Mary L. Marazita

According to our database, Mary L. Marazita authored at least 8 papers between 2014 and 2025.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2025

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., March, 2025

Fundamentals of FAIR biomedical data analyses in the cloud using custom pipelines.

Seth R. Berke, Kanika Kanchan, Mary L. Marazita, Eric Tobin, Ingo Ruczinski

PLoS Comput. Biol., 2025

Clustering individuals using INMTD: a novel versatile multi-view embedding framework integrating omics and imaging data.

Zuqi Li, Sam F. L. Windels, Noël Malod-Dognin, Seth M. Weinberg, Mary L. Marazita, Susan Walsh, Mark D. Shriver, David W. Fardo, Peter Claes, Natasa Przulj, Kristel Van Steen

Bioinform., 2025

2023

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

Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2023

2021

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

2020

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

2019

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

2014

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