AustinLarsonMD
Medical Genetics • Aurora, COClinical Biochemical Genetics, Clinical Genetics, Medical Biochemical Genetics, Pediatric Medical Genetics
Assistant Professor
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Office
13123 E 16th Ave
Aurora, CO 80045Phone+1 303-724-2338Fax+1 720-777-7321
Summary
- Dr. Austin Larson is a medical geneticist in Aurora, CO and is affiliated with Children's Hospital Colorado. He received his medical degree from The Warren Alpert Medical School of Brown University and has been in practice 7 years. He specializes in clinical biochemical genetics, clinical genetics, medical biochemical genetics, and pediatric medical genetics and is experienced in mitochondrial diseases and inborn errors of metabolism.
Education & Training
University of ColoradoFellowship, Medical Biochemical Genetics, 2015 - 2017- University of ColoradoResidency, Medical Genetics and Genomics, 2013 - 2015
- University of ColoradoResidency, Pediatrics, 2010 - 2013
The Warren Alpert Medical School of Brown UniversityClass of 2010
Certifications & Licensure
CO State Medical License 2013 - 2025
MT State Medical License 2017 - 2019- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Clinical and Basic Investigations Into Congenital Disorders of Glycosylation Start of enrollment: 2019 Oct 08
Publications & Presentations
PubMed
- The clinical utility in hospital-wide use of growth differentiation factor 15 as a biomarker for mitochondrial DNA-related disorders.Andrea Cortés Fernández, Jane Estrella, Devin Oglesbee, Austin A Larson, Johan L K Van Hove
Journal of Inherited Metabolic Disease. 2025-01-01 - 1 citationsAn integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with...Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, Sara Gracie, Marisa W Friederich
Mitochondrion. 2024-11-01 - 1 citationsACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis.Johan L K Van Hove, Marisa W Friederich, Daniella H Hock, David A Stroud, Nikeisha J Caruana
Mitochondrion. 2024-09-01
Journal Articles
- TRAPPC11 and GOSR2 Mutations Associate with Hypoglycosylation of Α-dystroglycan and Muscular DystrophyCharles A Williams, Steven A Moore, Craig A Press, Aaron D Bossler, Austin A Larson, BioMed Central
Press Mentions
Pueblo Girl Battles Rare Disease That Affects Neurological DevelopmentJuly 25th, 2018
University of Colorado Ophthalmologists Administer Novel Treatment for Single Patient Facing Rare Genetic ConditionSeptember 7th, 2023
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