Ohiko Hashimoto

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi et autres

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DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi et autres

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Development of a picture completion test for clinical research use: Relationships between individual differences in task performance and ASD/ADHD tendencies

Shinobu Matsunaga, Takanori MATSUNO, Ayano KIMURA, Keiichiro Watanabe et autres

Profound Mental Retardation

Chisaka Yamamoto, Ohiko Hashimoto

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Identification of Four Novel Synonymous Substitutions in the X-Linked GenesNeuroligin 3andNeuroligin 4Xin Japanese Patients with Autistic Spectrum Disorder

Kumiko Yanagi, Tadashi Kaname, Keiko Wakui, Ohiko Hashimoto et autres

Mutations in the X-linked genes neuroligin 3 (NLGN3) and neuroligin 4X (NLGN4X) were first implicated in the pathogenesis of X-linked autism in Swedish families. However, reports of mutations in these genes in autism spectrum disorder (ASD) patients from various ethnic backgrounds present …

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The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism

Tetsuya Marui, Ikuko Funatogawa, Shinko Koishi, Kenji Yamamoto et autres

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. The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism. Objective: Autism …

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Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population

Xiaoxi Liu, Yoshiya Kawamura, Takafumi Shimada, Takeshi Otowa et autres

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Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene

Tetsuya Marui, Ikuko Funatogawa, Shinko Koishi, Kenji Yamamoto et autres

Autism is a severe neurodevelopmental disorder with a complex genetic aetiology. The wingless-type MMTV integration site family member 2 (WNT2) gene has been considered as a candidate gene for autism. We conducted a case-control study and followed up with a transmission disequilibrium …

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Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism – Corrigendum

Tetsuya Marui, Ikuko Funatogawa, Shinko Koishi, Kenji Yamamoto et autres

doi:10.1017/S1461145708009127. Published online by Cambridge University Press, 30 July 2008. Owing to an oversight by the authors the paper by Marui et al. (2008), was published with the name of a co-author, Tsukasa Sasaki, being omitted. The correct version of the author …

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism

Tetsuya Marui, Ikuko Funatogawa, Shinko Koishi, Kenji Yamamoto et autres

Autism is a severe neurodevelopmental disorder of early childhood. Genetic factors play an important role in the aetiology of the disorder. In this study, we considered the NRCAM gene as a candidate gene of autism. This gene is expressed in the central …

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No association between the ryanodine receptor 3 gene and autism in a Japanese population

Mamoru Tochigi, Chieko Kato, Jun Ohashi, Shinko Koishi et autres

AIM: Autism is a neurodevelopmental disorder with a complex genetic etiology. Chromosome 15q11-q14 has been proposed to harbor a gene for autism susceptibility because deletion of the region leads to Prader-Willi syndrome or Angelman syndrome, having phenotypic overlap with autism. Here we …

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Association study of the commonly recognized breakpoints in chromosome 15q11–q13 in Japanese autistic patients

Chieko Kato, Mamoru Tochigi, Shinko Koishi, Yuki Kawakubo et autres

OBJECTIVE: Chromosome 15q11-q13 has been proposed to harbor a gene for autism susceptibility because deletions of the region lead to Prader-Willi syndrome and Angelman syndrome, whose phenotypes overlap with autism. These deletions generally occur with the use of three commonly recognized breakpoints …

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