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

PloS one, 2022-03, Vol.17 (3), p.e0265359-e0265359

2022

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Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease

Journal of the American Heart Association, 2015-05, Vol.4 (5), p.n/a

2015

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Identification of shared genomic aberrations between angiomatous and microcystic meningiomas

Neuro-oncology advances, 2019-05, Vol.1 (1), p.vdz028-vdz028

2019

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Molecular Cloning of a Novel Brain‐Type Na+‐Dependent Inorganic Phosphate Cotransporter

Journal of neurochemistry, 2000-06, Vol.74 (6), p.2622-2625

2000

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Genomewide-Linkage and Haplotype-Association Studies Map Intracranial Aneurysm to Chromosome 7q11

American journal of human genetics, 2001-10, Vol.69 (4), p.804-819

2001

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

Journal of stroke and cerebrovascular diseases, 2017-01, Vol.26 (1), p.150-161

2017

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

Journal of stroke and cerebrovascular diseases, 2016-12, Vol.25 (12), p.2900-2906

2016

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

Human genome variation, 2018-01, Vol.5 (1), p.17060-17060, Article 17060

2018

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Quantitative analysis of gene expressions related to inflammation in canine spastic artery after subarachnoid hemorrhage

Stroke (1970), 2001-01, Vol.32 (1), p.212-217

2001

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Role of p38 mitogen-activated protein kinase on cerebral vasospasm after subarachnoid hemorrhage

Stroke (1970), 2004-06, Vol.35 (6), p.1466-1470

2004

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Nicardipine Prolonged-Release Implants for Preventing Cerebral Vasospasm After Subarachnoid Hemorrhage: Effect and Outcome in the First 100 Patients

Neurologia medico-chirurgica, 2007, Vol.47(9), pp.389-396

2007

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Collagen type I α2 (COL1A2) is the susceptible gene for intracranial aneurysms

Stroke (1970), 2004-02, Vol.35 (2), p.443-448

2004

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Efficacy and safety of nicardipine prolonged-release implants for preventing vasospasm in humans

Stroke (1970), 2002-04, Vol.33 (4), p.1011-1015

2002

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Identification of Genes Differentially Expressed in Canine Vasospastic Cerebral Arteries After Subarachnoid Hemorrhage

Journal of cerebral blood flow and metabolism, 1999-11, Vol.19 (11), p.1279-1288

1999

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Bedside monitoring of circulating blood volume after subarachnoid hemorrhage

Stroke (1970), 2003-04, Vol.34 (4), p.956-960

2003

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Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm

Journal of human genetics, 2003-01, Vol.48 (6), p.309-314

2003

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

Journal of the neurological sciences, 2019-04, Vol.399, p.183-185

2019

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

Neurology India, 2019-01, Vol.67 (1), p.312-314

2019

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

PloS one, 2022-01, Vol.17 (3)

2022

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Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

Journal of human genetics, 2006-05, Vol.51 (5), p.491-494

2006

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Cerebral Hypermetabolism Demonstrated by FDG PET in Familial Creutzfeldt-Jakob Disease

Clinical nuclear medicine, 2011-08, Vol.36 (8), p.725-727

2011

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

Journal of the neurological sciences, 2016-03, Vol.362, p.144-146

2016

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Increased expression of ephrin A1 in brain arteriovenous malformation: DNA microarray analysis

Neurosurgical review, 2007-10, Vol.30 (4), p.299-305

2007

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Clinical features of intracranial aneurysms in siblings

Neurosurgery, 2000-06, Vol.46 (6), p.1301-1306

2000

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Spontaneous regression together with increased calcification of incidental meningioma

Surgical neurology international, 2014, Vol.5 (1), p.73

2014

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

Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease

Identification of shared genomic aberrations between angiomatous and microcystic meningiomas

Molecular Cloning of a Novel Brain‐Type Na+‐Dependent Inorganic Phosphate Cotransporter

Genomewide-Linkage and Haplotype-Association Studies Map Intracranial Aneurysm to Chromosome 7q11

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

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

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

Quantitative analysis of gene expressions related to inflammation in canine spastic artery after subarachnoid hemorrhage

Role of p38 mitogen-activated protein kinase on cerebral vasospasm after subarachnoid hemorrhage

Nicardipine Prolonged-Release Implants for Preventing Cerebral Vasospasm After Subarachnoid Hemorrhage: Effect and Outcome in the First 100 Patients

Collagen type I α2 (COL1A2) is the susceptible gene for intracranial aneurysms

Efficacy and safety of nicardipine prolonged-release implants for preventing vasospasm in humans

Identification of Genes Differentially Expressed in Canine Vasospastic Cerebral Arteries After Subarachnoid Hemorrhage

Bedside monitoring of circulating blood volume after subarachnoid hemorrhage

Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm

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

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

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

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

Cerebral Hypermetabolism Demonstrated by FDG PET in Familial Creutzfeldt-Jakob Disease

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

Increased expression of ephrin A1 in brain arteriovenous malformation: DNA microarray analysis

Clinical features of intracranial aneurysms in siblings

Spontaneous regression together with increased calcification of incidental meningioma

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