Tsz H. Wong

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 18 publications

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 23, 2025

Delayed Progression of Ataxia with a Static Cerebellar Lesion- Consider SCA27B.

Delayed Progression of Ataxia with a Static Cerebellar Lesion- Consider SCA27B.

Journal: Cerebellum (London, England)

Published: January 07, 2025

A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics.

A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics.

Journal: Acta neuropathologica communications

Published: September 27, 2021

Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.

Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.

Journal: Neurology. Genetics

Published: September 28, 2020

Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.

Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.

Journal: Neurobiology of aging

Published: April 17, 2020

LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands.

LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands.

Journal: Parkinsonism & related disorders

Published: February 07, 2019

Three VCP Mutations in Patients with Frontotemporal Dementia.

Three VCP Mutations in Patients with Frontotemporal Dementia.

Journal: Journal of Alzheimer's disease : JAD

Published: August 15, 2018

Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.

Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.

Journal: Neurobiology of aging

Published: April 20, 2018

EIF2AK3 variants in Dutch patients with Alzheimer's disease.

EIF2AK3 variants in Dutch patients with Alzheimer's disease.

Journal: Neurobiology of aging

Published: April 12, 2018

Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes.

Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes.

Journal: Neurobiology of aging

Published: December 18, 2017

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Journal: The Lancet. Neurology

Published: December 05, 2017

Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy.

Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy.

Journal: European journal of human genetics : EJHG

Published: April 02, 2017

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Last Updated: 09/26/2026