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C. Terao · SciRah

Researcher profile · Semantic Scholar

C. Terao

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C. Terao — researcher profile on SciRah

h-index: 40
Works: 230
Citations: 14K

Most-cited papers

Genomics yields biological and phenotypic insights into bipolar disorder
K. O'Connell, M. Koromina, Tracey van der Veen, T. Boltz +309 more
2025Nature215 citations Open access
Semantic Scholar
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Anqi Wang, Jiayi Shen, Alex A. Rodriguez, E. Saunders +309 more
2023Nature Genetics136 citations Open access
Semantic Scholar
Translational genomics of osteoarthritis in 1,962,069 individuals
K. Hatzikotoulas, L. Southam, L. Stefánsdóttir, C. Boer +169 more
2025Nature95 citations Open access
Semantic Scholar
Comparative evaluation of SNVs, indels, and structural variations detected with short- and long-read sequencing data
Shunichi Kosugi, C. Terao
2024Human Genome Variation56 citations Open access
Semantic Scholar
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
M. Purdue, Diptavo Dutta, M. Machiela, B. Gorman +128 more
2024Nature Genetics50 citations Open access
Semantic Scholar
Genetic drivers and cellular selection of female mosaic X chromosome loss
Ao-Xing Liu, G. Genovese, Ya-Jie Zhao, M. Pirinen +41 more
2024Nature45 citations Open access
Semantic Scholar
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
K. Kentistou, L. R. Kaisinger, S. Stankovic, Marc Vaudel +217 more
2024Nature Genetics40 citations Open access
Semantic Scholar
Neoself-antigens are the primary target for autoreactive T cells in human lupus.
Shunsuke Mori, M. Kohyama, Yoshiaki Yasumizu, Asa Tada +22 more
2024Cell38 citations Open access
Semantic Scholar
Protein-altering variants at copy number-variable regions influence diverse human phenotypes
M. Hujoel, R. Handsaker, Maxwell A. Sherman, Nolan Kamitaki +5 more
2024Nature Genetics36 citations Open access
Semantic Scholar
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Akiko Oguchi, A. Suzuki, Shuichiro Komatsu, Hiroyuki Yoshitomi +35 more
2024Science26 citations
Semantic Scholar
RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction
K. Hikino, S. Koyama, K. Ito, Yoshinao Koike +12 more
2024JAMA cardiology25 citations Open access
Semantic Scholar
Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing
Xiao-Xi Liu, S. Koyama, Kohei Tomizuka, Sadaaki Takata +15 more
2024Science Advances23 citations Open access
Semantic Scholar
Population-specific putative causal variants shape quantitative traits
S. Koyama, Xiao-Xi Liu, Yoshinao Koike, K. Hikino +26 more
2024Nature Genetics23 citations Open access
Semantic Scholar
Fine-mapping genomic loci refines bipolar disorder risk genes
M. Koromina, A. Ravi, G. Panagiotaropoulou, B. Schilder +129 more
2025Nature Neuroscience21 citations Open access
Semantic Scholar
Stem-like and effector peripheral helper T cells comprise distinct subsets in rheumatoid arthritis.
Masuo Yuki, A. Murakami, Rinko Akamine, Osamu Iri +17 more
2025Science immunology19 citations Open access
Semantic Scholar
Update of the FANTOM web resource: enhancement for studying noncoding genomes
Tomoe Nobusada, Chi-Wai Yip, Saumya Agrawal, Jessica Severin +19 more
2024Nucleic Acids Research17 citations Open access
Semantic Scholar
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Yuki Ishikawa, Nao Tanaka, Y. Asano, M. Kodera +68 more
2024Nature Communications17 citations Open access
Semantic Scholar
Mosaic loss of chromosome Y, tobacco smoking and risk of age-related lung diseases: insights from two prospective cohorts
Chenghao Weng, Yuxuan Zhao, Mi-Nam Song, Zi-Lun Shao +15 more
