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
- 2 citationsA novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype.Kimberly A. Kripps, Marisa W. Friederich, Ting Chen, Austin Larson, David M. Mirsky
Molecular Genetics and Metabolism. 2020-11-24 - 395 citationsPatient-Customized Oligonucleotide Therapy for a Rare Genetic DiseaseJinkuk Kim, Chunguang Hu, Christelle Moufawad El Achkar, Lauren E. Black, Julie Douville
The New England Journal of Medicine. 2019-10-09 - 1 citationsInsights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing.Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones
American Journal of Medical Genetics. Part A. 2023-04-01
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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