Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS05
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
Yamada Y et al.
International Journal of Molecular Medicine, 2019
Identification of four genes as novel susceptibility loci for early-onset type 2 diabetes mellitus, metabolic syndrome, or hyperuricemia.
Yamada Y et al.
Biomedical Reports, 2018
Identification of five genetic variants as novel determinants of type 2 diabetes mellitus in Japanese by exome-wide association studies.
Yamada Y et al.
Oncotarget, 2017
Identification of polymorphisms in 12q24.1, ACAD10, and BRAP as novel genetic determinants of blood pressure in Japanese by exome-wide association studies.
Yamada Y et al.
Oncotarget, 2017
Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.
Yamada Y et al.
Oncotarget, 2017
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