2024European Respiratory Journal17 citations Open access
Semantic Scholar
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
Kensuke Goto, Y. Koyanagi, M. Akiyama, Yusuke Murakami +30 more
2023Journal of Medical Genetics17 citations Open access
Semantic Scholar
Detection of trait-associated structural variations using short-read sequencing
Shunichi Kosugi, Y. Kamatani, K. Harada, Kohei Tomizuka +3 more
2023Cell Genomics17 citations Open access
Semantic Scholar
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Jack Flanagan, Xiao-Xi Liu, David Ortega-Reyes, Kohei Tomizuka +16 more
2024Communications Biology14 citations Open access
Semantic Scholar
Serum high-sensitivity C-reactive protein and dementia in a community-dwelling Japanese older population (JPSC-AD)
Ayumi Tachibana, J. Iga, Tomoki Ozaki, T. Yoshida +60 more
2024Scientific Reports14 citations Open access
Semantic Scholar
Improved genetic prediction of the risk of knee osteoarthritis using the risk factor-based polygenic score
Y. Morita, Y. Kamatani, H. Ito, S. Ikegawa +11 more
2023Arthritis Research & Therapy14 citations Open access
Semantic Scholar
Human CD4+ T cells regulate peripheral immune responses in rheumatoid arthritis via insulin-like growth factor-like family member 2.
A. Murakami, Rinko Akamine, Shiro Tanaka, K. Murata +17 more
2025Science immunology13 citations Open access
Semantic Scholar
The genome-wide association study of serum IgE levels demonstrated the shared genetic background in allergic diseases.
Hsing-Fang Lu, Chen-Hsing Chou, Ying-Ju Lin, Shunsuke Uchiyama +7 more
2024Clinical Immunology13 citations
Semantic Scholar
Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease
R. Malik, Nathalie Beaufort, Jiang Li, Koki Tanaka +9 more
2024Nature Cardiovascular Research12 citations Open access
Semantic Scholar
Fine-mapping genomic loci refines bipolar disorder risk genes
M. Koromina, A. Ravi, G. Panagiotaropoulou, B. Schilder +129 more
2024medRxiv12 citations Open access
Semantic Scholar
Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study
N. Otomo, Anas M. Khanshour, M. Koido, Kazuki Takeda +44 more
2023Frontiers in Endocrinology11 citations Open access
Semantic Scholar
Integrative spatial multiomics analysis reveals regulatory mechanisms of VCAM1+ proximal tubule cells in lupus nephritis.
Junyu Wang, Ao Zheng, Nian-Ping Liu, Zhen Tan +18 more
2025Annals of the Rheumatic Diseases10 citations Open access
Semantic Scholar
Adipokine dysregulation as an underlying pathology for diffuse ectopic ossification of spinal posterior longitudinal ligament in patients with obesity.
M. Takahata, Yoshinao Koike, Tsutomu Endo, S. Ikegawa +12 more
2024The spine journal10 citations Open access
Semantic Scholar
Distinguishing clinical and genetic risk factors for suicidal ideation and behavior in a diverse hospital population
Sarah M. C. Colbert, L. Lepow, B. Fennessy, Nakao Iwata +8 more
2024Translational Psychiatry9 citations Open access
Semantic Scholar
Mosaic loss of chromosome Y characterises late-onset rheumatoid arthritis and contrasting associations of polygenic risk score based on age at onset.
S. Uchiyama, Y. Ishikawa, K. Ikari, S. Honda +7 more
2025Annals of the Rheumatic Diseases8 citations Open access
Semantic Scholar
A single-cell atlas of transcribed cis-regulatory elements in the human genome
Jonathan Moody, Tsukasa Kouno, M. Kojima, Ikuko Koya +48 more
2023bioRxiv8 citations Open access
Semantic Scholar
Attenuation of HOIL-1L ligase activity promotes systemic autoimmune disorders by augmenting linear ubiquitin signaling
Yasuhiro Fuseya, K. Kadoba, Xiao-Xi Liu, H. Suetsugu +7 more
