Author

Karen L. DeBalsi

Observed names: Karen DeBalsi, Karen L. DeBalsi

Observed institutions: National Institutes of Health, Duke University, National Institute of Environmental Health Sciences, Metabolon (United States)

OpenAlex ID: A5061562256

Muscle-Specific Deletion of Carnitine Acetyltransferase Compromises Glucose Tolerance and Metabolic Flexibility

2012 · Deborah M. Muoio, Robert C. Noland, et al. · Cell Metabolism · 368

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Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases

2016 · Karen L. DeBalsi, Kirsten E. Hoff, et al. · Ageing Research Reviews · 180

Obesity and lipid stress inhibit carnitine acetyltransferase activity

2014 · Sarah E. Seiler, Ola J. Martin, et al. · Journal of Lipid Research · 104

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Carnitine Acetyltransferase Mitigates Metabolic Inertia and Muscle Fatigue during Exercise

2015 · Sarah E. Seiler, Timothy R. Koves, et al. · Cell Metabolism · 101

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PPARγ coactivator-1α contributes to exercise-induced regulation of intramuscular lipid droplet programming in mice and humans

2012 · Timothy R. Koves, Lauren M. Sparks, et al. · Journal of Lipid Research · 95

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Targeted Metabolomics Connects Thioredoxin-interacting Protein (TXNIP) to Mitochondrial Fuel Selection and Regulation of Specific Oxidoreductase Enzymes in Skeletal Muscle

2014 · Karen L. DeBalsi, Kari E. Wong, et al. · Journal of Biological Chemistry · 61

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Muscle-Specific Overexpression of PGC-1α Does Not Augment Metabolic Improvements in Response to Exercise and Caloric Restriction

2014 · Kari E. Wong, Catherine R. Mikus, et al. · Diabetes · 47

POLG2disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity

2015 · Matthew J. Young, Margaret M. Humble, et al. · Human Molecular Genetics · 34

Synergistic Effects of the in cis T251I and P587L Mitochondrial DNA Polymerase γ Disease Mutations

2017 · Karen L. DeBalsi, Matthew J. Longley, et al. · Journal of Biological Chemistry · 22

Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndrome

2018 · Kirsten E. Hoff, Karen L. DeBalsi, et al. · PLoS ONE · 18

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Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder

2024 · Rulan Shaath, Aljazi Al-Maraghi, et al. · Metabolites · 3

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Dried blood spots capture a wide range of metabolic pathways and biological changes associated with exercise

2025 · Karen L. DeBalsi, Kelli D. Goodman, et al. · Metabolomics · 2

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Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder

2025 · Aljazi Al-Maraghi, Rulan Shaath, et al. · International Journal of Molecular Sciences · 1

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Absence of malonyl-CoA decarboxylase (MCD) impacts endurance exercise capacity and reprograms skeletal muscle mitochondrial metabolism

2012 · Tim Koves, Sarah Seiler, et al. · Mitochondrion · 1

Expanding the ABCA2-associated neurodevelopmental phenotype

2026 · Kaisa T. Oja, Karit Reinson, et al. · Human Genetics and Genomics Advances

Dried Blood Spots Capture a Wide Range of Metabolic Pathways and Biological Characteristics Associated with Fish Oil Supplementation, Fasting, and the Postprandial State

2025 · Karen L. DeBalsi, Kelli D. Goodman, et al. · Metabolites

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A Case Study of Dysfunctional Nicotinamide Metabolism in a 20-Year-Old Male

2023 · Karen L. DeBalsi, John H. Newman, et al. · Metabolites

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Biochemical characterization of PolG exonuclease disease mutations

2015 · Karen L. DeBalsi, Matthew J. Longley, et al. · Mitochondrion

Role of Thioredoxin-Interacting Protein (TXNIP) in Regulating Redox Balance and Mitochondrial Function in Skeletal Muscle

2013 · Karen L. DeBalsi · DukeSpace (Duke University)

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Works count: 19

Citation count: 1,037

H-index: 10

I10-index: 10