1. Cheng-Jun Lin, Liang-Shuan Hu, Hao-Ping Chen, Yung-Hao Ching (2021, Oct). Functional Analysis of a Novel ALDH5A1 Allele Causing Succinic Semialdehyde Dehydrogenase Deficiency In Human. 2021 Annual Meeting of Buddhist Tzu Chi Medical Foundation, Hualein, Taiwan. 本人為通訊作者.
2. Cheng-Jun Lin, Liang-Shuan Hu, Hao-Ping Chen, Yung-Hao Ching (2021, Mar). Functional analysis of a novel ALDH5A1 allele causing Succinic semialdehyde dehydrogenase deficiency in human. The 93rd Annual Meeting of the Genetics Society of Japan, Tokyo, Japan. 本人為通訊作者. 3. Yung-Hao Ching, Liang-Shuan Hu, Ming-Der Lin, Wun-Ying Lin, Ben-Yang Liao, Chia-Yin Chiang (2020, Dec). Molecular Cloning and Functional Analysis of Three Taiwanese Usher Syndrome families. International Symposium on Evolutionary Genomics and Bioinformatics 2020, Taipei. 本人為第一作者、通訊作者.
4. Yung-Hao Ching, Chu-Ting Wu, Liang-Hsuan Hu, and Raymond Y. Lo (2020, Dec). Identification of a novel APOE p.Gly4Gly Mutation Causing Early-Onset Alzheimer’s Disease by Next Generation Sequencing. International Symposium on Evolutionary Genomics and Bioinformatics 2020, Taipei. 本人為第一作者.
5. Guan-Yu Chen1, Shih-Ying Huang, Yung-Hao Ching, Ming-Der Lin and HouFeng Li (2020, Feb). Monitoring the Hybridization of Two Notorious Termite Pests in Taiwan. The 13th Conference of the PRTRG, Taipei.
6. Yung-Hao Ching1, Vani Vennela1, Yi-Ning Chiu, Ming-Der Lin1, and Hou-Feng Li (2020, Feb). De novo Development and Polymorphism Analysis of Microsatellite Markers in Prorhinotermes flavus (Blattodea: Rhinotermitid). The 13 th Conference of the PRTRG, Taipei Zoo, Taipei, 本人為第一作者.
7. Yung-Hao Ching, Vani Vennela, Yi-Ning Chiu, Ming-Der Lin,Hou-Feng Li (2019, Oct). De novo development and polymorphism analysis of microsatellite markers in Prorhinotermes flavus (Blattodea: Rhinotermitidae). The 40th annual meeting of Taiwan Entomological Society., NTU Experimental Forest, Xitou Nature Education Area. 本人為第一作者.
8. Yung-Hao Ching, Wen-Ying Lin, Ming-Der Lin (2019, Aug). Identification and Functional analysis of a novel mutant MYO7A allele of Usher syndrome. 2 nd Thailand-Taiwan Forum on Medical Science and Technology, National Sun Yat Sen University. 本人為第一作者、通訊作者.
9. Wen-Ying Lin, Ming-Der Lin, Yung-Hao Ching (2019, Mar). Characterization of a novel mutant allele, MYO7A p.S2112*, of Usher syndrome type II. 2019 The 34th Joint Annual Conference of Biomedical Science, National Defense Medical Center, Taipei. MOST 104-2311-B-320-001. 本人為通訊作者.
10. Divya Suresh, Yung-Hao Ching, Ming-Der Lin, Ben-Yang Liao (2018, Jun). Functional analysis of a novel gene X causing small eye phenotype through JNK-dependent apoptotic pathway. 2018 European Human Genetics Conference, Milan, Italy. 本人為通訊作者.
11. Liang-shuan Hu, Cheng-der Liu, Jia-ying Chien,Chi-shuan Chung,Shum-ping Huang, Yung-hao Ching (2018, Jun). Eye-specific transcription factor PAX6 and CRX regulate the expression of a de novo pyrimidine biosynthesis gene Cad. 2018 European Human Genetics Conference, Milan, Italy. 本人為通訊作者.
12. Wen-Lang Fan, Ren-Hua Chung, Wen-Ying Lin, Wan-Hsuan Tsai, Liang-Hsuan Hu, Shun-Ping Huang, Yung-Hao Ching (2018, Jun). Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family. 2018 European Human Genetics Conference, Milan, Italy. 本人為通訊作者.
13. Wun-ying Lin, Cheng-der Liu, Liang-shuan Hu, Chi-hsuan Chung, Jia-ying Chien, Ming-der Lin, Shun-ping Huang, Yung-hao Ching (2018, Jun). Functional study of a PAX6 non-stop mutation causing autosomal dominant Retinitis Pigmentosa. 2018 European Human Genetics Conference, Milan, Italy. 本人為通訊作者.
14. Yi-Hsuan Kao, Wen-Lang Fan, Ren-Hua Chung, Wun-Ying Lin, Wan-Hsuan Tsai, Liang-Hsuan Hu, Shun-Ping Huang, Yung-Hao Ching (2018, Jun). In vitro functional analysis of a novel RP2 alleles. European Human Genetics Conference, Milan, Italy. 本人為通訊作者.
15. Yung-Hao Ching, Wun-Ying Lin, Lian-Hsuan Hu, Wen-Lang Fan, Ren-Hua Chung, Jia-ling Jiang, Shun-Ping Huan (2017, Mar). Using Use of HighThroughput Sequencing Combining Linkage Analysis to Positionally Clone the Causative Mutation for a Taiwanese X linked Recessive Retinitis Pigmentosa Family. The 32nd Joint Annual Conference of Biomedical Science, Taipei, Taiwan. MOST 104-2311-b-320-001. 本人為第一作者、通訊作者.