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Year Number of Results
2002 1
2005 1
2006 2
2007 1
2009 4
2011 1
2012 1
2016 1
2017 3
2018 1
2020 3
2021 5
2022 3
2023 3
2024 1

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Page 1
The Health History of First-Degree Relatives' Dyslipidemia Can Affect Preferences and Intentions following the Return of Genomic Results for Monogenic Familial Hypercholesterolemia.
Tokutomi T, Yoshida A, Fukushima A, Yamamoto K, Ishigaki Y, Kawame H, Fuse N, Nagami F, Suzuki Y, Sakurai-Yageta M, Uruno A, Suzuki K, Tanno K, Ohmomo H, Shimizu A, Yamamoto M, Sasaki M. Tokutomi T, et al. Genes (Basel). 2024 Mar 21;15(3):384. doi: 10.3390/genes15030384. Genes (Basel). 2024. PMID: 38540442 Free PMC article.
Recontact: a survey of current practices and BRCA1/2 testing in Japan.
Sakaguchi T, Tokutomi T, Yoshida A, Yamamoto K, Obata K, Carrieri D, Kelly SE, Fukushima A. Sakaguchi T, et al. Among authors: tokutomi t. J Hum Genet. 2023 Aug;68(8):551-557. doi: 10.1038/s10038-023-01149-x. Epub 2023 Apr 18. J Hum Genet. 2023. PMID: 37072622
De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experiments.
Suzuki H, Li S, Tokutomi T, Takeuchi C, Takahashi M, Yamada M, Okuno H, Miya F, Takenouchi T, Numabe H, Kosaki K, Ohshima T. Suzuki H, et al. Among authors: tokutomi t. Hum Mol Genet. 2022 Dec 16;31(24):4173-4182. doi: 10.1093/hmg/ddac166. Hum Mol Genet. 2022. PMID: 35861646
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number Variations.
Suzuki H, Nozaki M, Yoshihashi H, Imagawa K, Kajikawa D, Yamada M, Yamaguchi Y, Morisada N, Eguchi M, Ohashi S, Ninomiya S, Seto T, Tokutomi T, Hida M, Toyoshima K, Kondo M, Inui A, Kurosawa K, Kosaki R, Ito Y, Okamoto N, Kosaki K, Takenouchi T. Suzuki H, et al. Among authors: tokutomi t. J Pediatr. 2022 May;244:38-48.e1. doi: 10.1016/j.jpeds.2022.01.033. Epub 2022 Feb 4. J Pediatr. 2022. PMID: 35131284 Free article.
dbTMM: an integrated database of large-scale cohort, genome and clinical data for the Tohoku Medical Megabank Project.
Ogishima S, Nagaie S, Mizuno S, Ishiwata R, Iida K, Shimokawa K, Takai-Igarashi T, Nakamura N, Nagase S, Nakamura T, Tsuchiya N, Nakaya N, Murakami K, Ueno F, Onuma T, Ishikuro M, Obara T, Mugikura S, Tomita H, Uruno A, Kobayashi T, Tsuboi A, Tadaka S, Katsuoka F, Narita A, Sakurai M, Makino S, Tamiya G, Aoki Y, Shimizu R, Motoike IN, Koshiba S, Minegishi N, Kumada K, Nobukuni T, Suzuki K, Danjoh I, Nagami F, Tanno K, Ohmomo H, Asahi K, Shimizu A, Hozawa A, Kuriyama S; Tohoku Medical Megabank Project Study Group; Fuse N, Tominaga T, Kure S, Yaegashi N, Kinoshita K, Sasaki M, Tanaka H, Yamamoto M. Ogishima S, et al. Hum Genome Var. 2021 Dec 10;8(1):44. doi: 10.1038/s41439-021-00175-5. Hum Genome Var. 2021. PMID: 34887386 Free PMC article.
The return of individual genomic results to research participants: design and pilot study of Tohoku Medical Megabank Project.
Kawame H, Fukushima A, Fuse N, Nagami F, Suzuki Y, Sakurai-Yageta M, Yasuda J, Yamaguchi-Kabata Y, Kinoshita K, Ogishima S, Takai T, Kuriyama S, Hozawa A, Nakaya N, Nakamura T, Minegishi N, Sugawara J, Suzuki K, Tomita H, Uruno A, Kobayashi T, Aizawa Y, Tokutomi T, Yamamoto K, Ohneda K, Kure S, Aoki Y, Katagiri H, Ishigaki Y, Sawada S, Sasaki M, Yamamoto M. Kawame H, et al. Among authors: tokutomi t. J Hum Genet. 2022 Jan;67(1):9-17. doi: 10.1038/s10038-021-00952-8. Epub 2021 Jul 8. J Hum Genet. 2022. PMID: 34234266
GNAO1 mutation-related severe involuntary movements treated with gabapentin.
Akasaka M, Kamei A, Tanifuji S, Asami M, Ito J, Mizuma K, Oyama K, Tokutomi T, Yamamoto K, Fukushima A, Takenouchi T, Uehara T, Suzuki H, Kosaki K. Akasaka M, et al. Among authors: tokutomi t. Brain Dev. 2021 Apr;43(4):576-579. doi: 10.1016/j.braindev.2020.12.002. Epub 2020 Dec 23. Brain Dev. 2021. PMID: 33358199
25 results