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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

Journal of human genetics, 2021-04, Vol.66 (4), p.419-429

2021

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

Journal of human genetics, 2010-03, Vol.55 (3), p.137-141

2010

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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

Journal of human genetics, 2021-04, Vol.66 (4), p.449-450

2021

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Association between the neurofibromatosis-1 (NF1) locus and autism in the Japanese population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-11, Vol.131B (1), p.43-47

2004

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No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population

Journal of human genetics, 2007-12, Vol.52 (12), p.985-989

2007

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No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population

Neuroscience research, 2005-09, Vol.53 (1), p.91-94

2005

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Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: A case-control study

Brain & development (Tokyo. 1979), 2007-09, Vol.29 (8), p.510-513

2007

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Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder

Autism Research and Treatment, 2012-01, Vol.2012 (2012), p.1-5

2012

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

Psychiatry and clinical neurosciences, 2008-06, Vol.62 (3), p.341-344

2008

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Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism

Brain & development (Tokyo. 1979), 2004, Vol.26 (1), p.5-7

2004

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Antenatal Depression and Maternal-Fetal Attachment

Psychopathology, 2003-11, Vol.36 (6), p.304-311

2003

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

The international journal of neuropsychopharmacology, 2009-02, Vol.12 (1), p.1-10

2009

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Similarities and differences between the behavior of Asperger's syndrome and obsessive-compulsive disorder

Nihon rinshō, 2007-03, Vol.65 (3), p.506

Hashimoto, Ohiko

2007

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

The international journal of neuropsychopharmacology, 2010-05, Vol.13 (4), p.443-449

2010

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Delayed automatic detection of change in speech sounds in adults with autism: A magnetoencephalographic study

Clinical neurophysiology, 2005-07, Vol.116 (7), p.1655-1664

2005

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Association study of the 15q11-q13 maternal expression domain in Japanese autistic patients

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-10, Vol.147B (7), p.1008-1012

2008

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Polyhistidine tract expansions in HOXA1 result in intranuclear aggregation and increased cell death

Biochemical and biophysical research communications, 2005-11, Vol.336 (4), p.1033-1039

2005

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

Psychiatric genetics, 2008-06, Vol.18 (3), p.133-136

2008

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Human Leukocyte Antigen and Season of Birth in Japanese Patients With Schizophrenia

The American journal of psychiatry, 2000-07, Vol.157 (7), p.1173-1175

2000

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A Family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia

Movement disorders, 1999-03, Vol.14 (2), p.342-344

1999

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A Study on Verbal Memory Functions in Temporal Lobe Epilepsy with the Rey Auditory‐Verbal Learning Test

Epilepsia (Copenhagen), 1998-05, Vol.39 (S5), p.57-58

1998

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Unspecified mental retardation

Ryoikibetsu shokogun shirizu, 2003 (39), p.423

Hashimoto, Ohiko

2003

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Mixed specific developmental disorder

Ryoikibetsu shokogun shirizu, 2003 (39), p.513

Hashimoto, Ohiko

2003

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Support for the family from infancy

Psychiatria et neurologia Japonica, 2004, Vol.106 (5), p.602

2004

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Low Frequency of the Fragile X Syndrome among Japanese Autistic Subjects

Journal of autism and developmental disorders, 1993-03, Vol.23 (1), p.201-209

Hashimoto, Ohiko

1993

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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

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

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

Association between the neurofibromatosis-1 (NF1) locus and autism in the Japanese population

No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population

Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: A case-control study

Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder

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

Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism

Antenatal Depression and Maternal-Fetal Attachment

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

Similarities and differences between the behavior of Asperger's syndrome and obsessive-compulsive disorder

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

Delayed automatic detection of change in speech sounds in adults with autism: A magnetoencephalographic study

Association study of the 15q11-q13 maternal expression domain in Japanese autistic patients

Polyhistidine tract expansions in HOXA1 result in intranuclear aggregation and increased cell death

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

Human Leukocyte Antigen and Season of Birth in Japanese Patients With Schizophrenia

A Family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia

A Study on Verbal Memory Functions in Temporal Lobe Epilepsy with the Rey Auditory‐Verbal Learning Test

Unspecified mental retardation

Mixed specific developmental disorder

Support for the family from infancy

Low Frequency of the Fragile X Syndrome among Japanese Autistic Subjects

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