Rasika A. Mathias

发表

Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

Seunggeun Lee, Brian E. Cade, Tamar Sofer, 2018, bioRxiv.

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

Brian E. Cade, Thomas W. Blackwell, Yan Gao, 2020, bioRxiv.

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

Brian E. Cade, Jan Graffelman, Alex P. Reiner, 2020, bioRxiv.

Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data

Zachary A. Szpiech, Rasika A. Mathias, Ryan D. Hernandez, 2017, Bioinform..

Inheritance of Total Serum IgE in the Isolated Tangier Island Population from Virginia: Complexities Associated with Genealogical Depth of Pedigrees in Segregation Analyses

Rasika A. Mathias, Terri H. Beaty, Kathleen C. Barnes, 2005, Human Heredity.

Directional dominance on stature and cognition in diverse human populations

Laura J. Scott, Claude Bouchard, Christian Gieger, 2015, Nature.

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Scott T. Weiss, Hemant K. Tiwari, Donald W. Bowden, 2019, bioRxiv.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma

Scott T. Weiss, Rasika A. Mathias, Oren E. Livne, 2015, Nature Communications.

Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry

Zachary A. Szpiech, Michael Bamshad, Ingo Ruczinski, 2016, Nature Communications.

On the Analysis of Genome-Wide Association Studies in Family-Based Designs: A Universal, Robust Analysis Approach and an Application to Four Genome-Wide Association Studies

Scott T. Weiss, Christoph Lange, Sungho Won, 2009, PLoS genetics.