Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. - Alexandre Bureau; Samuel G. Younkin; Margaret M. Parker; Joan E. Bailey-Wilson; Mary L. Marazita; Jeffrey C. Murray; Elisabeth Mangold; Hasan Albacha-Hejazi; Terri H. Beaty; Ingo Ruczinski (Bioinform., 2014)

Unsupervised discovery of phenotype-specific multi-omics networks. - W. Jenny Shi; Yonghua Zhuang; Pamela H. Russell; Brian D. Hobbs; Margaret M. Parker; Peter J. Castaldi; Pratyaydipta Rudra; Brian Vestal; Craig P. Hersh; Laura M. Saba; Katerina J. Kechris (Bioinform., 2019)