Millie Young

Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes

Kevin A. Strauss, Vincent J. Carson, Kyle Soltys et al. · Molecular Genetics and Metabolism · 2020 · 140 citations · Full text

Metabolic Disorder, Pathology, Metabolic Syndrome +19

Genomic diagnostics within a medically underserved population: efficacy and implications

Kevin A. Strauss, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti et al. · Genetics in Medicine · 2017 · 57 citations · Full text

Genetic Testing, Medicine, Genetics +9

Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades

Kevin A. Strauss, Katie B. Williams, Vincent J. Carson et al. · Molecular Genetics and Metabolism · 2020 · 57 citations · Full text

Neonatology, Brain Development, Striatal Degeneration +17

Preliminary Safety and Tolerability of a Novel Subcutaneous Intrathecal Catheter System for Repeated Outpatient Dosing of Nusinersen to Children and Adults With Spinal Muscular Atrophy

Kevin A. Strauss, Vincent J. Carson, Karlla W. Brigatti et al. · Journal of Pediatric Orthopaedics · 2018 · 55 citations · Full text

Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier

Lauren E. Bowser, Millie Young, Olivia Wenger et al. · Molecular Genetics and Metabolism · 2019 · 53 citations

Developmental Biology, Genetic Disorder, Genetics +9