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 2021-11-01 to 2025-11-01.)
ArticleCitations
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Association between the interferon‐γ +874 T/A polymorphism and susceptibility to systemic lupus erythematosus and rheumatoid arthritis: A meta‐analysis26
Risk Genes and Anti‐C1q Autoantibodies in Upper Egyptian Patients With Systemic Lupus Erythromatosis—High Frequency of HLA‐DRB1*04:05–DQA1*03–DQB1*02 Risk Haplotype in Lupus Nephritis Patients22
HDAC3‐mediated lncRNA ZFAS1 inhibited IL‐13‐induced secretion of proinflammatory cytokines in nasal epithelial cells by regulating the miR‐7‐5p/SIRT1 pathway22
Comparison of HISTO SPOT HLA AB With Cross‐Match Results19
The correlation between soluble human leukocyte antigen (sHLA‐G) levels and +3010 polymorphism15
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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 Indians8
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Interleukin‐21 receptor gene polymorphism (rs2285452 A/G) is associated with susceptibility to Behçet's disease8
Systematic review of associations between HLA and renal function8
High plasma interleukin‐6 level, but not IL‐6 gene variants, as a predictive marker for the development of hepatocellular carcinoma in a Moroccan population7
Genetic epidemiology of human neutrophil antigen variants suggests significant global variability7
Association between STAT4 gene polymorphism and susceptibility to pulmonary tuberculosis in the Moldavian population6
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Association analysis of MALAT1 polymorphisms and risk of psoriasis among Iranian patients5
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Association of Vitamin D Deficiency and Vitamin D Receptor FokI Gene Polymorphism With Diabetic Retinopathy Complications in Ethiopian Patients With Type 2 Diabetes Mellitus5
CCR5 promoter region polymorphisms in systemic lupus erythematosus5
Nomenclature for Factors of the HLA System, Update October, November and December 20245
Cytokine and IRF5 Gene Polymorphisms Associated With Susceptibility and Organ Damage in Systemic Lupus Erythematosus4
Nomenclature for factors of the HLA system, update January, February and March 20234
High soluble HLA‐DQB2 levels in posttransplant serum are associated with kidney graft dysfunction3
Possible impact of HLA class I and class II on malignancies driven by a single germ‐line BRCA1 mutation3
Allelic and haplotypic data of MHC class II Alu insertions in Ngazidja (Comoros archipelago) and insight on its historical biology3
Immune and inflammation‐related gene polymorphisms and susceptibility to tuberculosis in Southern Xinjiang population: A case‐control analysis3
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Non‐invasive molecular biomarkers for monitoring solid organ transplantation: A comprehensive overview3
Investigation of cytokine polymorphisms on viral infections after renal transplantation exhibit association between IFN‐γ +874 A > T and CMV manifestations3
Nomenclature for factors of the HLA system, update October, November and December 20223
Professor Paul Dunn, 1958–20253
Association between gene polymorphisms of IL‐12, IL‐12 receptor and IL‐27 and organ involvement in Iranian endometriosis patients3
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HLA‐DQ7.5 and coeliac disease3
Human leukocyte antigen‐G in gynaecological tumours3
A susceptibility putative haplotype within NLRP3 inflammasome gene influences ischaemic stroke risk in the population of Punjab, India3
Association of TNFRSF13B Gene Polymorphisms With SARS‐CoV‐2 Infection, Severity, and Humoral Immune Response in a Moroccan Population2
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Nomenclature for factors of the HLA system, update April, May and June 20232
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Vitamin D receptor gene polymorphisms role in COVID‐19 severity: Results of a Mexican patients’ cohort2
Polymorphisms of HLA genes and hypersensitivity to penicillin among patients in a Taiwanese population2
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Associations between interleukin 17A and 17F polymorphisms and asthma susceptibility: A meta‐analysis2
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Association between interleukin‐1 receptor antagonist (IL‐1ra) VNTR, gene polymorphism and breast cancer susceptibility in Iranian population: Experimental and web‐based analysis2
Vitamin D receptor gene polymorphisms influence on clinical profile and bone mineral density at different skeletal sites in postmenopausal osteoporotic women2
