| Year |
Citation |
Score |
| 2024 |
Hiramoto T, Sumiyoshi A, Kato R, Yamauchi T, Takano T, Kang G, Esparza M, Matsumura B, Stevens LJ, Hiroi YJ, Tanifuji T, Ryoke R, Nonaka H, Machida A, Nomoto K, et al. Highly demarcated structural alterations in the brain and impaired social incentive learning in Tbx1 heterozygous mice. Molecular Psychiatry. PMID 39463450 DOI: 10.1038/s41380-024-02797-x |
0.667 |
|
| 2023 |
Hiroi N, Hiramoto T, Sumiyoshi A, Kato R, Yamauchi T, Kang G, Matsumura B, Stevens L, Ryoke R, Nonaka H, Machida A, Nomoto K, Mogi K, Kikusui T, Kawashima R. Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders. Research Square. PMID 37461714 DOI: 10.21203/rs.3.rs-3070199/v1 |
0.685 |
|
| 2023 |
Hiramoto T, Sumiyoshi A, Kato R, Yamauchi T, Kang G, Matsumura B, Stevens LJ, Ryoke R, Nonaka H, Machida A, Nomoto K, Mogi K, Kikusui T, Kawashima R, Hiroi N. 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. PMID 37398198 DOI: 10.1101/2023.06.14.545013 |
0.684 |
|
| 2021 |
Hiramoto T, Sumiyoshi A, Yamauchi T, Tanigaki K, Shi Q, Kang G, Ryoke R, Nonaka H, Enomoto S, Izumi T, Bhat MA, Kawashima R, Hiroi N. 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. PMID 34737458 DOI: 10.1038/s41380-021-01318-4 |
0.627 |
|
| 2021 |
Nakamura M, Ye K, E Silva MB, Yamauchi T, Hoeppner DJ, Fayyazuddin A, Kang G, Yuda EA, Nagashima M, Enomoto S, Hiramoto T, Sharp R, Kaneko I, Tajinda K, Adachi M, et al. Computational identification of variables in neonatal vocalizations predictive for postpubertal social behaviors in a mouse model of 16p11.2 deletion. Molecular Psychiatry. PMID 33859357 DOI: 10.1038/s41380-021-01089-y |
0.581 |
|
| 2020 |
Kato R, Machida A, Nomoto K, Kang G, Hiramoto T, Tanigaki K, Mogi K, Hiroi N, Kikusui T. Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism. Developmental Psychobiology. PMID 32573780 DOI: 10.1002/Dev.22006 |
0.519 |
|
| 2013 |
Hiroi N, Takahashi T, Hishimoto A, Izumi T, Boku S, Hiramoto T. Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders. Molecular Psychiatry. 18: 1153-65. PMID 23917946 DOI: 10.1038/Mp.2013.92 |
0.642 |
|
| 2012 |
Hiroi N, Hiramoto T, Harper KM, Suzuki G, Boku S. Mouse Models of 22q11.2-Associated Autism Spectrum Disorder. Autism-Open Access. 001. PMID 25089229 DOI: 10.4172/2165-7890.S1-001 |
0.751 |
|
| 2012 |
Harper KM, Hiramoto T, Tanigaki K, Kang G, Suzuki G, Trimble W, Hiroi N. 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. PMID 22589251 DOI: 10.1093/Hmg/Dds180 |
0.767 |
|
| 2012 |
Yoshida A, Yamamoto N, Kinoshita M, Hiroi N, Hiramoto T, Kang G, Trimble WS, Tanigaki K, Nakagawa T, Ito J. Localization of septin proteins in the mouse cochlea. Hearing Research. 289: 40-51. PMID 22575789 DOI: 10.1016/J.Heares.2012.04.015 |
0.555 |
|
| 2011 |
Hiramoto T, Kang G, Suzuki G, Satoh Y, Kucherlapati R, Watanabe Y, Hiroi N. 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. PMID 21908517 DOI: 10.1093/Hmg/Ddr404 |
0.762 |
|
| 2011 |
Satoh Y, Endo S, Nakata T, Kobayashi Y, Yamada K, Ikeda T, Takeuchi A, Hiramoto T, Watanabe Y, Kazama T. ERK2 contributes to the control of social behaviors in mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 11953-67. PMID 21849556 DOI: 10.1523/Jneurosci.2349-11.2011 |
0.486 |
|
| 2009 |
Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N. Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice. Human Molecular Genetics. 18: 3914-25. PMID 19617637 DOI: 10.1093/Hmg/Ddp334 |
0.729 |
|
| 2009 |
Suzuki G, Harper KM, Hiramoto T, Sawamura T, Lee M, Kang G, Tanigaki K, Buell M, Geyer MA, Trimble WS, Agatsuma S, Hiroi N. Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice. Human Molecular Genetics. 18: 1652-60. PMID 19240081 DOI: 10.1093/Hmg/Ddp086 |
0.721 |
|
| 2009 |
Hiramoto T, Suzuki G, Kang G, Funke B, Watanabe Y, Kucherlapati R, Morrow B, Hiroi N. Tbx1 heterozygosity impairs working memory in mice Neuroscience Research. 65: S121-S122. DOI: 10.1016/J.Neures.2009.09.576 |
0.641 |
|
| 2008 |
Kikuchi A, Shimizu K, Nibuya M, Hiramoto T, Kanda Y, Tanaka T, Watanabe Y, Takahashi Y, Nomura S. Relationship between post-traumatic stress disorder-like behavior and reduction of hippocampal 5-bromo-2'-deoxyuridine-positive cells after inescapable shock in rats. Psychiatry and Clinical Neurosciences. 62: 713-20. PMID 19068009 DOI: 10.1111/J.1440-1819.2008.01875.X |
0.33 |
|
| 2007 |
Suzuki G, Kanda Y, Nibuya M, Hiramoto T, Tanaka T, Shimizu K, Watanabe Y, Nomura S. Stress and electroconvulsive seizure differentially alter GPR56 expression in the adult rat brain. Brain Research. 1183: 21-31. PMID 17945200 DOI: 10.1016/J.Brainres.2007.09.020 |
0.469 |
|
| 2007 |
Satoh Y, Endo S, Ikeda T, Yamada K, Ito M, Kuroki M, Hiramoto T, Imamura O, Kobayashi Y, Watanabe Y, Itohara S, Takishima K. Extracellular signal-regulated kinase 2 (ERK2) knockdown mice show deficits in long-term memory; ERK2 has a specific function in learning and memory. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 10765-76. PMID 17913910 DOI: 10.1523/Jneurosci.0117-07.2007 |
0.387 |
|
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