The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases by Hui Wang, Hui Wang, Li-San Wang, Li-San Wang, Gerard Schellenberg, Gerard Schellenberg, Wan-Ping Lee, Wan-Ping Lee

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One reference genome is not enough by Xiaofei Yang, Wan-Ping Lee, Kai Ye, Charles Lee

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Persistence and clinical consequences of post-traumatic and dissociative symptoms in people with depressive symptoms: a one-year follow-up study by Hong Wang Fung, Anson Kai Chun Chau, Suet Lin Hung, Stanley Kam Ki Lam, Wai Tong Chien, Vincent Wan Ping Lee

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JAX-CNV: A Whole-genome Sequencing-based Algorithm for Copy Number Detection at Clinical Grade Level by Wan-Ping Lee, Qihui Zhu, Xiaofei Yang, Silvia Liu, Eliza Cerveira, Mallory Ryan, Adam Mil-Homens, Lauren Bellfy, Kai Ye, Charles Lee, Chengsheng Zhang

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The prediction of Alzheimer’s disease through multi-trait genetic modeling by Kaylyn Clark, Kaylyn Clark, Wei Fu, Chia-Lun Liu, Chia-Lun Liu, Pei-Chuan Ho, Pei-Chuan Ho, Pei-Chuan Ho, Hui Wang, Hui Wang, Wan-Ping Lee, Wan-Ping Lee, Shin-Yi Chou, Shin-Yi Chou, Shin-Yi Chou, Shin-Yi Chou, Li-San Wang, Li-San Wang, Jung-Ying Tzeng, Jung-Ying Tzeng, Jung-Ying Tzeng

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LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants by Jinfeng Lu, Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Cristiane Araujo Martins Moreno, Wan-Ping Lee, Yuk Yee Leung, Mathew B. Harms, Badri Vardarajan, Erin L. Heinzen

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Dissociative symptoms among community health service users in Hong Kong: a longitudinal study of clinical course and consequences by Hong Wang Fung, Stanley Kam Ki Lam, Wai Tong Chien, Albe Sin Ying Ng, Emily Nga Man Wong, Colin A. Ross, Suet Lin Hung, Vincent Wan Ping Lee

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SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data by Jocelyn T. Chi, Ilse C. F. Ipsen, Tzu-Hung Hsiao, Ching-Heng Lin, Li-San Wang, Wan-Ping Lee, Tzu-Pin Lu, Jung-Ying Tzeng, Jung-Ying Tzeng, Jung-Ying Tzeng

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FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods by Timothy Becker, Wan-Ping Lee, Joseph Leone, Qihui Zhu, Chengsheng Zhang, Silvia Liu, Jack Sargent, Kritika Shanker, Adam Mil-homens, Eliza Cerveira, Mallory Ryan, Jane Cha, Fabio C. P. Navarro, Timur Galeev, Mark Gerstein, Ryan E. Mills, Dong-Guk Shin, Charles Lee, Ankit Malhotra

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A comprehensive map of mobile element insertion polymorphisms in humans. by Chip Stewart, Deniz Kural, Michael P Strömberg, Jerilyn A Walker, Miriam K Konkel, Adrian M Stütz, Alexander E Urban, Fabian Grubert, Hugo Y K Lam, Wan-Ping Lee, Michele Busby, Amit R Indap, Erik Garrison, Chad Huff, Jinchuan Xing, Michael P Snyder, Lynn B Jorde, Mark A Batzer, Jan O Korbel, Gabor T Marth, 1000 Genomes Project

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Human whole-exome genotype data for Alzheimer’s disease by Yuk Yee Leung, Adam C. Naj, Yi-Fan Chou, Otto Valladares, Michael Schmidt, Kara Hamilton-Nelson, Nicholas Wheeler, Honghuang Lin, Prabhakaran Gangadharan, Liming Qu, Kaylyn Clark, Amanda B. Kuzma, Wan-Ping Lee, Laura Cantwell, Heather Nicaretta, Alzheimer’s Disease Sequencing Project, Jonathan Haines, Lindsay Farrer, Sudha Seshadri, Zoran Brkanac, Carlos Cruchaga, Margaret Pericak-Vance, Richard P. Mayeux, William S. Bush, Anita Destefano, Eden Martin, Gerard D. Schellenberg, Li-San Wang

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