Shoichiro Ando

Brain Science Branch
Niigata, Japan

Last Updated: 09/26/2026

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Found 19 publications

ABCC6 pathogenic variants are associated with hemorrhagic phenotypes in Japanese patients with severe cerebral small vessel disease.

ABCC6 pathogenic variants are associated with hemorrhagic phenotypes in Japanese patients with severe cerebral small vessel disease.

Journal: Scientific reports

Published: August 21, 2025

Hereditary Leukoencephalopathy: Overview to Definition, Diagnosis and Treatment

Hereditary Leukoencephalopathy: Overview to Definition, Diagnosis and Treatment

Journal: Brain and nerve = Shinkei kenkyu no shinpo

Published: May 12, 2025

The analysis of schizophrenia-like psychosis in dentatorubral-pallidoluysian atrophy.

The analysis of schizophrenia-like psychosis in dentatorubral-pallidoluysian atrophy.

Journal: Frontiers in neurology

Published: January 22, 2025

"Chocolate Chip Sign" on Susceptibility-Weighted Imaging: A Novel Neuroimaging Biomarker for HTRA1-Related Cerebral Small Vessel Disease.

"Chocolate Chip Sign" on Susceptibility-Weighted Imaging: A Novel Neuroimaging Biomarker for HTRA1-Related Cerebral Small Vessel Disease.

Journal: Neurology. Genetics

Published: August 05, 2024

Missense Variants in COL4A1/2 Are Associated with Cerebral Aneurysms: A Case Report and Literature Review.

Missense Variants in COL4A1/2 Are Associated with Cerebral Aneurysms: A Case Report and Literature Review.

Journal: Neurology international

Published: December 09, 2023

Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.

Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.

Journal: Nature communications

Published: November 03, 2023

Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.

Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.

Journal: Brain sciences

Published: May 19, 2023

Inappropriate interpretation of non-pathogenic HTRA1 variant as pathogenic.

Inappropriate interpretation of non-pathogenic HTRA1 variant as pathogenic.

Journal: Annals of clinical and translational neurology

Published: January 14, 2023

High frequency of HTRA1 AND ABCC6 mutations in Japanese patients with adult-onset cerebral small vessel disease.

High frequency of HTRA1 AND ABCC6 mutations in Japanese patients with adult-onset cerebral small vessel disease.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: July 04, 2022

Rethinking Lacunar Stroke: Beyond Fisher's Curse

Rethinking Lacunar Stroke: Beyond Fisher's Curse

Journal: Brain and nerve = Shinkei kenkyu no shinpo

Published: August 31, 2021

Corrigendum: HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.

Corrigendum: HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.

Journal: Frontiers in neurology

Published: August 09, 2021

Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.

Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.

Journal: Acta neuropathologica communications

Published: June 29, 2021

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Last Updated: 09/26/2026