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Kyoko Hoshino

Neocortical Layer Formation of Human Developing Brains and Lissencephalies: Consideration of Layer-Specific Marker Expression
2010 · Takashi Saito, Sae Hanai, et al. · Cerebral Cortex · 74
ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H+-ATPases is essential for brain development in humans and mice
2021 · Kazushi Aoto, Mitsuhiro Kato, et al. · Nature Communications · 73
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A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
2005 · Kazue Kimura, Takashi Sugawara, et al. · Brain and Development · 52
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing
2019 · Kazuhiro Iwama, Takeshi Mizuguchi, et al. · Journal of Medical Genetics · 40
Two hyperandrogenic adolescent girls with congenital portosystemic shunt
2001 · Mari Satoh, Susumu Yokoya, et al. · European Journal of Pediatrics · 37
Whole genome sequencing of 45 Japanese patients with intellectual disability
2021 · Chihiro Abe‐Hatano, Aritoshi Iida, et al. · American Journal of Medical Genetics Part A · 31
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Development of language in Rett syndrome
2001 · June Uchino, Michiyo Suzuki, et al. · Brain and Development · 29
PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia
2018 · Kishin Koh, Yuta Ichinose, et al. · Journal of Human Genetics · 27
GRIN2D variants in three cases of developmental and epileptic encephalopathy
2018 · Naomi Tsuchida, Keisuke Hamada, et al. · Clinical Genetics · 24
An Interactive Smartphone App, Nenne Navi, for Improving Children’s Sleep: Pilot Usability Study
2020 · Arika Yoshizaki, Ikuko Mohri, et al. · JMIR Pediatrics and Parenting · 23
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Correction: PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia
2018 · Kishin Koh, Yuta Ichinose, et al. · Journal of Human Genetics · 20
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Transitional Care for Young People with Movement Disorders: Consensus‐Based Recommendations from the MDS Task Force on Pediatrics
2023 · Tamara Pringsheim, Amit Batla, et al. · Movement Disorders Clinical Practice · 15
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Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies
2021 · Sachiko Miyamoto, Mitsuhiro Kato, et al. · Journal of Human Genetics · 15
Pyoderma gangrenosum of the skin and respiratory tract in a 5-year-old girl
2003 · Kuniko Takeuchi, Kyoko Hoshino, et al. · European Journal of Pediatrics · 14
Problems in the Development of the Sleep–Wake Rhythm Influence Neurodevelopmental Disorders in Children
2023 · Kyoko Hoshino · Diagnostics · 12
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A case of acute encephalopathy with biphasic seizures and late reduced diffusion associated with Streptococcus pneumoniae meningoencephalitis
2011 · Seiko Kuwata, Hideaki Senzaki, et al. · Brain and Development · 11
A Single Gene for Dystonia Involves Both or Either of the Two Striatal Pathways
2002 · Masaya Segawa, Kyoko Hoshino, et al. · Advances in behavioral biology · 9
Very-Low-Dose Levodopa Therapy for Pediatric Neurological Disorders: A Preliminary Questionnaire in Japan
2021 · Kyoko Hoshino, Masaharu Hayashi, et al. · Frontiers in Pediatrics · 6
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Pre-movement gating of somatosensory evoked potentials in Tourette syndrome
2023 · Kazue Kimura, Nagako Murase, et al. · Brain and Development · 5
Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations
2021 · Kyoko Hoshino, Kathleen J. Sweadner, et al. · Neurology Genetics · 4
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A randomized clinical trial of remote Group-Based comprehensive behavioral intervention for tics
2025 · Takeshi Inoue, Jumpei Iwanami, et al. · European Child & Adolescent Psychiatry · 3
Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
2009 · Yoshiaki Saito, Kenji Sugai, et al. · Brain and Development · 3
[Neurological involvements with transient gait disturbance in subacute phase of Kawasaki disease; a case report].
1995 · K Hoshino, K Morooka, et al. · PubMed · 3
The Pathophysiology of Gilles de la Tourette Syndrome: Changes in Saccade Performance by Low-Dose L-Dopa and Dopamine Receptor Blockers
2023 · Yasuo Terao, Yoshiko Nomura, et al. · Brain Sciences · 2
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Pathogenicity evaluation of variants of uncertain significance at exon-intron junction by splicing assay in patients with Mowat–Wilson syndrome
2023 · Yasuyo Suzuki, Noriko Nomura, et al. · European Journal of Medical Genetics · 2
Works count: 49
Citation count: 543
H-index: 14
I10-index: 16
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