Norio Ozaki spends much of his time researching Genetics, Internal medicine, Single-nucleotide polymorphism, Endocrinology and Psychiatry. His research is interdisciplinary, bridging the disciplines of Psychosis and Genetics. His studies in Internal medicine integrate themes in fields like Oncology, Sleep disorder, Major depressive disorder, Pharmacology and Candidate gene.
His Single-nucleotide polymorphism study incorporates themes from Genetic determinism and Haplotype. His work on Schizophrenia, Bipolar disorder, Depression and Mood is typically connected to Demography as part of general Psychiatry study, connecting several disciplines of science. His Schizophrenia research includes themes of Hippocampus and Bioinformatics.
His scientific interests lie mostly in Genetics, Internal medicine, Schizophrenia, Single-nucleotide polymorphism and Psychiatry. His study in Genetic association, Gene, Allele, Candidate gene and Allele frequency falls under the purview of Genetics. His Internal medicine research includes elements of Major depressive disorder, Endocrinology and Oncology.
Norio Ozaki interconnects Receptor and Serotonin in the investigation of issues within Endocrinology. As a member of one scientific family, Norio Ozaki mostly works in the field of Schizophrenia, focusing on Bipolar disorder and, on occasion, Mood disorders. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Psychosis and Haplotype.
The scientist’s investigation covers issues in Schizophrenia, Psychiatry, Autism spectrum disorder, Internal medicine and Neuroscience. His study on Schizophrenia also encompasses disciplines like
His research related to Gene, Copy-number variation, Missense mutation, Genetic association and Exome sequencing might be considered part of Genetics. He combines subjects such as Endocrinology, Protein kinase C and Oncology with his study of Internal medicine. The concepts of his Neuroscience study are interwoven with issues in Schizophrenia and Neurite.
Norio Ozaki mainly focuses on Autism spectrum disorder, Internal medicine, Schizophrenia, Phenotype and Psychiatry. His research in Internal medicine intersects with topics in Endocrinology, Depression and Oncology. His Schizophrenia research incorporates elements of Bipolar disorder, Eye movement and Copy-number variation.
His Copy-number variation study combines topics in areas such as Synapse, Neuroscience and Single-nucleotide polymorphism. His Exome sequencing study improves the overall literature in Genetics. As part of his studies on Genetics, he often connects relevant areas like Mechanisms of schizophrenia.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Nature (2014)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen.
Cell (2020)
Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome
Takashi Ebisawa;Makoto Uchiyama;Naofumi Kajimura;Kazuo Mishima.
EMBO Reports (2001)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S Breen;Michael S Breen.
Social Science Research Network (2019)
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report
Mirko Manchia;Mazda Adli;Nirmala Akula;Raffaella Ardau.
web science (2013)
Linkage of Antisocial Alcoholism to the Serotonin 5-HT1B Receptor Gene in 2 Populations
Jaakko Lappalainen;Jeffrey C. Long;Monica Eggert;Norio Ozaki.
Archives of General Psychiatry (1998)
Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia
Tadahiro Numakawa;Yuki Yagasaki;Tetsuya Ishimoto;Takeya Okada.
Human Molecular Genetics (2004)
DNA Methylation Profiles of the Brain-Derived Neurotrophic Factor (BDNF) Gene as a Potent Diagnostic Biomarker in Major Depression
Manabu Fuchikami;Shigeru Morinobu;Masahiro Segawa;Yasumasa Okamoto.
PLOS ONE (2011)
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Liping Hou;Urs Heilbronner;Urs Heilbronner;Franziska Degenhardt;Mazda Adli.
The Lancet (2016)
Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling
Ryota Hashimoto;Tadahiro Numakawa;Takashi Ohnishi;Emi Kumamaru.
Human Molecular Genetics (2006)
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