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Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese population.
Egawa J, Watanabe Y, Wang C, Inoue E, Sugimoto A, Sugiyama T, Igeta H, Nunokawa A, Shibuya M, Kushima I, Orime N, Hayashi T, Okada T, Uno Y, Ozaki N, Someya T. Egawa J, et al. Among authors: sugiyama t. PLoS One. 2015 Mar 25;10(3):e0119413. doi: 10.1371/journal.pone.0119413. eCollection 2015. PLoS One. 2015. PMID: 25806950 Free PMC article.
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Liu X, Shimada T, Otowa T, Wu YY, Kawamura Y, Tochigi M, Iwata Y, Umekage T, Toyota T, Maekawa M, Iwayama Y, Suzuki K, Kakiuchi C, Kuwabara H, Kano Y, Nishida H, Sugiyama T, Kato N, Chen CH, Mori N, Yamada K, Yoshikawa T, Kasai K, Tokunaga K, Sasaki T, Gau SS. Liu X, et al. Among authors: sugiyama t. Autism Res. 2016 Mar;9(3):340-9. doi: 10.1002/aur.1536. Epub 2015 Aug 28. Autism Res. 2016. PMID: 26314684
Association of transcription factor gene LMX1B with autism.
Thanseem I, Nakamura K, Anitha A, Suda S, Yamada K, Iwayama Y, Toyota T, Tsujii M, Iwata Y, Suzuki K, Matsuzaki H, Iwata K, Sugiyama T, Yoshikawa T, Mori N. Thanseem I, et al. Among authors: sugiyama t. PLoS One. 2011;6(8):e23738. doi: 10.1371/journal.pone.0023738. Epub 2011 Aug 25. PLoS One. 2011. PMID: 21901133 Free PMC article.
Further evidence for the role of MET in autism susceptibility.
Thanseem I, Nakamura K, Miyachi T, Toyota T, Yamada S, Tsujii M, Tsuchiya KJ, Anitha A, Iwayama Y, Yamada K, Hattori E, Matsuzaki H, Matsumoto K, Iwata Y, Suzuki K, Suda S, Kawai M, Sugihara G, Takebayashi K, Takei N, Ichikawa H, Sugiyama T, Yoshikawa T, Mori N. Thanseem I, et al. Among authors: sugiyama t. Neurosci Res. 2010 Oct;68(2):137-41. doi: 10.1016/j.neures.2010.06.014. Epub 2010 Jul 6. Neurosci Res. 2010. PMID: 20615438
3,905 results