Takeshi Hiramoto
Affiliations: | National Defense Medical College, Tokorozawa-shi, Saitama-ken, Japan |
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"Takeshi Hiramoto"Mean distance: 14.99 (cluster 6) | S | N | B | C | P |
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| Hiroi N, Hiramoto T, Sumiyoshi A, et al. (2023) Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders. Research Square |
| Hiramoto T, Sumiyoshi A, Kato R, et al. (2023) Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders. Biorxiv : the Preprint Server For Biology |
| Hiramoto T, Sumiyoshi A, Yamauchi T, et al. (2021) Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice. Molecular Psychiatry |
| Nakamura M, Ye K, E Silva MB, et al. (2021) Computational identification of variables in neonatal vocalizations predictive for postpubertal social behaviors in a mouse model of 16p11.2 deletion. Molecular Psychiatry |
| Kato R, Machida A, Nomoto K, et al. (2020) Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism. Developmental Psychobiology |
| Hiroi N, Takahashi T, Hishimoto A, et al. (2013) Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders. Molecular Psychiatry. 18: 1153-65 |
| Hiroi N, Hiramoto T, Harper KM, et al. (2012) Mouse Models of 22q11.2-Associated Autism Spectrum Disorder. Autism-Open Access. 001 |
| Harper KM, Hiramoto T, Tanigaki K, et al. (2012) Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain. Human Molecular Genetics. 21: 3489-99 |
| Yoshida A, Yamamoto N, Kinoshita M, et al. (2012) Localization of septin proteins in the mouse cochlea. Hearing Research. 289: 40-51 |
| Hiramoto T, Kang G, Suzuki G, et al. (2011) Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model. Human Molecular Genetics. 20: 4775-85 |