C K Powell

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.

Harold F. Sims, J C Brackett, C K Powell et al. · Proceedings of the National Academy of Sciences · 1995 · 221 citations · Full text

Metabolic Disorder, Genetics, Fetal Health +25

Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood.

Arnold W. Strauss, C K Powell, Daniel E. Hale et al. · Proceedings of the National Academy of Sciences · 1995 · 168 citations · Full text

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency.

J C Brackett, Harold F. Sims, Piero Rinaldo et al. · Journal of Clinical Investigation · 1995 · 100 citations · Full text

Beta Subunits, Transcriptional Regulation, Systems Biology +13

Maternal Acute Fatty Liver of Pregnancy Associated with Fetal Trifunctional Protein Deficiency: Molecular Characterization of a Novel Maternal Mutant Allele

John D. Isaacs, Harold F. Sims, C K Powell et al. · Pediatric Research · 1996 · 80 citations · Full text

Pregnancy Nutrition, Molecular Characterization, Hepatology +14

Multimarkerhaplotypes within the serotonin transporter gene suggest evidence of an association with bipolar disorder

L. Mynett‐Johnson, Carmel Kealey, E. Claffey et al. · American Journal of Medical Genetics · 2000 · 43 citations · Full text

Psychiatric Disorders, Genetics, Genetic Epidemiology +19