Last Updated: 09/26/2026
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Found 19 publications
Systematic evaluation of de novo mutation calling tools using whole genome sequencing data.
Journal: Briefings in bioinformatics
Published: January 23, 2025
Diagnostic Obscurity of Gastrointestinal Subepithelial Tumors: An Organizing Gastric Hematoma Requiring En Bloc Resection.
Journal: ACG case reports journal
Published: December 11, 2022
Mastalgia is Not An Indication for Mammogram.
Journal: Journal of the American Board of Family Medicine : JABFM
Published: November 29, 2021
Scarcity of Recurrent Regulatory Driver Mutations in Colorectal Cancer Revealed by Targeted Deep Sequencing.
Journal: JNCI cancer spectrum
Published: September 26, 2018
The non-coding RNA landscape of human hematopoiesis and leukemia.
Journal: Nature communications
Published: September 13, 2016
Alpha2A adrenergic receptor genetic variation contributes to hyperglycemia after myocardial infarction.
Journal: International journal of cardiology
Published: March 04, 2016
Differential DNA repair underlies mutation hotspots at active promoters in cancer genomes.
Journal: Nature
Published: June 12, 2015
Systematic Screening of Promoter Regions Pinpoints Functional Cis-Regulatory Mutations in a Cutaneous Melanoma Genome.
Journal: Molecular cancer research : MCR
Published: March 26, 2015
Validating drug repurposing signals using electronic health records: a case study of metformin associated with reduced cancer mortality.
Journal: Journal of the American Medical Informatics Association : JAMIA
Published: July 24, 2014
Last Updated: 09/26/2026