M. Thiri

High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese

K. Tokunaga, A. Mabuchi, K. Doi, 2016, Scientific Reports.

Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy

Khun Zaw Latt, M. Nagasaki, K. Tokunaga, 2018, Scientific Reports.

Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals

Khun Zaw Latt, N. Matsumoto, K. Tokunaga, 2015, Human Genome Variation.

Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals

Khun Zaw Latt, N. Kato, N. Matsumoto, 2016, Human Genome Variation.

Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy

Khun Zaw Latt, K. Tokunaga, H. Sawai, 2018, Scientific Reports.