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Author

Yohane Miyata

Observed name: Miyata, Yohane
Institution: Kyorin University
ORCID: 0000-0002-7767-7592
Observed ORCID: 0000-0002-7767-7592
OpenAlex ID: A5025317933
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy
2019 · Atsushi Takata, Mitsuko Nakashima, et al. · Nature Communications · 69
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Prenatal clinical manifestations in individuals with COL4A1/2 variants
2020 · Toshiyuki Itai, Satoko Miyatake, et al. · Journal of Medical Genetics · 45
Assessment and Rating of Motor Cerebellar Ataxias With the Kinect v2 Depth Sensor: Extending Our Appraisal
2020 · Takeru Honda, Hiroshi Mitoma, et al. · Frontiers in Neurology · 18
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Clinical and genetic characteristics of patients with Doose syndrome
2020 · Nodoka Hinokuma, Mitsuko Nakashima, et al. · Epilepsia Open · 17
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Long-Term Evaluation of Low-Dose Betamethasone for Ataxia Telangiectasia
2019 · Setsuko Hasegawa, Satoko Kumada, et al. · Pediatric Neurology · 13
Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene
2018 · Yohane Miyata, Ken Saida, et al. · Brain and Development · 6
An atypical case of KMT2B‐related dystonia manifesting asterixis and effect of deep brain stimulation of the globus pallidus
2019 · Yohane Miyata, Kohei Hamanaka, et al. · Neurology and Clinical Neuroscience · 5
Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield
2024 · Shogo Furukawa, Mitsuhiro Kato, et al. · Journal of Human Genetics · 4
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Fatal X-linked lymphoproliferative disease type 1-associated limbic encephalitis with positive anti-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antibody
2022 · Satoru Ochiai, Itaru Hayakawa, et al. · Brain and Development · 4
Completely resolved structural variants by optical genome mapping with adaptive sampling from CNV discovery
2026 · Li Fu, Chong Ae Kim, et al. · npj Genomic Medicine · 2
Ocular Manifestations of Peters Plus-Like Syndrome in 8q21.11 Microdeletion Syndrome
2023 · Chika Shigeyasu, Masakazu Yamada, et al. · Cornea · 2
A Japanese case of multisystem inflammatory syndrome in children
2021 · Ayumi Ogihara, Yohane Miyata, et al. · Pediatrics International · 2
Low excretor glutaric acidemia type 1 with transient lesions in the basal ganglia
2025 · Yohane Miyata, Kei Murayama, et al. · Brain and Development
Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield
2024 · 古川, 省悟, 中島, 光子, et al. · Institutional Repositories DataBase (IRDB)
The efficacy of GPi—DBS in two KMT2B mutation cases using the quantitative evaluation system
2018 · Yohane Miyata · Japanese Society of Child Neurology
Hippocampal injury caused by lipoteichoic acid of Staphylococcus aureus in immature rat brains
2017 · Yohane Miyata · Japanese Society of Child Neurology
Duplication of the Xq21.1 in two male siblings with neurodegeneration with brain iron accumulation
2017 · Yohane Miyata · Japanese Society of Child Neurology
Factors associated with antisocial behavior in patients with developmental disorder.
2016 · Yukiko Nakamura, Makiko Shimazaki, et al. · PubMed
[Nonconvulsive status epilepticus as an initial symptom in a boy with frontal lobe epilepsy].
2014 · Yohane Miyata, Makiko Shimazaki, et al. · PubMed
Works count: 19
Citation count: 187
H-index: 6
I10-index: 5
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