Ashlee R. Stiles

Associate Professor of Pediatrics

Pediatrics, Medical Genetics

ashlee.stiles@duke.edu

801-6 Capitola Dr, Durham, NC 27713

801-6 Capitola Drive, Durham, NC 27713

More About This Person

At a Glance

Credentials
1. Education

Academic Experience

Global Scholarship

Keywords

Research

Scholarly Works

Teaching & Mentoring
1. Teaching Summary
2. Advising & Mentoring Summary

Recognition

Professional Activities

Scholarly Works - Conferences

Rescue of glutaric aciduria type I mice by liver directed gene editing

Conference MOLECULAR THERAPY · April 28, 2025 Link to item Cite

Rescue of glutaric aciduria type I mice by liver directed therapies

Conference HUMAN GENE THERAPY · February 1, 2025 Link to item Cite

Critical sample collection delayed? Urine organic acid analysis can still save the day!

Conference Molecular Genetics and Metabolism · April 2024 Full text Cite

Early presentation of Morquio B syndrome identified via skeletal et biochemical findings

Conference Molecular Genetics and Metabolism · April 2024 Full text Cite

Rescue of Glutaric Aciduria Type I Mice by Liver Directed Therapies

Conference MOLECULAR THERAPY · May 1, 2023 Link to item Cite

RESCUE OF GLUTARIC ACIDURIA TYPE I MICE BY LIVER DIRECTED THERAPIES

Conference Molecular Genetics and Metabolism · March 2023 Full text Cite

TRIHEPTANOIN FOR PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE I (GSDI): PILOT CLINICAL TRIAL RESULTS

Conference Molecular Genetics and Metabolism · March 2023 Full text Cite

Validation of therapeutic strategies in a novel compound heterozygote model of Methylmalonic Acidemia

Conference HUMAN GENE THERAPY · December 1, 2022 Link to item Cite

Urinary glucose tetrasaccharide correlates with phenotype in Pompe disease in the newborn period

Conference MOLECULAR GENETICS AND METABOLISM · April 2021 Link to item Cite

Utilization of in-patient genetic testing services at Duke University Health System

Conference MOLECULAR GENETICS AND METABOLISM · April 2021 Link to item Cite

Phenotypic target organ and biomarker variation within a family with late onset Fabry disease

Conference Molecular Genetics and Metabolism · February 2021 Full text Cite

EVALUATION OF PLASMA GLUCOSYLSPHINGOSINE AND GALACTOSYLSPHINGOSINE IN PATIENTS WITH GAUCHER DISEASE

Conference MOLECULAR GENETICS AND METABOLISM · July 1, 2019 Link to item Cite

Ashlee R. Stiles

Scholarly Works - Conferences

Rescue of glutaric aciduria type I mice by liver directed gene editing

Rescue of glutaric aciduria type I mice by liver directed therapies

Critical sample collection delayed? Urine organic acid analysis can still save the day!

Early presentation of Morquio B syndrome identified via skeletal et biochemical findings

Rescue of Glutaric Aciduria Type I Mice by Liver Directed Therapies

RESCUE OF GLUTARIC ACIDURIA TYPE I MICE BY LIVER DIRECTED THERAPIES

TRIHEPTANOIN FOR PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE I (GSDI): PILOT CLINICAL TRIAL RESULTS

Validation of therapeutic strategies in a novel compound heterozygote model of Methylmalonic Acidemia

Urinary glucose tetrasaccharide correlates with phenotype in Pompe disease in the newborn period

Utilization of in-patient genetic testing services at Duke University Health System

Phenotypic target organ and biomarker variation within a family with late onset Fabry disease

EVALUATION OF PLASMA GLUCOSYLSPHINGOSINE AND GALACTOSYLSPHINGOSINE IN PATIENTS WITH GAUCHER DISEASE

EVALUATION OF PLASMA GLUCOSYLSPHINGOSINE AND GALACTOSYLSPHINGOSINE IN PATIENTS WITH GAUCHER DISEASE

Quantification of glucosylsphingosine in plasma/serum by UPLC-MS/MS

Plasma lyso-Gb3 as a diagnostic marker for Fabry disease