2024JCI Insight7 citations Open access
Semantic Scholar
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
N. Enzan, K. Miyazawa, S. Koyama, R. Kurosawa +26 more
2024Nature Communications7 citations Open access
Semantic Scholar
Pan-cancer prevalence, risk, and clinical and demographic characteristics of Lynch Syndrome-associated variants in BioBank Japan
Keijiro Mizukami, Yoshiaki Usui, Y. Iwasaki, K. Shiraishi +17 more
2025Communications Medicine6 citations Open access
Semantic Scholar
Green tea consumption and cerebral white matter lesions in community-dwelling older adults without dementia
Shutaro Shibata, M. Noguchi-Shinohara, Ayano Shima, Taro Ozaki +61 more
2025npj Science of Food6 citations Open access
Semantic Scholar
A longitudinal population-based study identifies THBS2 as a susceptibility gene for intervertebral disc degeneration
Tsuyoshi Deguchi, H. Hashizume, C. Terao, M. Nakajima +6 more
2024European spine journal6 citations
Semantic Scholar
Increased somatic mosaicism in autosomal and X chromosomes for suicide death
Ikuo Otsuka, Shunsuke Uchiyama, Toshiyuki Shirai, Xiao-Xi Liu +4 more
2024Molecular Psychiatry5 citations Open access
Semantic Scholar
Genotype imputation accuracy and the quality metrics of the minor ancestry in multi-ancestry reference panels
Ming-Yang Shi, C. Tanikawa, H. Munter, Masato Akiyama +7 more
2023Briefings Bioinform.5 citations Open access
Semantic Scholar
Clinical characteristics of EYS-associated retinal dystrophy in 291 Japanese patients
Y. Koyanagi, Yusuke Murakami, T. Kominami, Masatoshi Fukushima +24 more
2025npj Genomic Medicine4 citations Open access
Semantic Scholar
Genome-wide association studies for pelvic organ prolapse in the Japanese population
M. Matsunami, Minako Imamura, A. Ashikari, Xiao-Xi Liu +40 more
2024Communications Biology4 citations Open access
Semantic Scholar
Fundamentals for predicting transcriptional regulations from DNA sequence patterns
M. Koido, Kohei Tomizuka, C. Terao
2024Journal of Human Genetics4 citations Open access
Semantic Scholar
Common protein-altering variant in GFAP is associated with white matter lesions in the older Japanese population
Y. Furuta, Masato Akiyama, Naoki Hirabayashi, T. Honda +15 more
2024npj Genomic Medicine4 citations Open access
Semantic Scholar
Genetic study identifies novel genes in developmental dysplasia of the hip
Soichiro Yoshino, Shi-Bo Chen, R. Yamaguchi, Taishi Kurakazu +39 more
2026Bone Research3 citations Open access
Semantic Scholar
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Fei-Fei Cheng, Xiao-Xi Liu, Hao Mi, Li-Zhong Wang +66 more
2026Nature Genetics3 citations Open access
Semantic Scholar
Deletion of neurosecretory proteins GL and GM drives dual anti-obesity effects via appetite suppression and enhanced energy expenditure
Kenshiro Shikano, M. Yoshimura, Takaki Yahiro, Taishi Kurakazu +15 more
2026Communications Biology3 citations Open access
Semantic Scholar
Local radiotherapy for cancer patients is associated with mosaic loss of chromosome Y, a hallmark of male aging
Takuro Kobayashi, Tsuyoshi Hachiya, Yan Lu, Yoshihiro Ikehata +15 more
2025npj Aging3 citations
Semantic Scholar
EPHA4 signaling dysregulation links abnormal locomotion and the development of idiopathic scoliosis
Lian-Lei Wang, Xinyu Yang, Sen Zhao, Pengfei Zheng +34 more
2025bioRxiv3 citations Open access
Semantic Scholar
Genomic architecture of bipolar disorder in Japan: Insights from genomic structural equation modeling
Hiroki Kimura, Yukako Nagasaki, Sawako Furukawa, Shiori Ogawa +4 more
2025Psychiatry and Clinical Neurosciences3 citations Open access
Semantic Scholar

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