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No association between the ryanodine receptor 3 gene and autism in a Japanese population.
Tochigi M, Kato C, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T. Tochigi M, et al. Among authors: watanabe k. Psychiatry Clin Neurosci. 2008 Jun;62(3):341-4. doi: 10.1111/j.1440-1819.2008.01802.x. Psychiatry Clin Neurosci. 2008. PMID: 18588595 Free article.
Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.
Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, Sasaki T. Marui T, et al. Among authors: watanabe k. Brain Dev. 2007 Sep;29(8):510-3. doi: 10.1016/j.braindev.2007.01.010. Epub 2007 Mar 21. Brain Dev. 2007. PMID: 17376622 Clinical Trial.
No association between the neuronal pentraxin II gene polymorphism and autism.
Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Ishijima M, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, Sasaki T. Marui T, et al. Among authors: watanabe k. Prog Neuropsychopharmacol Biol Psychiatry. 2007 May 9;31(4):940-3. doi: 10.1016/j.pnpbp.2007.02.016. Epub 2007 Mar 3. Prog Neuropsychopharmacol Biol Psychiatry. 2007. PMID: 17408830
Association study of the 15q11-q13 maternal expression domain in Japanese autistic patients.
Kato C, Tochigi M, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T. Kato C, et al. Among authors: watanabe k. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1008-12. doi: 10.1002/ajmg.b.30690. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18186074
Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.
Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Sasaki T, Kato N. Marui T, et al. Among authors: watanabe k. Int J Neuropsychopharmacol. 2009 Feb;12(1):1-10. doi: 10.1017/S1461145708009127. Epub 2008 Jul 30. Int J Neuropsychopharmacol. 2009. PMID: 18664314 Free article.
Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene.
Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Jinde S, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N. Marui T, et al. Among authors: watanabe k. Int J Neuropsychopharmacol. 2010 May;13(4):443-9. doi: 10.1017/S1461145709990903. Epub 2009 Nov 9. Int J Neuropsychopharmacol. 2010. PMID: 19895723 Free article.
Impaired prefrontal hemodynamic maturation in autism and unaffected siblings.
Kawakubo Y, Kuwabara H, Watanabe K, Minowa M, Someya T, Minowa I, Kono T, Nishida H, Sugiyama T, Kato N, Kasai K. Kawakubo Y, et al. Among authors: watanabe k. PLoS One. 2009 Sep 3;4(9):e6881. doi: 10.1371/journal.pone.0006881. PLoS One. 2009. PMID: 19727389 Free PMC article.
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