Sakae Takahashi

发表

Chronological changes of MRI findings on striatal damage after acute cyanide intoxication: Pathogenesis of the damage and its selectivity, and prevention for neurological sequelae: A case report

T. Kojima, Y. Okuhata, R. Satoh, 2005, European Archives of Psychiatry and Clinical Neuroscience.

Heterogeneity of schizophrenia: Genetic and symptomatic factors

Sakae Takahashi, Sakae Takahashi, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families

S. Faraone, M. Tsuang, J. Lasky-Su, 2005, Psychiatry Research.

Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia

Masato Matsuura, Eisuke Matsushima, Takuya Kojima, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Initial genome‐wide scan for linkage with schizophrenia in the Japanese schizophrenia sib‐pair linkage group (JSSLG) families

S. Tsuji, T. Shinkai, K. Yara, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Family-based association study of the NOTCH4 gene in schizophrenia using Japanese and Chinese samples

S. Faraone, M. Tsuang, K. Yara, 2003, Biological Psychiatry.

Failure to find association between PRODH deletion and schizophrenia

K. Yara, M. Matsuura, T. Arinami, 2004, Schizophrenia Research.

Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

Naoshi Kaneko, Hiroki Shibata, Takashi Asada, 2005, American journal of human genetics.

Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia

Makoto Uchiyama, Ming T. Tsuang, Takuya Kojima, 2008, Schizophrenia Research.

Family‐based association study of markers on chromosome 22 in schizophrenia using African‐American, European‐American, and Chinese families

S. Faraone, M. Tsuang, M. Matsuura, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Case history and genome‐wide scans for copy number variants in a family with patient having 15q11.1–q11.2 duplication and 22q11.2 deletion, and schizophrenia

M. Uchiyama, Takahiro Suzuki, Sakae Takahashi, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Eye movement and random number in NP lupus evaluation

Masato Matsuura, Takuya Kojima, Satoshi Kamei, 2008, Clinical Rheumatology.

Mutation screening and association study of the beta-adrenergic receptor kinase 2 gene in schizophrenia families

M. Matsuura, T. Arinami, E. Tanabe, 2004, Psychiatry Research.

The Relationship between Exploratory Eye Movement Dysfunction and Psychiatric Symptoms in Schizophrenia

T. Kojima, M. Uchiyama, Masahiro Suzuki, 2015 .

Relationships between exploratory eye movement dysfunction and clinical symptoms in schizophrenia

Y. Hirayasu, M. Kurachi, Y. Okubo, 2012, Psychiatry and clinical neurosciences.

Exploratory eye movement dysfunction as a discriminator for schizophrenia

Y. Hirayasu, M. Kurachi, Y. Okubo, 2009, European Archives of Psychiatry and Clinical Neuroscience.

Relationship between exploratory eye movement, P300, and reaction time in schizophrenia

S. Obayashi, M. Matsuura, E. Tanabe, 2008, Psychiatry and clinical neurosciences.