Miho Toyama
Overview
Explore the profile of Miho Toyama including associated specialties, affiliations and a list of published articles.
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10
Citations
73
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Recent Articles
1.
Furuta S, Aleksic B, Nawa Y, Kimura H, Kushima I, Ishizuka K, et al.
Nagoya J Med Sci
. 2022 Aug;
84(2):260-268.
PMID: 35967956
A number of genomic mutations that are thought to be strongly involved in the development of schizophrenia (SCZ) and autism spectrum disorder (ASD) have been identified. Abnormalities involving oligodendrocytes have...
2.
Kimura H, Nakatochi M, Aleksic B, Guevara J, Toyama M, Hayashi Y, et al.
Transl Psychiatry
. 2022 Jul;
12(1):265.
PMID: 35811316
Autism spectrum disorder (ASD) is a highly heritable, complex disorder in which rare variants contribute significantly to disease risk. Although many genes have been associated with ASD, there have been...
3.
Toyama M, Takasaki Y, Branko A, Kimura H, Kato H, Nawa Y, et al.
PLoS One
. 2022 May;
17(5):e0268321.
PMID: 35536790
Background: Most sequencing studies of schizophrenia (SCZ) have focused on de novo genetic variants due to interpretability. However, investigating shared rare variants among patients in the same multiplex family is...
4.
Nawa Y, Kimura H, Mori D, Kato H, Toyama M, Furuta S, et al.
Hum Genome Var
. 2020 Dec;
7(1):37.
PMID: 33298905
Disabled 1 (DAB1) is an intracellular adaptor protein in the Reelin signaling pathway and plays an essential role in correct neuronal migration and layer formation in the developing brain. DAB1...
5.
Kato H, Kushima I, Mori D, Yoshimi A, Aleksic B, Nawa Y, et al.
Transl Psychiatry
. 2020 Dec;
10(1):421.
PMID: 33279929
Dysregulation of epigenetic processes involving histone methylation induces neurodevelopmental impairments and has been implicated in schizophrenia (SCZ) and autism spectrum disorder (ASD). Variants in the gene encoding lysine demethylase 4C...
6.
Kato K, Mizuno S, Morton J, Toyama M, Hara Y, Wasmer E, et al.
Am J Med Genet A
. 2020 Oct;
185(1):282-285.
PMID: 33084202
The NSUN2 gene encodes a tRNA cytosine methyltransferase that functions in the maturation of leucyl tRNA (Leu) (CAA) precursors, which is crucial for the anticodon-codon pairing and correct translation of...
7.
Araki K, Nakamura R, Ito D, Kato K, Iguchi Y, Sahashi K, et al.
Epilepsy Res
. 2020 Jun;
164:106371.
PMID: 32485575
We report on familial 5 epilepsy patients with autosomal dominant inheritance of a novel heterozygous NUS1 frameshift mutation. All patients had cerebellar ataxia and tremor. Three patients were diagnosed with...
8.
Nagata T, Matsushita M, Mishima K, Kamiya Y, Kato K, Toyama M, et al.
Mol Genet Genomic Med
. 2020 Jan;
8(3):e1148.
PMID: 31975530
Background: Achondroplasia (ACH), the most common form of short-limbed skeletal dysplasia, is caused by gain-of-function mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. More than 97% of patients...
9.
Nakamura Y, Nakatochi M, Kunimoto S, Okada T, Aleksic B, Toyama M, et al.
BMC Psychiatry
. 2019 Jun;
19(1):190.
PMID: 31221108
Background: Postpartum depression (PPD) is a major depressive disorder that occurs after childbirth. Objective diagnostic and predictive methods for PPD are important for early detection and appropriate intervention. DNA methylation...
10.
Yu Y, Lin Y, Takasaki Y, Wang C, Kimura H, Xing J, et al.
Transl Psychiatry
. 2018 Jan;
8(1):12.
PMID: 29317596
In schizophrenia (SCZ) and autism spectrum disorder (ASD), the dysregulation of glutamate transmission through N-methyl-D-aspartate receptors (NMDARs) has been implicated as a potential etiological mechanism. Previous studies have accumulated evidence...