Selected Peer-reviewed Publications
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Link to Google Scholar
- Kimura R, Lardenoije R, Tomiwa K, Funabiki Y, Nakata M, Suzuki S, Awaya T, Kato T, Okazaki S, Murai T, Heike T, Rutten BPF, Hagiwara M. Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome. Neuropsychopharmacology. 45:1627-1636, 2020
- Kimura R, Swarup V, Tomiwa K, Gandal MJ, Parikshak NN, Funabiki Y, Nakata M, Awaya T, Kato T, Iida K, Okazaki S, Matsushima K, Kato T, Murai T, Heike T, Geschwind DH, Hagiwara M. Integrative network analysis reveals biological pathways associated with Williams syndrome. Journal of Child Psychology and Psychiatry, 60 (5), 585-598, 2019
- Kimura R, Ishii Y, Tomiwa K, Awaya T, Nakata M, Kato T, Okazaki S, Heike T, Hagiwara M. Williams-Beuren syndrome as a potential risk factor for Burkitt lymphoma. Frontiers in Genetics (2018) 9:368. doi: 10.3389/fgene.2018.00368.
- Morihara T, Hayashi N, Yokokoji M, Akatsu H, Silverman MA, Kimura N, Sato M, Saito Y, Suzuki T, Yanagida K, Kodama TS, Tanaka T, Okochi M, Tagami S, Kazui H, Kudo T, Hashimoto R, Itoh N, Nishitomi K, Yamaguchi-Kabata Y, Tsunoda T, Takamura H, Katayama T, Kimura R, Kamino K, Hashizume Y, Takeda M. Transcriptome analysis of distinct mouse strains reveals kinesin light chain-1 splicing as an amyloid beta accumulation modifier. Proc Natl Acad Sci U S A. 111(7): 2638-2643, 2014
- Kimura R, Ikeda S, Kumazaki H, Yanagida M, Matsunaga H. Comparison of the clinical features of suicide attempters by jumping from a height and those by self-stabbing in Japan. Journal of Affective Disorders. 150: 695-698, 2013
- Kimura R., Mori K., Kumazaki H., Yanagida M., Taguchi S., Matsunaga H. Treatment of delirium with ramelteon: initial experience in three patients. General Hospital Psychiatry. 33:407-409, 2011
- Kimura R., Yamamoto M., Morihara T., Akatsu H., Kudo T., Kamino K., Takeda M. SORL1 is genetically associated with Alzheimer disease in a Japanese population. Neuroscience Letters. 461:177-80, 2009
- Kimura R., Kamino K., Yamamoto M, Nuripa A, Kida T, Kazui H, Hashimoto R, Tanaka T, Kudo T, Yamagata H, Tabara Y, Miki T, Akatsu H, Kosaka K, Funakoshi E, Nishitomi K, Sakaguchi G, Kato A, Hattori H, Uema T, Takeda M. The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between beta-amyloid production and tau phosphorylation in Alzheimer disease. Human Molecular Genetics. 16:15-23, 2007
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