Jarmo Ritari

This paper performs fine-mapping of HLA effects in lichen planus subtypes, identifying specific HLA haplotypes associated with increased or decreased risk in oral and non-oral forms.

This study identifies 2,973 genetic loci associated with health outcomes in blood donors, suggesting genetic factors contribute to the healthier donor effect.

The paper investigates the impact of CFHR gene deletions on kidney transplant rejection risk and identifies associated SNPs and protein expression changes.

The paper identifies genetic loci associated with female infertility through a GWAS, revealing a rare recessive mutation in TBPL2 and age-dependent risk factors.

The paper develops imputation models for non-classical HLA genes using SNP data, achieving high accuracy and providing accessible tools for research.

The paper develops a machine learning method to predict blood group antigens and HPA-1 from genotyping data, achieving high accuracy in multiple cohorts.

The paper imputes KIR gene content from SNPs in the Finnish population with high accuracy using a stand-alone model trained on biobank data.