Associated Papers
Genetic and Epigenetic Characterization of a Discordant KMT2A/AFF1-Rearranged Infant Monozygotic Twin Pair.
Russo A et al.
International Journal of Molecular Sciences, 2021
34575904 (PubMed )
Supplement: ijms-22-09740-s001.zip › ijms-1351727-supplementary › Supplementary_Table_S1-rev.xlsx › Foglio1
Tumor mutation burden and recurrent tumors in hereditary lung cancer.
Hsu YC et al.
Cancer Medicine, 2019
30941903 (PubMed )
Supplement: CAM4-8-2179-s001.xlsx › S2
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
Yamada Y et al.
International Journal of Molecular Medicine, 2019
Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
Yamada Y et al.
International Journal of Molecular Medicine, 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 C21orf59 and ATG2A as novel determinants of renal function-related traits 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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