The contribution of de novo coding mutations to autism spectrum disorder. - Ivan Iossifov; Brian J. O'Roak; Stephan J. Sanders; Michael Ronemus; Niklas Krumm; Dan Levy; Holly A. Stessman; Kali T. Witherspoon; Laura Vives; Karynne E. Patterson; Joshua D. Smith; Bryan Paeper; et al. (Nat., 2014)

A Biomedical Open Knowledge Network Harnesses the Power of AI to Understand Deep Human Biology. - Sergio E. Baranzini; Katy Börner; John H. Morris; Charlotte A. Nelson; Karthik Soman; Erica Schleimer; Michael J. Keiser; Mark A. Musen; Roger Pearce; Tahsin Reza; Brett Smith; Bruce William Herr II; et al. (AI Mag., 2022)

CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. - Yujin Kim; Minwoo Jeong; In Gyeong Koh; Chanhee Kim; Hyeji Lee; Jae Hyun Kim; Ronald Yurko; Il Bin Kim; Jeongbin Park; Donna M. Werling; Stephan J. Sanders; Joon-Yong An (Briefings Bioinform., 2024)

Artificial intelligence-assisted quantification and assessment of whole slide images for pediatric kidney disease diagnosis. - Chunyue Feng; Kok Haur Ong; David M. Young; Bingxian Chen; Longjie Li 004; Xinmi Huo; Haoda Lu; Weizhong Gu; Fei Liu; Hongfeng Tang; Manli Zhao; Min Yang; et al. (Bioinform., 2024)