Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease by Wei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang

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Genome-wide association study identifies DRAM1 associated with Tourette syndrome in Taiwan by Wei-De Lin, Ting-Yuan Liu, Yu-Chia Chen, I-Ching Chou, Fuu-Jen Tsai

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Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?—A Retrospective Study by Chien-Heng Lin, Wei-De Lin, I-Ching Chou, Inn-Chi Lee, Syuan-Yu Hong

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Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population by Wei-De Lin, Wen-Ling Liao, Wei-Cheng Chen, Ting-Yuan Liu, Yu-Chia Chen, Fuu-Jen Tsai

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Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study by Wei-De Lin, Chu-Chyn Ou, Shih-Hao Hsiao, Chih-Han Chang, Fuu-Jen Tsai, Jiunn-Wang Liao, Yng-Tay Chen

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Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics by Yu-Tzu Chang, Syuan-Yu Hong, Wei-De Lin, Chien-Heng Lin, Sheng-Shing Lin, Fuu-Jen Tsai, I-Ching Chou

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GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease by Chung-Hsing Wang, Yu‐Nan Huang, Wen-Ling Liao, Ai-Ru Hsieh, Wei-De Lin, Kai-Wen Liu, Wen-Li Lu, Chieh‐Chen Huang, Yin-Hsiu Chien, Ni-Chung Lee, Pen-Hua Su, Fuu-Jen Tsai

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