Gene polymorphisms of an interleukin‐23 receptor associated with susceptibility to rheumatoid arthritis in the Western Chinese Han population2
Research progress of B subfamily of leucocyte immunoglobulin‐like receptors in inflammation2
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Genetic Variations in TLR2 and TLR4 Genes and Their Association With COVID‐19 Severity and Inflammatory Markers in the Moroccan Population1
Polymorphism Analysis as Biomarker in Genes AIRE, CD40, HLA‐DRB1 and TRAF1/C5 SNPs in Rheumatoid Arthritis Patients1
Correlation of TBX21 gene polymorphisms with ankylosing spondylitis in a Chinese population1
Poster Abstract1
Extended Typing of Common Erythrocyte Antigens in Tunisian Blood Donors and Its Usefulness in Transfusion Immunology1
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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 (NGS1
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Redundancy and absurd names in immunology1
Immunological drivers of IgA nephropathy: Exploring the mucosa–kidney link1
Association study of TAP and HLA‐I gene combination with chronic hepatitis C virus infection in a Han population in China1
HLA‐G 3′UTR haplotype analyses in HCV infection and HCV‐derived cirrhosis, hepatocellular carcinoma and fibrosis1
Association of HLA‐G 14‐bp Insertion/Deletion Polymorphism With Recurrent Spontaneous Abortion: A Meta‐Analysis1
Are the cut‐offs of the rheumatoid factor and anti‐cyclic citrullinated peptide antibody different to distinguish rheumatoid arthritis from their primary differential diagnoses?1
A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population1
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Replication Study and Meta‐Analysis of the Contribution of Seven Genetic Polymorphisms in Immune‐Related Genes to the Risk of Gastric and Colorectal Cancers1
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Forming a new perspective: Post‐structural approaches to determination of donor compatibility and post‐transplant assessment of allograft health1
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Forming a new perspective: Post‐structural approaches to determination of donor compatibility and post‐transplant assessment of allograft health1
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Association of IL‐13 Gene Polymorphism (rs20541) With Chronic Inflammatory Diseases: A Systematic Review and Meta‐Analysis1
Association of class II HLA alleles with susceptibility to develop immune‐mediated diseases in Paraguayan patients1
Author Index1
Association of SOCS6 Gene Polymorphisms and Promoter Hypermethylation With the Progression of Hepatitis B Virus Infection1
Association of C4 Null Alleles and Persistently Low C4 in Asian Indian Patients With Systemic Lupus Erythematosus1
Interleukin 6 Promoter Region Polymorphism in Patients With Type 2 Diabetes Mellitus, Study in One Egyptian Centre1
UK NEQAS and BSHI guideline: Laboratory testing and clinical interpretation of HLA genotyping results supporting the diagnosis of coeliac disease1
Differential distribution of vitamin D receptor (VDR) gene variants and its expression in systemic lupus erythematosus1
Genetic associations with lymphomas in Polish patients: A pooled‐DNA genome‐wide association analysis1
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Unrepresented human leucocyte antigen alleles in single‐antigen bead assays: A single‐centre cohort study1
Response to “Unaddressed Confounding Factors Undermine Causal Inference in the Study on IL‐6 Promoter Region Polymorphism and Type 2 Diabetes Mellitus in an Egyptian Centre”0
HLA‐C*01:02 and ‐C*04:03 May Confer Susceptibility to Treponema pallidum Infection in the Chinese Han Population0
Nomenclature for factors of the HLA system, update July, August and September 20230
A Prospective Pilot Study to Investigate Whether Donor‐Derived Cell‐Free DNA Can Be Used as a Biomarker of Recurrent IgA Nephropathy Post–Kidney Transplantation0
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The Quest for Antibodies and Other Acquired Immune Receptors: A Historical Perspective0
Analysis of null deletion polymorphism of glutathione S‐transferase theta (GSTT‐1), associated with anti‐GSTT‐1 antibodies development in transplantation0
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
High‐resolution HLA sequencing and hypocretin receptor 2 autoantibodies in narcolepsy type 1 and type 20
High‐resolution HLA class II sequencing of Swedish multiple sclerosis patients0
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Oral Abstract0
Exploring the immunological relevance of pre‐transplant donor‐specific antibody in intestinal transplantation, with special consideration to the liver0
