Author

Iori Ohmori

Okayama UniversityORCID 0000-0001-6823-2762Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:differential expression· 2 Organism:mouse· 2 Organism:rat· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Kazuhiro YamakawaiD· 2 shared Mamoru OuchidaiD· 2 shared Matthieu RaveauiD· 2 shared Shinya ToyokuniiD· 2 shared Tetsuya TatsukawaiD· 2 shared Tomoji MashimoiD· 2 shared Adrian Walton MooreiD· 1 shared Akiko Hayashi‐TakagiiD· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersNeuroscience

Kazuhiro YamakawaORCID

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4 papers

Recent·Most cited

NeuroscienceeLifePeer-reviewedSep 1, 2023

Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment

Hideo Hagihara, Hirotaka Shoji, Satoko Hattori…·Michihiro Igarashi

The paper investigates brain pH and lactate levels in animal models of neuropsychiatric disorders, finding decreased pH and increased lactate levels as common features across multiple models.

18 citations

mousestatistical model

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PhysiologybioRxivPreprintAug 14, 2023

Txn1 mutation is a monogenic cause of chronic kidney disease associated with mitochondrial dysfunction in rats

Iori Ohmori, Mamoru Ouchida, Yoshiko Hada…·Tomoji Mashimo

1 citation

ratbulk RNA-seq

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NeuroscienceScientific ReportsPeer-reviewedMay 17, 2022

CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate

Toshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo…·Kazuhiro Yamakawa

This study identifies CUX2 and CASP variants in temporal lobe epilepsy patients and shows they increase seizure susceptibility and excitatory synaptic transmission.

13 citations

humanmouse

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NeurosciencebioRxivPreprintOct 7, 2021

Txn1 mutation causes epilepsy associated with vacuolar degeneration in the midbrain

Iori Ohmori, Mamoru Ouchida, Hirohiko Imai…·Tomoji Mashimo

This study identifies a Txn1 mutation causing epilepsy and midbrain vacuolar degeneration in rats, with age-dependent neuronal and oligodendrocyte cell death and repair.

DOI 10.1101/2021.10.07.463470

ratexperimental assay

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