Tsu-Yen Wu

Detection of mycobacteria in Crohn's disease by a broad spectrum polymerase chain reaction.

C. Tzen, Tsu-Yen Wu, Tsu‐Yen Wu, 2006, Journal of the Formosan Medical Association = Taiwan yi zhi.

A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a family

D. Lin, Hsuan-Liang Liu, Shuan-Pei Lin, 2011, American journal of medical genetics. Part A.

Impairment of Proteasome and Autophagy Underlying the Pathogenesis of Leukodystrophy

D. Lin, C. Ho, M. Chiang, 2020, Cells.

Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndrome

D. Lin, Hsuan-Liang Liu, Shuan-Pei Lin, 2011, American journal of medical genetics. Part A.

Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial disease

D. Lin, Yau-Huei Wei, C. Ho, 2017, Oncotarget.