Immunogenetics

Papers
(The TQCC of Immunogenetics is 6. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
The KIR2DL1 intermediate upstream element participates in gene activation73
Causal effect of interleukin (IL)-6 on blood pressure and hypertension: A mendelian randomization study32
iTTCA-MFF: identifying tumor T cell antigens based on multiple feature fusion30
Evolutionary divergence of TLR9 through ancestral sequence reconstruction27
Dysregulated PD-L2 is correlated with disease activity and inflammation in rheumatoid arthritis26
Prognostic value of the WT-1 gene combined with recurrent cytogenetic genes in acute myeloid leukemia22
Correction to: C. elegans: out on an evolutionary limb21
Factors regulating the differences in frequency of infiltration of Th17 and Treg of the blood–brain barrier19
Distinct frequency patterns of LILRB3 and LILRA6 allelic variants in Europeans19
Increased circulating Th17 cell populations in patients with pancreatic ductal adenocarcinoma17
The characteristic of HLA-A, HLA-B, HLA-C, HLA-DRB1, HLA-DRB3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1 alleles in Zhejiang Han population16
Evaluation of miRNA-16–2-3P, miRNA-618 levels and their diagnostic and prognostic value in the regulation of immune response during SARS Cov-2 infection15
Erik Thorsby (1938–2021)14
Resolving unknown nucleotides in the IPD-IMGT/HLA database by extended and full-length sequencing of HLA class I and II alleles12
SNHG3 regulates NEIL3 via transcription factor E2F1 to mediate malignant proliferation of hepatocellular carcinoma11
Compound heterozygous DCLRE1C mutations lead to clinically typical Severe Combined Immunodeficiency presenting with Graft Versus Host Disease11
VaxOptiML: leveraging machine learning for accurate prediction of MHC-I and II epitopes for optimized cancer immunotherapy11
High-resolution characterization of the structural features and genetic variation of six feline leukocyte antigen class I loci via single molecule, real-time (SMRT) sequencing11
Bioinformatics analysis of structural protein to approach a vaccine candidate against Vibrio cholerae infection10
Correlation between human leukocyte antigen ligands and killer cell immunoglobulin-like receptors in aplastic anemia patients from Shaanxi Han10
Evolution of immunogenetic components encoding ultralong CDR H310
The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurat10
The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearing10
HLA-G expression in Merkel cell carcinoma and the correlation with Merkel cell polyomavirus infection10
Oncogenic signaling pathway mediated by Notch pathway-related genes induces immunosuppression and immunotherapy resistance in hepatocellular carcinoma9
HLA alleles, haplotypes frequencies, and their association with hematological disorders: a report from 1550 families whose patients underwent allogeneic bone marrow transplantation in Egypt9
Exploring the therapeutic potential of interleukin-6 receptor blockade in autoimmune diseases using drug target mendelian randomization9
The immunogenetics of tuberculosis (TB) susceptibility9
Macroevolution of avian T cell receptor C segments using genomic data9
Functional consequences of allotypic polymorphisms in human immunoglobulin G subclasses8
Single-cell RNA-seq profiling of individual Biomphalaria glabrata immune cells with a focus on immunologically relevant transcripts8
Determination for KIR genotype and allele copy number via real-time quantitative PCR method8
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides8
Innate receptors modulating adaptive T cell responses: KIR-HLA interactions and T cell-mediated control of chronic viral infections7
Bioinformatic analysis predicts the regulatory function of noncoding SNPs associated with Long COVID-19 syndrome7
Kirsten Falk 1963-20246
Full-length mRNA sequencing resolves novel variation in 5′ UTR length for genes expressed during human CD4 T-cell activation6
Primary regulatory T cell activator FOXP3 is present across Amphibia6
Immunological assessment of a patient with Omenn syndrome resulting from compound heterozygous mutations in the RAG1 gene6
Assessment of regulatory T cells (Tregs) and Foxp3 methylation level in chronic myeloid leukemia patients on tyrosine kinase inhibitor therapy6
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