E H Ludwig

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

George Papanikolaou, Mark Samuels, E H Ludwig et al. · Nature Genetics · 2003 · 976 citations · Full text

Juvenile Hemochromatosis, Heme Homeostasis, Iron Metabolism +8

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

L. F. SORIA, E H Ludwig, Howard R. G. Clarke et al. · Proceedings of the National Academy of Sciences · 1989 · 634 citations · Full text

Familial Defective Apolipoprotein, Genetics, Genetic Epidemiology +18

Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

Roger R. Williams, Steven C. Hunt, Mary Catherine Schumacher et al. · The American Journal of Cardiology · 1993 · 563 citations

Metabolic Syndrome, Lipid Disorder, Genetic Testing +11

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.

Ikuo Inoue, Toshiaki Nakajima, Christopher S. Williams et al. · Journal of Clinical Investigation · 1997 · 548 citations · Full text

Hypertension, Promoter Activity, Genetics +18

High-resolution analysis of a hypervariable region in the human apolipoprotein B gene.

E H Ludwig, W Friedl, Brian J. McCarthy · PubMed · 1989 · 177 citations