Miyano, Satoru

The repertoire of mutational signatures in human cancer

Alexandrov, L. B., Kim, J., Haradhvala, N. J., Huang, M. N., Tian Ng, A. W., Wu, Y., Boot, A., Covington, K. R., Gordenin, D. A., Bergstrom, E. N., et al. (2020) · Nature

Cancer Genomics and DiagnosticsChromatin Remodeling and Cancer

Cited by 3,496

Pan-cancer analysis of whole genomes

The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Aaltonen, L. A., Abascal, F., Abeshouse, A., Aburatani, H., Adams, D. J., Agrawal, N., Ahn, K. S., Ahn, S.-M., Aikata, H., et al. (2020) · Nature

Cancer Genomics and DiagnosticsChromatin Remodeling and Cancer

Cited by 3,064

Frequent pathway mutations of splicing machinery in myelodysplasia

Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., et al. (2011) · Nature

RNA Research and SplicingAcute Myeloid Leukemia Research

Cited by 2,029

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

Haferlach, T., Nagata, Y., Grossmann, V, Okuno, Y., Bacher, U., Nagae, G., Schnittger, S., Sanada, M., Kon, A., Alpermann, T., et al. (2014) · Leukemia

Acute Myeloid Leukemia ResearchCancer Genomics and Diagnostics

Cited by 1,532

The evolutionary history of 2,658 cancers

Gerstung, M., Jolly, C., Leshchiner, I., Dentro, S. C., Gonzalez, S., Rosebrock, D., Mitchell, T. J., Rubanova, Y., Anur, P., Yu, K., et al. (2020) · Nature

Cancer Genomics and DiagnosticsChromatin Remodeling and Cancer

Cited by 1,057

Mutational landscape and clonal architecture in grade II and III gliomas

Suzuki, H., Aoki, K., Chiba, K., Sato, Y., Shiozawa, Y., Shiraishi, Y., Shimamura, T., Niida, A., Motomura, K., Ohka, F., et al. (2015) · Nature Genetics

Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics

Cited by 831

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia

Yoshizato, T., Dumitriu, B., Hosokawa, K., Makishima, H., Yoshida, K., Townsley, D., Sato-Otsubo, A., Sato, Y., Liu, D., Suzuki, H., et al. (2015) · New England Journal of Medicine

Acute Myeloid Leukemia ResearchBlood disorders and treatments

Cited by 646

Age-related remodelling of oesophageal epithelia by mutated cancer drivers

Yokoyama, A., Kakiuchi, N., Yoshizato, T., Nannya, Y., Suzuki, H., Takeuchi, Y., Shiozawa, Y., Sato, Y., Aoki, K., Kim, S. K., et al. (2019) · Nature

Cancer Genomics and DiagnosticsEsophageal Cancer Research and Treatment

Cited by 628

Prognostic relevance of genetic alterations in diffuse lower-grade gliomas

Aoki, K., Nakamura, H., Suzuki, H., Matsuo, K., Kataoka, K., Shimamura, T., Motomura, K., Ohka, F., Shiina, S., Yamamoto, T., et al. (2018) · Neuro-Oncology

Glioma Diagnosis and TreatmentAcute Myeloid Leukemia Research

Cited by 307

Identification of novel adrenomedullin in mammals: a potent cardiovascular and renal regulator

Takei, Y., Inoue, K., Ogoshi, M., Kawahara, T., Bannai, H., & Miyano, S. (2004) · FEBS Letters

Neuropeptides and Animal PhysiologyCardiovascular, Neuropeptides, and Oxidative Stress Research

Cited by 268

Dynamic Bayesian network and nonparametric regression for nonlinear modeling of gene networks from time series gene expression data

Kim, S., Imoto, S., & Miyano, S. (2004) · Biosystems

Gene Regulatory Network AnalysisGene expression and cancer classification

Cited by 224

Recurrent somatic mutations underlie corticotropin-independent Cushing’s syndrome

Sato, Y., Maekawa, S., Ishii, R., Sanada, M., Morikawa, T., Shiraishi, Y., Yoshida, K., Nagata, Y., Sato-Otsubo, A., Yoshizato, T., et al. (2014) · Science

Adrenal and Paraganglionic TumorsPituitary Gland Disorders and Treatments

Cited by 209

Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia

Seki, M., Kimura, S., Isobe, T., Yoshida, K., Ueno, H., Nakajima-Takagi, Y., Wang, C., Lin, L., Kon, A., Suzuki, H., et al. (2017) · Nature Genetics

Acute Lymphoblastic Leukemia researchT-cell and Retrovirus Studies

Cited by 138

Comprehensive phosphoproteome analysis unravels the core signaling network that initiates the earliest synapse pathology in preclinical Alzheimer's disease brain

Tagawa, K., Homma, H., Saito, A., Fujita, K., Chen, X., Imoto, S., Oka, T., Ito, H., Motoki, K., Yoshida, C., et al. (2015) · Human Molecular Genetics

Alzheimer's disease research and treatmentsAdvanced Proteomics Techniques and Applications

Cited by 86

Comparing Pearson, Spearman and Hoeffding’s D measure for gene expression association analysis

FUJITA, A., SATO, J. R., DEMASI, M. A. A., SOGAYAR, M. C., FERREIRA, C. E., & MIYANO, S. (2009) · Journal of Bioinformatics and Computational Biology

Gene expression and cancer classificationBioinformatics and Genomic Networks

Cited by 64

Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance

Wang, Q. S., Hasegawa, T., Namkoong, H., Saiki, R., Edahiro, R., Sonehara, K., Tanaka, H., Azekawa, S., Chubachi, S., Takahashi, Y., et al. (2024) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 43

Exploring temporal transcription regulation structure of Aspergillus fumigatus in heat shock by state space model

Do, J. H., Yamaguchi, R., & Miyano, S. (2009) · BMC Genomics

Fungal and yeast genetics researchGene Regulatory Network Analysis

Cited by 42