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Circulation. Genomic and Precision Medicine|October 5, 2022
Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian ChannelopathiesMatthew J O'Neill, Yuko Wada, Lynn D Hall, et al.Plos One|February 14, 2013
Enabling genomic-phenomic association discovery without sacrificing anonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.American Journal of Human Genetics|May 14, 2025
Benefits and barriers to broad implementation of genomic sequencing in the NICUMelissa R Goldin, Douglas M Ruderfer, Alexander Bick, et al.Plos Genetics|June 23, 2020
A Bayesian method to estimate variant-induced disease penetranceBrett M Kroncke, Derek K Smith, Yi Zuo, et al.Pharmacogenomics|June 18, 2009
Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmiasWilliam S Bush, Dana C Crawford, Charles Alexander, et al.Plos One|July 5, 2013
Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing AnonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.Pediatrics|November 25, 2020
Pharmacogenetics to Predict Adverse Events Associated With AntidepressantsKatelyn M Rossow, Ida T Aka, Angela C Maxwell-Horn, et al.Pharmacology & Therapeutics|April 27, 2018
Anticancer drug-induced cardiac rhythm disorders: Current knowledge and basic underlying mechanismsJoachim Alexandre, Javid J Moslehi, Kevin R Bersell, et al.Medrxiv : the Preprint Server for Health Sciences|September 21, 2023
ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering VariantsMatthew J O'Neill, Tao Yang, Julie Laudeman, et al.Epidemiology (Cambridge, Mass.)|November 22, 2013
On the validity of the case-time-control design for autocorrelated exposure historiesAksel Karl Georg Jensen, Thomas Alexander Gerds, Peter Weeke, et al.Pageof 54