Nakamura, Yusuke

Complete sequencing and characterization of 21,243 full-length human cDNAs

Ota, T., Suzuki, Y., Nishikawa, T., Otsuki, T., Sugiyama, T., Irie, R., Wakamatsu, A., Hayashi, K., Sato, H., Nagai, K., et al. (2004) · Nature Genetics

Genomics and Phylogenetic StudiesRNA Research and Splicing

Cited by 925

A ribonucleotide reductase gene involved in a p53-dependent cell-cycle checkpoint for DNA damage

Tanaka, H., Arakawa, H., Yamaguchi, T., Shiraishi, K., Fukuda, S., Matsui, K., Takei, Y., & Nakamura, Y. (2000) · Nature

Cancer-related Molecular PathwaysDNA Repair Mechanisms

Cited by 904

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus

Yasuda, K., Miyake, K., Horikawa, Y., Hara, K., Osawa, H., Furuta, H., Hirota, Y., Mori, H., Jonsson, A., Sato, Y., et al. (2008) · Nature Genetics

Genetic Associations and EpidemiologyPancreatic function and diabetes

Cited by 776

Overview of the BioBank Japan Project: Study design and profile

Nagai, A., Hirata, M., Kamatani, Y., Muto, K., Matsuda, K., Kiyohara, Y., Ninomiya, T., Tamakoshi, A., Yamagata, Z., Mushiroda, T., et al. (2017) · Journal of Epidemiology

Health, Environment, Cognitive AgingGenetic Associations and Epidemiology

Cited by 739

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

Unoki, H., Takahashi, A., Kawaguchi, T., Hara, K., Horikoshi, M., Andersen, G., Ng, D. P. K., Holmkvist, J., Borch-Johnsen, K., Jørgensen, T., et al. (2008) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 725

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Ellinor, P. T., Lunetta, K. L., Albert, C. M., Glazer, N. L., Ritchie, M. D., Smith, A. V., Arking, D. E., Müller-Nurasyid, M., Krijthe, B. P., Lubitz, S. A., et al. (2012) · Nature Genetics

Atrial Fibrillation Management and OutcomesGenetic Associations and Epidemiology

Cited by 601

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

Ishigaki, K., Akiyama, M., Kanai, M., Takahashi, A., Kawakami, E., Sugishita, H., Sakaue, S., Matoba, N., Low, S.-K., Okada, Y., et al. (2020) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 508

Overexpression of LSD1 contributes to human carcinogenesis through chromatin regulation in various cancers

Hayami, S., Kelly, J. D., Cho, H., Yoshimatsu, M., Unoki, M., Tsunoda, T., Field, H. I., Neal, D. E., Yamaue, H., Ponder, B. A. J., et al. (2011) · International Journal of Cancer

Epigenetics and DNA MethylationCancer-related gene regulation

Cited by 489

Critical roles of non-histone protein lysine methylation in human tumorigenesis

Hamamoto, R., Saloura, V., & Nakamura, Y. (2015) · Nature Reviews Cancer

Cancer-related gene regulationEpigenetics and DNA Methylation

Cited by 376

Genome-wide association meta-analysis identifies new endometriosis risk loci

Nyholt, D. R., Low, S.-K., Anderson, C. A., Painter, J. N., Uno, S., Morris, A. P., MacGregor, S., Gordon, S. D., Henders, A. K., Martin, N. G., et al. (2012) · Nature Genetics

Endometriosis Research and TreatmentGenetic Associations and Epidemiology

Cited by 315

Novel 5α‐steroid reductase (SRD5A3, type‐3) is overexpressed in hormone‐refractory prostate cancer

Uemura, M., Tamura, K., Chung, S., Honma, S., Okuyama, A., Nakamura, Y., & Nakagawa, H. (2008) · Cancer Science

Prostate Cancer Treatment and ResearchCancer, Lipids, and Metabolism

Cited by 263

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

Uno, S., Zembutsu, H., Hirasawa, A., Takahashi, A., Kubo, M., Akahane, T., Aoki, D., Kamatani, N., Hirata, K., & Nakamura, Y. (2010) · Nature Genetics

Endometriosis Research and TreatmentGenetic Associations and Epidemiology

Cited by 259

Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations

GIANT consortium, Okada, Y., Kubo, M., Ohmiya, H., Takahashi, A., Kumasaka, N., Hosono, N., Maeda, S., Wen, W., Dorajoo, R., et al. (2012) · Nature Genetics

Genetic Associations and EpidemiologyGenetics and Physical Performance

Cited by 256

Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population

Arakawa, S., Takahashi, A., Ashikawa, K., Hosono, N., Aoi, T., Yasuda, M., Oshima, Y., Yoshida, S., Enaida, H., Tsuchihashi, T., et al. (2011) · Nature Genetics

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 149

p53CSV, a Novel p53-Inducible Gene Involved in the p53-Dependent Cell-Survival Pathway

Park, W.-R., & Nakamura, Y. (2005) · Cancer Research

Cancer-related Molecular PathwaysCell death mechanisms and regulation

Cited by 72

p53RFP, a p53-inducible RING-finger protein, regulates the stability of p21WAF1

Ng, C.-C., Arakawa, H., Fukuda, S., Kondoh, H., & Nakamura, Y. (2003) · Oncogene

Cancer-related Molecular PathwaysUbiquitin and proteasome pathways

Cited by 54

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis

Jongjaroenprasert, W., Phusantisampan, T., Mahasirimongkol, S., Mushiroda, T., Hirankarn, N., Snabboon, T., Chanprasertyotin, S., Tantiwong, P., Soonthornpun, S., Rattanapichart, P., et al. (2012) · Journal of Human Genetics

Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology

Cited by 33

Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population

Kamatani, Y., Matsuda, K., Ohishi, T., Ohtsubo, S., Yamazaki, K., Iida, A., Hosono, N., Kubo, M., Yumura, W., Nitta, K., et al. (2008) · Journal of Human Genetics

Systemic Lupus Erythematosus ResearchGenetic Associations and Epidemiology

Cited by 31