Daniel E. Hale

The genetic architecture of type 2 diabetes

Christian Fuchsberger, Jason Flannick, Tanya M. Teslovich et al. · Nature · 2016 · 1.1K citations · Full text

Genetic Determinant, Genetics, Diabetes +6

Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts

William R. Treem, Charles A. Stanley, David N. Finegold et al. · New England Journal of Medicine · 1988 · 308 citations

Metabolic Disorder, Oxidative Stress, Metabolic Syndrome +22

A quantitative scale of acanthosis nigricans.

J. P. Burke, Daniel E. Hale, Helen P. Hazuda et al. · Diabetes Care · 1999 · 270 citations

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

An acyl-coenzyme a dehydrogenase assay utilizing the ferricenium ion

Thomas Lehman, Daniel E. Hale, A. Bhala et al. · Analytical Biochemistry · 1990 · 218 citations

Ferricenium Ion, Biosynthesis, Aldehyde Dehydrogenase +4