Yi‐Chun Lu

Mutations in <i>KCND3</i> cause spinocerebellar ataxia type 22

Yi‐Chung Lee, Alexandra Dürr, Karen Majczenko et al. · Annals of Neurology · 2012 · 151 citations · Full text

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21‐q23

Ming‐Yi Chung, Yi‐Chun Lu, Bing‐Wen Soong · Brain · 2003 · 102 citations · Full text

Allelic Variant, Molecular Neuroscience, Engineering +14

Metabolic Characterization of Spinocerebellar Ataxia Type 6

Bing‐Wen Soong, Liang-Chih Wu, Yi‐Chun Lu et al. · Archives of Neurology · 2001 · 44 citations

Metabolic Syndrome, Neurodegenerative Diseases, Molecular Neuroscience +15

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Two novel mutations in the NOTCH3 gene in Chinese

Yi‐Chung Lee, An‐Hang Yang, Hsiu-Chih Liu et al. · Journal of the Neurological Sciences · 2006 · 20 citations

Subcortical Infarcts, Genetic Disorder, Genetics +10

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan

Yi‐Chung Lee, Yi‐Chun Lu, Ming-Hon Chang et al. · Journal of the Neurological Sciences · 2007 · 16 citations

Adult-onset Ataxia, Mendelian Disorder, Genetic Disorder +9