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Characterizing rare and low-frequency height-associated variants in the Japanese population.
Akiyama M, Ishigaki K, Sakaue S, Momozawa Y, Horikoshi M, Hirata M, Matsuda K, Ikegawa S, Takahashi A, Kanai M, Suzuki S, Matsui D, Naito M, Yamaji T, Iwasaki M, Sawada N, Tanno K, Sasaki M, Hozawa A, Minegishi N, Wakai K, Tsugane S, Shimizu A, Yamamoto M, Okada Y, Murakami Y, Kubo M, Kamatani Y. Akiyama M, et al. Among authors: minegishi n. Nat Commun. 2019 Sep 27;10(1):4393. doi: 10.1038/s41467-019-12276-5. Nat Commun. 2019. PMID: 31562340 Free PMC article.
Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population.
Motoike IN, Matsumoto M, Danjoh I, Katsuoka F, Kojima K, Nariai N, Sato Y, Yamaguchi-Kabata Y, Ito S, Kudo H, Nishijima I, Nishikawa S, Pan X, Saito R, Saito S, Saito T, Shirota M, Tsuda K, Yokozawa J, Igarashi K, Minegishi N, Tanabe O, Fuse N, Nagasaki M, Kinoshita K, Yasuda J, Yamamoto M. Motoike IN, et al. Among authors: minegishi n. BMC Genomics. 2014 Aug 10;15(1):673. doi: 10.1186/1471-2164-15-673. BMC Genomics. 2014. PMID: 25109789 Free PMC article.
117 results