| TMEM173 variants and potential importance to human biology and disease |
19 |
| Yersinia pestis and plague: an updated view on evolution, virulence determinants, immune subversion, vaccination, and diagnostics |
13 |
| Mutations in RNA Polymerase III genes and defective DNA sensing in adults with varicella-zoster virus CNS infection |
8 |
| Adults with septic shock and extreme hyperferritinemia exhibit pathogenic immune variation |
8 |
| Studying fungal pathogens of humans and fungal infections: fungal diversity and diversity of approaches |
7 |
| Choriodecidual leukocytes display a unique gene expression signature in spontaneous labor at term |
7 |
| Cell death pathologies: targeting death pathways and the immune system for cancer therapy |
6 |
| The IL-23/IL-17 pathway in human chronic inflammatory diseases-new insight from genetics and targeted therapies |
5 |
| Novel mechanistic insights into physiological signaling pathways mediated by mycobacterial Ser/Thr protein kinases |
5 |
| CRISPR/cas9 mediated knockout of an intergenic variant rs6927172 identified IL-20RA as a new risk gene for multiple autoimmune diseases |
5 |
| Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort |
5 |
| MHC haplotype diversity in Icelandic horses determined by polymorphic microsatellites |
5 |
| IFN-lambda s inhibit Hantaan virus infection through the JAK-STAT pathway and expression of Mx2 protein |
4 |
| Akkermansia muciniphila is permissive to arthritis in the K/BxN mouse model of arthritis |
4 |
| The many faces of tumor necrosis factor signaling in the intestinal epithelium |
4 |
| Extra-adrenal glucocorticoid synthesis at epithelial barriers |
4 |
| Elevated T cell levels in peripheral blood predict poor clinical response following rituximab treatment in new-onset type 1 diabetes |
4 |
| Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis |
4 |
| CRISPR/Cas9-mediated deletion of miR-146a enhances antiviral response in HIV-1 infected cells |
4 |
| Ecto-Calreticulin is essential for an efficient immunogenic cell death stimulation in mouse melanoma |
3 |
| Relationship between human leukocyte antigen alleles and risk of Kaposi's sarcoma in Cameroon |
3 |
| Inhibitor of apoptosis proteins in human health and disease |
3 |
| Frequently used bioinformatics tools overestimate the damaging effect of allelic variants |
3 |
| Human IL12RB1 expression is allele-biased and produces a novel IL12 response regulator |
2 |
| Identification of additional EHMT2 variant associated with the risk of chronic hepatitis B by GWAS follow-up study |
2 |
| Cell death in cancer in the era of precision medicine |
2 |
| Intestinal glucocorticoid synthesis enzymes in pediatric inflammatory bowel disease patients |
2 |
| Prioritizing Crohn's disease genes by integrating association signals with gene expression implicates monocyte subsets |
2 |
| MICA and NKG2D variants as risk factors in spondyloarthritis: a case-control study |
2 |
| Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants |
2 |
| Effects of an Fc gamma RIIA polymorphism on leukocyte gene expression and cytokine responses to anti-CD3 and anti-CD28 antibodies |
2 |
| An IL7RA exon 5 polymorphism is associated with impaired IL-7R alpha splicing and protection against tuberculosis in Ghana |
2 |
| High resolution HLA analysis reveals independent class I haplotypes and amino-acid motifs protective for multiple sclerosis |
2 |
| Intracellular parasitism, the driving force of evolution of Legionella pneumophila and the genus Legionella |
2 |
| The remarkable history of the hepatitis C virus |
2 |
| From septicemia to sepsis 3.0-from Ignaz Semmelweis to Louis Pasteur |
1 |
| Regulation of invariant NKT cell development and function by a 0.14 Mbp locus on chromosome 1: a possible role for Fcgr3 |
1 |
| Association between thyroglobulin polymorphisms and autoimmune thyroid disease: a systematic review and meta-analysis of case-control studies |
1 |
| System network analysis of genomics and transcriptomics data identified type 1 diabetes-associated pathway and genes |
1 |
| Polymorphism of FCGR3A gene in chronic beryllium disease |
1 |
| Prognostic role of the systemic immune-inflammation index in brain metastases from lung adenocarcinoma with different EGFR mutations |
1 |
| Primary immunodeficiency diseases in a tuberculosis endemic region: challenges and opportunities |
1 |
| Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling |
1 |
| Evaluation of the TLR negative regulatory network in CVID patients |
1 |
| Memory CD4(+) T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatus |
1 |
| The Act1 D10N missense variant impairs CD40 signaling in human B-cells |
1 |
| Structure-based selection of human metabolite binding P4 pocket of DRB1*15:01 and DRB1*15: with implications for multiple sclerosis |
1 |
| Frequency analysis of the g.7081T>G/A and g.10872T>G polymorphisms in the FCGR3A gene (CD16A) using nested PCR and their functional specific effects |
1 |
| HLA-DQB1*06 is a risk marker for chlamydia reinfection in African American women |
1 |
| Association between interleukin family gene polymorphisms and recurrent aphthous stomatitis risk |
1 |
