Kent E. Kruckeberg

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

Karen Snow, David J. Tester, Kent E. Kruckeberg et al. · Human Molecular Genetics · 1994 · 156 citations

Genetics, Molecular Biology, Molecular Genetics +21

Iron overload in cirrhosis— HFE genotypes and outcome after liver transplantation

David J. Brandhagen, William Alvarez, Terry M. Therneau et al. · Hepatology · 2000 · 99 citations · Full text

Liver Transplant Recipients, Iron Metabolism, Genetics +23

The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C4-acylcarnitine concentration in newborn blood spots

Narasimhan Nagan, Kent E. Kruckeberg, Angela L. Tauscher et al. · Molecular Genetics and Metabolism · 2003 · 62 citations

Aldehyde Dehydrogenase, Genetics, Inherited Metabolic Disease +8

Analysis of hMLH1 and hMSH2 Gene Dosage Alterations in Hereditary Nonpolyposis Colorectal Cancer Patients by Novel Methods

Linnea M. Baudhuin, Ming Mai, Amy J. French et al. · Journal of Molecular Diagnostics · 2005 · 30 citations

Novel Methods, Oncology, Medicine +10

Familial Splenomegaly: Macrophage Hypercatabolism of Lipoproteins Associated with Apolipoprotein E Mutation [Apolipoprotein E (Δ149 Leu)]

Tu T. Nguyen, Kent E. Kruckeberg, John F. O’Brien et al. · The Journal of Clinical Endocrinology & Metabolism · 2000 · 28 citations · Full text