Hideaki Onda

Kofu, Japan

Last Updated: 09/26/2026

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Found 14 publications

Biallelic loss-of-function variants in PTGIS cause recurrent cervical internal carotid artery vasospasm.

Biallelic loss-of-function variants in PTGIS cause recurrent cervical internal carotid artery vasospasm.

Journal: International journal of stroke : official journal of the International Stroke Society

Published: April 25, 2026

Recurrent Hemorrhagic Stroke in a Patient with Neurosarcoidosis.

Recurrent Hemorrhagic Stroke in a Patient with Neurosarcoidosis.

Journal: Internal medicine (Tokyo, Japan)

Published: August 20, 2025

Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.

Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.

Journal: PloS one

Published: November 03, 2021

Identification of shared genomic aberrations between angiomatous and microcystic meningiomas.

Identification of shared genomic aberrations between angiomatous and microcystic meningiomas.

Journal: Neuro-oncology advances

Published: July 10, 2020

A case of delayed-onset hereditary hemorrhagic telangiectasia with a frameshift ENG mutation.

A case of delayed-onset hereditary hemorrhagic telangiectasia with a frameshift ENG mutation.

Journal: Neurology India

Published: March 13, 2019

Novel SLC20A2 mutation in a Japanese pedigree with primary familial brain calcification.

Novel SLC20A2 mutation in a Japanese pedigree with primary familial brain calcification.

Journal: Journal of the neurological sciences

Published: January 22, 2019

Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease.

Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease.

Journal: Human genome variation

Published: September 16, 2017

KRIT1 mutations in three Japanese pedigrees with hereditary cavernous malformation.

KRIT1 mutations in three Japanese pedigrees with hereditary cavernous malformation.

Journal: Human genome variation

Published: August 02, 2016

Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease.

Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: May 31, 2016

Association of Rare Nonsynonymous Variants in PKD1 and PKD2 with Familial Intracranial Aneurysms in a Japanese Population.

Association of Rare Nonsynonymous Variants in PKD1 and PKD2 with Familial Intracranial Aneurysms in a Japanese Population.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: May 23, 2016

Unusual case of cerebral small vessel disease with a heterozygous nonsense mutation in HTRA1.

Unusual case of cerebral small vessel disease with a heterozygous nonsense mutation in HTRA1.

Journal: Journal of the neurological sciences

Published: November 12, 2015

Two Cases of Primary Intracranial Solitary Fibrous Tumor:Genetic Examination of NAB2-STAT6 Fusion and Its Association with Hemangiopericytoma

Two Cases of Primary Intracranial Solitary Fibrous Tumor:Genetic Examination of NAB2-STAT6 Fusion and Its Association with Hemangiopericytoma

Journal: No shinkei geka. Neurological surgery

Published: July 03, 2015

Showing 1-12 of 14

Last Updated: 09/26/2026