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Archives of Pathology & Laboratory Medicine|October 31, 2018
Proficiency Testing of Standardized Samples Shows Very High Interlaboratory Agreement for Clinical Next-Generation Sequencing-Based Oncology AssaysJason D Merker, Kelly Devereaux, A John Iafrate, et al.Family Practice|October 7, 2017
Recruiting primary care practices for practice-based research: a case study of a group-randomized study (TRANSLATE CKD) recruitment processNatalia Y Loskutova, Craig Smail, Kemi Ajayi, et al.Nucleic Acids Research|November 9, 2022
Deep learning-assisted genome-wide characterization of massively parallel reporter assaysFred Lu, Aaron Sossin, Nathan Abell, et al.American Journal of Human Genetics|September 13, 2011
Epistatic selection between coding and regulatory variation in human evolution and diseaseTuuli Lappalainen, Stephen B Montgomery, Alexandra C Nica, et al.Plos Genetics|August 4, 2011
Rare and common regulatory variation in population-scale sequenced human genomesStephen B Montgomery, Tuuli Lappalainen, Maria Gutierrez-Arcelus, et al.Current Atherosclerosis Reports|March 14, 2014
Dissecting the causal genetic mechanisms of coronary heart diseaseClint L Miller, Themistocles L Assimes, Stephen B Montgomery, et al.Methods in Molecular Biology (Clifton, N.J.)|September 10, 2010
Annotating the regulatory genomeStephen B Montgomery, Katayoon Kasaian, Steven J M Jones, et al.American Journal of Human Genetics|December 19, 2012
Integrating GWAS and expression data for functional characterization of disease-associated SNPs: an application to follicular lymphomaLucia Conde, Paige M Bracci, Rhea Richardson, et al.Journal of Patient Safety|September 14, 2020
Stimulant Prescribing Error Assessment Rubric DevelopmentNatalia Y Loskutova, Cory Lutgen, Craig Smail, et al.Pageof 20