Hiroshi Ujike
Okayama, Japan
Last Updated: 09/26/2026
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Found 34 publications
A Single Medical Marker for Diagnosis of Methamphetamine Addiction - DNA Methylation of SHATI/NAT8L Promoter Sites from Patient Blood.
Journal: Current pharmaceutical design
Published: August 12, 2019
Enrichment of deleterious variants of mitochondrial DNA polymerase gene (POLG1) in bipolar disorder.
Enrichment of deleterious variants of mitochondrial DNA polymerase gene (POLG1) in bipolar disorder.
Journal: Psychiatry and clinical neurosciences
Published: August 25, 2016
The regulation of soluble receptor for AGEs contributes to carbonyl stress in schizophrenia.
Journal: Biochemical and biophysical research communications
Published: August 16, 2016
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Journal: Scientific reports
Published: January 28, 2016
Individual risk alleles of susceptibility to schizophrenia are associated with poor clinical and social outcomes.
Journal: Journal of human genetics
Published: September 30, 2015
JSNP Excellent Presentation Award for CINP2014
Journal: Nihon shinkei seishin yakurigaku zasshi = Japanese journal of psychopharmacology
Published: June 02, 2015
Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies.
Journal: Molecular brain
Published: June 01, 2015
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
Journal: Schizophrenia bulletin
Published: October 22, 2014
The Piccolo Intronic Single Nucleotide Polymorphism rs13438494 Regulates Dopamine and Serotonin Uptake and Shows Associations with Dependence-Like Behavior in Genomic Association Study.
Journal: Current molecular medicine
Published: October 04, 2014
Aripiprazole is effective for treatment of delayed sleep phase syndrome.
Journal: Clinical neuropharmacology
Published: July 04, 2014
Frontotemporal dementia with parkinsonism linked to chromosome 17 with the MAPT R406W mutation presenting with a broad distribution of abundant senile plaques.
Journal: Neuropathology : official journal of the Japanese Society of Neuropathology
Published: March 29, 2014
Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: February 14, 2014
Last Updated: 09/26/2026