A functional immunology study characterizing HLA-B*57:01-restricted CD8 T-cell proliferation, cytokine release, and degranulation in abacavir-sensitive HIV-1 patients.
A case control study evaluating the influence of acetylcholinesterase variants on north indian women experiencing unexplained recurrent pregnancy loss.
A case–control genetic study evaluating adipokine (leptin, adiponectin, resistin) and UCP2 polymorphisms in non-obese women with recurrent miscarriage.
A 200-patient cohort study exploring AML mutational profiles and survival correlations.
A 200-patient case–control study evaluating whether APOE (E2, E3, E4) allele and genotype frequencies are associated with unexplained recurrent pregnancy loss in North Indian women.
A laboratory validation study testing whether whole-genome amplification preserves genotyping fidelity across clinical histocompatibility and immunogenetics assays.
A case-control genetic study evaluating CYP1A1, CYP2D6, GSTM1, GSTT1, and GSTP1 polymorphisms in unexplained recurrent miscarriage.
A cohort-based immunogenetic study evaluating donor cytokine gene variants and their impact on acute GVHD outcomes following allogeneic HCT.
A case-control molecular study assessing six endothelial nitric oxide synthase (eNOS) polymorphisms and their haplotypes in unexplained recurrent miscarriage.
An ex vivo trophoblast study assessing whether dexamethasone and hydrocortisone enhance HLA-G mRNA and protein expression in recurrent miscarriage placental tissue.
An in-vitro study evaluating whether dexamethasone and hydrocortisone can enhance HLA-G transcription and protein expression in trophoblast-derived and non-trophoblast cell lines.
A large-scale NGS-based cohort study evaluating the frequency, linkage disequilibrium, and haplotypic diversity of HLA-DRB1*15:03 with absent DRB5 in transplant populations.
A transplant-outcome study assessing whether FLT3-ITD and NPM1 mutations retain their prognostic value in AML patients treated with allogeneic hematopoietic cell transplantation.
A case-control study evaluating how maternal activating and inhibitory KIR gene content shapes predisposition to recurrent miscarriage.
A retrospective study and meta-analysis examining IL-1 pathway variants as inflammatory genetic risk factors for recurrent pregnancy loss in North Indian women.
A population immunogenetics study mapping KIR gene frequencies, framework patterns, and centromeric/telomeric haplotypes in a Northern Indian cohort.
A case-control immunogenetic study showing that activating KIR/HLA-C combinations linked to dominant NK-cell activation are enriched among women with recurrent miscarriages.
A clinical metagenomics study evaluating SARS-CoV-2 detection, respiratory co-pathogens, microbiome diversity, and variant identification.
A 284-patient cohort study exploring donor and recipient KIR genotypes and post-HCT outcomes.
A translational immunology study analyzing NK-cell counts, cytolytic function, and cytokine signatures in hospitalized patients with severe COVID-19.
A VEGF polymorphism study examining whether angiogenesis-related genetic variants are associated with end stage renal disease in a North Indian cohort.
A reproductive genetics study evaluating VEGF variants as contributors to uteroplacental insufficiency and recurrent miscarriage risk in North Indian women.