Liao, Yi-Chu

Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles

Liao, Y.-C., Hsiao, C.-T., Fuh, J.-L., Chern, C.-M., Lee, W.-J., Guo, Y.-C., Wang, S.-J., Lee, I.-H., Liu, Y.-T., Wang, Y.-F., et al. (2015) · PLOS ONE

Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases

Cited by 123

Prolonged Excretion of Poliovirus among Individuals with Primary Immunodeficiency Disorder: An Analysis of the World Health Organization Registry

Macklin, G., Liao, Y., Takane, M., Dooling, K., Gilmour, S., Mach, O., Kew, O. M., Sutter, R. W., & The iVDPV Working Group (2017) · Frontiers in Immunology

Viral Infections and Immunology ResearchImmunodeficiency and Autoimmune Disorders

Cited by 47

Disease Severity Staging System for NOTCH3 -Associated Small Vessel Disease, Including CADASIL

Gravesteijn, G., Rutten, J. W., Cerfontaine, M. N., Hack, R. J., Liao, Y.-C., Jolly, A. A., Guey, S., Hsu, S.-L., Park, J.-Y., Yuan, Y., et al. (2025) · JAMA Neurology

Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases

Cited by 25

Plasma biomarkers are associated with agitation and regional brain atrophy in Alzheimer’s disease

Hsu, J.-L., Lee, W.-J., Liao, Y.-C., Lirng, J.-F., Wang, S.-J., & Fuh, J.-L. (2017) · Scientific Reports

Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Cited by 18

Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype

Hsu, S.-L., Chen, Y.-H., Chou, C.-T., Chou, Y.-T., Tsai, Y.-S., Hsiao, C.-T., Liao, Y.-C., & Lee, Y.-C. (2021) · Parkinsonism & Related Disorders

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 3