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Genetic variations in low‐to‐medium‐affinity Fcγ receptors and autoimmune neutropenia in early childhood in a Danish cohort0
Association between a single‐nucleotide polymorphism of the angiotensin‐converting enzyme gene and susceptibility to systemic lupus erythematosus in the Hainanese population of China0
Study of HLA class II loci reveals DQB1*03:03:02 as a risk factor for asthma in a Pakistani population0
Nomenclature for factors of the HLA system, update April, May and June 20220
Association of PADI4 Gene Polymorphisms With Susceptibility to Rheumatoid Arthritis: Evidence From 24 Case–Control Studies0
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Associations Between Interleukin‐10 Polymorphisms and Susceptibility to Sjögren's Syndrome: A Meta‐Analysis0
Familial Mediterranean fever and microRNAs0
Nomenclature for factors of the HLA System, update October, November and December 20210
CCR5 promoter polymorphisms associated with nonsmall cell lung cancer0
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Homozygous HLA‐DQB1*06:02 combined with T‐cell receptor alpha polymorphism results in narcolepsy onset – A familial case report0
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Epigenome‐wide methylation haplotype association analysis identified HLA‐DRB1, HLA‐DRB5 and HLA‐DQB1 as risk factors for rheumatoid arthritis0
Role of C–C chemokine receptor type 5 in pathogenesis of malaria and its severe forms0
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
An NLRP3 Variant Protects Against Severe COVID‐19: An Unexpected Contribution of Inflammasome Genetics in SARS‐CoV‐2 Infection0
Unaddressed Confounding Factors Undermine Causal Inference in the Study on IL‐6 Promoter Region Polymorphism and Type 2 Diabetes Mellitus in an Egyptian Centre0
BSHI and BTS UK guideline on the detection of alloantibodies in solid organ (and islet) transplantation0
Association between PTPN22 C1858T polymorphism and juvenile idiopathic arthritis: A meta‐analysis update with trial sequential analysis0
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ICOS gene polymorphisms in systemic lupus erythematosus: A case–control study0
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Abstracts0
Nomenclature for Factors of the HLA System, Update April, May and June 20250
Solute carrier family 11 member 1 genetic polymorphisms rs17235409 and rs3731865 associate with susceptibility to extremity post‐traumatic osteomyelitis in a Chinese Han population0
IL‐17A and IL‐17F polymorphisms and asthma risk: A meta‐analysis0
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Association Between Pathogenic Variants in NLRP12 and Autoinflammatory Disease: A Comprehensive Systematic Review0
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IKZF1 rs4132601 and rs11978267 gene polymorphisms and paediatric systemic lupus erythematosus; relation to lupus nephritis0
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
MALAT1 polymorphisms and psoriasis risk: Correspondence0
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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Human leukocyte antigen epitope mismatch loads and the development of de novo donor‐specific antibodies in cardiothoracic organ transplantation0
Association between the interleukin‐1B polymorphism at rs16944 T>C and diabetic retinopathy0
Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20‐year single centre experience0
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Author Index0
An early evaluation of the HISTO SPOT® AB ID Class I & II test in cardiothoracic transplant patients0
The role of monocyte/macrophage chemokines in pathogenesis of osteoarthritis: A review0
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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ELISpot assay and prediction of organ transplant rejection0
Oral Abstracts0
The importance of establishing genetic phase in clinical medicine0
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Correlation of single nucleotide polymorphisms in the AGT gene with susceptibility to systemic lupus erythematosus in Northeast China0
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Nomenclature for factors of the HLA system, update January, February and March 20220
VDR gene polymorphisms and susceptibility to COVID‐19: Correspondence0
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Leukocyte immunoglobulin‐like receptor A3 gene deletion in five Chinese populations and protective association with nasopharyngeal carcinoma0
Nomenclature for Factors of the HLA System, Update January, February and March 20250
