trial sequential analysis0
A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population0
Distribution of HLA‐DQA1, ‐DQB1 and ‐DRB1 genes and haplotypes in Han, Uyghur, Kazakh and Hui populations inhabiting Xinjiang Uyghur Autonomous Region, China0
RNA receptors, TLR3 and TLR7, are potentially associated with SLE clinical features0
IL1R2 polymorphisms and their interaction are associated with osteoporosis susceptibility in the Chinese Han population0
Genetic variations in low‐to‐medium‐affinity Fcγ receptors and autoimmune neutropenia in early childhood in a Danish cohort0
Investigations of associations between TNF‐α promoter polymorphisms and genetic susceptibility to type 2 diabetes mellitus: A cross‐sectional study in Chinese Han population0
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