Dr. Olson is interested in medical education utilizing team-based in-situ simulations as well as how non-cognitive traits effect physician training and education. In addition, he is interested in exploring ways to integrate evidence-based principles of mastery learning into undergraduate and graduate medical education.
Central Michigan University
Michigan
MAEd - Education, Curriculum, Instruction
2018
Northwestern University, Mcgaw Medical Center
Illinois
- Emergency Medicine Residency
2014
Drexel University College of Medicine
Pennsylvania
MD - Medicine
2010
University of California, San Diego
California
BS - Microbiology
2004
Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair.
Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. Sci Data. 2025 Aug 08; 12(1):1385.
PMID: 40781089
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair.
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. Sci Data. 2025 07 16; 12(1):1195.
PMID: 40670386
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair.
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. bioRxiv. 2025 Jun 14.
PMID: 39345378
Assessment of Emergency Medicine Residents' Situational Awareness and Perception of Patient Safety Culture in the Emergency Department.
Assessment of Emergency Medicine Residents' Situational Awareness and Perception of Patient Safety Culture in the Emergency Department. AEM Educ Train. 2025 Jun; 9(3):e70060.
PMID: 40510557
Small variant benchmark from a complete assembly of X and Y chromosomes.
Small variant benchmark from a complete assembly of X and Y chromosomes. Nat Commun. 2025 Jan 08; 16(1):497.
PMID: 39779690
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation.
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 11 20; 34(11):2061-2073.
PMID: 39358015
The GIAB genomic stratifications resource for human reference genomes.
The GIAB genomic stratifications resource for human reference genomes. Nat Commun. 2024 10 19; 15(1):9029.
PMID: 39424793
Analysis and benchmarking of small and large genomic variants across tandem repeats.
Analysis and benchmarking of small and large genomic variants across tandem repeats. Nat Biotechnol. 2025 Mar; 43(3):431-442.
PMID: 38671154
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation. medRxiv. 2024 Mar 07.
PMID: 38496498
The complete sequence of a human Y chromosome.
The complete sequence of a human Y chromosome. Nature. 2023 09; 621(7978):344-354.
PMID: 37612512