Nomenclature for factors of the HLA system, update July, August and September 20210
Co‐Occurrence of HIV‐Susceptibility and ‐Protective HLA Alleles Is a Possible Contributor to the Development of Primary HIV‐Associated Thrombocytopenia (PHAT): A Cross‐Sectional Study0
Correlation analysis of IL‐37 gene polymorphisms and susceptibility to chronic HBV infection among Han people in Central China0
HLA‐A*02:06 allele may be susceptible to myelodysplastic syndrome in Zhejiang Han population, China0
Prevalence of Rh and K phenotypes among blood donors from different ethnicities in Samtah (Southwestern Region) Saudi Arabia0
Correlation of CTLA‐4 polymorphism and the risk of gastric cancer in a Chinese Bai population0
Correction to Abstracts from the 34th BSHI Annual Conference (2024), 24 September 2024, Manchester0
Erythropoiesis signature and ubiquitin‐mediated proteolysis are enriched in systematic juvenile idiopathic arthritis0
Nomenclature for factors of the HLA system, update July, August and September 20240
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Evaluation of Hardy–Weinberg equilibrium in genetic association studies0
The Distribution of HLA‐DRB4 Alleles Among HLA‐DRB1*07:01‐Positive Haplotypes in Saudi Arabia0
Genetic landscape of human platelet antigen variants in the Indian population analysed from 1029 whole genomes0
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TCR gene segment usage and HLA alleles that are associated with cancer survival rates also represent racial disparities0
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Angiotensin‐converting enzyme 2 rs2285666 polymorphism and clinical parameters as the determinants of COVID‐19 severity in Iranian population0
Interleukin 17A and 17F polymorphisms and asthma susceptibility: Correspondence0
Frequency and distribution of HLA‐DQB1 alleles from 2076 cord blood samples of the Vietnamese cohort0
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Author Index0
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The Association of IL‐17RC Polymorphisms rs708567 and rs76999397 With Acute Lymphoblastic Leukaemia0
New Evidence of TLR4 and TLR9 Variants Influencing Parasitaemia and Symptoms of Plasmodium vivax Infection0
Commentary on review: Forming new perspective approaches to determination of donor compatibility0
Predicting flow cytometry crossmatch results from single‐antigen bead testing0
Nomenclature for factors of the HLA system, update April, May and June 20240
Analysis of Rare Coding Variants in 470,000 UK Biobank Participants Reveals Genetic Associations With Childhood Asthma Predisposition0
Identification of a Novel Homozygous C1QB Mutation in an Iranian Girl: Expanding the Clinical Spectrum of C1q Deficiency0
Nomenclature for Factors of the HLA System, Update July, August and September 20250
Nomenclature for factors of the HLA system, update October, November and December 20230
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Author Index0
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HLAtools, Searching Shared HLA Amino Acid Residue Prevalence, and the Global Frequency Browsers: New Computational Resources for Working With HLA Data and Visualizing Global Patterns of HLA Variation0
Impact of IRGM gene promoter polymorphisms on susceptibility to chronic HBV infection0
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Does HLA‐DQA1*05 carriage have a greater impact on the outcome of infliximab therapy for isolated small‐bowel Crohn's disease?0
Rheumatoid arthritis‐associated antibodies in healthy first‐degree relatives of RA patients0
VDR gene polymorphisms are associated with the increased susceptibility to COVID‐19 among iranian population: A case‐control study0
Response to MALAT1 polymorphisms and psoriasis risk: Correspondence0
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Saliva direct PCR protocol for HLA‐DQB1*02 genotyping0
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Reduced human leukocyte antigen mismatching is associated with more favourable outcomes after unrelated donor haematopoietic stem cell transplantation0
Nomenclature for factors of the HLA system, update July, August and September 20220
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Genetic polymorphisms of IL6 gene –174G > C and –597G > A are associated with the risk of COVID‐19 severity0
Nomenclature for factors of the HLA system, update January, February and March 20240
Genetic polymorphisms of TLR1, TLR2, TLR3 and TLR4 in patients with recurrent or severe infections0
A Potential Link Between HLA‐DRB1/DQB1 Alleles and Response to Treatment in Rheumatoid Arthritis Patients0
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