K. Bartlett
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, Peroxisome Proliferator-Activated Receptors, Diet and metabolism studies, Biotin and Related Studies
Most-Cited Works
- → Mammalian mitochondrial β-oxidation(1996)413 cited
- → Mitochondrial β‐oxidation(2004)401 cited
- → Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency(1999)300 cited
- → Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.(1998)234 cited
- → Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with a Lipid-Storage Myopathy and Secondary Carnitine Deficiency(1984)135 cited
- → Combined enzyme defect of mitochondrial fatty acid oxidation.(1992)128 cited
- → The Factorial Survey: An Approach to Defining Sexual Harassment on Campus(1982)114 cited
- → Very long‐chain acyl coenzyme A dehydrogenase deficiency presenting with exercise‐induced myoglobinuria(1994)109 cited
- → Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency(1991)107 cited
- → Fatal Lactic Acidosis in Infancy with a Defect of Complex III of the Respiratory Chain(1989)107 cited