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Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
Communications Medicine|February 6, 2026
Machine learning to infer neurocognitive testing scores among adolescents and young adults with congenital heart diseaseMohammad Arafat Hussain, Sheng He, Heather R Adams, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Journal of Pathology Informatics|November 26, 2015
Practical considerations in genomic decision support: The eMERGE experienceTimothy M Herr, Suzette J Bielinski, Erwin Bottinger, et al.
AJOB Empirical Bioethics|September 22, 2018
Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental surveyArmand H Matheny Antommaria, Kyle B Brothers, John A Myers, et al.
Plos One|June 2, 2015
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin TherapySara L Van Driest, Tracy L McGregor, Digna R Velez Edwards, et al.
BMC Medical Research Methodology|November 25, 2016
Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutionsMaureen E Smith, Saskia C Sanderson, Kyle B Brothers, et al.
American Journal of Human Genetics|February 14, 2017
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the USSaskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, et al.
Neuroimage|July 5, 2024
Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structureMarlee M Vandewouw, Ami Norris-Brilliant, Anum Rahman, et al.
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