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Gen Tamiya

Showing results (121-130 of 169) with videos related to

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Scientific Reports|October 6, 2018
Potential identification of vitamin B6 responsiveness in autism spectrum disorder utilizing phenotype variables and machine learning methodsTaku Obara, Mami Ishikuro, Gen Tamiya, et al.
Journal of Bone and Mineral Metabolism|December 15, 2022
Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27)Akiko Saito-Hakoda, Atsuo Kikuchi, Tadahisa Takahashi, et al.
Journal of Biochemistry|June 16, 2021
Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPsMika Sakurai-Yageta, Kazuki Kumada, Chinatsu Gocho, et al.
Plos Genetics|August 11, 2020
Endogenization and excision of human herpesvirus 6 in human genomesXiaoxi Liu, Shunichi Kosugi, Rie Koide, et al.
Translational Psychiatry|February 17, 2026
Genome-wide association study of social isolation in 63,497 Japanese individuals from the general populationHisashi Ohseto, Kosuke Inoue, Ippei Takahashi, et al.
Nucleic Acids Research|November 6, 2023
jMorp: Japanese Multi-Omics Reference Panel update report 2023Shu Tadaka, Junko Kawashima, Eiji Hishinuma, et al.
BMC Genomics|July 26, 2018
Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank ProjectJun Yasuda, Fumiki Katsuoka, Inaho Danjoh, et al.
Human Genome Variation|June 27, 2019
3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosomeShu Tadaka, Fumiki Katsuoka, Masao Ueki, et al.
Translational Psychiatry|August 19, 2020
Clustering by phenotype and genome-wide association study in autismAkira Narita, Masato Nagai, Satoshi Mizuno, et al.
Heart Rhythm|March 25, 2025
Sex difference in genetic risk in the prevalence of atrial fibrillationSayuri Tokioka, Masato Takase, Naoki Nakaya, et al.
Pageof 17

Showing results (121-130 of 169) with videos related to

Sort By:
Pageof 17
Scientific Reports|October 6, 2018
Potential identification of vitamin B6 responsiveness in autism spectrum disorder utilizing phenotype variables and machine learning methodsTaku Obara, Mami Ishikuro, Gen Tamiya, et al.
Journal of Bone and Mineral Metabolism|December 15, 2022
Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27)Akiko Saito-Hakoda, Atsuo Kikuchi, Tadahisa Takahashi, et al.
Journal of Biochemistry|June 16, 2021
Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPsMika Sakurai-Yageta, Kazuki Kumada, Chinatsu Gocho, et al.
Plos Genetics|August 11, 2020
Endogenization and excision of human herpesvirus 6 in human genomesXiaoxi Liu, Shunichi Kosugi, Rie Koide, et al.
Translational Psychiatry|February 17, 2026
Genome-wide association study of social isolation in 63,497 Japanese individuals from the general populationHisashi Ohseto, Kosuke Inoue, Ippei Takahashi, et al.
Nucleic Acids Research|November 6, 2023
jMorp: Japanese Multi-Omics Reference Panel update report 2023Shu Tadaka, Junko Kawashima, Eiji Hishinuma, et al.
BMC Genomics|July 26, 2018
Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank ProjectJun Yasuda, Fumiki Katsuoka, Inaho Danjoh, et al.
Human Genome Variation|June 27, 2019
3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosomeShu Tadaka, Fumiki Katsuoka, Masao Ueki, et al.
Translational Psychiatry|August 19, 2020
Clustering by phenotype and genome-wide association study in autismAkira Narita, Masato Nagai, Satoshi Mizuno, et al.
Heart Rhythm|March 25, 2025
Sex difference in genetic risk in the prevalence of atrial fibrillationSayuri Tokioka, Masato Takase, Naoki Nakaya, et al.
Pageof 17