Matthew A. Deardorff
Medical Genetics | Pediatrics
4650 W Sunset Blvd # Ms 43
Los Angeles, CA 90027
Los Angeles, CA 90027
Last Updated: 09/26/2026
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Found 131 publications
Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylation.
Journal: European journal of human genetics : EJHG
Published: February 10, 2026
Impact of SARS-CoV-2 variants and demographic factors on COVID-19 severity in pediatric patients.
Journal: BMC infectious diseases
Published: December 03, 2025
Identification of a novel TLR7 gain-of-function variant that underlies systemic lupus erythematosus.
Identification of a novel TLR7 gain-of-function variant that underlies systemic lupus erythematosus.
Journal: Journal of human immunity
Published: September 05, 2025
The role of pharmacogenomics and opioid prescribing for infants with surgical congenital heart disease.
Journal: Pharmacogenetics and genomics
Published: June 30, 2025
Isolated lateralized overgrowth and the need for tumor screening: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 04, 2025
Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing.
Journal: Frontiers in genetics
Published: February 10, 2025
Opioid-Related Pharmacogenomic Variants in a Retrospective Cohort of High-Risk Hospitalized Infants.
Opioid-Related Pharmacogenomic Variants in a Retrospective Cohort of High-Risk Hospitalized Infants.
Journal: The Journal of pediatrics
Published: December 20, 2024
16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome.
Journal: Genes
Published: December 19, 2024
Copy number variant analysis improves diagnostic yield in a diverse pediatric exome sequencing cohort.
Journal: NPJ genomic medicine
Published: October 24, 2024
Optical genome mapping improves clinical interpretation of constitutional copy-number gains and reduces their VUS burden.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 28, 2024
Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome.
Journal: Annals of clinical and translational neurology
Published: June 04, 2024
Last Updated: 09/26/2026