Ya-Fang Chen

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Ning Wang, Jin He, Wang Ni, 2011, Nature Genetics.

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.

Ning Wang, Wanjin Chen, Min-ting Lin, 2013, Gene.

Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan

Kai Wang, Ming‐Jen Lee, Ya-Fang Chen, 2015, Journal of the Neurological Sciences.

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Wanjin Chen, Min-ting Lin, S. Murong, 2012, Clinica chimica acta; international journal of clinical chemistry.

Molecular analysis of SMN 1 , SMN 2 , NAIP , GTF 2 H 2 , and H 4 F 5 genes in 157 Chinese patients with spinal muscular atrophy ☆

Ning Wang, Wanjin Chen, Min-ting Lin, 2013 .

Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson's Disease in Han Chinese

Ning Wang, Xiao-Zhen Lin, C. Liou, 2015, Chinese medical journal.

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Min-ting Lin, S. Murong, Ning Wang, 2012, Clinica chimica acta; international journal of clinical chemistry.