J. Vockley
Genetics in Medicine · 2010–2014
A researcher in the Science corpus: 3 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Papers from J. Vockley's perspective
Ordered by how strongly the researchers J. Vockley trusts endorse each paper. Same corpus, a different order for every researcher.
- Lipotoxic diseases. (Annual Review of Medicine)
- Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. (Diabetes)
- Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes. (Diabetes)
- Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns. (Clinical Chemistry)
- Mitochondrial overload and incomplete fatty acid oxidation contribute to skeletal muscle insulin resistance. (Cell Metabolism)
- Faculty Opinions recommendation of PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes.
- Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1 (Proceedings of the National Academy of Sciences of the United States of America)
- Regulation of Mitochondrial Biogenesis in Skeletal Muscle by CaMK (Science)
- Lipid oxidation is reduced in obese human skeletal muscle. (American Journal of Physiology. Endocrinology and Metabolism)
- Mitochondrial Dysfunction in the Elderly: Possible Role in Insulin Resistance (Science)
Their papers
- BLOOD AMMONIA AND GLUTAMINE AS PREDICTORS OF HYPERAMMONEMIC CRISES IN UREA CYCLE DISORDER PATIENTS (2014) — 818 citations
- Phenylalanine hydroxylase deficiency: diagnosis and management guideline (2013) — 641 citations
- Increased Levels of Plasma Acylcarnitines in Obesity and Type 2 Diabetes and Identification of a Marker of Glucolipotoxicity (2010) — 625 citations