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)

Detection of de novo copy number deletions from targeted sequencing of trios. - Jack M. Fu; Elizabeth J. Leslie; Alan F. Scott; Jeffrey C. Murray; Mary L. Marazita; Terri H. Beaty; Robert B. Scharpf; Ingo Ruczinski (Bioinform., 2019)

A Multivariate Approach to Determine the Dimensionality of Human Facial Asymmetry. - Omid Ekrami; Peter Claes; Julie D. White; Seth M. Weinberg; Mary L. Marazita; Susan Walsh; Mark D. Shriver; Stefan Van Dongen (Symmetry, 2020)

Fluctuating Asymmetry and Sexual Dimorphism in Human Facial Morphology: A Multi-Variate Study. - Omid Ekrami; Peter Claes; Ellen Van Assche; Mark D. Shriver; Seth M. Weinberg; Mary L. Marazita; Susan Walsh; Stefan Van Dongen (Symmetry, 2021)

Data-driven trait heritability-based extraction of human facial phenotypes. - Meng Yuan; Seppe Goovaerts; Hanne Hoskens; Stephen Richmond; Susan Walsh; Mark D. Shriver; John R. Shaffer; Mary L. Marazita; Seth M. Weinberg; Hilde Peeters; Peter Claes (BIBM, 2023)

Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variants. - Meng Yuan; Seppe Goovaerts; Myoung K. Lee; Jay Devine; Stephen Richmond; Susan Walsh; Mark D. Shriver; John R. Shaffer; Mary L. Marazita; Hilde Peeters; Seth M. Weinberg; Peter Claes (Briefings Bioinform., 2025)